Sage Journals: Discover world-class research

Abstract

Background:

Irritable bowel syndrome (IBS) is characterized by abdominal pain and altered bowel habits. Further, IBS patients experience a high degree of extraintestinal symptoms.

Objectives:

The aim of this review was to describe the relation between IBS and extraintestinal manifestations and mechanisms and treatments of these extraintestinal manifestations.

Design:

The study was performed as a systematic review.

Data Sources and Methods:

Search terms including extraintestinal manifestations or somatization and IBS were used to scrutinize for publications in Pubmed. In total, 630 publications were identified and 80 were finally included in this review.

Results:

About 50% of all IBS patients have extraintestinal manifestations in addition to gastrointestinal symptoms. Somatic pain, fatigue, and sleeping disturbances are most common, and most often described in women. Both extraintestinal manifestations and psychological distress are associated with exaggerated gastrointestinal symptoms, impaired quality of life, and difficulties to treat IBS symptoms. The extraintestinal manifestations render an excess of healthcare costs. Varying etiology and pathophysiology to IBS are discussed, and many patients express a general hypersensitivity. Extraintestinal symptoms are seldom documented at clinical healthcare or included in the assessment of treatment outcomes. A good patient-physician relationship and strengthening of coping mechanisms have rendered less gastrointestinal symptoms, psychological distress, and somatization. Altered lifestyle habits may improve both gastrointestinal and extraintestinal symptoms. Pharmacological treatment, including antidepressant drugs, should be considered when lifestyle advice fails. Teamwork between different specialists and healthcare providers may be of importance in the wide range of symptoms and extraintestinal manifestations.

Conclusion:

Extraintestinal manifestations are common in IBS patients and is associated with worse suffering and difficulties to treat symptoms. Evaluation and treatment of IBS patients should consider also extraintestinal manifestations and their treatment outcome. Establishment of good relationship, strengthening of coping mechanisms, and education in healthier lifestyle habits are crucial in the management of these patients.

Keywords

disorder of gut–brain interaction extraintestinal manifestations irritable bowel syndrome somatization visceral hypersensitivity

Background

Irritable bowel syndrome (IBS) is defined as abdominal pain at least once weekly, associated with defecation, altered stool frequency, and/or altered stool consistency.¹ IBS is the most frequent and well known of the disorders of gut–brain interaction (DGBI), with a worldwide pooled prevalence of 4.1% (range: 1.3–7.6%) according to the Rome IV criteria.² The prevalence of IBS was higher when Rome II and Rome III criteria were used to define the condition,³ and the most studies in the literature reflect these former criteria. Female sex, lower middle age, stress, psychological factors, and certain lifestyle habits are associated with IBS.⁴ The etiology to IBS is unknown but suspected to be multifactorial. Dietary intake of unabsorbed carbohydrates, gut microbiota dysbiosis, and low-grade inflammation are some factors that have been considered in the pathophysiology.⁵ Visceral and somatic hypersensitivity has been widely discussed in IBS,⁶ especially since IBS is associated with chronic fatigue, fibromyalgia, and other extraintestinal pain syndromes.^7,8 A term often referred to in these circumstances is somatization disorders, a psychiatric diagnosis defined by explicit criteria. This should be distinguished from the tendency to report somatic complaints, measured by psychological tests of somatization. The present overview about extraintestinal manifestations in IBS is to report somatic complaints and not somatization disorders.^7,8

IBS patients may be referred to several departments for their extraintestinal manifestations to undergo invasive investigations, before IBS is recognized, which may further aggravate their symptoms.⁹ Thus, extraintestinal symptoms in IBS need to be recognized and handled appropriately. The aims of the present review were (a) to describe the comorbidity between IBS and extraintestinal manifestations; (b) to explore the mechanisms behind this comorbidity; and (c) to discuss the treatment of extraintestinal manifestations.

Methods

A search was performed on 15 October 2021 in Pubmed with the research terms ‘extraintestinal symptoms and IBS’ which rendered 114 publications. The term ‘symptoms’ rendered more publications than ‘manifestations’ (20 publications), why the term symptoms was used. A new search strategy was performed on 21 October with the term ‘treatment of extraintestinal symptoms in IBS’ which rendered 49 publications. On 30 May 2022, the search strategies ‘somatization and irritable bowel syndrome’ rendered 261 publications, ‘extraintestinal symptoms and irritable bowel syndrome’ rendered 173 publications, ‘non-colonic symptoms and irritable bowel syndrome’ rendered 15 publications, and ‘extra-colonic symptoms and irritable bowel syndrome’ rendered 6 publications. Altogether, 618 articles were found in the search strategies. In all, 12 further publications were found from their reference lists or other sources. After scrutinizing titles and abstracts, 99 full-length-articles were read by the author and evaluated according to the Newcastle–Ottawa Scale for cohort and case–control studies when applicable.¹⁰ Inclusion criteria were original or review articles written in English describing the presence of extraintestinal symptoms in IBS, mechanisms behind extraintestinal symptoms in IBS, and/or treatment of extraintestinal symptoms in IBS. Extraintestinal symptoms referred to somatic complaints including fatigue. Exclusion criteria were animal studies, articles not available in full length, conference abstracts, editorials, letters to the editor, or articles describing only psychological or psychiatric diseases. After removal of duplicates and publications not fulfilling the inclusion criteria, 80 remained which were finally included in the review (Figure 1). Articles describing the prevalence of extraintestinal manifestations in IBS cohorts are listed in Table 1. Other articles not including the prevalence of the manifestations in the cohorts are listed in Table 2.

Figure 1.

Flow chart according to PRISMA.

Table 1.

Description of studies that report the prevalence of extraintestinal manifestations.

Study	Country	Study design	Manifestation
Whitehead et al.⁷	USA	Systematic review	Back/low back pain, bad breath, fatigue, decreased libido, dizziness, dyspareunia, dyspnea, headache, incomplete bladder emptying, muscle aches or soreness, nocturia, palpitations, poor sleep, pruritus, sensitivity to heat or cold, stiffness, subjective fever, tummy butterflies, urinary frequency, urinary urgency, urinary hesitancy, nocturia, wheezing
Riedl et al.⁸	Germany	Systematic review	Bronchopulmonary syndromes, cardiac syndromes, cerebral-, musculoskeletal-, and urogenital pain syndromes, urogenital syndromes, fatigue, sleeping disturbances
Maxton et al.¹¹	UK	Cross-sectional case–control study	Lethargy, headaches, backpain, bad breath, urinary frequency, urgency of micturition
Whorwell et al.¹²	UK	Cross-sectional case–control study	Back pain, headaches, pruritis, bad breath, poor sleeping, tiredness
Si et al.¹³	China	Cross-sectional cohort study	Poor appetite, headache, back pain, difficulty in urination, fatigue
Spiller et al.¹⁴	UK	Guidelines	Guidelines
Alpers¹⁵	USA	Review	Extraintestinal comorbidities of IBS
Talley¹⁶	USA	Review	Extraintestinal comorbidities of IBS
Choung et al. ¹⁷	USA	Population-based study	Chronic pelvic pain
Sperber and Dekel¹⁸	Israel	Review	Fibromyalgia, chronic fatigue syndrome, chronic pelvic pain, sexual dysfunction
Shiha and Aziz¹⁹	UK	Review	Asthma and bronchial hypersensitivity, chronic back pain, chronic fatigue, chronic pelvic pain, endometriosis, fibromyalgia, interstitial cystitis, migraine, sexual dysfunction, sleep disorders, temporomandibular disorder
Koloski et al.²⁰	Australia	Population-based case–control study	Somatization
Patel et al.²¹	Multicenter	Cross-sectional case–control study	Somatization
Devanarayana et al.²²	Sri Lanka	Population-based case–control study	Headache, sleeping difficulty, limb pain, photophobia, light-headed
Rajindrajith and Devanarayana²³	Sri Lanka	Population-based case–control study	Headache, sleeping difficulty, limb pain, photophobia, light-headed
Agrawal et al.²⁴	UK	Cross-sectional case–control study	Lethargy, headaches, backache, chest pain, urinary frequency, nausea, joint and muscle pain, heartburn
Poulsen et al.²⁵	Denmark	Prospective population-based study	Functional somatic syndromes
Han and Yang²⁶	USA	Systematic review	Fatigue
Hausteiner-Whiele and Henningsen²⁷	Germany	Review	Fatigue, fibromyalgia, temporomandibular disorder
Kamp et al.²⁸	USA	Randomized clinical trial	Backache, fatigue, headache, joint pain, muscle pain, sleeping disturbances
Vu et al.²⁹	USA	Cross-sectional case–control study	All extraintestinal manifestations grouped together
Marcuzzi et al.³⁰	Australia	Systematic review	Fatigue
Norlin et al.³¹	Multicenter	Cross-sectional case–control study	Fatigue
Svedberg et al.³²	Multicenter	Cross-sectional twin-pair study	Headache, migraine, muscle pain, urinary tract problems

IBS, irritable bowel syndrome.

Table 2.

Description of the other studies included in the review.

Study	Country	Study design	Subject studied
Houghton et al.⁴	Multicenter	Review	Gender aspects in IBS
Van den Houte et al.⁵	Belgium	Review	Diagnosis and management of IBS
Zhou et al.⁶	USA	Interventional case–control study	Hypersensitivity in IBS
Aziz et al.³³	Sweden	Cross-sectional cohort study	Fatigue, somatization
Chang and Lu³⁴	Taiwan	Review	Asian perspective of IBS
Spiller et al.¹⁴	UK	Guidelines	Guidelines
Chang and Lu³⁵	Taiwan	Review	Asian perspective of IBS
Choung et al.³⁶	USA	Population-based study	Somatization
Park et al.³⁷	Korea	Cross-sectional case–control study	Somatization
Zimmerman³⁸	Israel	Cross-sectional case–control study	Coexistence of extraintestinal symptoms and IBS
Noble et al.³⁹	UK	Cross-sectional cohort study	COVID-19 and IBS
Guthrie et al.⁴⁰	UK	Cross-sectional study	Backache, urinary frequency, leg pains, headaches, dysmenorrhea, premenstrual tension, lethargy
Björkman et al.⁴¹	Sweden	Cross-sectional cohort study	Gender and IBS
Prior and Whorwhell⁴²	UK	Prospective cohort study	Gynecological symptoms in IBS
Vege et al.⁴³	USA	Population-based study	Sleeping disturbances and IBS
Rey de Castro et al.⁴⁴	UK	Cross-sectional cohort study	Symptoms in relation to subtypes of IBS
Shiha et al.⁴⁵	UK	Cross-sectional case–control study	Psychological distress and somatization in IBS
Sperber et al.⁴⁶	Multicenter	Population-based study	Somatization related to overlap of gut–brain interaction disorders
Bennet et al.⁴⁷	Australia	Cross-sectional cohort study	Coexistence of extraintestinal symptoms and IBS
Creed et al.⁴⁸	USA	Cross-sectional cohort study	Somatization
Andresen et al.⁴⁹	Multicenter	Prospective cohort study	Post-infectious IBS
Klem et al.⁵⁰	Multicenter	Systematic review	Post-infectious IBS
Gwee et al.⁵¹	UK	Prospective cohort study	Post-infectious IBS
Schwille-Kiuntke et al.⁵²	Germany	Cross-sectional cohort study	Post-infectious IBS and somatization
Schwille-Kiuntke et al.⁵³	Germany	Cross-sectional cohort study	Post-infectious IBS and somatization
Card et al.⁵⁴	Multicenter	Cross-sectional cohort study	Post-infectious IBS and somatization
Arisè et al.⁵⁵	Italy	Cross-sectional cohort study	Somatization
Lackner et al.⁵⁶	USA	Cross-sectional cohort study	Self-ratings of health and IBS
Levy et al.⁵⁷	USA	Cross-sectional case–control study	Illness behavior
Black et al.⁵⁸	UK	Cross-sectional cohort study	Awareness of GI and extraintestinal symptoms is associated with severity
Van Tilburg et al.⁵⁹	USA	Cross-sectional case–control study	Somatization
Wilpart et al.⁶⁰	Multicenter	Cross-sectional cohort study	Coping skills
Feng et al.⁶¹	USA	Review	Mechanisms of visceral hypersensitivity
Hollister et al.⁶²	USA	Cross-sectional cohort study	Fecal microbiota in IBS
Undseth et al.⁶³	Norway	Experimental study	Symptoms before and after a lactulose test
Verne et al.⁶⁴		Interventional case–control study	Visceral and cutaneous hyperalgesia
Tardy et al.⁶⁵	Multicenter	Review	Micronutrients
Roth et al.⁶⁶	Sweden	Randomized clinical trial	Dietary intervention
Nilholm et al.⁶⁷	Sweden	Randomized clinical trial	Dietary intervention
Han et al.⁶⁸	Multicenter	Randomized clinical trial	Genetics in IBS
Lembo et al.⁶⁹	UK	Cross-sectional twin-pair study	Genetics in IBS
Moayyedi et al.⁷⁰	Multicenter	Algorithm for clinical practice	Algorithm for clinical practice
Black et al.⁷¹	UK	Follow-up cohort study	Patients with high psychological burden were more likely to consult a doctor
Johannesson et al.⁷²	Sweden	Cross-sectional cohort study	Experience of physical activity
Palsson et al.⁷³	USA	Intervention	Hypnotherapy
Lövdahl et al.⁷⁴	Sweden	Intervention	Hypnotherapy
Vasant et al.⁷⁵	UK	Intervention	Hypnotherapy
Gillan⁷⁶	UK	Review	Hypnotherapy
Lakhan and Schofield⁷⁷	USA	Systematic review	Mindfulness and IBS
Rothmore⁷⁸	Australia	Review	Antidepressant drugs and sexuality
Levy et al.⁷⁹	USA	Cross-sectional case–control study	Care costs
Loftus et al.⁸⁰	USA	Cross-sectional cohort study	Multispecialty teamwork
Koloski et al.⁸¹	Australia	Prospective population-based study	Gut–brain pathways
Atkinson et al.⁸²	UK	Randomized clinical trial	Food elimination
Buchanan et al.⁸³	USA	Explorative cohort study	Sleeping habits and IBS
Lackner et al.⁸⁴	USA	Cross-sectional cohort study	Treatment expectancy and motivation

COVID-19, corona virus disease 2019; GI, gastrointestinal; IBS, irritable bowel syndrome.

Main text

Extraintestinal manifestations

The criteria and diagnosis of IBS are based on symptoms in the absence of organic alterations. IBS is divided into constipation-predominant IBS (IBS-C), diarrhea-predominant IBS (IBS-D), IBS with mixed bowel habits (IBS-M), and unclassified IBS.¹ The Rome criteria have changed over time, rendering some differences between IBS patients diagnosed at different time points.² Thus, IBS patients diagnosed according to Rome IV had increased severity of gastrointestinal (GI) symptoms, somatization, and fatigue than those diagnosed according to Rome III.³³ About 50% of all IBS patients have sole IBS; the rest have any kind of additional somatic and/or mental symptoms.⁷ A list of common extraintestinal manifestations (syndromes and symptoms) in IBS is shown in Table 3.

Table 3.

Extraintestinal syndromes and symptoms reported in increased prevalence in IBS.

Syndromes	Prevalence in IBS patients (%)
Asthma	15.8
Bronchial hyperreactivity	22.7
Chronic back pain	29–37.3
Chronic fatigue syndrome	14–54.2
Chronic headaches	34–72
Chronic migraine	6
Chronic pelvic pain	35–49.9
Detrusor dysfunction	30
Dysmenorrhea	10–50
Dysuria	36–50
Fibromyalgia	26–65
Interstitial cystitis	Not described
Premenstrual syndrome	10–50
Sexual function disturbances	24–83
Sleeping disturbances	37.6
Temporomandibular joint disorder	9.16–64
Urinary stones	Not described
Symptoms
Back pain	27.6–81
Low back pain	37.1–88
Bad breath	16.3–65
Fatigue	36.3–63
Decreased libido	13.4–26.9
Dizziness	11–27
Dyspareunia	9.3–42
Dyspnea/shortness of breath	25
Headache	23.1–45
Incomplete bladder emptying	50
Muscle aches or soreness	29–36.3
Nocturia	53
Palpitations	13–44
Poor sleep	30
Pruritus	32
Sensitivity to heat or cold	14
Sleep difficulties	30
Stiffness	27.1
Subjective fever	6
Urinary frequency	20.5–61
Urinary urgency	60
Urinary hesitancy	11
Nocturia	53
Tummy butterflies	13
Wheezing	Not described

Syndromes and symptoms from Whitehead et al.,⁷ Riedl et al.,⁸ and Shiha and Aziz.¹⁹

IBS, irritable bowel syndrome.

The prevalence of extraintestinal manifestations is much higher in IBS than in organic GI disorders,^8,11 and about twice as common as compared to control groups in adults.^{7,12–19,34,35} Not only the prevalence of somatization is increased, also the severity of somatization is higher in IBS than in controls^20,21,36 and in organic GI disorders.³⁷ The prevalence of extraintestinal manifestations is also much higher in children and adolescents with IBS compared to controls, especially in girls and in children exposed to stressful events.^22,23 In a cohort of elder patients (65–94 years), the prevalence of extraintestinal symptoms was much higher in IBS patients than in other patient groups.²⁴ The intestinal symptom reflux was the strongest predictor of extraintestinal symptoms.³⁷ Both GI and extraintestinal symptoms were scored higher after the corona virus disease 2019 pandemic than prior to the pandemic.³⁸ In general, there is an increased risk for IBS individuals to develop any extraintestinal manifestations over time.²⁵ In accordance, both GI symptoms and extraintestinal symptoms are perceived more severe in chronic attenders to a tertiary center than in first-time attenders.³⁹ Not only the prevalence of IBS is more frequent in women than in men, also the prevalence and severity of extraintestinal manifestations in IBS is highest in women.^4,37,40

Back pain, chronic fatigue, fibromyalgia, headache, pelvic pain, sleeping disturbances, and urogenital symptoms are the most common manifestations, occurring in 34–50% of IBS patients (Table 3).^7,8,21 Many IBS patients attend to a gynecologic department because of pelvic pain, without having any gynecologic diagnosis.⁴¹ Fatigue is by some authors suggested to be the most common extraintestinal manifestation and has great impact on GI symptoms, psychological stress, and quality of life.²⁶ Fatigue is more common in IBS patients from tertiary centers than from primary centers, and more common in females and at younger age.²⁶

On the other hand, patients with chronic fatigue syndrome have a 35–92% prevalence of IBS.^18,27 Fibromyalgia was associated with a 1.54-fold increased risk of having IBS according to a national database,¹⁹ whereas a review showed that 32% of women with fibromyalgia had IBS.¹⁸ Up to 40% of patients with chronic pelvic pain fulfilled diagnostic criteria for IBS, and patients with migraine had IBS twice as often than those without migraine.^17–19 Patients with endometriosis have a two- to three-fold increased risk of IBS compared with controls and patients with interstitial cystitis have an 11-fold increased risk to have IBS compared with controls.¹⁹ About half of the patients with sexual dysfunction also suffered from IBS.^18,19 Furthermore, 40–50% of patients attending a urologic department also suffered from IBS, in addition to urologic symptoms.⁸⁵ Asthma patients reported a 20% increase in the incidence of IBS, whereas patients with anxiety and depression have a two-fold increased risk for the onset of IBS.¹⁹ In a population-based study, those reporting sleeping disturbances had an IBS prevalence of 33% compared to 13% in the others.⁴²

Most studies have shown that the distribution of extraintestinal manifestations is equal between subgroups,^23,28,43 whereas one study reported that somatization was most pronounced in IBS-M,²¹ and one study showed that sleeping disturbances were associated with IBS-D but not IBS-C.⁴² One study showed that IBS patients had a greater number of somatic symptoms and higher somatization level than patients with functional constipation and functional diarrhea.⁴⁴ IBS diagnosed according to Rome IV criteria exhibited more severe disease and more somatoform symptoms than IBS diagnosed by a physician.⁸⁶ Overlap of DGBI-affected GI regions was associated with extraintestinal symptoms.^45,84 In line with this, extraintestinal manifestations were predictive for the combination of functional dyspepsia and IBS.⁴⁶ IBS patients at tertiary centers have more severe disease and other comorbidities compared with IBS patients at primary care.²⁶ The patients with highest degree of somatization were older with less education and were more likely to be unemployed compared with those IBS patients with lower scores of somatizations.⁴⁷

Infectious enteritis is a well-known risk factor to develop IBS. Somatization at the time point for the infection was associated with an increased risk to develop post-infectious IBS in two studies^48,49 but not in a third study.⁵⁰ In follow-up of patient cohorts with infectious enteritis, those who had developed IBS scored higher in somatization than those who had not developed IBS.^51,52 Patients with post-infectious IBS had higher somatization scores than other IBS patients, and those post-infectious IBS patients with high somatization scores had lower recovery rates than those with low somatization scores.⁵³

The more comorbidity, the worse quality of life and psychological distress; and the more extraintestinal and psychiatric comorbidity, the more GI symptoms and difficulties to successfully treat the IBS symptoms.^{7,8,18,27,29,47,54} The patients’ self-ratings of health were associated with fatigue and the number of medically unexplained somatic complaints.⁵⁵ The high levels of symptom burden render twice as many healthcare visits for IBS patients compared with age-matched controls, and 78% of extra healthcare visits from IBS patients depend on extraintestinal manifestations and not GI symptoms.^36,56

Mechanisms of extraintestinal manifestations

Etiology

The etiology behind IBS and extraintestinal manifestations are multifactorial. Several hypotheses have been proposed to explain the overlap and comorbidity between IBS and other syndromes. One hypothesis is that they are all vague syndromes with overlapping symptoms but without specific organic characteristics. A visit to a gastroenterologist renders the IBS diagnosis, but a visit to another specialist renders another diagnosis.

Both physiological and cognitive/psychological processes may give rise to GI and extraintestinal symptoms. IBS patients and other patients with extraintestinal manifestations have a high degree of psychological distress and psychiatric diseases, which can affect the experience of different somatic symptoms.^7,8,27,29 The tendency to report or experience both GI and extraintestinal symptoms seems to be the central driver to severity of IBS symptoms.⁵⁷ The tendency of somatization may depend on social and behavior learning during childhood, which play a great role in these conditions.⁷ Children to mothers with IBS had higher somatization scores than children to mothers without IBS.⁵⁸ However, the occurrence of several IBS cases within the same family may also include genetic components.^87,88 Different subgroups may have varying etiology, but the body may react similarly to several different stimuli. On the other hand, all patient groups may get anxiety and depression secondary to other symptoms. Theoretically, there may be a more obvious biological etiology to IBS without comorbidity, and more psychological etiology to IBS with symptoms from multiple organs. However, this dualistic mind–body dichotomization is complex, and many researchers are approaching a more holistic biopsychosocial view. Phenomenon in the central nervous system involved in central sensitization involves etiological mechanisms that might explain multisystem symptoms, which can not only be viewed as psychological features.

Studies report that IBS patients with several extraintestinal manifestations have more often a history of sexual or physical abuse than IBS patients with sole GI symptoms.^7,8 Coping is defined as a process of efforts to manage stressful life events.⁸⁹ Coping resources are both individual psychological resources within the subject and interindividual resources in the form of social support and acceptance, and the possibility to practice activities that gain the health, like exercise and healthy lifestyle habits. Coping mechanisms may be adaptive or maladaptive. Impaired coping mechanisms have been reported in IBS patients, with more escape-avoiding strategies than planful problem solving.⁹⁰ Anxiety, GI-specific anxiety, and depression were associated with less efficient coping mechanisms.⁵⁹

Pathophysiology

Regarding the pathophysiology, several biological models have been suggested, such as low-grade inflammation, altered microbiome, increased intestinal permeability, and motility disturbances.^1,5 Activation of nociceptive receptors is a physiological protection from harm. The International Association for the Study of Pain⁹¹ defines pain as an unpleasant sensory and emotional experience associated with actual or potential tissue damage, which means that experience of pain does not necessarily mean a true tissue damage. Afferent signals are transmitted through the dorsal horn and further trunks into the cortex. In cortex, the information is interpreted in relation to other sources of information and cognitive and psychological factors.³⁰ Efferent pain trunks then inhibit or facilitate the afferent transmission of pain, to modulate the nociceptive pathways at different levels.^92,93 Higher levels of anxiety, stress, and pain catastrophizing are associated with reduced conditioned pain modulation in IBS.³⁰ When normal stimulus is experienced as pain, it is called allodynia, whereas exaggerated pain is called hyperalgesia. Hypersensitivity is a collective description of abnormal pain modulation and may be peripheral, due to increased excitability (i.e. sensitization) of nociceptors, or central, the latter divided into spinal cord processes or descending pain modulation.^6,92,94 Low-grade inflammation is described in multiple studies of IBS, which may render peripheral hypersensitivity through neuroendocrine and immunological imbalance that may influence pain modulation and perception.⁶⁰ Pro-inflammatory and lipotoxic lipids, mast cells and their products, enteroendocrine cells, and mononuclear phagocytes are involved, and among many neurotransmitters, substance P, calcitonin gene-related peptide, 5-hydroxytrytamine, transient receptor potential vanilloid, and glutamate deserve to be mentioned.⁶⁰ Other mechanisms may be traumatic neuropathy or myopathy. Even extraintestinal manifestations, for example, fatigue is associated with low-grade inflammation and related biomarkers.^26,31 Associations have also been found between increased urgency and extraintestinal pain and lower microbial diversity and richness in feces in women with IBS.⁶¹ Nevertheless, studies have failed to explain the increased extraintestinal symptoms after a lactulose test to be caused by mucosal damage.⁶²

Cognitive functions, mood disorders, and fatigue are more involved in central than in peripheral hypersensitivity.^26,30 Widespread hypersensitivity in IBS with comorbidity and extraintestinal manifestations suggest central rather than peripheral hypersensitivity. However, almost all chronic complaints are initiated by peripheral sensory neurons.⁶⁰ Central hypersensitivity is characterized by an increased membrane excitability, a facilitated synaptic strength, and/or a decreased inhibitory influence on dorsal horn neurons and contributes to abnormal responsiveness to noxious and innocuous stimuli and a tenderness in several visceral and somatic organs.^92,94 Functional magnetic resonance imaging has described involvement of augmented pain processing also in cortical and subcortical structures,⁹⁴ and associations between fatigue and connectivity within a mesocorticolimbic network.³¹

In IBS, both widespread visceral and somatic hypersensitivity may be present,^6,60 and somatization is associated with more visceral hypersensitivity⁹⁵ and anxiety and depression.⁵⁴ When examining cold and heat pain, pressure pain, and ischemic pain, IBS patients could be divided into one group with normal pain thresholds and one group with reduced thresholds. Interestingly, the thresholds were lower in foot than in hand, and the lower cold and ischemic thresholds were accompanied with higher systolic blood pressure and higher circulating levels of corticotrophin and cortisol.⁶ Associations between blood pressure, cortisol, and hypersensitivity suggest a disturbed hypothalamic–pituitary–adrenal axis in IBS patients,⁹⁶ possibly due to a higher stress level. The coexistence of hypersensitivity in several visceral organs, that is, cross sensitization, along with somatic hypersensitivity, is explained by the proximity between visceral organs and the organization of the enteric nervous system, and a viscerosomatic convergence at the spinal cord level and at higher brain centers.⁹⁷ The more pronounced hypersensitivity in lower extremities may be explained by more afferent convergence at spinal cord level with colon and lower extremities than with upper extremities.⁶³

Several animal models have shown that high intake of fat and/or sugar has led to hyperglycemia, insulin resistance, metabolic disturbances, and histopathological changes with nerve super excitability.⁹⁸ Recently, poor dietary habits have been described in IBS patients in several countries.^65,99–101 Vitamins and minerals act as cofactors in multiple processes in the cells. It is well described how micronutrient deficiency leads to impaired cognitive and psychological functions, including mental and physical fatigue, weakness, and muscle pain.⁶⁴ Improvement of dietary habits in IBS with lower intake of candies and sugar rendered lower levels of weight, GI symptoms, extraintestinal symptoms, and levels of C-peptide, insulin, gastric inhibitory polypeptide, and leptin,^66,100,102 in parallel with reduced weight and improved endocrine and metabolic profile during a similar diet in type 2 diabetes.¹⁰³ Thus, the painful syndromes may depend on neuropathy secondary to disturbed homeostasis in the nerves and surrounding tissues.⁹⁸

Even if the extraintestinal manifestations are not primarily explained by genetic influences, there is evidence of a genetic component in the associations between IBS and extraintestinal symptoms.⁶⁷ The associations between IBS and extraintestinal manifestations in twins may depend on both genetic and environmental conditions.^32,68 Recently, a genome-wide analysis of 53,400 subjects with IBS showed shared genetic pathways for IBS, anxiety, depression, and neuroticism.¹⁰⁴

Treatment of extraintestinal manifestations

Classification systems of IBS and treatment guidelines do not consider extraintestinal or psychological symptoms in their statements.^1,69 Although it has been shown that both presence of extraintestinal manifestations and psychological comorbidity are associated with more severe GI symptoms,^7,8,29,85 few studies assess the effect of the treatment on extraintestinal manifestations in addition to the GI symptoms.¹⁹ Most studies only use GI symptoms to measure the outcome of efficiency, but many also include psychological assessments. Furthermore, the varying definitions of IBS and extraintestinal manifestations, as well as varying evaluation scores of extraintestinal manifestations, may complicate the conclusions of efficiency of different treatments.²⁶ The parallel severity between GI and extraintestinal symptoms suggest that treatments improving GI symptoms should also improve extraintestinal symptoms. However, this must be proven. In prospective follow-up studies, it has been shown that about half of the IBS patients remained in their original clusters over time, when the clusters were stratified by stool pattern.⁷⁰ On the contrary, 84% of IBS patients in the cluster with a high psychological comorbidity remained in this cluster at follow-up, with more severe GI symptoms and a higher number of consultations and treatments commenced.⁷⁰ Still, very few of these patients are considered for psychological treatment in daily practice.

The most important in all IBS treatment is to establish a strong patient–physician relationship.⁶⁹ It is important to inform the patient about the physiological and pathophysiological mechanisms, and to explain the mechanisms in a patient-friendly way. Better physical coping was associated with less GI symptoms, and lower levels of physical and psychological coping were associated with more extraintestinal symptoms, mediated through anxiety and depressive symptoms.⁵⁹

Next step is to penetrate lifestyle habits and give advice about healthy dietary habits and physical activity. In the IBS-severity scoring system (IBS-SSS) questionnaire, also 10 extraintestinal symptoms are measured, namely, nausea, early satiety/difficulty to eat a whole portion, reflux/heartburn, belching/excess wind, headache, back pain, thigh pain, muscle/joint pain, urinary emergency, and tiredness/lethargy.^66,105 In a clinical trial with starch and sucrose-reduced diet, 74% of the patients were responders regarding GI symptoms. In addition, the total IBS-SSS for extraintestinal symptoms was reduced in the intervention group compared with the control group, as were the individual symptoms belching/excess wind, muscle/joint pain, urinary emergency, and tiredness/lethargy.⁶⁶ The improvement of extraintestinal symptoms correlated with the improvement of total GI symptoms and psychological well-being. Decreased cereal intake correlated with decreased belching/excess wind, and decreased intake of sweets/soft drinks correlated with decreased belching/excess wind and tiredness/lethargy.⁶⁶ Treatment with low Fermentable Oligo-, Di-, Mono- saccharides And Polyols has shown similar results in the effect on fibromyalgia.¹⁹ Physical activity has documented effect both on GI and on extraintestinal symptoms.⁷¹

If lifestyle advice is not enough, pharmacological treatment could be prescribed; the choice of treatment depending on the most prominent symptom.⁶⁹ Antidepressants are widely used to treat abdominal pain, global IBS symptoms, and several extraintestinal manifestations.^8,69

A comprehensive self-management (CSM) intervention model in IBS covered the topics education, diet, relaxation, and cognitive-behavioral strategies. The effect of this intervention on extraintestinal pain, fatigue, and sleep disturbances was studied in a randomized controlled trial. CSM led to almost as large effects on backache, headache, and joint pain, as well as decreased fatigue and sleeping disturbances as on GI symptoms.²⁸

The use of individual hypnotherapy has been shown to be efficient to decrease extraintestinal symptoms and somatization, although performed without any control group.^72–74 In a systematic review of group and self-help hypnotherapy, only one of the found studies had assessed the outcome on extraintestinal symptoms and could not demonstrate any effect of hypnotherapy on somatization or extraintestinal symptoms.⁷⁵ Mindfulness-based therapy has been found to be efficient in several entities: GI symptoms in IBS, fibromyalgia, and fatigue.⁷⁶ Psychological treatment of somatic complaints is more effective in patients at tertiary healthcare centers than in the community,¹⁴ and most efficient in IBS patients with the highest scores of somatization and symptoms.⁴⁷

Regarding the treatment of fibromyalgia, exercise, psychological therapy, pharmacotherapy, and/or multimodal rehabilitation programs are suggested by rheumatic guidelines.¹⁹ Observational studies have proposed fecal transplantation as a treatment of fatigue,¹⁹ but the close relationship between fatigue and eating habits and low physical activity suggests changes in lifestyle habits as an important treatment option.²⁶ Patients with both temporomandibular disorders and IBS have high levels of anxiety, depression, fatigue, and sleeping disturbances, and a multidisciplinary treatment is more successful than separate treatments.¹⁹ Concerning interstitial cystitis, a multidisciplinary team involving urologists, gastroenterologists, and psychologists is recommended.¹⁹ IBS is many times treated with antidepressants, which may lead to sexual dysfunction.⁷⁷ Thus, withdrawal of medicals may be the first treatment option in sexual dysfunction. Due to a relationship between poor sleeping quality and visceral hypersensitivity, a low dose of tricyclic antidepressants may be efficient against sleeping disorders.¹⁹

Future treatment

Independent of etiology and pathophysiology, we must handle these patients without any organic abnormalities at routine care examinations but with a general high level of stress and pain. These conditions render a high degree of suffering from the patients, and they constitute a great part of healthcare costs. Since extraintestinal manifestations have greater impact on quality of life and treatment responsiveness than GI symptoms,^27,29 and most of the excess in healthcare costs for IBS patients resulted from care not directly related to GI symptoms,⁷⁸ it is of great interest both for the patients and for the society to consider extraintestinal manifestations as well as GI symptoms.¹⁵

A clear discrepancy between the patients’ experience of symptoms and the physicians’ views of the symptoms is at hand.^4,106 The most important in the handling of the patients is to confirm the patient and mediate that the patient’s symptoms are taken seriously.¹⁰⁷ All mental and somatic symptoms must be considered, documented, and borne in mind when planning the treatment.^{27,29,105,108} A holistic approach with a team representing different professions is needed to objectively assess the most troublesome symptom/disease and to create a proper therapeutic attitude toward the patients.¹⁰⁷ Not only specialists in gastroenterology should be involved, also specialists in gynecology, neurology, psychiatry, and rheumatology may be of importance to create a full picture of the patient’s need.⁷⁹

The question is whether we are talking about one disease with several different aspects and modes of presentation, or whether we are talking about different diseases. The explanations of sensitization and hypersensitivity point to a common, generalized increase in experience of pain and discomfort. Central sensitization, mood disturbances, learned behavior, the autonomic nervous system, the immune system, and the gut–brain axis may be involved.^6,7,30 The presence of concomitant multiple disorders characterized by pain and subjective experiences point to psychological influences in the etiology.⁷ Even if some of the extraintestinal manifestations have independent etiologies, they must have something in common since they overlap to such a high degree regarding female predominance, fatigue, sleeping disturbances, and anxiety.⁷ The important question is what comes first, IBS or psychological discomfort. In efforts to prospectively study these mechanisms in IBS, independent gut-to-brain and brain-to-gut pathways have been described. Both anxiety and depression at baseline were predictors to develop IBS, and IBS patients without anxiety and depression at baseline reported higher levels of these conditions at follow-up.⁸⁰ The common genetic pathways to IBS and mood disorders may explain the coexistence of IBS and psychological discomfort.³² Apart from different subgroups of IBS,¹ there are also differences between IBS patients depending on the mode of recruitment and inclusion in clinical trials, and whether the patients are recruited from primary or tertiary healthcare centers.^2,26,86

A dietary intervention with less sugar and starch improved both GI symptoms and extraintestinal symptoms, as well as psychological well-being.^65,66 Elimination of foods, which the patients expressed directed antibodies against, also reduced both GI and extraintestinal symptoms.⁸¹ Furthermore, increased physical activity has also led to improvement of extraintestinal symptoms.⁷¹ These improvements stress how important it is to improve poor lifestyle habits described in the IBS populations with low intake of important nutrients,^65,99–101 especially before more potential investigations and treatments are prescribed. In the future, more efforts must be done to enhance the knowledge about healthy lifestyle habits, which is crucial for the general health in the whole society. Thus, exclusion of malnutrition, especially micronutrients, is of great importance in these entities.⁶⁴

The efficacy of group and self-help hypnotherapy on extraintestinal manifestations in IBS has not been settled.⁷⁵ Reductions in extraintestinal symptoms may indirectly improve GI symptoms, since for example, sleep measures predict next-day symptoms of IBS.⁸² The effect of cognitive behavioral therapy and mindfulness have not been studied sufficiently but could be of interest to improve coping mechanisms, since the most predictive factors for a positive treatment were interpersonal support, motivation for improvement of symptoms, and expectancy of improvement.^76,83 Thus, more efforts should be put into treatments to strengthen the individual coping mechanisms and enhance the motivation for self-management.^28,59

Linaclotide, efficient in constipation treatment, also normalized the bladder function through indirect inhibition of bladder afferents in a mouse model,¹⁰⁹ supporting the concepts that pharmaceutical treatments may inhibit cross-organ sensitization through common sensory pathways. Further studies are warranted in this area to prove evidence in clinical practice.

Conclusion

Future research studies and healthcare must consider not only GI symptoms, but also extraintestinal manifestations in IBS, and assess both the magnitude of extraintestinal symptoms and the effect of interventions on these symptoms. Both the subjective experience for the patients and the healthcare resources and costs for the society are considerable for extraintestinal manifestations and must be considered. Good relationship between caregivers and patients and support of coping mechanisms in the patients are crucial. More efforts are needed to bring the society into a healthier lifestyle regarding diet and physical activity to prevent or improve IBS and related extraintestinal manifestations. The efficiency of pharmacological treatment on extraintestinal manifestations must be evaluated.

Supplemental Material

sj-docx-1-tag-10.1177_17562848221114558 – Supplemental material for Extraintestinal manifestations in irritable bowel syndrome: A systematic review

Supplemental material, sj-docx-1-tag-10.1177_17562848221114558 for Extraintestinal manifestations in irritable bowel syndrome: A systematic review by Bodil Ohlsson in Therapeutic Advances in Gastroenterology

Footnotes

Acknowledgements

None.

Declarations

ORCID iD

Bodil Ohlsson

Supplemental material

Supplemental material for this article is available online.

References

Lacy

Mearin

Chang

Bowel disorders. Gastroenterology 2016; 150: 1393–1407.

Sperber

Bangdiwala

Drossman

, et al. Worldwide prevalence and burden of functional gastrointestinal disorders, results of Rome Foundation Global Study. Gastroenterology 2021; 160: 99–114.e3.

Barberio

Judge

Savarino

, et al. Global prevalence of functional constipation according to the Rome criteria: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol 2021; 6: 638–648.

Houghton

Heitkemper

Crowell

, et al. Age, gender and women’s health and the patient. Gastroenterology 2016; 150: 1332–1343.

Van den Houte

Colomier

Schol

, et al. Recent advances in diagnosis and management of irritable bowel syndrome. Curr Opin Psychiatry 2020; 33: 460–466.

Zhou

Fillingim

Riley

3rd , et al. Central and peripheral hypersensitivity in the irritable bowel syndrome. Pain 2010; 148: 454–461.

Whitehead

Palsson

Jones

KR.

Systematic review of the comorbidity of irritable bowel syndrome with other disorders: what are the causes and implications?

Gastroenterology 2002; 122: 1140–1156.

Riedl

Schmidtmann

Stengel

, et al. Somatic comorbidities of irritable bowel syndrome: a systematic analysis. J Psychosom Res 2008; 64: 573–582.

Whorwell

PJ.

Editorial: preventing unnecessary investigation and surgery in the irritable bowel syndrome—the critical role of the general practitioner. Aliment Pharmacol Ther 2018; 47: 1558–1559.

10.

The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomized studies in meta-analyses, ohri.ca (accessed 15 October 2021).

11.

Maxton

Morris

Whorwell

PJ.

More accurate diagnosis of irritable bowel syndrome by the use of ‘non-colonic’ symptomatology. Gut 1991; 32: 784–786.

12.

Whorwell

McCallum

Creed

, et al. Non-colonic features of irritable bowel syndrome. Gut 1986; 27: 37–40.

13.

Wang

Chen

, et al. Irritable bowel syndrome consulters in Zhejiang province: the symptoms pattern, predominant bowel habit subgroups and quality of life. World J Gastroenterol 2004; 10: 1059–1064.

14.

Spiller

Aziz

Creed

, et al. Guidelines on the irritable bowel syndrome: mechanisms and practical management. Gut 2007; 56: 1770–1798.

15.

Alpers

DH.

Multidimensionality of symptom complexes in irritable bowel syndrome and other functional gastrointestinal disorders. J Psychosom Res 2008; 64: 567–572.

16.

Talley

NJ.

Functional gastrointestinal disorders as a public health problem. Neurogastroenterol Motil 2008; 20 Suppl 1: 121–129.

17.

Choung

Herrick

Locke

, et al. Irritable bowel syndrome and chronic pelvic pain: a population-based study. J Clin Gastroentreol 2010; 44: 696–701.

18.

Sperber

Dekel

Irritable bowel syndrome and co-morbid gastrointestinal and extra-gastrointestinal functional syndromes. J Neurogastroenterol Motil 2010; 16: 113–119.

19.

Shiha

Aziz

Review article: physical and psychological comorbidities associated with irritable bowel syndrome. Aliment Pharmacol Ther 2021; 54: S12–S23.

20.

Koloski

Boyce

Talley

NJ.

Somatization an independent psychosocial risk factor for irritable bowel syndrome but not dyspepsia: a population-based study. Eur J Gastroenterol Hepatol 2006; 18: 1101–1109.

21.

Patel

Bercik

Morgan

, et al. Irritable bowel syndrome is significantly associated with somatisation in 840 patients, which may drive bloating. Aliment Pharmacol Ther 2015; 41: 449–458.

22.

Devanarayana

Mettananda

Liyanarachchi

, et al. Abdominal pain-predominant functional gastrointestinal diseases in children and adolescents: prevalence, symptomatology, and association with emotional stress. J Pediatr Gastroenterol Nutr 2011; 53: 659–665.

23.

Rajindrajith

Devanarayana

NM.

Subtypes and symptomatology of Irritable Bowel Syndrome in children and adolescents: a school-based survey using Rome III criteria. J Neurogastroenterol Motil 2012; 18: 298–304.

24.

Agrawal

Khan

Whorwell

PJ.

Irritable bowel syndrome in the elderly: an overlooked problem?

Dig Liver Dis 2009; 41: 721–724.

25.

Poulsen

Eplov

Hjorthøj

, et al. Irritable bowel symptoms and the development of common mental disorders and functional somatic syndromes identified in secondary care - a long-term, population-based study. Clin Epidemiol 2017; 9: 393–402.

26.

Han

Yang

GS.

Fatigue in irritable bowel syndrome: a systematic review and meta-analysis of pooled frequency and severity of fatigue. Asian Nurs Res 2016; 10: 1–10.

27.

Hausteiner-Wiehle

Henningsen

Irritable bowel syndrome: relations with functional, mental, and somatoform disorders. World J Gastroenterol 2014; 20: 6024–6030.

28.

Kamp

Weaver

Sherwin

, et al. Effects of a comprehensive self-management intervention on extraintestinal symptoms among patients with IBS. J Psychosom Res 2019; 126: 109821.

29.

Kushnir

Cassell

, et al. The impact of psychiatric and extraintestinal comorbidity on quality of life and bowel symptom burden in functional GI disorders. Neurogastroenterol Motil 2014; 26: 1323–1332.

30.

Marcuzzi

Chakiath

Siddall

, et al. Conditioned pain modulation (CPM) is reduced in irritable bowel syndrome: a systematic review and meta-analysis of CPM and the role of psychological factors. J Clin Gastroenterol 2019; 53: 399–408.

31.

Norlin

Walter

Icenhour

, et al. Fatigue in irritable bowel syndrome is associated with plasma levels of TNF-α and mesocorticolimbic connectivity. Brain Behav Immun 2021; 92: 211–220.

32.

Svedberg

Johansson

Wallander

, et al. Extra-intestinal manifestations associated with irritable bowel syndrome: a twin study. Aliment Pharmacol Ther 2002; 16: 975–983.

33.

Aziz

Törnblom

Palsson

, et al. How the change in IBS criteria from Rome III to Rome IV impacts on clinical characteristics and key pathophysiological factors. Am J Gastroenterol 2018; 113: 1017–1025.

34.

Chang

CL.

Irritable bowel syndrome in the 21st century: perspectives from Asia or South-East Asia. J Gastroenterol Hepatol 2007; 22: 4–12.

35.

Chang

CL.

The clinical significances of irritable bowel syndrome in Taiwan. J Gastroenterol Hepatol 2011; 26 Suppl 3: 102–105.

36.

Choung

Locke

3rd Zinsmeister

, et al. Psychosocial distress and somatic symptoms in community subjects with irritable bowel syndrome: a psychological component is the rule. Am J Gastroenterol 2009; 104: 1772–1779.

37.

Park

Choi

Cho

, et al. Functional gastrointestinal disorders diagnosed by Rome III questionnaire in Korea. J Neurogastroenterol Motil 2011; 17: 279–286.

38.

Zimmerman

Extraintestinal symptoms in irritable bowel syndrome and inflammatory bowel diseases: nature, severity, and relationship to gastrointestinal symptoms. Dig Dis Sci 2003; 48: 743–749.

39.

Noble

Hasan

Whorwell

, et al. The symptom burden of irritable bowel syndrome in tertiary care during the COVID-19 pandemic. Neurogastroenterol Motil 2022; e14347.

40.

Guthrie

Creed

Whorwell

, et al. Outpatients with irritable bowel syndrome: a comparison of first time and chronic attenders. Gut 1992; 33: 361–363.

41.

Björkman

Jakobsson Ung

Ringström

, et al. More similarities than differences between men and women with irritable bowel syndrome. Neurogastroenterol Motil 2015; 27: 796–804.

42.

Prior

Whorwell

PJ.

Gynaecological consultation in patients with the irritable bowel syndrome. Gut 1989; 30: 996–998.

43.

Vege

Locke

3rd Weaver

, et al. Functional gastrointestinal disorders among people with sleep disturbances: a population-based study. Mayo Clin Proc 2004; 79: 1501–1506.

44.

Rey

Castro

Miller

Carruthers

, et al. Irritable bowel syndrome: a comparison of subtypes. J Gastroenterol Hepatol 2015; 30: 279–285.

45.

Shiha

Asghar

Thoufeeq

, et al. Increased psychological distress and somatization in patients with irritable bowel syndrome compared with functional diarrhea or functional constipation, based on Rome IV criteria. Neurogastroenterol Motil 2021; 33: e14121.

46.

Sperber

Freud

Aziz

, et al. Greater overlap of Rome IV disorders of Gut-Brain interactions leads to increased disease severity and poorer quality of life. Clin Gastroenterol Hepatol 2022; 20: e945–e956.

47.

Bennett

Piesse

Palmer

, et al. Functional gastrointestinal disorders: psychological, social, and somatic features. Gut 1998; 42: 414–420.

48.

Creed

Tomenson

Guthrie

, et al. The relationship between somatisation and outcome in patients with severe irritable bowel syndrome. J Psychosom Res 2008; 64: 613–620.

49.

Andresen

Löwe

Broicher

, et al. Post-infectious irritable bowel syndrome (PI-IBS) after infection with Shiga-like toxin-producing Escherichia coli (STEC) O104:H4: a cohort study with prospective follow-up. United Eur Gastroenterol J 2016; 4: 121–131.

50.

Klem

Wadhwa

Prokop

, et al. Prevalence, risk factors, and outcomes of irritable bowel syndrome after infectious enteritis: a systematic review and meta-analysis. Gastroenterology 2017; 152: 1042–1054.e1.

51.

Gwee

Leong

Graham

, et al. The role of psychological and biological factors in postinfective gut dysfunction. Gut 1999; 44: 400–406.

52.

Schwille-Kiuntke

Enck

Zendler

, et al. Postinfectious irritable bowel syndrome: follow-up of a patient cohort of confirmed cases of bacterial infection with Salmonella or Campylobacter. Neurogastroenterol Motil 2011; 23: e479–e488.

53.

Schwille-Kiuntke

Enck

Polster

, et al. Postinfectious irritable bowel syndrome after travelers’ diarrhea: a cohort study. Neurogastroenterol Motil 2015; 27: 1147–1155.

54.

Card

Enck

Barbara

, et al. Post-infectious IBS: Defining its clinical features and prognosis using an internet-based survey. United Eur Gastroenterol J 2018; 6: 1245–1253.

55.

Arsiè

Coletta

Cesana

, et al. Symptom-association probability between meal ingestion and abdominal pain in patients with irritable bowel syndrome. Does somatization play a role? Neurogastroenterol Motil 2015; 27: 416–422.

56.

Lackner

Gudleski

Thakur

, et al. The impact of physical complaints, social environment, and psychological functioning on IBS patients’ health perceptions: looking beyond GI symptom severity. Am J Gastroenterol 2014; 109: 224–233.

57.

Levy

Whitehead

Von Korff

, et al. Intergenerational transmission of gastrointestinal illness behavior. Am J Gastroenterol 2000; 95: 451–456.

58.

Black

Yiannakou

Houghton

, et al. Anxiety-related factors associated with symptom severity in irritable bowel syndrome. Neurogastroenterol Motil 2020; 32: e13872.

59.

van Tilburg

Levy

Walker

, et al. Psychosocial mechanisms for the transmission of somatic symptoms from parents to children. World J Gastroenterol 2015; 21: 5532–5541.

60.

Wilpart

Törnblom

Svedlund

, et al. Coping skills are associated with gastrointestinal symptom severity and somatization in patients with irritable bowel syndrome. Clin Gastroenterol Hepatol 2017; 15: 1565–1571.e3.

61.

Feng

Schwartz

, et al. Irritable bowel syndrome: methods, mechanisms, and pathophysiology.Neural and neuro-immune mechanisms of visceral hypersensitivity in irritable bowel syndrome. Am J Physiol Gastrointest Liver Physiol 2012; 302: G1085–G1098.

62.

Hollister

Cain

Shulman

, et al. Relationships of microbiome markers with extraintestinal, psychological distress and gastrointestinal symptoms, and quality of life in women with irritable bowel syndrome. J Clin Gastroenterol 2020; 54: 175–183.

63.

Undseth

Berstad

Valeur

Systemic symptoms in irritable bowel syndrome: an investigative study on the role of enterocyte disintegrity, endotoxemia and inflammation. Mol Med Rep 2016; 14: 5072–5076.

64.

Verne

Robinson

Vase

, et al. Reversal of visceral and cutaneous hyper-algesia by local rectal anesthesia in irritable bowel syndrome (IBS) patients. Pain 2003; 105: 223–230.

65.

Tardy

Pouteau

Marquez

, et al. Vitamins and minerals for energy, fatigue and cognition: a narrative review of the biochemical and clinical evidence. Nutrients 2020; 12: 228.

66.

Roth

Larsson

Ohlsson

Poor intake of vitamins and minerals is associated with symptoms among patients with irritable bowel syndrome. J Gastroenterol Hepatol. Epub ahead of print March 2022. DOI: 10.1111/jgh.15830.

67.

Nilholm

Roth

Ohlsson

A dietary intervention with reduction of starch and sucrose leads to reduced gastrointestinal and extra-intestinal symptoms in IBS patients. Nutrients 2019; 11: 1662.

68.

Han

Jarrett

Cain

, et al. Association of fatigue with TPH2 genetic polymorphisms in women with irritable bowel syndrome. Biol Res Nurs 2019; 21: 72–79.

69.

Lembo

Zaman

Krueger

, et al. Psychiatric disorder, irritable bowel syndrome, and extraintestinal symptoms in a population-based sample of twins. Am J Gastroenterol 2009; 104: 686–694.

70.

Moayyedi

Mearin

Azpiroz

, et al. Irritable bowel syndrome diagnosis and management: a simplified algorithm for clinical practice. United Eur Gastroenterol J 2017; 5: 773–788.

71.

Black

Yiannakou

Guthrie

, et al. Longitudinal follow-up of a novel classification system for irritable bowel syndrome: natural history and prognostic value. Aliment Pharmacol Ther 2021; 53: 1126–1137.

72.

Johannesson

Jakobsson Ung

Sadik

, et al. Experiences of the effects of physical activity in persons with irritable bowel syndrome (IBS): a qualitative content analysis. Scand J Gastroenterol 2018; 53: 1194–1200.

73.

Palsson

Turner

Johnson

, et al. Hypnosis treatment for severe irritable bowel syndrome. Investigation of mechanism and effects on symptoms. Dig Dis Sci 2002; 47: 2605–2614.

74.

Lövdahl

Ringström

Agerforz

, et al. Nurse-Administered, Gut-Directed hypnotherapy in IBS: efficacy and factors predicting a positive response. Am J Clin Hypn 2015; 58: 100–114.

75.

Vasant

Hasan

Cruickshanks

, et al. Gut-focused hypnotherapy for children and adolescents with irritable bowel syndrome. Front Gastroenterol 2021; 12: 570–577.

76.

Gillan

Review article: the effectiveness of group and self-help hypnotherapy for irritable bowel syndrome and the implications for improving patients’ choice and access to treatment. Aliment Pharmacol Ther 2021; 54: 1389–1404.

77.

Lakhan

Schofield

KL.

Mindfulness-based therapies in the treatment of somatization disorders: a systematic review and meta-analysis. PLoS One 2013; 8: e71834.

78.

Rothmore

Antidepressant-induced sexual dysfunction. Med J Aust 2020; 212: 329–334.

79.

Levy

Korff

Whitehead

, et al. Costs of care for irritable bowel syndrome patients in a health maintenance organization. Am J Gastroenterol 2001; 96: 3122–3129.

80.

Loftus

Ebbert

Aakre

, et al. Creation of a multispecialty clinic for patients with central sensitization-based chronic pain conditions. Mayo Clin Proc Innov Qual Outcomes 2022; 6: 45–54.

81.

Koloski

Jones

Talley

NJ.

Evidence that independent gut-to-brain and brain-to-gut pathways operate in the irritable bowel syndrome and functional dyspepsia: a 1-year population-based prospective study. Aliment Pharmacol Ther 2016; 44: 592–600.

82.

Atkinson

Sheldon

Shaath

, et al. Food elimination based on IgG antibodies in irritable bowel syndrome: a randomised controlled trial. Gut 2004; 53: 1459–1464.

83.

Buchanan

Cain

Heitkemper

, et al. Sleep measures predict next-day symptoms in women with irritable bowel syndrome. J Clin Sleep Med 2014; 10: 1003–1009.

84.

Lackner

Quigley

Radziwon

, et al. IBS patients’ treatment expectancy and motivation impacts quality of the therapeutic alliance with provider: results of the IBS Outcome Study. J Clin Gastroenterol 2021; 55: 411–421.

85.

Francis

Duffy

Whorwell

, et al. High prevalence of irritable bowel syndrome in patients attending urological outpatient departments. Dig Dis Sci 1997; 42: 404–407.

86.

Goodoory

Craig

Gracie

, et al. Prognosis of patients with Rome IV-defined versus physician-diagnosed irritable bowel syndrome: longitudinal follow-up study. Neurogastroenterol Motil 2022; 34: e14282.

87.

Bengtson

Rønning

Vatn

, et al. Irritable bowel syndrome in twins: genes and environment. Gut 2006; 55: 1754–1759.

88.

Waehrens

Ohlsson

Sundquist

, et al. Risk of irritable bowel syndrome in first-degree, second-degree and third-degree relatives of affected individuals: a nationwide family study in Sweden. Gut 2015; 64: 215–221.

89.

Taylor

Stanton

AL.

Coping resources, coping processes, and mental health. Annu Rev Clin Psychol 2007; 3: 377–401.

90.

Jones

Wessinger

Crowell

MD.

Coping strategies and interpersonal support in patients with irritable bowel syndrome and inflammatory bowel disease. Clin Gastroenterol Hepatol 2006; 4: 474–481.

91.

International Association for the Study of Pain (IASP). IASP terminology, https://www.iasp-pain.org/Education/Content.aspx?ItemNumber=1698&navItemNumber=576 (2017, assessed 5 June 2022).

92.

Ossipov

Morimura

Porreca

Descending pain modulation and chronification of pain. Curr Opin Support Palliat Care 2014; 8: 143–151.

93.

Chakiath

Siddall

Kellow

, et al. Descending pain modulation in irritable bowel syndrome (IBS): a systematic review and meta-analysis. Syst Rev 2015; 4: 175.

94.

Latremoliere

Woolf

CJ.

Central sensitization: a generator of pain hypersensitivity by central neural plasticity. J Pain 2009; 10: 895–926.

95.

Grinsvall

Törnblom

Tack

, et al. Relationships between psychological state, abuse, somatization and visceral pain sensitivity in irritable bowel syndrome. United Eur Gastroenterol J 2018; 6: 300–309.

96.

Chang

Sundaresh

Elliott

, et al. Dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis in irritable bowel syndrome. Neurogastroenterol Motil 2009; 21: 149–159.

97.

Pezzone

Liang

Fraser

MO.

A model of neural cross-talk and irritation in the pelvis: implications for the overlap of chronic pelvic pain disorders. Gastroenterology 2005; 128: 1953–1964.

98.

Ohlsson

Theories behind the effect of starch- and sucrose-reduced diets on gastrointestinal symptoms in irritable bowel syndrome (review). Mol Med Rep 2021; 24: 732.

99.

Tigchelaar

Mujagic

Zhernakova

, et al. Habitual diet and diet quality in irritable bowel syndrome: a case-control study. Neurogastroenterol Motil 2017; 29: e13151.

100.

Nilholm

Larsson

Roth

, et al. Irregular dietary habits with a high intake of cereals and sweets are associated with more severe gastrointestinal symptoms in IBS patients. Nutrients 2019; 11: 1279.

101.

Staudacher

Ralph

FSE

Irving

, et al. Nutrient intake, diet quality, and diet diversity in irritable bowel syndrome and the impact of the low FODMAP diet. J Acad Nutr Diet 2020; 120: 535–547.

102.

Saidi

Nilholm

Roth

, et al. Introduction of a starch- and sucrose-reduced diet to patients with irritable bowel syndrome influences plasma hormone levels. Nutr Res 2021; 86: 23–36.

103.

Darwiche

Höglund

Roth

, et al. An Okinawan-based Nordic diet improves anthropometry, metabolic control, and health-related quality of life in Scandinavian patients with type 2 diabetes: a pilot trial. Food Nutr Res 2016; 60: 32594.

104.

Eijsbouts

Zheng

Kennedy

, et al. Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders. Nat Genet 2021; 53: 1543–1552.

105.

Francis

Morris

Whorwell

PJ.

The irritable bowel severity scoring system: A simple method of monitoring irritable bowel syndrome and its progress. Aliment Pharmacol Ther 1997; 11: 395–402.

106.

Bengtsson

Hammar

Mandl

, et al. Evaluation of gastrointestinal symptoms in different patient groups using the visual analogue scale for irritable bowel syndrome (VAS-IBS). BMC Gastroenterol 2011; 11: 122.

107.

Bengtsson

Ulander

Börgdal

, et al. A holistic approach for planning care of patients with irritable bowel syndrome. Gastroenterol Nurs 2010; 33: 98–108.

108.

Bengtsson

Ohlsson

Ulander

Development and psychometric testing of the visual analogue scale for irritable bowel syndrome (VAS-IBS). BMC Gastroenterol 2007; 7: 16.

109.

Grundy

Harrington

Castro

, et al. Chronic linaclotide treatment reduces colitis-induced neuroplasticity and reverses persistent bladder dysfunction. JCI Insight 2018; 3: e121841.

Supplementary Material

Please find the following supplemental material available below.

For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.

For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.

0.00 MB

0.03 MB