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Abstract

French

Purpose of review:

Nephrologists are increasingly providing care to transgender individuals with chronic kidney disease (CKD). However, they may lack familiarity with this patient population that faces unique challenges. The purpose of this review is to discuss the care of transgender persons and what nephrologists should be aware of when providing care to their transgender patients.

Sources of information:

Original research articles were identified from MEDLINE and Google Scholar using the search terms “transgender,” “gender,” “sex,” “chronic kidney disease,” “end stage kidney disease,” “dialysis,” “transplant,” and “nephrology.”

Methods:

A focused review and critical appraisal of existing literature regarding the provision of care to transgender men and women with CKD including dialysis and transplant to identify specific issues related to gender-affirming therapy and chronic disease management in transgender persons.

Key findings:

Transgender persons are at an increased risk of adverse outcomes compared with the cisgender population including mental health, cardiovascular disease, malignancy, sexually transmitted infections, and mortality. Individuals with CKD have a degree of hypogonadotropic hypogonadism and decreased levels of endogenous sex hormones; therefore, transgender persons with CKD may require reduced exogenous sex hormone dosing. Exogenous estradiol therapy increases the risk of venous thromboembolism and cardiovascular disease which may be further increased in CKD. Exogenous testosterone therapy increases the risk of polycythemia which should be closely monitored. The impact of gender-affirming hormone therapy on glomerular filtration rate (GFR) trajectory in CKD is unclear. Gender-affirming hormone therapy with testosterone, estradiol, and anti-androgen therapies changes body composition and lean body mass which influences creatinine generation and the performance for estimated glomerular filtration rate (eGFR) equations in transgender persons. Confirmation of eGFR with measured GFR is reasonable if an accurate knowledge of GFR is needed for clinical decision-making.

Limitations:

There are limited studies regarding the intersection of transgender persons and kidney disease and those that exist are mostly case reports. Randomized controlled trials and observational studies in nephrology do not routinely differentiate between cisgender and transgender participants.

Implications:

This review highlights important considerations for providing care to transgender persons with kidney disease. Additional research is needed to evaluate the performance of eGFR equations in transgender persons, the effects of gender-affirming hormone therapy, and the impact of being transgender on outcomes in persons with kidney disease.

Keywords

transgender transmen transwomen kidney disease gender-affirming therapy

Introduction

Nephrologists are increasingly providing care to transgender patients with chronic kidney disease (CKD) including those with end-stage kidney disease (ESKD) treated with dialysis or kidney transplantation. However, clinicians may lack familiarity with this patient population that faces unique challenges. There are several issues that need to be considered when providing nephrology care to transgender patients given that sex and gender differences exist within the cisgender (non-transgender) population regarding kidney disease but it is unknown how this applies to transgender individuals with kidney disease who may be undergoing gender-affirming hormone therapy or surgery.

Scope and Purpose

The purpose of this review is to discuss the provision of kidney care to adult transgender persons and the issues nephrologists should be aware of when interacting with and treating their transgender patients.

Methods

MEDLINE and Google Scholar were searched using the terms “transgender” on its own or in combination with “chronic kidney disease,” “end stage kidney disease,” “dialysis,” “transplant” and “nephrology” by the first author (D.C.) to identify relevant literature. We also searched “sex” and “gender” in combination with the same MeSH terms. The searches were completed in May 2020. References of key articles were reviewed for additional papers relevant to the care of transgender with and without kidney disease. This was supplemented by key articles from other authors who either provide gender-affirming hormone therapy to transgender persons (N.S.) or are experts in sex and gender in kidney disease (S.A.). We prioritized the inclusion of clinical practice guidelines, systematic reviews, meta-analyses, and large observational studies given the lack of randomized controlled trials in this patient population.

Review

The Nomenclature of Gender Identity

Every person goes through a process of gender identity development starting in infancy and develops their gender identity over time which refers to one’s internal, deeply held sense of gender such as being a male or a female or an alternative gender that may or may not correspond to a person’s sex assigned at birth.^1-3 Gender includes gender expression (physical appearance and behavior related to gender), gender identity (a person’s perception of their gender), and gender roles (behaviors, values, and attitudes that a society considers appropriate to gender). In general, umbrella terms such as “cisgender” and “transgender” are used to classify gender identities.³ A cisgender person is an individual whose gender identity aligns with their sex assigned at birth and a transgender person¹ is an individual whose gender identity does not align with their sex assigned at birth.¹ Specifically, a transgender man is an individual who was assigned female at birth but who identifies and lives as a man² and a transgender woman is an individual who was assigned male at birth but who identifies and lives as a woman.² Importantly, gender identities and their expression are diverse beyond the binary framework; while this review focuses on transgender men and women, it also applies to other gender diverse individuals⁴ including those who identify as without gender or “agender.” Furthermore, it is crucial to create a safe and welcoming clinical environment for transgender patients with culturally competent care.⁵ In clinical practice and for research purposes, it is important to document gender identity data and to use patients’ preferred name and pronouns.⁵ In addition, other important aspects to consider include appropriate staff training, bathrooms, waiting areas, and having a basic understanding of transgender terminology.⁵ All of this is important in acknowledging and respecting individuals’ gender identity and fostering trust in the patient-physician relationship.⁵

The Epidemiology of Transgender Persons

It is estimated that 0.3% to 0.6% of the adult population⁶ is transgender and that there are more than 150 000 transgender persons in Canada, 1 million transgender persons in the United States,⁷ and 25 million transgender persons worldwide.⁶ The prevalence of transgender individuals in a population depends on the definition of transgender and its classification by self-report, the use of sex hormone therapy, or the receipt of gender-affirming surgery.⁸ In the Behavioral Risk Factor Surveillance System which included more than 500 000 random respondents from across the United States, 0.24% identified as male-to-female, 0.14% identified as female-to-male, and 0.10% identified as gender nonconforming.⁹

Transgender persons have a higher burden of chronic diseases when compared with the cisgender population¹⁰ and have worse overall health outcomes due to many different factors.¹¹ Coexisting mental health comorbidities¹² are common including mood disorders, substance abuse and dependency, and self-harm behaviors¹³ that all negatively impact health-related quality of life.^14-16 Many of these factors can influence or contribute to underlying CKD including nonadherence, HIV, highly active antiretroviral therapy, illicit drugs, renovascular disease, and gender-affirming hormone therapy.

Gender-Affirming Care

When transgender individuals experience gender dysphoria or incongruence, they have distress or discomfort associated with their gender identity being incongruent with their sex assigned at birth and may seek treatment to alleviate this.^1,2,17 The World Professional Association for Transgender Health (WPATH) clearly outlines the importance of mental health support and treatment as well as the medical necessity for providing gender-affirming hormone and/or surgical therapy in many transgender individuals with gender dysphoria.¹⁷ Gender-affirming care includes providing mental health support as well as support in transition-related care such as with a social transition, coping with transphobia, changing legal documents, and connecting patients to accessing gender services. It also involves supporting transgender individuals interested in gender-affirming hormone therapy and/or surgical therapy² in addition to general medical care¹ which includes addressing mental health issues, malignancy screening, the prevention and treatment of HIV¹⁸ and other sexually transmitted infections, cardiovascular (CV) risk reduction,^19,20 and vaccinations.²¹ Inclusive²² and culturally competent care²³ of transgender persons is typically provided by a network of physicians that includes primary care physicians, mental health professionals, endocrinologists, and surgeons but barriers to accessing care^24,25 resulting in health inequities²⁶ and unmet healthcare needs²⁷ are common, especially outside of larger cities and urban settings.

Gender-Affirming Hormone Therapy in Transgender Persons

There are 2 main objectives of gender-affirming hormone therapy in transgender individuals. The first is to decrease the levels of endogenous sex hormones and their associated secondary sex characteristics of the sex assigned at birth.² The second is to then replace and shift the individual’s biochemical sex hormone configuration to reflect their affirmed gender in a way that mimics physiology as best as possible using the principles from hormone replacement therapy in hypogonadal cisgender individuals.² This is guided by the individual’s gender-affirming goals as well as providing this hormonal therapy in a risk reduction manner depending on the clinical scenario and presence of medical comorbidities. Gender-affirming hormone therapy is associated with an improvement in quality of life,^28,29 psychological outcomes,³⁰ and sexual function² in transgender persons. Data also suggest that the overall satisfaction is high after gender-affirming treatment.³¹

Masculinizing Hormone Therapy in Transgender Men

For transgender men, the general goal of masculinizing hormone therapy is virilization with the development of masculine secondary sexual characteristics that match their masculine gender identity.^1,31 This is accomplished by using exogenous testosterone therapy to raise testosterone levels into the male physiological range by using either injectable or transdermal testosterone formulations.^1,2 This leads to masculine changes which typically include voice deepening, menstrual suppression, facial and body hair growth, and increased muscle mass.^1,31 In particular, exogenous testosterone therapy leads to changes in body composition with increased body weight, decreased body fat, and increased lean body mass usually by several kilograms.³¹ Adverse effects of exogenous testosterone therapy include erythrocytosis³² and a risk of polycythemia especially with additional risk factors,¹ acne, scalp hair loss, unexpected menstrual bleeding, hypertriglyceridemia, and infertility.³¹

Feminizing Hormone Therapy in Transgender Women

For transgender women, the general goal of feminizing hormone therapy is to decrease the effects of endogenous testosterone and to induce feminine secondary sex characteristics that match their feminine gender identity.³¹ This is achieved by adding estrogen and by reducing endogenous testosterone to attain estradiol and testosterone levels within the female physiological range. This is accomplished by using exogenous estradiol therapy which in itself can suppress endogenous testosterone production via central feedback mechanism as well as anti-androgen therapy that suppresses either the secretion or action of androgens³³ such as spironolactone, cyproterone acetate, or gonadotropin-releasing hormone (GnRH) agonists.^1,2,31 Guidelines recommend using oral, transdermal, or injectable exogenous estradiol therapy in this clinical setting.² Feminizing hormone therapy generally leads to skin softening, breast development, decrease in body hair,³¹ as well as changes in body composition³¹ with increased body fat and decreased lean body mass which usually increases body weight by several kilograms without any negative effects on bone mineral density.³⁴ Adverse effects of estrogens include venous thromboembolism (VTE),^35,36 malignancy,^37,38 hypertriglyceridemia, CV disease,^19,20 and infertility.³¹ Progesterone may also be used for breast development in transgender women but may have side effects and increase the risk of breast cancer³⁷ and vascular disease.

Gender-Affirming Surgery

Gender-affirming surgery refers to any surgery in which a transgender individual uses to align their body with their affirmed gender identity.³⁹ Among these gender-affirming surgeries, there is a group of surgeries that do not affect fertility which include facial feminization, breast augmentation, bilateral mastectomy, and metoidioplasty.^1,2 The other group of surgeries that directly affect fertility include orchiectomy, penectomy, vaginoplasty, hysterectomy, oophorectomy, vaginectomy, and phalloplasty.^1,2 Gender-affirming surgeries affecting fertility are irreversible and guidelines recommend first having used gender-affirming hormone therapy continuously for 1 year and having successfully been living full-time in one’s affirmed gender role for 1 year.² Obstructive uropathy is a complication of gender-affirming surgery and altered anatomy may result in challenges in the management of specific urological issues and kidney transplantation. After gender-affirming surgery, transgender persons remain at an increased risk of psychiatric morbidity, suicidality, and death.⁴⁰

Special Considerations for Transgender Care in the Setting of Kidney Disease

CKD and Hypogonadotropic Hypogonadism

It is believed that there is proportional increase in hypothalamic-pituitary-gonadal (HPG) dysfunction as glomerular filtration rate (GFR) decreases in individuals with CKD that results in testosterone deficiency in men⁴¹ and estrogen deficiency and functional menopause in females.⁴² However, postmenopausal females with kidney disease have similar estrogen levels as postmenopausal females without kidney disease.⁴³ How kidney disease suppresses the HPG axis is not entirely clear but is thought to be due to the reduction in cyclic release of GnRH leading to the loss of pulsatile luteinizing hormone and follicular stimulating hormone release with subsequent decrease in the secretion of sex hormones.⁴⁴ Another potential factor is the presence of hyperprolactinemia which is also common in CKD and dialysis as a result of increased pituitary production due to resistance from dopamine inhibition and decreased excretion by the kidneys.^45,46 Transgender persons with CKD may have decreased levels of endogenous sex hormones and may thus potentially require lower dosages of gender-affirming hormone therapy to meet their gender-affirming goals but there is no evidence to support this beyond the presumed hypogonadotropic hypogonadism of patients with kidney disease.

The Role of Sex Hormones in Kidney Disease

The effects of sex on kidney function are uncertain because in human studies, unlike animal studies, it is challenging to separate sex and gender as prognostic factors for the development and progression of CKD. In a meta-analysis of studies in the Chronic Kidney Disease-Prognosis Consortium, there was no difference in the progression of kidney disease between men and women even after stratifying by age to account for menopause.⁴⁷ This is different from previous meta-analyses where female sex was associated with either improved or deleterious kidney outcomes,^48,49 which in addition to differences in menopausal status in the included populations likely reflects dissimilarities in definitions of kidney outcomes in the different studies.

Estrogen and Kidney Disease

Estrogen has been shown to be renoprotective in animal studies with estrogen receptors located in mesangial, endothelial, and endothelial cells of the kidney where it affects the synthesis and activity of cytokines, growth factors, vasoactive mediators, renin-angiotensin aldosterone system (RAAS) activity, and transforming growth factor-β signal transduction.⁵⁰ However, the renoprotective effects of estrogen in human prospective and observational studies have been inconsistent. If in fact female sex is renoprotective, is not clear whether this is because of a protective effect of endogenous estrogen or due to decreased exposure to the potentially harmful effects of testosterone. However, exogenous estrogen may also be harmful. Oral contraceptives with estrogen are associated with the development of microalbuminuria⁵¹ and macroalbuminuria⁵² as well as RAAS and an increase in blood pressure.⁵³ Postmenopausal hormone therapy in the setting of kidney disease is associated with a lower low-density lipoprotein and higher high-density lipoprotein without any effects on triglycerides or blood pressure.⁵⁴ Studies examining the effect of postmenopausal hormone therapy on long-term CV outcomes in CKD and ESKD are lacking with those examining the effects of exogenous estrogen on albuminuria and GFR showing conflicting results^55-57 which likely reflect differences in estrogen doses, routes, concurrent use of progestins, and timing of initiation of therapy relative to menopausal onset.

Whether the potential benefits and harms of exogenous estrogen in transgender women and decreased estrogen in transgender men are similar to that of cisgender individuals are unclear. The pharmacokinetics of estrogen differs in cisgender women with CKD,^58,59 in that while little estradiol and estrone are excreted in the urine and neither is dialyzed, free and total estradiol plasma concentrations are still higher in cisgender women with ESKD so it is recommended that only 50% of its dose is administered. The absolute risks of VTE from estrogen are likely increased in CKD and dialysis⁶⁰ so its benefit to risk ratio should be revaluated as CKD progresses. The development of additional risk factors such as surgery and immobilization, as is in the setting of kidney transplantation, may further increase VTE risk so that it may be reasonable to temporarily discontinue estrogen to prevent the risk of VTE (and graft thrombosis) until additional risk factors have resolved but there is no evidence to guide this approach. The route of estrogen (ie, transdermal vs oral vs other) may influence the risk of VTE as transdermal estrogen may be safer in transgender⁶¹ and postmenopausal women.⁶² Similarly, given the already increased CV risk in the setting of CKD, the use of estrogen in transgender women may further increase the of CV events.⁶³ In an electronic medical record–based cohort study of 2842 transwomen and 2118 transmen from Kaiser Permanente integrated health systems, the incidences of ischemic stroke and myocardial infarction were higher in transwomen than cisgender men and women controls but eGFR and eGFR/proteinuria estrogen interactions were not considered.¹⁹ Observational studies that accurately identify transgender women, estrogen exposure, and both VTE and CV events across the spectrum of CKD are needed to determine the degree of effect modification by GFR and proteinuria.

Testosterone and Kidney Outcomes

Low testosterone is common in CKD⁶⁴ as a result of aging, comorbidities such as diabetes, obesity, liver disease, and medications (eg, glucocorticoids, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, statins, opioids) with many adverse outcomes including low muscle mass,⁶⁵ frailty,⁶⁶ arterial stiffness,⁶⁷ CV events,⁶⁸ and mortality.^64,69-71 It is unknown whether low testosterone levels from the effects of feminizing hormone therapy or as a result of gonadectomy in transgender women are associated with similar risks. Similarly, it is also unknown whether the goal of gender-affirming hormone therapy in transgender men with CKD should be that of mimicking normal physiology or targeting the lower testosterone levels seen in the cismale CKD population.

If accurate testosterone levels are needed to guide clinical decision-making, a measurement method that takes into account sex hormone–binding globulin levels which are altered in CKD and influence total testosterone levels is recommended. This may include bioavailable testosterone, free androgen index, or free testosterone measured using a validated equilibrium dialysis assay. The treatment of low testosterone in cisgender men with hypogonadism not only results in virilization and improves sexual function, muscle strength, fat-free mass, bone density but might also increase the risk of CV events.⁷² Exogenous testosterone therapy increases erythropoiesis and so hemoglobin should be carefully monitored in all patients on testosterone⁷³ given the potential risk of iatrogenic polycythemia, especially if there is the concurrent use of iron, erythropoietin-stimulating agents, or post-transplant polycythemia. It appears that exogenous testosterone is not significantly removed by hemodialysis as total and free testosterone levels do not differ before and after dialysis in men using transdermal testosterone.⁷⁴

Cyproterone acetate and GnRH agonists do not need to be dose adjusted in CKD and dialysis but this has not been formally studied. However, spironolactone should be dosed reduced for eGFR < 30 mL/min/1.73m² although lower doses may not be effective as an anti-androgen. As spironolactone may increase the risk of hyperkalemia, especially in individuals approaching or currently being treated with dialysis,⁷⁵ replacement by another anti-androgen may be necessary in transgender women. Alternatively, pharmacologic (eg, diuretics, novel potassium binding resins) and nonpharmacologic treatments (strict dietary restriction, frequent dialysis) for hyperkalemia may need to be initiated or intensified. Androgen deprivation therapy for nonmetastatic prostate cancer with GnRH agonists and combination therapy with oral antiandrogens or estrogens increases the risk of acute kidney injury⁷⁶ but its mechanism and whether this is the case in transgender persons are not known. In a retrospective study of weightlifters that included 57 current anabolic-androgenic steroid (AAS) users, 28 past AAS users, and 52 nonusers, adjusted eGFR was the lowest in current users, intermediate in past users, and the highest in nonusers suggesting either a direct nephrotoxic effect or an indirect effect mediated by AAS-induced CV dysfunction.⁷⁷

Estimating GFR in Transgender Persons

GFR is routinely estimated⁷⁸ using creatinine and equations developed from linear regression models including the Modification of Diet in Renal Disease (MDRD)⁷⁹ and the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI)⁸⁰ equations. Creatinine is a biomarker of GFR that is derived from diet and skeletal muscle metabolism so it is influenced not only by GFR but also by diet and muscle mass which is dependent on age, sex/gender, and race but the latter is controversial.⁸¹ For this reason, estimated GFR equations typically adjust for these non-GFR-related factors to improve their performance. The eGFR equations include sex as a covariate because cisgender females generate less creatinine than cisgender males due to having lower muscle mass and there may also be sex/gender differences in diet and creatinine production.⁸² If sex and gender factors are not considered, eGFR is systematically overestimated in cisgender females.

The adjustment in eGFR for female sex in the MDRD equation is × 0.742. The adjustment in eGFR for female sex in CKD-EPI equation⁸³ is more complicated and is based on sex differences in the (SCr/B)^C term of the equation where SCr is serum creatinine, B is 0.7 and 0.9 in cisgender females and males, respectively, and C is either −0.329 or −0.411 if SCr is ≤62 and ≤80 µmol/L in cisgender females and males (and 1.209 for both sexes above these SCr thresholds). The issue with using sex in eGFR equations in transgender persons is that it is unclear which adjustment to input into the equation for transgender men and women because their muscle mass and thus creatinine may not be the same as their respective cisgender counterparts. It should be noted that the MDRD and CKD-EPI populations used to derive and validate their eGFR formulas did not specifically report if any transgender persons were included or how sex and/or gender were captured in the initial datasets. The differences in eGFR estimation of using both sexes in the MDRD and CKD-EPI equations across ages and serum creatinine are shown in Figure 1. The absolute difference in eGFR between sexes decreases as serum creatinine increases and is lower in the elderly as compared with younger individuals. The bias between measured GFR and eGFR may be larger in women compared with men⁸⁴ (ie, −14.2 [−16.5 to −10.9] in women and −3.4 [−6.3 to 0] in men using CKD-EPI) but how this compares with transgender men and women is not known.

Figure 1.

Differences in eGFR by sex and age in MDRD and CKD-EPI equations.

This potential bias (i.e., the difference in measured GFR and eGFR) in transgender persons is most problematic in the setting of gender-affirming hormone therapy, where body composition and muscle mass change as described above with a corresponding change in creatinine generation and serum creatinine^85,86; whether there is any true difference in actual GFR is unknown. In a systematic review and meta-analysis, testosterone therapy increased lean mass by 3.9kg (95% confidence interval [CI]: 3.2-4.5) in transgender men and estradiol therapy with or without anti-androgen therapy decreased lean mass by 2.4 kg (95% CI: 2.8-2.1).^87,88 The effects of gender-affirming hormone therapy on serum creatinine in transgender men and women before and after its initiation or between cisgender and transgender groups are shown in Table 1. On average, creatinine increases approximately 5 to 10 µmol/L in transgender men and decreases 5 to 10 µmol/L in transgender women which may or may not be clinically relevant as the minimally important difference in eGFR bias across GFR levels and clinical decision-making is unknown. The degree to which cystatin C is affected by gender-affirming hormone therapy is not known, but is presumably less than creatinine given that CKD-EPI equations that incorporate cystatin C with or creatinine are less influenced by sex (ie, the sex coefficient is .932 if female for the cystatin C only equation and the male and female values for [cystatin/B]^C are identical for the combined creatinine and cystatin C equation). To our knowledge, there are no studies that have examined if there are any differences in cystatin C between cisgender and transgender persons or pre/post gender-affirming hormone therapy.

Table 1.

Changes in Transgender Men and Women on Sex Hormone Therapy.

Study	Population	Duration	Prehormone therapy serum creatinine	Posthormone therapy serum creatinine	P value (between group)(pre/post*)
Ruestche⁸⁹	24 transwomen 15 transmen	12.5 y 7.6 y	Not applicable Not applicable	80 µmol/L (10) 90 µmol/L (6)	Not reported
Lapauw⁹⁰	23 transwomen 46 age, height Matched cismales	>3 y	Not applicable Not applicable	0.78 mg/dL ± 0.11 (69 µmol/L ± 10) 0.94 mg/dL ± 0.12 (83 µmol/L ± 11)	P < .001*
Wierckx⁹¹	50 transmen 50 transwomen	6.3 y 8.7 y	Not applicable Not applicable	0.9 mg/dL (0.9-1.0) (80 µmol/L) 0.8 mg/dL (0.7-0.9) (71 µmol/L)	P < .001*
Sorelle⁸⁵	133 transwomen 89 transmen	>6 mo	0.98 mg/dL (87 µmol/L) 0.74 mg/dL (65 µmol/L)	0.86 mg/dL (76 µmol/L) 0.90 mg/dL (80 µmol/L)	P < .0001 P < .0001
Fernandez⁹²	33 transwomen 19 transmen	18 mo	0.90 mg/dL (0.03) (80 µmol/L [3]) 0.73 mg/dL (0.03) (65 µmol/L [3])	0.83 mg/dL (0.03) (73 µmol/L [3]) 0.82 mg/dL (0.04) (73 µmol/L [4])	Not reported
Jarin⁹³	72 transmen 44 transwomen	6 mo	Not reported	Not reported	P > .05
Scharff⁸⁶	249 transwomen 278 transmen	12 mo	78.5 µmol/L (10.8) 66.0 µmol/L (9.0)	73.1 µmol/L (10.6) 77.4 µmol/L (10.6)	−5.0 (95% CI: −6.2 to −3.8) 11.1 (95% CI: 10.1 to 12.2)
Wierckx⁹⁴	53 transmen 53 transwomen	1 y	0.74 mg/dL (0.1) (65 µmol/L [9]) 0.9 mg/dL (0.1) (80 µmol/L [9])	0.84 mg/dL (0.1) (74 µmol/L [9]) 0.8 mg/dL (0.1) (71 µmol/L [9])	P < .001 P < .001
van Kesteren⁹⁵	20 transwomen 19 transmen	1 y	81 µmol/L (7) 72 µmol/L (8)	77 µmol/L (7) 79 µmol/L (9)	P = .048 P < .001

Note. CI = confidence interval.

Gandhi et al⁹⁶ report the case of a 36-year-old transgender man whose creatinine increased from 0.94 mg/dL (83 µmol/L) to 1.3 mg/dL (115 µmol/L) 2 years after the initiation of testosterone. A 24-hour urine for CrCl was 92 mL/min which, as expected, was higher than eGFR estimated by CKD-EPI due to tubular secretion Cr using either male sex (81 mL/min/1.73 m²) or female sex (61 mL/min/1.73 m²). Whitley and Greene⁹⁷ report the case of a 33-year-old transgender man on testosterone therapy with CKD and eGFR of 31 mL/min/1.73 m² or 23 mL/min/1.73 m² using male or female sex, respectively, in the MDRD equation. The eGFR equation performance in transgender persons is limited to case reports and there are no specific data regarding transgender women.

Given that the performance of eGFR equations has never been evaluated in any transgender populations, we recommend that both male and female sexes are inputted into eGFR equations for transgender persons on gender-affirming hormone therapy. This will give a range of eGFR by sex that can be narrowed by deciding on which value likely reflects the muscle mass of the patient to which the calculations were applied. In situations in which an accurate knowledge of GFR is needed (eg, living donor suitability, dosing of medications with a narrow therapeutic index, referral for pre-emptive kidney transplantation, the initiation of dialysis with vague but potentially uremic symptoms), measured GFR can be obtained by use of non-Cr exogenous filtration markers such as iothalamate or iohexol, or radionuclide imaging with diethylenetriaminepentaacetic acid or ethylenediaminetetraacetic acid. Ideally, Cr measurements before the initiation of gender-affirming hormone therapy are available in most patients so that accurate and precise baseline eGFR levels can be referenced as well. For transgender persons not on gender-affirming hormone therapy, because their muscle mass is likely reflective of their sex assigned at birth, we recommend that their sex assigned at birth and not their affirmed gender be used in all eGFR equations. Additional research is needed to determine the role of cystatin C instead of or in addition to Cr for eGFR in transgender persons as well as the performance (and possibly modification) of current eGFR equations in transgender persons with and without gender-affirming hormone therapy.

Inaccuracy in eGFR values on an individual level in transgender persons can be harmful depending on the level of GFR, the clinical decision at hand, and the availability of confirmatory measured GFR testing. For any population with a potential non-GFR determinant of an eGFR biomarker, bias and systemic overestimation in eGFR may result in delays in accessing care (eg, referrals to nephrology, vascular access, and transplant) and systemic underestimation could lead to the overdiagnosis of CKD, earlier initiation of dialysis, the inadequate use or dosing of drugs excreted by the kidney, limit access to diagnostic imaging (contrast, gadolinium), and result in exclusion from research.⁹⁸ Thus, the potential lack of precision, accuracy, and bias in any transgender eGFR calculation requires full disclosure by health care providers and shared decision-making⁹⁹ not only by nephrologists but also by all clinicians who provide care to transgender persons in addition to the patient. Ultimately, if eGFR equations were validated in transgender persons on gender-affirming hormone therapy and modified as necessary to optimize their performance, this could improve clinical decision-making and potentially avoid the need for measured GFR testing which is invasive, time-consuming, impractical, and costly. Potential differences in creatinine and eGFR equations in transgender persons warrant better awareness among clinicians and researchers. For example, in the iPrEX study of preexposure prophylaxis for HIV prevention in cisgender men who have sex with men and transgender women^100,101 (who comprised 14% of the trial population, 20% of whom were on gender-affirming hormone therapy), a creatinine >1.2 mg/dL (106 µmol/L) or “the upper limit of normal” and a CrCl <60 mL/min were both exclusion criteria and safety events independent of sex or gender. While this remains speculative, it is possible that thresholds of creatinine or eGFR that differed by gender may have modified the trial recruitment and population and altered its results regarding efficacy and safety.

Limitations

There is little research dedicated to the intersection of transgender persons and kidney disease unlike other priority areas for transgender persons such as HIV/AIDS, mood disorders, CV disease, malignancy, and fertility.¹⁰² However, even in these areas, there are unique methodologic and operational challenges¹⁰³ to research. These barriers¹⁰⁴ include recruitment, retention, efficiency,¹⁰⁵ mistrust,¹⁰⁶ a lack of individual and community engagement by researchers, and an overall concern for perceived more pressing issues such as personal safety, police violence,¹⁰⁷ poverty, unemployment,¹⁰⁸ and homelessness¹⁰⁹ instead of research that may or may not directly impact transgender health. The nephrology community needs to prioritize including transgender persons in research by at minimum collecting sex and gender separately to identify transgender persons in studies as well as perform dedicated epidemiologic studies dedicated to pertinent questions such as eGFR measurement and the safety of gender-affirming hormone therapy in transgender persons with kidney disease.

Conclusions

This review highlights important considerations for providing care to transgender persons with kidney disease. Additional research is needed to evaluate the performance of eGFR equations in transgender persons, the effects of gender-affirming hormone therapy on the kidney, and the impact of gender identity on outcomes of persons living with kidney disease.

Footnotes

Ethics Approval and Consent to Participate

Not applicable.

Consent for Publication

All authors provided consent for publication

Availability of Data and MaterialsNot applicable.

Not applicable.

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iD

David Collister

References

Safer

Tangpricha

Care of transgender persons. N Engl J Med. 2019;381(25):2451-2460. doi:10.1056/NEJMcp1903650.

Hembree

Cohen-Kettenis

Gooren

, et al. Endocrine treatment of gender-dysphoric/gender-incongruent persons: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2017;102(11):3869-3903. doi:10.1210/jc.2017-01658.

Polderman

TJC

Kreukels

BPC

Irwig

, et al. The biological contributions to gender identity and gender diversity: bringing data to the table. Behav Genet. 2018;48(2):95-108. doi:10.1007/s10519-018-9889-z.

Mohottige

Lunn

MR.

Ensuring gender-affirming care in nephrology: improving care for transgender and gender-expansive individuals. Clin J Am Soc Nephrol. 2020;15:1195-1197. doi:10.2215/cjn.14471119.

Deutsch

. Guidelines for the primary and gender-affirming care of transgender and gender nonbinary people. https://transcare.ucsf.edu/guidelines. Accessed December 21, 2020.

Reisner

Poteat

Keatley

, et al. Global health burden and needs of transgender populations: a review. Lancet. 2016;388(10042):412-436. doi:10.1016/s0140-6736(16)00684-x.

Meerwijk

Sevelius

JM.

Transgender population size in the United States: a meta-regression of population-based probability samples. Am J Public Health. 2017;107(2):e1-e8. doi:10.2105/AJPH.2016.303578.

Collin

Reisner

Tangpricha

Goodman

Prevalence of transgender depends on the “case” definition: a systematic review. J Sex Med. 2016;13(4):613-626. doi:10.1016/j.jsxm.2016.02.001.

Downing

Przedworski

JM.

Health of transgender adults in the U.S., 2014-2016. Am J Prev Med. 2018;55(3):336-344. doi:10.1016/j.amepre.2018.04.045.

10.

Dragon

Guerino

Ewald

Laffan

AM.

Transgender Medicare beneficiaries and chronic conditions: exploring fee-for-service claims data. LGBT Health. 2017;4(6):404-411. doi:10.1089/lgbt.2016.0208.

11.

Townsend

Jaffer

Goldman

Adverse health outcomes in transgender people. CMAJ. 2017;32:E1046.

12.

Beckwith

McDowell

Reisner

, et al. Psychiatric epidemiology of transgender and nonbinary adult patients at an urban health center. LGBT Health. 2019;6(2):51-61. doi:10.1089/lgbt.2018.0136.

13.

Adams

Vincent

Suicidal thoughts and behaviors among transgender adults in relation to education, ethnicity, and income: a systematic review. Transgend Health. 2019;4(1):226-246. doi:10.1089/trgh.2019.0009.

14.

Baker

KE.

Findings from the behavioral risk factor surveillance system on health-related quality of life among US transgender adults, 2014-2017. JAMA Intern Med. 2019;179(8):1141-1144. doi:10.1001/jamainternmed.2018.7931.

15.

Cicero

Reisner

Merwin

Humphreys

Silva

SG.

The health status of transgender and gender nonbinary adults in the United States. PLoS One. 2020;15(2):e0228765. doi:10.1371/journal.pone.0228765.

16.

Valashany

Janghorbani

Quality of life of men and women with gender identity disorder. Health Qual Life Outcomes. 2018;16(1):167. doi:10.1186/s12955-018-0995-7.

17.

Standards of Care for the Health of Transsexual, Transgender, and Gender-Nonconforming People, Version 7; 2012. World Professional Association for Transgender Health (WPATH). https://www.tandfonline.com/doi/abs/10.1080/15532739.2011.700873.

18.

Baral

Poteat

Strömdahl

Wirtz

Guadamuz

Beyrer

Worldwide burden of HIV in transgender women: a systematic review and meta-analysis. Lancet Infect Dis. 2013;13(3):214-222. doi:10.1016/S1473-3099(12)70315-8.

19.

Getahun

Nash

Flanders

, et al. Cross-sex hormones and acute cardiovascular events in transgender persons: a cohort study. Ann Intern Med. 2018;169(4):205-213. doi:10.7326/m17-2785.

20.

Connelly

Marie Freel

Perry

, et al. Gender-affirming hormone therapy, vascular health and cardiovascular disease in transgender adults. Hypertension. 2019;74(6):1266-1274. doi:10.1161/hypertensionaha.119.13080.

21.

Edmiston

Donald

Sattler

Peebles

Ehrenfeld

Eckstrand

KL.

Opportunities and gaps in primary care preventative health services for transgender patients: a systemic review. Transgend Health. 2016;1(1):216-230. doi:10.1089/trgh.2016.0019.

22.

Lam

JSH

Abramovich

Transgender-inclusive care. CMAJ. 2019;191(3):E79. doi:10.1503/cmaj.180954.

23.

Arnold

LM.

Promoting culturally competent care for the lesbian, gay, bisexual, and transgender population. Am J Public Health. 2001;91(11):1731.

24.

Alencar Albuquerque

de Lima Garcia

da Silva Quirino

, et al. Access to health services by lesbian, gay, bisexual, and transgender persons: systematic literature review. BMC Int Health Hum Rights. 2016;16:2. doi:10.1186/s12914-015-0072-9.

25.

Collier

Addressing transgender discrimination in health. CMAJ. 2015;17:E493.

26.

Kauth

Shipherd

Lindsay

Blosnich

Brown

Jones

. Access to care for transgender veterans in the Veterans Health Administration: 2006-2013. Am J Public Health. 2014;104(suppl. 4):S532-S534. doi:10.2105/ajph.2014.302086.

27.

Giblon

Bauer

GR.

Health care availability, quality, and unmet need: a comparison of transgender and cisgender residents of Ontario, Canada. BMC Health Serv Res. 2017;17(1):283. doi:10.1186/s12913-017-2226-z.

28.

Costa

Colizzi

The effect of cross-sex hormonal treatment on gender dysphoria individuals’ mental health: a systematic review. Neuropsychiatr Dis Treat. 2016;12:1953-1966. doi:10.2147/NDT.S95310.

29.

Nobili

Glazebrook

Arcelus

Quality of life of treatment-seeking transgender adults: a systematic review and meta-analysis. Rev Endocr Metab Disord. 2018;19(3):199-220. doi:10.1007/s11154-018-9459-y.

30.

White Hughto

Reisner

SL.

A systematic review of the effects of hormone therapy on psychological functioning and quality of life in transgender individuals. Transgend Health. 2016;1(1):21-31. doi:10.1089/trgh.2015.0008.

31.

T’Sjoen

Arcelus

Gooren

Klink

Tangpricha

Endocrinology of transgender medicine. Endocr Rev. 2019;40(1):97-117. doi:10.1210/er.2018-00011.

32.

Defreyne

Vantomme

Van Caenegem

, et al. Prospective evaluation of hematocrit in gender-affirming hormone treatment: results from European Network for the Investigation of Gender Incongruence. Andrology. 2018;6(3):446-454. doi:10.1111/andr.12485.

33.

Tangpricha

den Heijer

Oestrogen and anti-androgen therapy for transgender women. Lancet Diabetes Endocrinol. 2017;5(4):291-300. doi:10.1016/S2213-8587(16)30319-9.

34.

Fighera

Ziegelmann

Rasia

Silva

Spritzer

PM.

Bone mass effects of cross-sex hormone therapy in transgender people: updated systematic review and meta-analysis. J Endocr Soc. 2019;5:943-964.

35.

Chan

Drummond

Kelly

Deep vein thrombosis in a transgender woman. CMAJ. 2017;189(13):e502-e504. doi:10.1503/cmaj.160408.

36.

Shatzel

Connelly

DeLoughery

TG.

Thrombotic issues in transgender medicine: a review. Am J Hematol. 2017;92(2):204-208. doi:10.1002/ajh.24593.

37.

de Blok

CJM

Wiepjes

Nota

, et al. Breast cancer risk in transgender people receiving hormone treatment: nationwide cohort study in the Netherlands. BMJ. 2019;365:l1652. doi:10.1136/bmj.l1652.

38.

Joint

Chen

Cameron

Breast and reproductive cancers in the transgender population: a systematic review. BJOG. 2018;125(12):1505-1512. doi:10.1111/1471-0528.15258.

39.

Canner

Harfouch

Kodadek

, et al. Temporal trends in gender-affirming surgery among transgender patients in the United States. JAMA Surg. 2018;153(7):609-616. doi:10.1001/jamasurg.2017.6231.

40.

Dhejne

Lichtenstein

Boman

Johansson

Långström

Landén

Long-term follow-up of transsexual persons undergoing sex reassignment surgery: cohort study in Sweden. PLoS One. 2011;6(2):e16885. doi:10.1371/journal.pone.0016885.

41.

Lehtihet

Hylander

Semen quality in men with chronic kidney disease and its correlation with chronic kidney disease stages. Andrologia. 2015;47(10):1103-1108. doi:10.1111/and.12388.

42.

Lim

Henriquez

Sievertsen

Frohman

LA.

Ovarian function in chronic renal failure: evidence suggesting hypothalamic anovulation. Ann Intern Med. 1980;93(1):21-27. doi:10.7326/0003-4819-93-1-21.

43.

Kramer

Curhan

Singh

Hemodialysis and estrogen levels in postmenopausal (HELP) patients: the multicenter HELP study. Am J Kidney Dis. 2003;41(6):1240-1246. doi:10.1016/s0272-6386(03)00357-3.

44.

Ahmed

Ramesh

Sex hormones in women with kidney disease. Nephrol Dial Transplant. 2016;31(11):1787-1795. doi:10.1093/ndt/gfw084.

45.

Hou

Grossman

Molitch

ME.

Hyperprolactinemia in patients with renal insufficiency and chronic renal failure requiring hemodialysis or chronic ambulatory peritoneal dialysis. Am J Kidney Dis. 1985;6(4):245-249. doi:10.1016/s0272-6386(85)80181-5.

46.

Sievertsen

Lim

Nakawatase

Frohman

LA.

Metabolic clearance and secretion rates of human prolactin in normal subjects and in patients with chronic renal failure. J Clin Endocrinol Metab. 1980;50(5):846-852. doi:10.1210/jcem-50-5-846.

47.

Nitsch

Grams

Sang

, et al. Associations of estimated glomerular filtration rate and albuminuria with mortality and renal failure by sex: a meta-analysis. BMJ. 2013;346:f324. doi:10.1136/bmj.f324.

48.

Jafar

Schmid

Stark

, et al. The rate of progression of renal disease may not be slower in women compared with men: a patient-level meta-analysis. Nephrol Dial Transplant. 2003;18(10):2047-2053. doi:10.1093/ndt/gfg317.

49.

Neugarten

Acharya

Silbiger

SR.

Effect of gender on the progression of nondiabetic renal disease: a meta-analysis. J Am Soc Nephrol. 2000;11(2):319-329.

50.

Neugarten

Golestaneh

Gender and the prevalence and progression of renal disease. Adv Chronic Kidney Dis. 2013;20(5):390-395. doi:10.1053/j.ackd.2013.05.004.

51.

Monster

Janssen

de Jong

de Jong-van den Berg

LT.

Oral contraceptive use and hormone replacement therapy are associated with microalbuminuria. Arch Intern Med. 2001;161(16):2000-2005. doi:10.1001/archinte.161.16.2000.

52.

Ahmed

Hovind

Parving

, et al. Oral contraceptives, angiotensin-dependent renal vasoconstriction, and risk of diabetic nephropathy. Diabetes Care. 2005;28(8):1988-1994. doi:10.2337/diacare.28.8.1988.

53.

Burgner

Hladunewich

MA.

Contraception and CKD. Clin J Am Soc Nephrol. 2020;15(4):563-565. doi:10.2215/cjn.09770819.

54.

Ramesh

Mann

Holroyd-Leduc

, et al. Hormone therapy and clinical and surrogate cardiovascular endpoints in women with chronic kidney disease: a systematic review and meta-analysis. Menopause. 2016;23(9):1028-1037. doi:10.1097/GME.0000000000000657.

55.

Ahmed

Culleton

Tonelli

, et al. Oral estrogen therapy in postmenopausal women is associated with loss of kidney function. Kidney Int. 2008;74(3):370-376. doi:10.1038/ki.2008.205.

56.

Kattah

Suarez

MLG

Milic

, et al. Hormone therapy and urine protein excretion: a multiracial cohort study, systematic review, and meta-analysis. Menopause. 2018;25(6):625-634. doi:10.1097/GME.0000000000001062.

57.

Fung

Poddar

Bettencourt

Jassal

Barrett-Connor

. A cross-sectional and 10-year prospective study of postmenopausal estrogen therapy and blood pressure, renal function, and albuminuria: the Rancho Bernardo Study. Menopause. 2011;18(6):629-637. doi:10.1097/gme.0b013e3181fca9c4.

58.

Ginsburg

Owen

Jr. Greenberg

Shea

Lazarus

Walsh

BW.

Estrogen absorption and metabolism in postmenopausal women with end-stage renal disease. J Clin Endocrinol Metab. 1996;81(12):4414-4417. doi:10.1210/jcem.81.12.8954051.

59.

Stehman-Breen

Anderson

Gibson

Kausz

Ott

Pharmacokinetics of oral micronized beta-estradiol in postmenopausal women receiving maintenance hemodialysis. Kidney Int. 2003;64(1):290-294. doi:10.1046/j.1523-1755.2003.00073.x.

60.

Molnar

Bota

McArthur

, et al. Risk and complications of venous thromboembolism in dialysis patients. Nephrol Dial Transplant. May 1. 2018;33(5):874-880. doi:10.1093/ndt/gfx212.

61.

Asscheman

Giltay

Megens

de Ronde

van Trotsenburg

Gooren

LJ.

A long-term follow-up study of mortality in transsexuals receiving treatment with cross-sex hormones. Eur J Endocrinol. 2011;164(4):635-642. doi:10.1530/EJE-10-1038.

62.

Vinogradova

Coupland

Hippisley-Cox

Use of hormone replacement therapy and risk of venous thromboembolism: nested case-control studies using the QResearch and CPRD databases. BMJ. 2019;364:k4810. doi:10.1136/bmj.k4810.

63.

Chertow

Fan

McCulloch

Hsu

CY.

Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization. N Engl J Med. 2004;351(13):1296-1305. doi:10.1056/NEJMoa041031.

64.

Khurana

Navaneethan

Arrigain

Schold

Nally

Jr. Shoskes

DA.

Serum testosterone levels and mortality in men with CKD stages 3-4. Am J Kidney Dis. 2014;64(3):367-374. doi:10.1053/j.ajkd.2014.03.010.

65.

Chiang

Kaysen

Segal

Chertow

Delgado

Johansen

KL.

Low testosterone is associated with frailty, muscle wasting and physical dysfunction among men receiving hemodialysis: a longitudinal analysis. Nephrol Dial Transplant. 2019;34(5):802-810. doi:10.1093/ndt/gfy252.

66.

Yilmaz

Sonmez

Qureshi

, et al. Endogenous testosterone, endothelial dysfunction, and cardiovascular events in men with nondialysis chronic kidney disease. Clin J Am Soc Nephrol. 2011;6(7):1617-1625. doi:10.2215/CJN.10681210.

67.

Kyriazis

Tzanakis

Stylianou

, et al. Low serum testosterone, arterial stiffness and mortality in male haemodialysis patients. Nephrol Dial Transplant. 2011;26(9):2971-2977. doi:10.1093/ndt/gfq847.

68.

Carrero

Qureshi

Nakashima

, et al. Prevalence and clinical implications of testosterone deficiency in men with end-stage renal disease. Nephrol Dial Transplant. 2011;26(1):184-190. doi:10.1093/ndt/gfq397.

69.

Gungor

Kircelli

Carrero

, et al. Endogenous testosterone and mortality in male hemodialysis patients: is it the result of aging? Clin J Am Soc Nephrol. 2010;5(11):2018-2023. doi:10.2215/cjn.03600410.

70.

Carrero

Qureshi

Parini

, et al. Low serum testosterone increases mortality risk among male dialysis patients. J Am Soc Nephrol. 2009;20(3):613-620. doi:10.1681/ASN.2008060664.

71.

Bello

Stenvinkel

Lin

, et al. Serum testosterone levels and clinical outcomes in male hemodialysis patients. Am J Kidney Dis. 2014;63(2):268-275. doi:10.1053/j.ajkd.2013.06.010.

72.

Bhasin

Brito

Cunningham

, et al. Testosterone therapy in men with hypogonadism: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2018;103(5):1715-1744. doi:10.1210/jc.2018-00229.

73.

Ponce

Spencer-Bonilla

Alvarez-Villalobos

, et al. The efficacy and adverse events of testosterone replacement therapy in hypogonadal men: a systematic review and meta-analysis of randomized, placebo-controlled trials. J Clin Endocrinol Metab. 2018;103:1745-1754. doi:10.1210/jc.2018-00404.

74.

Singh

Norris

Modi

, et al. Pharmacokinetics of a transdermal testosterone system in men with end stage renal disease receiving maintenance hemodialysis and healthy hypogonadal men. J Clin Endocrinol Metab. 2001;86(6):2437-2445. doi:10.1210/jcem.86.6.7525.

75.

Quach

Lvtvyn

Baigent

, et al. The safety and efficacy of mineralocorticoid receptor antagonists in patients who require dialysis: a systematic review and meta-analysis. Am J Kidney Dis. 2016;68(4):591-598. doi:10.1053/j.ajkd.2016.04.011.

76.

Lapi

Azoulay

Niazi

Yin

Benayoun

Suissa

Androgen deprivation therapy and risk of acute kidney injury in patients with prostate cancer. JAMA. 2013;310(3):289-296. doi:10.1001/jama.2013.8638.

77.

Hudson

Kanayama

Pope

Jr. , et al. Glomerular filtration rate and supraphysiologic-dose anabolic-androgenic steroid use: a cross-sectional cohort study. Am J Kidney Dis. Jul. 2020;76(1):152-155. doi:10.1053/j.ajkd.2020.01.012.

78.

Levey

Inker

Coresh

GFR estimation: from physiology to public health. Am J Kidney Dis. 2014;63(5):820-834. doi:10.1053/j.ajkd.2013.12.006.

79.

Levey

Bosch

Lewis

Greene

Rogers

Roth

A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group. Ann Intern Med. 1999;130(6):461-470. doi:199903160-00002.

80.

Inker

Schmid

Tighiouart

, et al. Estimating glomerular filtration rate from serum creatinine and cystatin C. N Engl J Med. Jul 5. 2012;367(1):20-29. doi:10.1056/NEJMoa1114248.

81.

National Kidney Foundation ASoN. https://www.kidney.org/news/establishing-task-force-to-reassess-inclusion-race-diagnosing-kidney-diseases. Accessed December 21, 2020.

82.

Nitsch

Is there a difference in metabolic burden between men and women?

Nephrol Dial Transpl. 2014;29(6):1110-1112. doi:10.1093/ndt/gft518.

83.

Levey

Stevens

Schmid

, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150(9):604-612. doi:10.7326/0003-4819-150-9-200905050-00006.

84.

Inker

Levey

Tighiouart

, et al. Performance of glomerular filtration rate estimating equations in a community-based sample of Blacks and Whites: the multiethnic study of atherosclerosis. Nephrol Dial Transplant. 2018;33(3):417-425. doi:10.1093/ndt/gfx042.

85.

SoRelle

Jiao

Gao

, et al. Impact of hormone therapy on laboratory values in transgender patients. Clin Chem. Jan. 2019;65(1):170-179. doi:10.1373/clinchem.2018.292730.

86.

Scharff

Wiepjes

Klaver

Schreiner

T’Sjoen

den Heijer

Change in grip strength in trans people and its association with lean body mass and bone density. Endocr Connect. 2019;8(7):1020-1028. doi:10.1530/EC-19-0196.

87.

Spanos

Bretherton

Zajac

Cheung

AS.

Effects of gender-affirming hormone therapy on insulin resistance and body composition in transgender individuals: a systematic review. World J Diabetes. 2020;11(3):66-77. doi:10.4239/wjd.v11.i3.66.

88.

Klaver

Dekker

de Mutsert

Twisk

JWR

den Heijer

Cross-sex hormone therapy in transgender persons affects total body weight, body fat and lean body mass: a meta-analysis. Andrologia. 2017;49(5). doi:10.1111/and.12660.

89.

Ruetsche

Kneubuehl

Birkhaeuser

Lippuner

Cortical and trabecular bone mineral density in transsexuals after long-term cross-sex hormonal treatment: a cross-sectional study. Osteoporos Int. 2005;16(7):791-798. doi:10.1007/s00198-004-1754-7.

90.

Lapauw

Taes

Simoens

, et al. Body composition, volumetric and areal bone parameters in male-to-female transsexual persons. Bone. 2008;43(6):1016-1021. doi:10.1016/j.bone.2008.09.001.

91.

Wierckx

Mueller

Weyers

, et al. Long-term evaluation of cross-sex hormone treatment in transsexual persons. J Sex Med. 2012;9(10):2641-2651. doi:10.1111/j.1743-6109.2012.02876.x.

92.

Fernandez

Tannock

LR.

Metabolic effects of hormone therapy in transgender patients. Endocr Pract. 2016;22(4):383-388. doi:10.4158/EP15950.OR.

93.

Jarin

Pine-Twaddell

Trotman

, et al. Cross-sex hormones and metabolic parameters in adolescents with gender dysphoria. Pediatrics. 2017;139(5). doi:10.1542/peds.2016-3173.

94.

Wierckx

Van Caenegem

Schreiner

, et al. Cross-sex hormone therapy in trans persons is safe and effective at short-time follow-up: results from the European network for the investigation of gender incongruence. J Sex Med. 2014;11(8):1999-2011. doi:10.1111/jsm.12571.

95.

van Kesteren

Lips

Gooren

Asscheman

Megens

Long-term follow-up of bone mineral density and bone metabolism in transsexuals treated with cross-sex hormones. Clin Endocrinol (Oxf). 1998;48(3):347-354. doi:10.1046/j.1365-2265.1998.00396.x.

96.

Gandhi

Medeiros

Shah

AD.

Physiology or pathology? elevated serum creatinine in a female-to-male transgender patient. Am J Kidney Dis. Apr. 2020;75(4):A13-A14. doi:10.1053/j.ajkd.2019.10.018.

97.

Whitley

Greene

DN.

Transgender man being evaluated for a kidney transplant. Clin Chem. 2017;63(11):1680-1683. doi:10.1373/clinchem.2016.268839.

98.

Grubbs

Precision in GFR reporting: let’s stop playing the race card. Clin J Am Soc Nephrol. 2020;15:1201-1202. doi:10.2215/cjn.00690120.

99.

Levey

Titan

Powe

Coresh

Inker

LA.

Kidney disease, race, and GFR estimation. Clin J Am Soc Nephrol. 2020;15:1203-1212. doi:10.2215/cjn.12791019.

100.

Buchbinder

Glidden

Liu

, et al. HIV pre-exposure prophylaxis in men who have sex with men and transgender women: a secondary analysis of a phase 3 randomised controlled efficacy trial. Lancet Infect Dis. 2014;14(6):468-475. doi:10.1016/S1473-3099(14)70025-8.

101.

Deutsch

Glidden

Sevelius

, et al. HIV pre-exposure prophylaxis in transgender women: a subgroup analysis of the iPrEx trial. Lancet HIV. 2015;2(12):e512-e519. doi:10.1016/S2352-3018(15)00206-4.

102.

Feldman

Brown

Deutsch

, et al. Priorities for transgender medical and healthcare research. Curr Opin Endocrinol Diabetes Obes. 2016;23(2):180-187. doi:10.1097/MED.0000000000000231.

103.

Matthews

Rak

Anderson

, et al. White paper from a CTSA workshop series on special and underserved populations: enhancing investigator readiness to conduct research involving LGBT populations. J Clin Transl Sci. 2018;2(4):193-200. doi:10.1017/cts.2018.317.

104.

Reisner

Deutsch

Bhasin

, et al. Advancing methods for US transgender health research. Curr Opin Endocrinol Diabetes Obes. 2016;23(2):198-207. doi:10.1097/MED.0000000000000229.

105.

Hughes

Emel

Hanscom

Zangeneh

Design issues in transgender studies. J Acquir Immune Defic Syndr. 2016;72 (suppl 3):S248-S251. doi:10.1097/qai.0000000000001077.

106.

Owen-Smith

Woodyatt

Sineath

, et al. Perceptions of barriers to and facilitators of participation in health research among transgender people. Transgend Health. 2016;1(1):187-196. doi:10.1089/trgh.2016.0023.

107.

DeVylder

Jun

Fedina

, et al. Association of exposure to police violence with prevalence of mental health symptoms among urban residents in the United States. JAMA Netw Open. 2018;1(7):e184945. doi:10.1001/jamanetworkopen.2018.4945.

108.

Conron

Scott

Stowell

Landers

SJ.

Transgender health in Massachusetts: results from a household probability sample of adults. Am J Public Health. 2012;102(1):118-122. doi:10.2105/AJPH.2011.300315.

109.

Fraser

Pierse

Chisholm

Cook

LGBTIQ+ homelessness: a review of the literature. Int J Environ Res Public Health. 2019;16(15). doi:10.3390/ijerph16152677.

Providing Care for Transgender Persons With Kidney Disease: A Narrative Review

Abstract

Purpose of review:

Sources of information:

Methods:

Key findings:

Limitations:

Implications:

Keywords

Introduction

Scope and Purpose

Methods

Review

The Nomenclature of Gender Identity

The Epidemiology of Transgender Persons

Gender-Affirming Care

Gender-Affirming Hormone Therapy in Transgender Persons

Masculinizing Hormone Therapy in Transgender Men

Feminizing Hormone Therapy in Transgender Women

Gender-Affirming Surgery

Special Considerations for Transgender Care in the Setting of Kidney Disease

CKD and Hypogonadotropic Hypogonadism

The Role of Sex Hormones in Kidney Disease

Estrogen and Kidney Disease

Testosterone and Kidney Outcomes

Estimating GFR in Transgender Persons

Limitations

Conclusions

Footnotes

Ethics Approval and Consent to Participate

Consent for Publication

Availability of Data and MaterialsNot applicable.

Declaration of Conflicting Interests

Funding

ORCID iD

References