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Abstract

The age at diagnosis of pulmonary arterial hypertension (PAH) and the prevalence of cardiovascular (CV) risk factors are increasing. We sought to determine whether the response to drug therapy was influenced by CV risk factors in PAH patients. We studied consecutive incident PAH patients (n = 146) between January 1, 2008, and July 15, 2011. Patients were divided into two groups: the PAH–No CV group included patients with no CV risk factors (obesity, systemic hypertension, type 2 diabetes mellitus, permanent atrial fibrillation, mitral and/or aortic valve disease, and coronary artery disease), and the PAH-CV group included patients with at least one. The response to PAH treatment was analyzed in all the patients who received PAH drug therapy. The PAH–No CV group included 43 patients, and the PAH-CV group included 69 patients. Patients in the PAH–No CV group were younger than those in the PAH-CV group (P < 0.0001). In the PAH–No CV group, 16 patients (37%) improved on treatment and 27 (63%) did not improve, compared with 11 (16%) and 58 (84%) in the PAH-CV group, respectively (P = 0.027 after adjustment for age). There was no difference in survival at 30 months (P = 0.218). In conclusion, in addition to older age, CV risk factors may predict a reduced response to PAH drug therapy in patients with PAH.

Keywords

pulmonary arterial hypertension cardiovascular risk factors pulmonary arterial hypertension–targeted treatment

INTRODUCTION

Pulmonary arterial hypertension (PAH) is a rare progressive disease that leads to right heart failure and death.¹ PAH drug therapies have significantly improved symptoms, hemodynamics, and exercise capacity in patients with PAH.^2–4 The age at diagnosis of PAH has been gradually shifting to older age over the last decade,^5–8 while the United Kingdom and Ireland registry has identified a less good outcome in older compared with younger patients,⁷ and COMPERA (Comparative, Prospective Registry of Newly Initiated Therapies for Pulmonary Hypertension) has shown that older patients respond less well to PAH drugs.⁸

As patients age, there is an increase in the prevalence of cardiovascular (CV) risk factors predisposing to left heart disease.^6–8 Postcapillary pulmonary hypertension (PH) is driven by left heart disease and according to current guidelines should not be treated by PAH drugs.^9,10 Given that most of the randomized controlled trials of PAH drug therapies have included younger patients,^2–4 it is an open question whether these therapies are equally beneficial in patients with coexisting CV risk factors that may affect the left heart.

In this study, we sought to determine whether the response to PAH drug therapy in patients with PAH was influenced by conventional CV risk factors. We compared PAH patients to those without CV risk factors as well as to patients with PH due to left heart disease to examine whether they share some of the characteristics of left heart disease.

METHODS

Study design: definitions

This study was conducted in the National Pulmonary Hypertension Service at Hammersmith Hospital, London, which is one of seven nationally designated referral centers in the United Kingdom. We collected and examined data on consecutive, incident PH patients seen and investigated between January 1, 2008, and July 15, 2011. Incident PH patients were defined as patients with PH presenting for the first time to a specialist PH center who had never received PAH drug therapy. All patients underwent investigation of PH according to current guidelines.^9,10 PH was defined by mean pulmonary arterial pressure (mPAP) of ≥25 mmHg on cardiac catheterization.^9,10

We divided the patients into two groups according to the presence of CV risk factors: group 1 had no risk factors, and group 2 had at least one risk factor (Fig. 1). These risk factors included obesity, systemic hypertension, type 2 diabetes mellitus, permanent atrial fibrillation, aortic and/or mitral valve disease, and coronary artery disease.^11–16

Figure 1.

Consort diagram of the study. PH: pulmonary hypertension; CV: cardiovascular; PVH: pulmonary venous hypertension; CTEPH: chronic thromboembolic pulmonary hypertension; PAH: pulmonary arterial hypertension.

Systemic hypertension was defined by systolic blood pressure of >140 mmHg and/or diastolic blood pressure of >90 mmHg recorded in more than two measurements, by physician-documented history of hypertension, or by chronic use of antihypertensive medications. Diabetes mellitus was defined by the presence of a physician-documented history or prescription of oral hypoglycemic agents or insulin for the treatment of hyperglycemia. Permanent atrial fibrillation was defined as atrial fibrillation accepted by patient and physician.¹⁷ Coronary artery disease was defined by the presence of physician-documented history, known coronary stenosis of >50%, prior history of myocardial infarction, previous percutaneous coronary intervention, coronary artery bypass grafting, or abnormal stress test consistent with myocardial ischemia. Obesity was defined by a body mass index of ≥30 (calculated as the weight in kilograms divided by the square of height in meters). Valve disease was defined by at least moderate mitral stenosis, mitral regurgitation, aortic stenosis, and/or aortic regurgitation demonstrated by echocardiography according to current guidelines.¹⁸

We further divided the patients of groups 1 and 2 into two additional groups according to the presence of pre- or postcapillary PH (Fig. 1). Precapillary PH was defined by mPAP of ≥25 mmHg, pulmonary arterial wedge pressure (PAWP) of ≤15 mmHg, and/or left ventricular end-diastolic pressure (LVEDP) of ≤16 mmHg and normal or reduced cardiac output, and postcapillary PH was defined as mPAP of ≥25 mmHg, PAWP of >15 mmHg, and/or LVEDP of >16 mmHg and normal or reduced cardiac output.^10,19

As the number of patients with left ventricular systolic dysfunction who were referred to our center was small, we excluded them on the basis of left ventricular ejection fraction of ≤50% measured on the echocardiogram by Simpson's method.¹⁹ We also excluded patients with chronic thromboembolic PH and PH due to lung disease and/or hypoxia.

Variables analyzed

We analyzed parameters identified and obtained during the first visit to the clinic with the exception of hemodynamic data. As the time between the first visit to the clinic and catheterization did not exceed 3 weeks, we assumed that these variables had not significantly changed in this time.

We conducted a 6-minute walk test (6MWT) according to American Thoracic Society guidelines.²⁰ We examined the electrocardiogram (ECG) and determined heart rhythm, the presence of complete right bundle branch block (defined by rSR′ or qRs morphology in V₁ lead and QRS duration of >120 ms), a dominant R wave in V₁ lead (R > S), right ventricular strain (ST segment deviation and T-wave inversion in V₁–V₃),²¹ and right axis deviation (QRS axis of >100°).

All echocardiograms recorded at the first visit were reviewed. The measurements were made according to American Society of Echocardiography guidelines.²² We also calculated the ratio of end-diastolic basal right ventricular diameter (at the tips of the tricuspid valve) to end-diastolic basal left ventricular diameter (at the tips of the mitral valve) in the 4-chamber view (RV/LV ratio) as a marker of the ventricular predominance in terms of dimensions.²³ The echocardiographic variables that had not been measured in the first instance were measured retrospectively off-line, on stored images. All of the echocardiographic variables were measured independently by two echocardiographers who were masked to the hemodynamic data.

Finally, we analyzed hemodynamics. Cardiac output was measured using the Fick principle with estimated oxygen consumption, cardiac index was calculated as cardiac output divided by body surface area, and pulmonary vascular resistance (PVR) was calculated as the difference between mPAP and PAWP divided by pulmonary flow. Transpulmonary gradient was calculated as mPAP minus PAWP, and diastolic pulmonary pressure difference was calculated as diastolic pulmonary arterial pressure minus PAWP.

Response to treatment

The majority of patients with PAH received PAH drug therapies. The reasons why some of the PAH patients were not started on treatment included drug therapy not being funded at that time in England for New York Heart Association (NYHA) functional class II or patients having PAH related to conditions in which the underlying cause needed to be treated prior to considering PAH drugs (e.g., closure of atrial septal defects, immunosuppression for systemic lupus erythematosus).

We identified the response to PAH drugs at the last available patient visit to the PH clinic compared with the baseline before treatment was commenced. Improvement on treatment was defined as a combined improvement in NYHA functional class plus an increase in 6MWT distance (6MWTD) of ≥15% compared with baseline. Patients who failed to meet these criteria were classified as having no improvement on treatment.

Worsening on treatment was defined as a combined deterioration of NYHA functional class after treatment or failure to improve from NYHA functional class IV plus a decrease in 6MWTD of ≥15% or death. The patients who did not meet the criteria of improvement or worsening were considered to be stable.

Combination therapy included a phosphodiesterase 5 inhibitor plus an endothelin receptor antagonist or a phosphodiesterase 5 inhibitor and/or an endothelin receptor antagonist plus prostacyclin.

Statistical analysis

PH patients were assigned to one of four groups: PAH with no CV risk factors (PAH–No CV group), PAH with CV risk factors (PAH-CV group), PH related to left heart disease with CV risk factors (PVH-CV group), and PH with postcapillary hemodynamics and no CV risk factors (PVH–No CV group; Fig. 1).

We compared the groups as follows: PAH–No CV to PAH-CV and PAH-CV to PVH-CV. The PVH–No CV group included only a small number of patients (7 patients) with variable etiology of left heart disease and was not analyzed further.

Categorical data are expressed as number of patients (%), while continuous data are presented as median (inter quartile range), as some were not normally distributed. Between-group differences were assessed by the χ² test for categorical variables and by the Kruskal-Wallis test for continuous variables.

As we compared a large number of variables between the groups, we applied a post hoc Bonferroni correction for multiple comparisons, which raised the threshold of statistical significance to 0.001. We report a trend toward a difference when a P value was <0.05. We did not apply a Bonferroni correction for the comparison of response to treatment.

As patients in the PAH-CV group were significantly older than those in the PAH–No CV group, we performed age adjustment using logistic regression to determine differences in clinical characteristics, response to PAH treatment, and survival between these groups.

Survival was estimated from the time of PH diagnosis to all-cause mortality or end of study. Univariate Cox regression was used to test for differences between survival probabilities of different PH groups. For the survival analysis, all patients were censored at a fixed date (March 13, 2013) or on the date of death if earlier. All statistical analyses were performed using SPSS (ver. 10).

RESULTS

PAH–No CV group versus PAH-CV group

Differences between the PAH–No CV and PAH-CV groups are listed in Tables 1and 2. Patients in the PAH-CV group were significantly older than those without CV risk factors. There was no difference in the types of PAH, symptoms, clinical signs, or 6MWTD across the groups (Table 1). The ECG findings were not different after adjustment for age and Bonferroni correction (Table 2). There was no significant difference in medications, brain natriuretic peptide levels, and echocardiographic variables. On echocardiogram there was a trend toward greater left ventricular posterior wall thickness and left atrial diameter in the PAH-CV group, while for hemodynamics there was a trend toward higher PAWP and LVEDP (Table 2).

Table 1.

Comparison of demographic and clinical data

				P value
Variable	PAH–No CV (n = 50)	PAH-CV (n = 96)	PVH-CV (n = 110)	PAH–No CV vs. PAH-CV	PAH-CV vs. PVH-CV
Demographics
Age, years	46 (34–64)	65 (59–73)	70 (60–76)	<0.0001	0.045
Female, no. (%)	30 (60)	57 (59.4)	69 (62.7)	0.942	0.622
BMI	25 (21.2–26.8)	30.5 (24.6–35.5)	29.7 (26–38)	<0.0001/<0.0001	0.215
BSA, m²	1.73 (1.6–1.9)	1.83 (1.7–2.05)	1.91 (1.78–2.12)	<0.0001/<0.0001	0.043
Cardiovascular comorbidities, no. (%)
Obesity		49 (52.7)	46/92 (50)		0.715
Systemic hypertension		56 (58.3)	88 (80)		0.001
Diabetes mellitus		28 (29.2)	48 (43.6)		0.032
Atrial fibrillation		21 (21.9)	45 (40.9)		0.003
Valve disease		9 (9.4)	17 (15.5)		0.190
Coronary artery disease		25 (26)	34 (30.9)		0.441
No. of cardiovascular risk factors		1.5 (1–3)	2 (2–4)		<0.0001
PAH type, no. (%)
Idiopathic PAH	23 (46)	59 (61.5)		0.222/0.874a
Associated with connective tissue disease	9 (18)	19 (19.8)
Associated with congenital heart disease	5 (10)	6 (6.3)
Portopulmonary	5 (10)	5 (5.2)
PVOD	2 (4)	3 (3.1)
Other	6 (12)	4 (4.2)
NYHA functional class, no. (%)
I	0 (0)	1 (1)	1 (0.9)	0.003/0.043b	0.051b
II	15 (30)	7 (7.3)	16 (14.7)
III	22 (44)	59 (61.5)	76 (68.8)
IV	13 (26)	29 (30.2)	17 (15.6)
Clinical symptoms and signs
Orthopnea, no. (%)	3/28 (10.7)	17/69 (24.6)	23/74 (31.1)	0.125/0.314	0.391
Heart rate, bpm	82 (75–98)	80 (72–92)	79 (69–89)	0.247/0.517	0.085
Systolic blood pressure, mmHg	128 (115–133)	138 (120–158)	147 (132–160)	0.003/0.042	0.024
Peripheral edema, no. (%)	19 (38)	42/95 (44.2)	66 (60)	0.472/0.908	0.020
Six-minute walk test
Distance, m	276 (78–405)	180 (96–276)	180 (93–310)	0.021/0.321	0.976
Pretest SpO₂, %	97 (93–98)	95 (91–98)	96 (93–97)	0.153/0.713	0.356
Posttest SpO₂, %	94 (85–97)	91 (86–97)	93 (90–96)	0.520	0.424
BNP, ng/L	274 (124–762)	395 (101.4–1127)	324 (185–817)	0.280	0.467
Medications, no. (%)
Diuretics	22 (44)	62 (64.6)	88 (80)	0.017/0.335	0.013
Warfarin	15 (30)	33 (34.4)	49 (44.5)	0.593/0.795	0.137
Angiotensin-converting enzyme inhibitors	5 (10)	35 (36.5)	41 (37.3)	0.001/0.054	0.904
Angiotensin II AT1 receptor blockers	0 (0)	13 (13.5)	38 (34.5)	0.006/0.999	<0.0001
Digoxin	3 (6)	9 (9.5)	24 (21.8)	0.471/0.553	0.016
β-Blockers	3 (6)	21 (21.9)	47 (42.7)	0.014/0.179	0.001
Statins	4 (8)	36 (37.5)	61 (56)	0.0001/0.007	0.008

Refers to all types of PAH.

Refers to all World Health Organization functional classes.

Table 2.

Comparison of electrocardiographic, echocardiographic, and hemodynamic data

				P value
Variable	PAH–No CV (n = 50)	PAH-CV (n = 96)	PVH-CV (n = 110)	PAH–No CV vs. PAH-CV	PAH-CV vs. PVH-CV
Electrocardiography
Sinus rhythm, no. (%)	49/49 (100)a	72/93 (77.4)b	61/105 (57.5)c	<0.0001/0.998	0.003
RBBB, no. (%)	5/49 (10.2)	7/93 (7.5)	5/105 (4.8)	0.586/0.337	0.416
R wave dominant in lead V₁, no. (%)	30/49 (61.2)	37/93 (39.8)	19/105 (18.1)	0.015/0.424	0.001
Right ventricular strain, no. (%)	31/49 (63.3)	40/93 (43)	23/105 (21.9)	0.022/0.541	0.001
Right axis deviation, no. (%)	31/49 (63.3)	32/93 (34.4)	15/105 (14.3)	0.001/0.011	0.001
PR interval, ms	152 (143–161)	164 (150–182)	154 (140–179)	0.006/0.045	0.110
QRS duration, ms	97 (84–108)	94 (86–104)	94 (84–106)	0.607/0.845	0.934
Echocardiography
Left ventricular end-diastolic diameter, cm	4.3 (3.8–4.6)	4.2 (3.9–4.6)	4.7 (4.2–5.1)	0.901/0.678	<0.0001
Interventricular septal thickness, cm	0.9 (0.7–1)	1.0 (0.9–1.1)	1.0 (0.9–1.1)	0.007/0.387	0.462
Left ventricular posterior wall thickness, cm	0.9 (0.8–1)	1.0 (0.9–1.1)	1.0 (0.9–1.1)	<0.0001/0.014	0.353
E/E′ ratio	5 (3.9–7.3)	7.5 (5–11)	9.1 (7–14)	0.091/0.547	0.009
RV/LV ratio	1.35 (1.07–1.68)	1.22 (0.84–1.5)	0.92 (0.79–1.15)	0.120/0.303	<0.0001
Peak velocity of tricuspid regurgitation, m/s	4.2 (3.7–4.6)	4.1 (3.6–4.5)	3.7 (3.3–4.1)	0.147/0.375	<0.0001
Right atrial volume, mL	80 (65–100)	105 (76–136)	105 (78–124)	0.029/0.507	0.713
Left atrial diameter, cm	3 (3–4)	4 (3–4)	5 (4–5)	0.001/0.024	<0.0001
LAVI	36 (26–47)	44 (31–57)	55 (38–70)	0.046/0.921	0.001
TAPSE, mm	15 (11–19)	15 (13–20)	16 (13–21)	0.608/0.587	0.803
Right ventricular TDI S wave, cm/s	9 (8.6–11)	11 (9–12)	9 (8–12)	0.073/0.195	0.041
Right ventricular Tei index	0.7 (0.57–0.8)	0.6 (0.47–0.74)	0.5 (0.38–0.65)	0.142/0.338	0.067
Pericardial effusion, no. (%)	9 (18)	23 (24)	9 (8.2)	0.409/0.739	0.002
Hemodynamics
mPAP, mmHg	51 (44–59)	43 (33–56)	41 (33–53)	0.023/0.998	0.284
LVEDP, mmHg	8 (6–10)	10 (8–13)	18 (17–22)	0.001/0.007
PAWP, mmHg	10 (8–12)	12 (9–15)	21 (17–25)	0.002/0.008
mRAP, mmHg	7 (5–10)	10 (7–14)	15 (11–18)	0.023/0.016	<0.0001
RVEDP, mmHg	10 (6–14)	10 (7–15)	15 (9–18)	0.602/0.196	<0.0001
Transpulmonary gradient, mmHg	40 (32–47)	34 (20–44)	18 (12–28)	0.006/0.372
Diastolic pulmonary pressure difference, mmHg	22 (11–30)	18 (9–27)	2 (–3 to 11)	0.248/0.375
Cardiac index	2.2 (1.8–2.9)	2.2 (1.9–2.8)	2.1 (1.8–2.8)	0.893/0.926	0.564
Pulmonary vascular resistance, Wood units	11 (6–15)	8 (5–13)	5 (3–8)	0.039/0.732	<0.0001

Note: All continuous variables are expressed as median (interquartile range). In the P value column for PAH–No CV versus PAH-CV, the second P value is after age adjustment. After Bonferroni correction, the statistical threshold is P ≤ 0.001. P values in boldface type indicate statistically significant differences. PAH: pulmonary arterial hypertension; CV: cardiovascular risk factors; PVH: pulmonary venous hypertension; RBBB: right bundle branch block; RV/LV ratio: right ventricular basal end-diastolic/left ventricular basal end-diastolic diameter (in the 4-chamber view); LAVI: left atrial volume index; TAPSE: tricuspid annular plane systolic excursion; TDI: tissue Doppler imaging; mPAP: mean pulmonary arterial pressure; LVEDP: left ventricular end-diastolic pressure; PAWP: pulmonary arterial wedge pressure; mRAP: mean right atrial pressure; RVEDP: right ventricular end-diastolic pressure.

One patient had paced rhythm.

Two patients had paced rhythm, and in one case an electrocardiogram was not available.

Five patients had paced rhythm.

Response to treatment: survival analysis

Forty-three (86%) of 50 patients were started on PAH-targeted treatment in the PAH–No CV group, while 75 (78%) of 96 were started in the PAH-CV group. The mean follow-up time was 20 ± 11.3 months in the PAH–No CV group and 16.4 ± 10.9 months in the PAH-CV group (P = 0.290). Patients in the PAH–No CV group were 3.3 times more likely to show improvement on treatment than were patients in the PAH-CV group (odds ratio, 3.294 [95% confidence interval, 1.11–9.72]; P = 0.002 before and 0.027 after adjustment for age; Table 3). The difference in response to treatment was driven by less improvement in the PAH-CV group rather than more worsening. The number of CV risk factors did not significantly affect the response to PAH therapies. There was no difference between PAH-specific medications (monotherapy or combination therapy) prescribed in the two groups (Table 4).

Table 3.

Response to pulmonary arterial hypertension (PAH) drug therapy

	PAH–No CV group (n = 43)	PAH-CV group (n = 69)	P value for improvement vs. no improvement
Improvement	16 (37)	11 (16)	0.002/0.027a
No improvement	27 (63)	58 (84)
Stable	14 (33)	31 (45)
Worsening	13 (30)	27 (39)

Note: Data are no. (%). CV: cardiovascular risk factors.

After adjustment for age.

Table 4.

Pulmonary arterial hypertension (PAH) medications

Medication	PAH–No CV (n = 43)	PAH-CV (n = 75)	P value
Phosphodiesterase 5 inhibitors	36 (84)	62 (83)	0.356
Endothelin receptor antagonists	21 (49)	39 (52)	0.289
Prostacyclin analogues	6 (14)	14 (19)	0.125
Combination therapy	19 (44)	38 (51)	0.176

Note: Data are no. (%). CV: cardiovascular risk factors.

The mean follow-up time for survival analysis was 32.8 ± 16.3 months for the PAH–No CV group and 28.2 ± 13 months for the PAH-CV group. Over 3 years, there were 13 deaths (26%) and the mean survival time was 30 months (SE, 1.529) in the PAH–No CV group, while there were 34 deaths (35.4%) with a mean survival time of 28.7 months (SE, 1.119) in the PAH-CV group (P = 0.245). Over 5 years, there were 15 deaths (30%) and the mean survival time was 46.2 months (SE, 2.962) in the PAH–No CV group, while there were 38 deaths (39.5%) and the mean survival time was 42 months (SE, 2.290) in the PAH-CV group. The difference between the groups was not significant (P = 0.218).

PAH-CV group versus PVH-CV group

There was no significant difference in age and sex distribution between the PAH-CV and PVH-CV groups. Patients in the PVH-CV group had a significantly greater number of CV comorbidities (median, 2 vs. 1.5; P < 0.0001; Fig. 2). The two groups had no difference in symptoms, symptom severity, or clinical signs. Differences in ECG, echocardiogram, and hemodynamics are shown in Table 2.

Figure 2.

Number of cardiovascular comorbidities. Shown is the number of cardiovascular risk factors in the PAH-CV and PVH-CV groups. PAH: pulmonary arterial hypertension; CV: cardiovascular risk factors; PVH-CV: PH related to left heart disease with CV factors; PH: pulmonary hypertension; count: number of patients.

The mean follow-up time for the PVH-CV group was 26.2 ± 13 months. There were 29 deaths (26.3%), and the mean survival time was 47.7 months (SE, 2.330). Compared with the PAH-CV group, there was a trend toward better survival, although not statistically significant, in the PVH-CV group (P = 0.075).

DISCUSSION

This is the first study to examine the response to PAH therapies according to the presence of CV risk factors related to left heart disease. This study showed that PAH patients with CV risk factors are less likely to respond well in terms of their symptom severity and exercise capacity 16 months after starting PAH drug therapies than are PAH patients without CV risk factors. Data from COMPERA⁸ have shown that elderly idiopathic PAH patients respond less well to PAH therapies than younger ones. Age difference and less aggressive PAH treatment in the elderly group were mentioned as possible reasons for this difference. In our study, even after adjustment for age the less effective response to treatment in the older PAH group with CV comorbidities remained, while there was no difference in the drugs prescribed for the two groups.

right ventricular ischemia (in addition to ischemia caused by increased afterload), and diastolic dysfunction, exactly as CV risk factors do in the left ventricle,^39–41 resulting in right ventricular dysfunction and exercise limitation not responding to PAH drugs, which mainly act on pulmonary vasculature. Sildenafil, in additional to its beneficial effect on pulmonary vasculature, has been shown to have a positive direct effect on hypertrophied right ventricular myocardium by increasing its contractility in humans,⁴² but it was unable to prevent right ventricular diastolic dysfunction in animal models.⁴³ Of note, sildenafil seems to play a beneficial role in microvascular coronary dysfunction of the left ventricle in women after a single dose, although its long-term effects are not known.⁴⁴

Our study has shown that some of the phenotypic features of the PAH-CV group lie between those of the PAH–No CV and PVH-CV groups: compared with the PAH–No CV group, the PAH-CV group had a trend toward higher PAWP and LVEDP, which by definition are lower in the PVH-CV group. Increasing PAWP may increase right ventricular afterload and contribute to right ventricular dysfunction.²⁴ In addition, the PAH-CV group had values for PVR and left atrial size between those of the PAH–No CV and PVH-CV groups.

One possible interpretation for the different response to PAH therapies in our study would be a possible deleterious effect of these drugs in the presence of left heart disease. The trials of intravenous epoprostenol and bosentan in patients with left ventricular systolic dysfunction have shown either a negative or no effect on clinical outcomes.^25–27 On the contrary, sildenafil in patients with left ventricular systolic dysfunction has been shown to improve exercise capacity and hemodynamics.^28,29 The recent LEPHT study (Study to Test the Effects of Riociguat in Patients with Pulmonary Hypertension Associated with Left Ventricular Systolic Dysfunction) with riociguat, a novel soluble guanylate cyclase stimulator, in patients with left systolic heart failure did not achieve its primary end point (decrease in mPAP) despite an improvement in other hemodynamic parameters (cardiac index, PVR), while it was not powered to detect any clinical outcomes in the study groups.³⁰ In our study, patients with left ventricular systolic dysfunction were excluded; however, PAH patients with CV risk factors may have masked left ventricular diastolic dysfunction. Some of the PAH-CV group characteristics, such as age, CV risk factors, heart failure symptoms, left ventricular ejection fraction of >50%, and dilated left atrium, meet the inclusion criteria used in randomized clinical trials in patients with heart failure with preserved ejection fraction (HFpEF).^31–33 This suggests that the PAH-CV group overlapped or may have consisted of a subpopulation of patients with HFpEF who also have precapillary PH at rest. The relatively poor efficacy of PAH drugs in such patients would then be consistent with the findings of the RELAX (Evaluating the Effectiveness of Sildenafil at Improving Health Outcomes and Exercise Ability in People with Diastolic Heart Failure) trial, which showed that sildenafil failed to improve clinical status and exercise capacity in patients with HFpEF but not specifically with PH.³⁴ Whether the natural history of some of the patients in the PAH-CV group is to develop postcapillary hemodynamics at a later stage is not clear. Our results would not be consistent, however, with the positive results of sildenafil in selected patients with left ventricular hypertrophy, HFpEF, and PH, although exercise capacity was not investigated in this study.³⁵

The role of sildenafil has also been explored in the presence of CV comorbidities in animal models. In animals with diabetic cardiomyopathy, impaired glucose intolerance, triglyceridemia, and hypertensive cardiomyopathy, sildenafil has had a beneficial effect on left ventricular function.^36–38 Although the effect on the function of the right ventricle is not known, in light of these studies the potential harmful effect of PAH drugs in the presence of CV comorbidities seems to be a less likely explanation.

If the drugs themselves are not responsible for the less good response of exercise capacity to them, then a more restrained myocardium might provide an explanation. In the PAH-CV group, the presence of CV risk factors may have caused coronary microvascular dysfunction,

The worse response to treatment did not lead to worse survival in our study. On the contrary, in COMPERA⁸ survival was significantly worse among elderly idiopathic PAH patients than among younger ones after adjustment for age. This difference could be attributed to the smaller size and the shorter time of follow-up of our population or to a much older population in COMPERA.

This study also examined whether the PAH-CV group shared some common characteristics with the patients with PVH-CV. The two groups had no age or sex differences. The PVH-CV group had a significantly greater prevalence of systemic hypertension and a trend toward more atrial fibrillation, while the total number of CV risk factors was significantly higher than in the PAH group (Fig. 2). The PVH-CV patients were less likely to have a dominant R wave on the ECG, while they had a larger left ventricle with a smaller RV/LV ratio, a more dilated left atrium, and a lower peak velocity of tricuspid regurgitation on the echocardiogram. Finally, on cardiac catheterization the PVH-CV patients had higher mean right atrial pressure and right ventricular end-diastolic pressure but lower PVR, with no difference in mPAP and cardiac index. These findings are consistent with other studies examining pulmonary venous hypertension⁴⁵ and HFpEF⁴⁶ with PH populations. In terms of survival, the patients with postcapillary PH had a trend toward better survival than the two PAH groups, which is consistent with the ASPIRE (Assessing the Spectrum of Pulmonary Hypertension Identified at a Referral Centre) registry.⁴⁷

Study limitations

This is a single-center retrospective study, and for this reason we recognize that the findings require verification in other patient cohorts. Nevertheless, the findings concerning less treatment efficacy in the PAH-CV group are broadly consistent with registry data and add to an understanding of why some patients respond less well to drug therapy for PAH.

We chose to assess the response to treatment at the patient's last hospital visit rather than at a set time to describe at least a medium-term rather than simply a short-term response. While this does mean we followed up patients after different periods on treatment, we did not do so within 3 months of commencing PAH drug treatment. Finally, we did not measure the blood levels of PAH drugs to check patients' adherence to taking their medications or for unexpected drug interactions. It is possible that older patients taking more medications may not have taken their prescribed PAH drugs, and for this reason future studies should confirm that these drugs have been ingested.

Conclusions

This study shows that PAH patients with CV risk factors have a less satisfactory response to PAH drug therapies in terms of symptom severity and exercise capacity compared with PAH patients without CV risk factors and that this difference is not simply a result of age. With the diagnosis of PAH being made with increasing frequency in older patients, there is a need to further elucidate the mechanisms influencing the response to PAH drug therapies and to define the best management strategies in this population.

Footnotes

Source of Support: Nil.

Conflict of Interest: None declared.

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Response to Pulmonary Arterial Hypertension Drug Therapies in Patients with Pulmonary Arterial Hypertension and Cardiovascular Risk Factors

Abstract

Keywords

INTRODUCTION

METHODS

Study design: definitions

Variables analyzed

Response to treatment

Statistical analysis

RESULTS

PAH–No CV group versus PAH-CV group

Response to treatment: survival analysis

PAH-CV group versus PVH-CV group

DISCUSSION

Study limitations

Conclusions

Footnotes

References