Skip to main content
PMC home page
Frontiers in Cardiovascular Medicine logoLink to Frontiers in Cardiovascular Medicine
. 2022 Jan 17;8:809594. doi: 10.3389/fcvm.2021.809594

Prevalence of Sarcoidosis-Associated Pulmonary Hypertension: A Systematic Review and Meta-Analysis

Shijie Zhang 1,†, Xiang Tong 1,†, Tianli Zhang 1, Dongguang Wang 1, Sitong Liu 1, Lian Wang 1, Hong Fan 1,*
PMCID: PMC8801498  PMID: 35111830

Abstract

Background

Sarcoidosis-associated pulmonary hypertension (SAPH) is associated with poor prognosis, conferring up to a 10-fold increase in mortality in patients with sarcoidosis, but the actual prevalence of SAPH is unknown.

Methods

The PubMed, Embase, and Cochrane Library databases were systematically searched for epidemiological studies reporting the prevalence of SAPH up to July 2021. Two reviewers independently performed the study selection, data extraction, and quality assessment. Studies were pooled using random-effects meta-analysis.

Results

This meta-analysis included 25 high-quality studies from 12 countries, with a pooled sample of 632,368 patients with sarcoidosis. The prevalence of SAPH by transthoracic echocardiography in Europe, the United States and Asia was 18.8% [95% confidence interval (CI): 11.1–26.5%], 13.9% (95% CI: 5.4–22.4%) and 16.2% (95% CI: 7.1–25.4%) separately, and the overall pooled prevalence was 16.4% (95%CI: 12.2–20.5%). By right heart catheterization (RHC), the pooled prevalence of SAPH was 6.4% (95% CI: 3.6–9.1%) in general sarcoidosis population, and subgroup analyses showed that the prevalence of SAPH was 6.7% (95% CI: 2.4–11.0%) in Europe and 8.6% (95% CI: −4.1 to 21.3%) in the United States. Further, the prevalence of pre-capillary PH was 6.5% (95% CI: 2.9–10.2%). For the population with advanced sarcoidosis, the pooled prevalence of SAPH and pre-capillary PH by RHC was as high as 62.3% (95% CI: 46.9–77.6%) and 55.9% (95% CI: 20.1–91.7%), respectively. Finally, the pooled prevalence of SAPH in large databases with documented diagnoses (6.1%, 95% CI: 2.6–9.5%) was similar to that of RHC. Substantial heterogeneity across studies was observed for all analyses (I2 > 80%, P < 0.001).

Conclusions

The sarcoidosis population has a relatively low burden of PH, mainly pre-capillary PH. However, as the disease progresses to advanced sarcoidosis, the prevalence of SAPH increases significantly.

Keywords: sarcoidosis-associated pulmonary hypertension, sarcoidosis, pulmonary hypertension, prevalence, meta-analysis

Introduction

Sarcoidosis is an inflammatory disease characterized by multisystem non-caseating granulomas with unknown causes, which most commonly affects the lungs and its surrounding lymph nodes but can also involve other organs, including the liver, kidneys, brain, heart, eyes, skin, and sinuses (1). The prevalence of sarcoidosis and its clinical presentation vary greatly according to patient sex, age group, ethnicity, and geographical region (2, 3). Consistently, the incidence of sarcoidosis is the highest among African Americans and lowest among Asians (4). Many patients with sarcoidosis have favorable outcomes, with a significant proportion showing spontaneous remission without systemic therapy. However, a small number of cases progress to advanced sarcoidosis, which is the end-stage of sarcoidosis associated with significant mortality (5, 6). The mortality rate of sarcoidosis is ~5% (5, 7).

Pulmonary hypertension (PH) is a hemodynamic and pathophysiological state characterized by an increase in the mean pulmonary arterial pressure (≥25 mmHg); a subgroup of pre-capillary PH is defined by an additional criterion of a pulmonary arterial wedge pressure of ≤ 15 mmHg (8). PH is a well-recognized complication of sarcoidosis, resulting in poor prognosis (9–11). The development of sarcoidosis-associated PH (SAPH) confers up to a 10-fold increase in mortality in patients with sarcoidosis (7, 12). SAPH is also an independent cause of death in patients with advanced pulmonary sarcoidosis (5). Therefore, it is important to know the actual prevalence of PH in patients with sarcoidosis for timely screening and treatment.

To date, the actual prevalence of SAPH is unknown; however, the condition is associated with the stage at which patients are assessed for PH. In recent years, researchers have been interested in the prevalence of SAPH and extensive related studies have been conducted worldwide. However, the results are somewhat different for the limited sample sizes and these studies are individually underpowered to effectively address this issue. Although there are relevant literatures describing and discussing this topic (13, 14), there are no meta-analysis reporting the epidemiology of SAPH globally. Therefore, we performed a systematic review and meta-analysis to comprehensively calculate the prevalence of SAPH in general and advanced sarcoidosis populations.

Methods

Data Source and Search Strategy

This systematic review and meta-analysis followed the Meta-analysis of Observational Studies in Epidemiology (MOOSE) (Supplementary Table 1) (15) and Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) guidelines (Supplementary Table 2) (16) guidelines. We performed a systematic literature search of the PubMed, Embase, and Cochrane Library databases up to July 6, 2021. The search strategy was as follows: (sarcoidosis) AND [(pulmonary hypertension) OR (pulmonary arterial hypertension) OR (PH) OR (PAH)]. The language of the searched papers was English. All reference lists of the included studies were manually searched for additional studies. Moreover, we conducted a web-based search in Internet search engines (such as Baidu Scholar and Google Scholar). As the current meta-analysis was based on previously published studies, no ethical approval or patient consent was required.

Inclusion and Exclusion Criteria

The inclusion criteria were as follows: (1) observational study, including cross-sectional, prospective, and retrospective studies; (2) study involving the prevalence of SAPH (including pre-capillary PH and post-capillary PH); and (3) study providing the total number of sarcoidosis cases to calculate the standard error. The exclusion criteria were as follows: (1) missing essential information; (2) duplicated data used in different studies; and (3) reviews, meta-analyses, in vitro studies, and study protocols.

Data Extraction

Two authors (Zhang and Tong) used a pre-designed data extraction form to independently extract data from all eligible studies. A third investigator intervened when there was any disagreement or doubt. We extracted the following information: first author; year of publication; country; sample size; number of SAPH cases identified by transthoracic echocardiography (TTE); number of SAPH cases identified by right heart catheterization (RHC); and patient age, sex, ethnicity, smoking status, and sarcoidosis stage. Notably, in the included studies, if the probability of PH was judged to be high, intermediate, or low (or the PH severity was classified as mild, moderate, and severe), the high and intermediate probabilities (or moderate and severe PH) were defined as the presence of PH. The diagnostic criteria of SAPH in included studies are shown in Supplementary Table 3. Advanced disease is mainly for patients who are at risk for death or loss of organ function (5), so in our analysis, advanced sarcoidosis refers mainly to patients with Stage IV sarcoidosis, those for lung transplantation, and those with severe life-threatening symptoms. In the study that only provided medians and ranges for several groups, we transformed the data into mean and standard deviation (SD) according to the validated methods described by Wan et al. (17), and then combined the mean and SD of multiple groups. When necessary, we also requested further information from the corresponding authors of the original studies.

Quality Assessments

For the quality assessments, two authors (Zhang and Tong) independently assessed the risk of bias of the included studies using an adapted risk of bias tool for prevalence studies (Supplementary Table 4) (18). Selection, non-response, measurement, and analysis biases were assessed using this tool. The possible answers for every item were “low risk” or “high risk,” which were scored as “0” or “1.” Scores of 0–3, 4–6, and 7–10 were defined as low, moderate, and high risk of bias, respectively. Any disagreement was clarified and confirmed by a third investigator.

Data Analysis and Statistical Methods

In this study, all analyses were performed using Stata 12.0, with statistical significance set at P < 0.05. We applied a random-effects model to obtain a pooled prevalence and a corresponding 95% confidence interval (CI) from various studies. Heterogeneity was tested using χ2 and I2 tests. A P < 0.10 suggested significant between-study heterogeneity. Thresholds for the interpretation of I2 were as follows: 0– 40%: might not be important; 30–60%: may represent moderate heterogeneity; 50–90%: may represent substantial heterogeneity; 75–100%: considerable heterogeneity (19). Sensitivity analyses were conducted to explore the sources of heterogeneity of results across studies by sequentially excluding eligible studies. Publication bias was assessed by Egger's and Begg's tests, with P < 0.05, indicating potential bias. A trim-and-fill analysis was performed to identify possible asymmetry and assess the robustness of the conclusions. Publication bias was not assessed when fewer than 10 studies were included in our analysis. If there was significant heterogeneity, subgroup analysis was further performed.

Results

Study Characteristics

As shown in Figure 1, the initial literature search in the PubMed, Embase, and Cochrane Library databases and other sources identified 1,857 studies. After checking for duplicates, 575 studies were excluded. And 1,202 studies were removed after title and abstract review. Furthermore, three articles were excluded because they were reviews. The remaining 77 studies were further assessed for eligibility through a full-text review. Of these, 49 studies were subsequently excluded for a lack of usable data. Three studies were removed for duplicated data used in another study (13, 20, 21). Finally, the analysis included 25 studies (7, 11, 12, 22–43). The studies were conducted in the United States (n = 10), Europe (n = 9), and Asia (n = 6). Of these, 14 studies reported the prevalence of SAPH by TTE, 11 studies reported the prevalence of SAPH by RHC, and eight studies reported the prevalence of pre-capillary PH by RHC. Furthermore, four other studies were conducted using large databases with only documented records for the diagnosis of sarcoidosis and PH (25, 26, 28, 29). In addition, five studies included patients with advanced sarcoidosis (11, 12, 27, 37, 43); the others included the general sarcoidosis population. The basic characteristics of the included studies are shown in Table 1. The quality score of all included studies was 1–3 points, and all studies were deemed to have low risks of selection, non-response, measurement, and analysis biases (Supplementary Table 5).

Figure 1.

Figure 1

Open in a new tab

Flow diagram of the selection of studies for inclusion.

Table 1.

Characteristics of included studies.

Study Country Sarcoidosis SAPH
N Age Sex (M/F) Ethnicity Smoking (yes/no) SAPH by TTE (N) SAPH by RHC (N) Pre-capillary PH by RHC (N) SAPH from database (N) Age* Sex* (M/F) Sarcoidosis* stage (0/1/2/3/4)
Pabst et al. (34) Germany 111 52.2 ± 14.9 65/56 NR NR 23 5 4 N/A 66.25 ± 7.80 NR 0/0/0/3/1
Shorr et al. (43) USA 363 46 127/236 71.6% A-A NR NR 268 NR N/A 46.5 ± 7.8 97/171 NR
Huitema et al. (24) Netherlands 479 NR NR NR NR 42 17 NR N/A 58.7 ± 12.9 13/4 NR
Rapti et al. (33) Greece 313 54.08 ± 13.39 121/192 NR 110/203 37 9 NR N/A NR NR NR
Milman et al. (37) Demark 24 NR 16/8 Danish NR NR 19 18 N/A 46.61 ± 6.87 14/5 0/0/3/0/16
Sulica et al. (42) USA 354 NR NR NR NR 54 NR NR N/A 50.3 ± 1.6 17/37 2/2/7/4/23
Handa et al. (40) Japan 212 57.67 ± 14.30 55/157 Japanese 46/166 12 NR NR N/A 58.9 ± 13.0 7/5 2/3/1/4/2
Maimon et al. (35) Israel 127 56.70 ± 13.46 37/91 NR 39/88 36 NR NR N/A 64.3 ± 11 12/25 1/5/13/17/0
Baughman et al. (12) USA 130 53.04 ± 11.43 39/91 50.77% white NR NR 70 50 N/A 52 (24–76) 17/33 1/7/10/7/25
Gangemi et al. (27) USA 28 59.23 ± 6.35 13/15 78.57% black NR NR 11 NR N/A NR NR NR
Kirkil et al. (7) USA 452 50 (25–78) 139/313 68.8% white;
30.1% A-A		 NR NR NR 29 N/A NR NR NR
Huitema et al. (32) Netherlands 89 51.69 ± 11.19 60/29 NR NR 37 25 NR N/A 55.8 ± 9.0 16/9 0/0/0/0/25
Smedema et al. (30) Netherlands 87 53.27 ± 10.04 57/30 NR NR 15 NR NR N/A NR NR NR
Baughman et al. (39) USA 142 51 (26–81) 41/101 61.97% A-A NR NR NR 14 N/A NR NR NR
Nardi et al. (11) France 111 NR NR NR NR 33 NR NR N/A NR NR NR
Mirsaeidi et al. (31) USA 108 NR NR NR NR 6 NR NR N/A NR NR NR
Baughman et al. (41) USA 1,223 NR 370/853 56.50% white,
43.50% A-A		 NR NR 30 25 N/A NR NR NR
Bourbonnais et al. (38) USA 162 47 ± 12 38/124 88.3% A-A,
11.7% White		 23/139 35 25 22 N/A NR NR NR
Alhamad et al. (36) Saudi Arabia 96 50.47 ± 13.75 32/64 NR NR 20 NR NR N/A 49.2 ± 14.2 3/17 0/2/6/3/9
Utpat et al. (22) India 68 42.7 27/41 NR NR 9 NR NR N/A NR NR NR
Özen et al. (23) Turkish 55 52.7 ± 10.1 10/45 NR 6/49 8 3 0 N/A 64 ± 2.646 0/3 0/1/0/0/2
Tiosano et al. (25) Israel 3,993 64.2 ± 15.7 1,471/2,522 NR 1,342/2,651 N/A N/A N/A 269 NR NR NR
Serrano et al. (26) Spain 5,484 60.62 ± 16.28 2,395/3,089 NR NR N/A N/A N/A 337 NR NR NR
Frank et al. (28) Germany 9,106 55.4 ± 15.5 4,288/4,818 NR NR N/A N/A N/A 254 NR NR NR
Patel et al. (29) USA 609,051 55 ± 14 199,769/409,282 43.9% white,
49.5% black		 NR N/A N/A N/A 52,442 NR NR NR
Open in a new tab

NR, not reported; N/A, not applicable; A-A, African-American.

*

Data were extracted in the priority order of pre-capillary PH by RHC, SAPH by RHC, and SAPH by TTE.

Prevalence of Sarcoidosis-Associated Pulmonary Hypertension by Transthoracic Echocardiography

Fourteen studies (11, 22–24, 30–36, 38, 40, 42) reported the prevalence of SAPH by TTE. Among them, one study targeted a population with advanced sarcoidosis, among which the prevalence of SAPH by TTE was 29.7% (11). In the general sarcoidosis population, the prevalence of SAPH by TTE in Europe, the United States, and Asia were 18.8% (95% CI: 11.1–26.5%), 13.9% (95% CI: 5.4–22.4%), and 16.2% (95% CI: 7.1–25.4%), separately. Overall, 334 of 2,261 sarcoidosis patients had SAPH by TTE and the pooled prevalence of SAPH by TTE was 16.4% (95% CI: 12.2–20.5%) (Figure 2). However, the heterogeneity between studies was substantial (I2 = 88.3%, P < 0.001). A sensitivity analysis to explore the effect of each study on the pooled meta-results showed no substantial changes in the pooled prevalence, indicating the stability of our meta-analysis (Supplementary Figure 1). In terms of publication bias, Begg's and Egger's tests revealed P-values of 0.059 and 0.003, respectively, indicating some publication bias. However, there was no indication of publication bias by trim-and-fill method (no trimming was performed, and the data were unchanged) (Supplementary Figure 2).

Figure 2.

Figure 2

Open in a new tab

Forest plot of the pooled prevalence of SAPH by TTE in the general sarcoidosis population. SAPH, sarcoidosis-associated pulmonary hypertension; TTE, transthoracic echocardiography.

Prevalence of Sarcoidosis-Associated Pulmonary Hypertension by Right Heart Catheterization

Eleven studies (12, 23, 24, 27, 32–34, 37, 38, 41, 43) described the prevalence of SAPH by RHC. Of these, seven studies focused on the general sarcoidosis population, while four studies focused on the population with advanced sarcoidosis. In 2,432 general sarcoidosis patients, 114 had SAPH by RHC, with an estimated prevalence of SAPH by RHC of 6.4% (95% CI: 3.6–9.1%) (Figure 3). Among the population with advanced sarcoidosis, the estimated prevalence of SAPH by RHC was 62.3% (95% CI: 46.9–77.6%) (Figure 4). Significant heterogeneity across studies was observed for both the general (I2 = 88.0%, P < 0.001) and advanced sarcoidosis (I2 = 89.4%, P < 0.001) populations. Sensitivity analysis revealed that our meta-results were stable in both groups (Supplementary Figures 3, 4).

Figure 3.

Figure 3

Open in a new tab

Forest plot of the pooled prevalence of SAPH by RHC in general sarcoidosis population. SAPH, sarcoidosis-associated pulmonary hypertension; RHC, right heart catheterization.

Figure 4.

Figure 4

Open in a new tab

Forest plot of the pooled prevalence of SAPH by RHC in advanced sarcoidosis population. SAPH, sarcoidosis-associated pulmonary hypertension; RHC, right heart catheterization.

Subgroup analyses by geographical region showed persisting heterogeneity. The pooled prevalence of SAPH by RHC was 6.7% (95% CI: 2.4–11.0%) in Europe and 8.6% (95% CI: −4.1 to 21.3%) in the United States for the general sarcoidosis population (Figure 5).

Figure 5.

Figure 5

Open in a new tab

Subgroup analysis of the prevalence of SAPH by RHC in the general sarcoidosis population by geographical regions. SAPH, sarcoidosis-associated pulmonary hypertension; RHC, right heart catheterization.

Prevalence of Sarcoidosis Associated Pre-capillary Pulmonary Hypertension by Right Heart Catheterization

Eight studies (7, 12, 23, 34, 37–39, 41) showed the prevalence of pre-capillary PH by RHC in patients with sarcoidosis, six of which focused on the general sarcoidosis population. In the general sarcoidosis population, the estimated prevalence of pre-capillary PH by RHC was 6.5% (95% CI: 2.9–10.2%) (Figure 6), with a high degree of heterogeneity across studies (I2 = 89.3%, P < 0.001). Sensitivity analysis revealed that our meta-results were stable (Supplementary Figure 5). In addition, two studies reported the prevalence of advanced sarcoidosis, with a pooled prevalence of pre-capillary PH by RHC of 55.9% (95% CI: 20.1–91.7%) (Figure 7).

Figure 6.

Figure 6

Open in a new tab

Forest plot of the pooled prevalence of pre-capillary PH by RHC in general sarcoidosis population. PH, pulmonary hypertension; RHC, right heart catheterization.

Figure 7.

Figure 7

Open in a new tab

Forest plot of the pooled prevalence of pre-capillary PH by RHC in the population with advanced sarcoidosis. PH, pulmonary hypertension; RHC, right heart catheterization.

Prevalence of Sarcoidosis-Associated Pulmonary Hypertension in Large Databases With Documented Records for Diagnoses

Four studies (25, 26, 28, 29) used data on the prevalence of SAPH in large databases with documented records for diagnoses of sarcoidosis and PH (i.e., the chronic disease registry of Clalit Health Services in Israel, the Spanish National Hospital Discharge Database, the patient-individual health insurance claims data in Germany, and the National Inpatient Sample database in the United States). Among 627,634 sarcoidosis records, 53,302 had PH. The pooled prevalence of SAPH was 6.1% (95% CI: 2.6–9.5%) (Figure 8), with a non-negligible heterogeneity (I2 = 99.7%, P < 0.001). Sensitivity analysis revealed the stability of our meta-analysis results (Supplementary Figure 6).

Figure 8.

Figure 8

Open in a new tab

Forest plot of the pooled prevalence of SAPH in large databases with documented diagnoses. SAPH, sarcoidosis-associated pulmonary hypertension.

Discussion

Sarcoidosis can affect multiple organs, including the lungs, liver, kidneys, brain, heart, eyes, skin, and sinuses, and can cause a variety of complications. Among them, cardiovascular complications, such as conduction abnormalities, arrhythmias, heart failure, and PH, are associated with higher mortality (14, 44, 45). SAPH is closely associated with poor prognosis, conferring up to a 10-fold increase in mortality in patients with sarcoidosis. Therefore, estimating the prevalence of SAPH is critical to the treatment and prognosis of sarcoidosis and essential for adequate health services planning and organization.

This is the first comprehensive meta-analysis to estimate the prevalence of SAPH in patients with sarcoidosis. Twenty-five high-quality studies from 12 countries met the inclusion criteria, with a pooled sample of 632,368 patients with sarcoidosis. In the general sarcoidosis population, the pooled prevalence of SAPH was 16.4% by TTE and 6.4% by RHC but was as high as 62.3% by RHC in the population with advanced sarcoidosis. Furthermore, the estimated prevalence of pre-capillary PH by RHC was 6.5% in the general sarcoidosis population and 55.9% in the population with advanced sarcoidosis. The prevalence of SAPH in large databases with documented diagnoses was 6.1%.

The mechanisms of PH in sarcoidosis patients are unclear and multifactorial. The possible triggers include progressive pulmonary fibrosis and hypoxic vasoconstriction (46), small vessel inflammatory vasculopathy (46, 47), diffuse alveolar-capillary multiplication (48, 49), pulmonary veno-occlusive disease (50), chronic thromboembolism and non-thromboembolic pulmonary embolism (51–53), extrinsic compression of pulmonary vessels caused by lymphadenopathy (54), myocardial involvement (55), sleep-disordered breathing (56), and liver dysfunction causing portopulmonary hypertension and anemia (14). Many confounders also affect the prevalence of SAPH, particularly the stage at which sarcoidosis patients are assessed (14). In our study, SAPH occurred much more frequently in patients with advanced sarcoidosis.

Surprisingly, our meta-analysis showed that the prevalence of pre-capillary PH by RHC (6.5%) was similar to that for SAPH by RHC (6.4%), or even slightly higher in general sarcoidosis patients, mainly because the studies included in each analysis were not completely consistent. To address this problem, we performed a meta-analysis of four studies (23, 34, 38, 41) that reported both the prevalence of PH and pre-capillary PH by RHC for general sarcoidosis patients, the results of which showed that the prevalence of SAPH by RHC (6.5%) (Supplementary Figure 7) was higher than that of pre-capillary PH (5.8%) (Supplementary Figure 8). In all included studies, only two studies (31, 33) excluded patients with cardiac dysfunction. Thus, our results showed that SAPH was mostly pre-capillary PH to some extent, with few parts related to cardiovascular conditions (mainly left heart disease) (57).

We also estimated the prevalence of SAPH in large databases with documented records for diagnoses. Surprisingly, the prevalence of SAPH in the large databases (6.1%) was similar to that by RHC (6.4%). These results indicated that the clinical diagnosis of SAPH mainly depends on RHC rather than TTE. The higher prevalence of PH by TTE than that by RHC is mainly based on the peak tricuspid regurgitation velocity or an estimated systolic pulmonary arterial pressure, which can only assign the echocardiographic probability of PH. Finally, the gold standard for the diagnosis of PH is RHC (8). When interpreted in a clinical context, TTE should always be performed initially in cases of suspected PH because TTE is non-invasive and cheaper, and if there are indications of PH, RHC should be considered to confirm the diagnosis of PH. In addition, TTE can help detect the cause of PH.

The presence of SAPH is an independent risk factor for poor prognosis in patients with sarcoidosis (46, 58, 59). As this meta-analysis aimed to calculate the prevalence of SAPH to inform clinic settings, attention should be paid to therapy after the confirmation of SAPH. The pathophysiology of SAPH is relevant to individual treatment. Currently, the approved medical therapies for PH are mainly for patients with group 1 pulmonary arterial hypertension (PAH); however, SAPH may be somewhat similar to PAH (54). Studies on PAH-directed therapies in the treatment of SAPH have demonstrated that pulmonary vasodilators (mainly referred to as endothelin receptor antagonists, phosphodiesterase inhibitors, and prostacyclins) can improve hemodynamics and functional status (21, 60–64). Additional treatments for SAPH include combination therapy with pulmonary vasodilators and immunomodulation, diuretics for volume optimization, stenting for mechanical vascular obstruction, pulmonary endarterectomy, balloon pulmonary angioplasty, and even lung transplantation (14, 54).

In our meta-analysis, the heterogeneity between studies was substantial, with many analyses showing I2 > 80%. Previous meta-analyses on prevalence studies have reported similar results (65, 66). The subgroup analyses failed to determine the reasons for this significant heterogeneity. There was insufficient information or quantity of studies to conduct subgroups according to sex, smoking, and the stage of sarcoidosis. The incidence of sarcoidosis in different races is different and evaluating the impact of ethnicity on SAPH is of significance. However, few included studies reported information on ethnicity and detailed data on the prevalence of SAPH in different races were not available. Thus, this study could not conduct a subgroup analysis by ethnicity. SAPH is also related to the severity of lung disease and chronic hypoxemia, but there was insufficient information to analyze the severity of PH based on current published literature. In addition, the inconsistent use of TTE and RHC to confirm the diagnosis of PH in all included studies contributed to the heterogeneity.

This study has several strengths. First, this was the first meta-analysis to estimate the prevalence of SAPH. Second, the 25 high-quality included studies from 12 countries provided a sufficient sample size with a pooled sample of 632,368 patients with sarcoidosis, which is powered to effectively address this issue. Third, our study assessed the prevalence of SAPH from multiple perspectives, including TTE, RHC, and data from a large database with documented records for diagnoses, as well as the prevalence of pre-capillary PH (a subgroup of PH) in patients with sarcoidosis. Nevertheless, this study also has some limitations arising from the included studies. First, because the prevalence of SAPH was not the main focus but was rather integrated into some studies, the reporting was often suboptimal for the purpose of this meta-analysis. Second, our meta-analysis identified significant publication bias, particularly regarding the prevalence of SAPH by TTE, which might be associated with the small sample sizes in most of the included studies and the English language restriction during study screening. Third, the included studies were concentrated in the United States (n = 10), Europe (n = 9), and Asia (n = 6), which might affect the generalizability of the findings. Finally, some analyses included small numbers of studies, resulting in limited statistical confidence. Despite these limitations, we were able to minimize bias throughout the entire analysis process.

Conclusions

Estimating the prevalence of SAPH is essential for adequate planning and organizing health services. Based on the available literature, the pooled prevalence of SAPH was 16.4% by TTE and 6.4% by RHC in the general sarcoidosis population but was as high as 62.3% by RHC in the population with advanced sarcoidosis. The estimated prevalence of pre-capillary PH by RHC was 6.5% in the general sarcoidosis population and 55.9% in the population with advanced sarcoidosis. To yield more accurate prevalence estimates, more high-quality cohort studies are warranted and procedures and prevalence studies should be standardized.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Author Contributions

HF and XT conceived of the study. SZ, XT, and TZ performed the literature search and selection, data extraction, and assessment of risk of bias. SZ, TZ, DW, SL, and LW carried out the data analysis. SZ drafted the manuscript. All authors critically revised the article and approved the final draft for publication.

Funding

This study was supported by China Postdoctoral Science Foundation (2020M673259), Post-Doctor Research Project, West China Hospital, Sichuan University (2020HXBH013), and 1•3•5 project for disciplines of excellence–Clinical Research Incubation Project, West China Hospital, Sichuan University (2019HXFH008).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcvm.2021.809594/full#supplementary-material

Supplementary Figure 1

Results of the sensitivity analysis of the prevalence of SAPH by TTE. SAPH, sarcoidosis-associated pulmonary hypertension; TTE, transthoracic echocardiography.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 2

Results of the trim-and-fill analysis of SAPH by TTE in the general sarcoidosis population. SAPH, sarcoidosis-associated pulmonary hypertension; TTE, transthoracic echocardiography.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 3

Results of the sensitivity analysis of the prevalence of SAPH by RHC in the general sarcoidosis population. SAPH, sarcoidosis-associated pulmonary hypertension; RHC, right heart catheterization.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 4

Results of the sensitivity analysis of the prevalence of SAPH by RHC in the population with advanced sarcoidosis. SAPH, sarcoidosis-associated pulmonary hypertension; RHC, right heart catheterization.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 5

Results of the sensitivity analysis of the prevalence of pre-capillary PH by RHC in the general sarcoidosis population. PH, pulmonary hypertension; RHC, right heart catheterization.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 6

Results of sensitivity analysis of the prevalence of SAPH based on documented diagnoses in large databases. SAPH, sarcoidosis-associated pulmonary hypertension.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 7

Forest plot of the pooled prevalence of SAPH for studies reporting both PH and pre-capillary PH. SAPH, sarcoidosis-associated pulmonary hypertension; PH, pulmonary hypertension.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 8

Forest plot of the pooled prevalence of pre-capillary PH in sarcoidosis patients for studies reporting both PH and pre-capillary PH. PH, pulmonary hypertension.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Table 1

MOOSE checklist (15).

Click here for additional data file. (2.3MB, zip)
Supplementary Table 2

PRISMA checklist.

Click here for additional data file. (2.3MB, zip)
Supplementary Table 3

Diagnostic criteria of pulmonary hypertension in included studies.

Click here for additional data file. (2.3MB, zip)
Supplementary Table 4

Risk of bias quality assessment tool.

Click here for additional data file. (2.3MB, zip)
Supplementary Table 5

Quality assessment of included studies.

Click here for additional data file. (2.3MB, zip)

References

  • 1.Raghu G, Berman JS, Govender P. Treatment of sarcoidosis. Am J Resp Crit Care Med. (2018) 197:P9–10. 10.1164/rccm.1976P9 [DOI] [PubMed] [Google Scholar]
  • 2.Zhou Y, Gerke AK, Lower EE, Vizel A, Talwar D, Strambu I, et al. The impact of demographic disparities in the presentation of sarcoidosis: a multicenter prospective study. Respir Med. (2021) 187:106564. 10.1016/j.rmed.2021.106564 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Judson MA, Boan AD, Lackland DT. The clinical course of sarcoidosis: presentation, diagnosis, and treatment in a large white and black cohort in the United States. Sarcoid Vasc Diffuse Lung Dis. (2012) 29:119–27. [PubMed] [Google Scholar]
  • 4.Grunewald J, Grutters JC, Arkema EV, Saketkoo LA, Moller DR, Muller-Quernheim J. Sarcoidosis. Nat Rev Dis Primers. (2019) 5:45. 10.1038/s41572-019-0096-x [DOI] [PubMed] [Google Scholar]
  • 5.Baughman RP, Wells A. Advanced sarcoidosis. Curr Opin Pulm Med. (2019) 25:497–504. 10.1097/MCP.0000000000000612 [DOI] [PubMed] [Google Scholar]
  • 6.Shlobin OA, Nathan SD. Management of end-stage sarcoidosis: pulmonary hypertension and lung transplantation. Eur Respir J. (2012) 39:1520–33. 10.1183/09031936.00175511 [DOI] [PubMed] [Google Scholar]
  • 7.Kirkil G, Lower EE, Baughman RP. Predictors of mortality in pulmonary sarcoidosis. Chest. (2018) 153:105–13. 10.1016/j.chest.2017.07.008 [DOI] [PubMed] [Google Scholar]
  • 8.Galie N, Humbert M, Vachiery JL, Gibbs S, Lang I, Torbicki A, et al. 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: the joint task force for the diagnosis and treatment of pulmonary hypertension of the European society of cardiology (ESC) and the European respiratory society (ERS): Endorsed by: association for European paediatric and congenital cardiology (AEPC), international society for heart and lung transplantation (ISHLT). Eur Respir J. (2015) 46:903–75. 10.1183/13993003.01032-2015 [DOI] [PubMed] [Google Scholar]
  • 9.Shlobin OA, Kouranos V, Barnett SD, Alhamad EH, Culver DA, Barney J, et al. Physiological predictors of survival in patients with sarcoidosis-associated pulmonary hypertension: results from an international registry. Eur Respir J. (2020) 55:1901747. 10.1183/13993003.01747-2019 [DOI] [PubMed] [Google Scholar]
  • 10.Boucly A, Cottin V, Nunes H, Jaïs X, Tazi A, Prévôt G, et al. Management and long-term outcomes of sarcoidosis-associated pulmonary hypertension. Eur Respir J. (2017) 50:1700465. 10.1183/13993003.00465-2017 [DOI] [PubMed] [Google Scholar]
  • 11.Nardi A, Brillet PY, Letoumelin P, Girard F, Brauner M, Uzunhan Y, et al. Stage IV sarcoidosis: comparison of survival with the general population and causes of death. Eur Respir J. (2011) 38:1368–73. 10.1183/09031936.00187410 [DOI] [PubMed] [Google Scholar]
  • 12.Baughman RP, Engel PJ, Taylor L, Lower EE. Survival in sarcoidosis-associated pulmonary hypertension: the importance of hemodynamic evaluation. Chest. (2010) 138:1078–85. 10.1378/chest.09-2002 [DOI] [PubMed] [Google Scholar]
  • 13.Pabst S, Grohé C, Skowasch D. Prevalence of sarcoidosis-associated pulmonary hypertension: cumulative analysis of two PULSAR studies. Eur Respir J. (2020) 55:1902223. 10.1183/13993003.02223-2019 [DOI] [PubMed] [Google Scholar]
  • 14.Samaranayake CB, McCabe C, Wort SJ, Price LC. Sarcoidosis associated pulmonary hypertension. Curr Opin Pulm Med. (2021) 27:285–95. 10.1097/MCP.0000000000000793 [DOI] [PubMed] [Google Scholar]
  • 15.Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, et al. Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis of observational studies in epidemiology (MOOSE) group. JAMA. (2000) 283:2008–12. 10.1001/jama.283.15.2008 [DOI] [PubMed] [Google Scholar]
  • 16.Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J Clin Epidemiol. (2009) 62:1006–12. 10.1016/j.jclinepi.2009.06.005 [DOI] [PubMed] [Google Scholar]
  • 17.Wan X, Wang W, Liu J, Tong T. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol. (2014) 14:135. 10.1186/1471-2288-14-135 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Hoy D, Brooks P, Woolf A, Blyth F, March L, Bain C, et al. Assessing risk of bias in prevalence studies: modification of an existing tool and evidence of interrater agreement. J Clin Epidemiol. (2012) 65:934–9. 10.1016/j.jclinepi.2011.11.014 [DOI] [PubMed] [Google Scholar]
  • 19.Higgins J, Green S. Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0 [updated March 2011]. The Cochrane Collaboration. (2011). Available online at: www.cochrane-handbook.org (accessed October, 2021).
  • 20.Huitema MP, Bakker ALM, Mager JJ, Rensing B, Smits F, Snijder RJ, et al. Prevalence of pulmonary hypertension in pulmonary sarcoidosis: the first large European prospective study. Eur Respir J. (2019) 54:1900897. 10.1183/13993003.00897-2019 [DOI] [PubMed] [Google Scholar]
  • 21.Milman N, Burton CM, Iversen M, Videbaek R, Jensen CV, Carlsen J. Pulmonary hypertension in end-stage pulmonary sarcoidosis: therapeutic effect of sildenafil? J Heart Lung Transplant. (2008) 27:329–34. 10.1016/j.healun.2007.11.576 [DOI] [PubMed] [Google Scholar]
  • 22.Utpat K, Sasikumar C, Desai U, Joshi JM. Sarcoidosis at the pulmonary medicine department of a tertiary care hospital in Mumbai. Our experience and the new modified criteria clinical radiological physiological (TNMC CRP) score for sarcoidosis: a novel proposition to assess the functional status. Monaldi Arch Chest Dis. (2021) 91:1636. 10.4081/monaldi.2021.1636 [DOI] [PubMed] [Google Scholar]
  • 23.Kaptan Ozen D, Mutlu B, Kocakaya D, Turan B, Sert Sekerci S, Ceyhan B. Pulmonary hypertension in patients with sarcoidosis: a single-center experience. Anatol J Cardiol. (2021) 25:36–41. 10.14744/AnatolJCardiol.2020.88054 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Huitema MP, Bakker ALM, Mager JJ, Snijder RJ, Rensing B, Swaans MJ, et al. Predicting pulmonary hypertension in sarcoidosis; value of PH probability on echocardiography. Int J Cardiovasc Imag. (2020) 36:1497–505. 10.1007/s10554-020-01859-9 [DOI] [PubMed] [Google Scholar]
  • 25.Tiosano S, Versini M, Dar Antaki L, Spitzer L, Yavne Y, Watad A, et al. The long-term prognostic significance of sarcoidosis-associated pulmonary hypertension - a cohort study. Clin Immunol. (2019) 199:57–61. 10.1016/j.clim.2018.12.012 [DOI] [PubMed] [Google Scholar]
  • 26.Pedraza-Serrano F, Jimenez-Garcia R, Lopez-de-Andres A, Hernandez-Barrera V, Sanchez-Munoz G, Puente-Maestu L, et al. Characteristics and outcomes of patients hospitalized with interstitial lung diseases in Spain, 2014 to 2015. Medicine. (2019) 98:e15779. 10.1097/MD.0000000000015779 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Gangemi AJ, Myers CN, Zheng M, Brown J, Butler-LeBair M, Cordova F, et al. Mortality for sarcoidosis patients on the transplant wait list in the lung allocation score era: experience from a high volume center. Respir Med. (2019) 157:69–76. 10.1016/j.rmed.2019.09.001 [DOI] [PubMed] [Google Scholar]
  • 28.Frank AL, Kreuter M, Schwarzkopf L. Economic burden of incident interstitial lung disease (ILD) and the impact of comorbidity on costs of care. Respir Med. (2019) 152:25–31. 10.1016/j.rmed.2019.04.009 [DOI] [PubMed] [Google Scholar]
  • 29.Patel N, Kalra R, Doshi R, Arora H, Bajaj NS, Arora G, et al. Hospitalization rates, prevalence of cardiovascular manifestations, and outcomes associated with sarcoidosis in the United States. J Am Heart Assoc. (2018) 7:e007844. 10.1161/JAHA.117.007844 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Smedema JP, van Geuns RJ, Ainslie G, Ector J, Heidbuchel H, Crijns H. Right ventricular involvement in cardiac sarcoidosis demonstrated with cardiac magnetic resonance. ESC Heart Fail. (2017) 4:535–44. 10.1002/ehf2.12166 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Mirsaeidi M, Omar HR, Baughman R, Machado R, Sweiss N. The association between BNP, 6MWD test, DLCO% and pulmonary hypertension in sarcoidosis. Sarcoid Vasc Diffuse Lung Dis. (2016) 33:317–20. [PubMed] [Google Scholar]
  • 32.Huitema MP, Spee M, Vorselaars VM, Boerman S, Snijder RJ, van Es HW, et al. Pulmonary artery diameter to predict pulmonary hypertension in pulmonary sarcoidosis. Eur Respir J. (2016) 47:673–6. 10.1183/13993003.01319-2015 [DOI] [PubMed] [Google Scholar]
  • 33.Rapti A, Kouranos V, Gialafos E, Aggeli K, Moyssakis J, Kallianos A, et al. Elevated pulmonary arterial systolic pressure in patients with sarcoidosis: prevalence and risk factors. Lung. (2013) 191:61–7. 10.1007/s00408-012-9442-4 [DOI] [PubMed] [Google Scholar]
  • 34.Pabst S, Hammerstingl C, Grau N, Kreuz J, Grohe C, Juergens UR, et al. Pulmonary arterial hypertension in patients with sarcoidosis: the Pulsar single center experience. Adv Exp Med Biol. (2013) 755:299–305. 10.1007/978-94-007-4546-9_38 [DOI] [PubMed] [Google Scholar]
  • 35.Maimon N, Salz L, Shershevsky Y, Matveychuk A, Guber A, Shitrit D. Sarcoidosis-associated pulmonary hypertension in patients with near-normal lung function. Int J Tuberc Lung Dis. (2013) 17:406–11. 10.5588/ijtld.12.0428 [DOI] [PubMed] [Google Scholar]
  • 36.Alhamad EH, Idrees MM, Alanezi MO, Alboukai AA, Shaik SA. Sarcoidosis-associated pulmonary hypertension: clinical features and outcomes in Arab patients. Ann Thorac Med. (2010) 5:86–91. 10.4103/1817-1737.62471 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Milman N, Svendsen CB, Iversen M, Videbaek R, Carlsen J. Sarcoidosis-associated pulmonary hypertension: acute vasoresponsiveness to inhaled nitric oxide and the relation to long-term effect of sildenafil. Clin Respir J. (2009) 3:207–13. 10.1111/j.1752-699X.2008.00120.x [DOI] [PubMed] [Google Scholar]
  • 38.Bourbonnais JM, Samavati L. Clinical predictors of pulmonary hypertension in sarcoidosis. Eur Respir J. (2008) 32:296–302. 10.1183/09031936.00175907 [DOI] [PubMed] [Google Scholar]
  • 39.Baughman RP, Sparkman BK, Lower EE. Six-minute walk test and health status assessment in sarcoidosis. Chest. (2007) 132:207–13. 10.1378/chest.06-2822 [DOI] [PubMed] [Google Scholar]
  • 40.Handa T, Nagai S, Miki S, Fushimi Y, Ohta K, Mishima M, et al. Incidence of pulmonary hypertension and its clinical relevance in patients with sarcoidosis. Chest. (2006) 129:1246–52. 10.1378/chest.129.5.1246 [DOI] [PubMed] [Google Scholar]
  • 41.Baughman RP, Engel PJ, Meyer CA, Barrett AB, Lower EE. Pulmonary hypertension in sarcoidosis. Sarcoid Vasc Diffuse Lung Dis. (2006) 23:108–16. [PubMed] [Google Scholar]
  • 42.Sulica R, Teirstein AS, Kakarla S, Nemani N, Behnegar A, Padilla ML. Distinctive clinical, radiographic, and functional characteristics of patients with sarcoidosis-related pulmonary hypertension. Chest. (2005) 128:1483–9. 10.1378/chest.128.3.1483 [DOI] [PubMed] [Google Scholar]
  • 43.Shorr AF, Helman DL, Davies DB, Nathan SD. Pulmonary hypertension in advanced sarcoidosis: epidemiology and clinical characteristics. Eur Respir J. (2005) 25:783–8. 10.1183/09031936.05.00083404 [DOI] [PubMed] [Google Scholar]
  • 44.Shade JK, Prakosa A, Popescu DM, Yu R, Okada DR, Chrispin J, et al. Predicting risk of sudden cardiac death in patients with cardiac sarcoidosis using multimodality imaging and personalized heart modeling in a multivariable classifier. Sci Adv. (2021) 7:eabi8020. 10.1126/sciadv.abi8020 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Alba AC, Gupta S, Kugathasan L, Ha A, Ochoa A, Balter M, et al. Cardiac sarcoidosis: a clinical overview. Curr Prob Cardiol. (2021) 46:100936. 10.1016/j.cpcardiol.2021.100936 [DOI] [PubMed] [Google Scholar]
  • 46.Nunes H, Humbert M, Capron F, Brauner M, Sitbon O, Battesti JP, et al. Pulmonary hypertension associated with sarcoidosis: mechanisms, haemodynamics and prognosis. Thorax. (2006) 61:68–74. 10.1136/thx.2005.042838 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Takemura T, Matsui Y, Saiki S, Mikami R. Pulmonary vascular involvement in sarcoidosis: a report of 40 autopsy cases. Human Pathol. (1992) 23:1216–23. 10.1016/0046-8177(92)90288-E [DOI] [PubMed] [Google Scholar]
  • 48.Weatherald J, Dorfmüller P, Perros F, Ghigna MR, Girerd B, Humbert M, et al. Pulmonary capillary haemangiomatosis: a distinct entity? Eur Res Rev. (2020) 29:190168. 10.1183/16000617.0168-2019 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Ota H, Sugino K, Uekusa T, Takemura T, Homma S. An autopsy case of refractory pulmonary hypertension with sarcoidosis. Res Inv. (2016) 54:490–3. 10.1016/j.resinv.2016.05.005 [DOI] [PubMed] [Google Scholar]
  • 50.Hoffstein V, Ranganathan N, Mullen JB. Sarcoidosis simulating pulmonary veno-occlusive disease. Am Rev Res Dis. (1986) 134:809–11. [DOI] [PubMed] [Google Scholar]
  • 51.Ungprasert P, Crowson CS, Matteson EL. Association of sarcoidosis with increased risk of VTE: a population-based study, 1976 to 2013. Chest. (2017) 151:425–30. 10.1016/j.chest.2016.09.009 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Goljan-Geremek A, Geremek M, Puscinska E, Sliwinski P. Venous thromboembolism and sarcoidosis: co-incidence or coexistence? Cent Eur J Immunol. (2015) 40:477–80. 10.5114/ceji.2015.56972 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Swigris JJ, Olson AL, Huie TJ, Fernandez-Perez ER, Solomon JJ, Sprunger D, et al. Increased risk of pulmonary embolism among US decedents with sarcoidosis from 1988 to 2007. Chest. (2011) 140:1261–6. 10.1378/chest.11-0324 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Duong H, Bonham CA. Sarcoidosis-associated pulmonary hypertension: pathophysiology, diagnosis, and treatment. Clin Pulm Med. (2018) 25:52–60. 10.1097/CPM.0000000000000252 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Ozyilmaz E, Akilli R, Berk I, Deniz A, Ozturk OG, Baydar O, et al. The frequency of diastolic dysfunction in patients with sarcoidosis and it's relationship with HLA DRB1* alleles. Sarcoid Vasc Diffuse Lung Dis. (2019) 36:285–93. 10.36141/svdld.v36i4.8606 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Lal C, Medarov BI, Judson MA. Interrelationship between sleep-disordered breathing and sarcoidosis. Chest. (2015) 148:1105–14. 10.1378/chest.15-0584 [DOI] [PubMed] [Google Scholar]
  • 57.Simonneau G, Montani D, Celermajer DS, Denton CP, Gatzoulis MA, Krowka M, et al. Haemodynamic definitions and updated clinical classification of pulmonary hypertension. Eur Respir J. (2019) 53:1801913. 10.1183/13993003.01913-2018 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Shorr AF, Davies DB, Nathan SD. Predicting mortality in patients with sarcoidosis awaiting lung transplantation. Chest. (2003) 124:922–8. 10.1016/S0012-3692(15)37649-2 [DOI] [PubMed] [Google Scholar]
  • 59.Neville E, Walker AN, James DG. Prognostic factors predicting the outcome of sarcoidosis: an analysis of 818 patients. Quart J Med. (1983) 52:525–33. [PubMed] [Google Scholar]
  • 60.Mathijssen H, Huitema MP, Bakker ALM, Mager JJ, Snijder RJ, Grutters JC, et al. Safety of macitentan in sarcoidosis-associated pulmonary hypertension: a case-series. Sarcoid Vasc Diffuse Lung Dis. (2020) 37:74–8. 10.1093/ehjci/ehaa946.2231 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Keir GJ, Walsh SL, Gatzoulis MA, Marino PS, Dimopoulos K, Alonso R, et al. Treatment of sarcoidosis-associated pulmonary hypertension: a single centre retrospective experience using targeted therapies. Sarcoid Vasc Diffuse Lung Dis. (2014) 31:82–90. [PubMed] [Google Scholar]
  • 62.Baughman RP, Culver DA, Cordova FC, Padilla M, Gibson KF, Lower EE, et al. Bosentan for sarcoidosis-associated pulmonary hypertension: a double-blind placebo controlled randomized trial. Chest. (2014) 145:810–7. 10.1378/chest.13-1766 [DOI] [PubMed] [Google Scholar]
  • 63.Baughman RP, Judson MA, Lower EE, Highland K, Kwon S, Craft N, et al. Inhaled iloprost for sarcoidosis associated pulmonary hypertension. Sarcoid Vasc Diffuse Lung Dis. (2009) 26:110–20. [PubMed] [Google Scholar]
  • 64.Fisher KA, Serlin DM, Wilson KC, Walter RE, Berman JS, Farber HW. Sarcoidosis-associated pulmonary hypertension: outcome with long-term epoprostenol treatment. Chest. (2006) 130:1481–8. 10.1378/chest.130.5.1481 [DOI] [PubMed] [Google Scholar]
  • 65.Hendriks S, Peetoom K, Bakker C, van der Flier WM, Papma JM, Koopmans R, et al. Global prevalence of young-onset dementia: a systematic review and meta-analysis. JAMA Neurol. (2021) 78:1080–90. 10.1001/jamaneurol.2021.2161 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Wu M, Tong X, Liu S, Wang D, Wang L, Fan H. Prevalence of methicillin-resistant staphylococcus aureus in healthy Chinese population: a system review and meta-analysis. PLoS ONE. (2019) 14:e0223599. 10.1371/journal.pone.0223599 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Figure 1

Results of the sensitivity analysis of the prevalence of SAPH by TTE. SAPH, sarcoidosis-associated pulmonary hypertension; TTE, transthoracic echocardiography.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 2

Results of the trim-and-fill analysis of SAPH by TTE in the general sarcoidosis population. SAPH, sarcoidosis-associated pulmonary hypertension; TTE, transthoracic echocardiography.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 3

Results of the sensitivity analysis of the prevalence of SAPH by RHC in the general sarcoidosis population. SAPH, sarcoidosis-associated pulmonary hypertension; RHC, right heart catheterization.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 4

Results of the sensitivity analysis of the prevalence of SAPH by RHC in the population with advanced sarcoidosis. SAPH, sarcoidosis-associated pulmonary hypertension; RHC, right heart catheterization.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 5

Results of the sensitivity analysis of the prevalence of pre-capillary PH by RHC in the general sarcoidosis population. PH, pulmonary hypertension; RHC, right heart catheterization.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 6

Results of sensitivity analysis of the prevalence of SAPH based on documented diagnoses in large databases. SAPH, sarcoidosis-associated pulmonary hypertension.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 7

Forest plot of the pooled prevalence of SAPH for studies reporting both PH and pre-capillary PH. SAPH, sarcoidosis-associated pulmonary hypertension; PH, pulmonary hypertension.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Figure 8

Forest plot of the pooled prevalence of pre-capillary PH in sarcoidosis patients for studies reporting both PH and pre-capillary PH. PH, pulmonary hypertension.

Click here for additional data file. (9.2MB, ZIP)
Supplementary Table 1

MOOSE checklist (15).

Click here for additional data file. (2.3MB, zip)
Supplementary Table 2

PRISMA checklist.

Click here for additional data file. (2.3MB, zip)
Supplementary Table 3

Diagnostic criteria of pulmonary hypertension in included studies.

Click here for additional data file. (2.3MB, zip)
Supplementary Table 4

Risk of bias quality assessment tool.

Click here for additional data file. (2.3MB, zip)
Supplementary Table 5

Quality assessment of included studies.

Click here for additional data file. (2.3MB, zip)

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.

Articles from Frontiers in Cardiovascular Medicine are provided here courtesy of Frontiers Media SA

RESOURCES