Risk Factors for Pulmonary Arterial Hypertension in Patients With Systemic Lupus Erythematosus: A Systematic Review and Expert Consensus

Author:

Atsumi Tatsuya1,Bae Sang‐Cheol2ORCID,Gu Hong3,Huang Wen‐Nan4,Li Mengtao5ORCID,Nikpour Mandana6,Okada Masato7,Prior David6,Atanasov Petar8,Jiang Xiaobin9,Wilson Liam9,Bloomfield Paul10,Wu David Bin‐chia11,Makanji Yogeshwar10

Affiliation:

1. Hokkaido University Hospital Sapporo Japan

2. Hanyang University Hospital for Rheumatic Diseases, Hanyang University Institute for Rheumatology Research, and Hanyang Institute of Bioscience and Biotechnology Seoul Republic of Korea

3. Beijing Anzhen Hospital Beijing China

4. Taichung Veterans General Hospital, Ling‐Tung University, and College of Medicine National Chung Hsing University, Taichung, Taiwan, and School of Medicine, National Yang Ming Chiao Tung University Taipei Taiwan

5. Chinese Academy of Medical Sciences & Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Ministry of Science & Technology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Key Laboratory of Rheumatology and Clinical Immunology, and Ministry of Education Beijing China

6. St. Vincent's Hospital and University of Melbourne Melbourne Australia

7. St. Luke's International Hospital Tokyo Japan

8. Amaris Consulting Barcelona Spain

9. Amaris Consulting Shanghai China

10. Janssen Pharmaceuticals Asia Pacific Singapore

11. Janssen Pharmaceuticals Asia Pacific and Saw Swee Hock School of Public Health National University of Singapore Singapore

Abstract

ObjectiveThis study aimed to identify risk factors associated with the development of pulmonary arterial hypertension (PAH) in patients with systemic lupus erythematosus (SLE).MethodsWe conducted a systematic literature review of studies focusing on adult patients classified as having SLE‐related PAH by searching the electronic databases Embase, Medline, Medline in‐progress, Wanfang, China National Knowledge Infrastructure, Ichushi Web, Kmbase, and KoreaMed. Based on the findings, we conducted a Delphi survey to build expert consensus on issues related to screening for PAH in patients with SLE and on the importance and feasibility of measuring the identified factors in clinical practice.ResultsWe included 21 eligible studies for data synthesis. Sixteen factors were associated with an increased risk of SLE‐PAH: pericardial effusion, serositis, longer duration of SLE, arthritis, acute and subacute cutaneous lupus, scleroderma pattern on nailfold capillaroscopy, diffusion capacity of carbon monoxide in the lungs (DLCO) <70% predicted, interstitial lung disease, thrombocytopenia, and seven serological factors. Six factors were associated with a decreased risk of SLE‐PAH: malar/acute rash, hematologic disorder, renal disorder, higher Systemic Lupus Erythematosus Disease Activity Index score, and two serological factors. Among these, there were six risk factors on which the panelists reached strong or general consensus (peak tricuspid regurgitation velocity on echocardiography >2.8 m/s, pericardial effusion, DLCO <70% predicted, scleroderma pattern on nailfold capillaroscopy, brain natriuretic peptide >50 ng/l, and N‐terminal pro–brain natriuretic peptide >300 ng/l). The Delphi panel confirmed the need for a screening tool to identify patients with SLE at high risk of developing PAH and provided consensus on the importance and/or practicality of measuring the identified factors.ConclusionThe risk factors we identified could be used in a screening algorithm to identify patients with SLE with a high risk of developing PAH to facilitate early diagnosis, which could improve prognosis and management of these patients.

Funder

Janssen Pharmaceuticals

Publisher

Wiley

Subject

Rheumatology

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