A normal diffusing capacity of the lungs for carbon monoxide is rare in incidental pulmonary arterial hypertension in systemic sclerosis: Data from the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma cohort

被引:2
|
作者
Overbury, Rebecca S. [1 ,2 ]
Murtaugh, Maureen A. [1 ]
Frech, Tracy M. [1 ,2 ]
Steen, Virginia D. [3 ]
机构
[1] Univ Utah, Div Rheumatol, Dept Internal Med, 30 N 1900 E,SOM4B200, Salt Lake City, UT 84132 USA
[2] George E Wahlen Dept Vet Affairs Med Ctr, Salt Lake City, UT USA
[3] Georgetown Univ, Div Rheumatol, Dept Internal Med, Washington, DC USA
关键词
Systemic sclerosis; pulmonary arterial hypertension; diffusion capacity for carbon monoxide; cardiac manifestations of systemic sclerosis;
D O I
10.1177/2397198318778818
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Our purpose was to determine the frequency of normal diffusing capacity for carbon monoxide defined as 70% predicted, in those diagnosed with pulmonary arterial hypertension in the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma cohort. We compared those with normal diffusing capacity for carbon monoxide to those with reduced diffusing capacity for carbon monoxide <70% in order to better clarify the role of pulmonary function testing as a screening test for pulmonary arterial hypertension and to better understand this population. Methods: Entry criteria included a right heart catheterization with mean pulmonary artery pressure 25 mm Hg and pulmonary capillary wedge pressure 15 mm Hg. Demographics, echocardiogram variables, B-type natriuretic peptide levels, right heart catheterization findings, and survival were described for both groups. Results: Of (n = 202), 11 (5.4%) had a diffusing capacity for carbon monoxide of 70% versus 191 (94.6%) who had a diffusing capacity for carbon monoxide <70%. There were no identified statistical differences between the groups. Left atrium size was 4.1 cm in the normal diffusing capacity for carbon monoxide patients compared to 3.7 cm in the low diffusing capacity for carbon monoxide group but did not reach statistical significance. There were no statistically significant differences in survival. On repeat testing, seven patients subsequently developed a diffusing capacity for carbon monoxide <70%. Conclusion: Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma data suggest that it is very rare for a patient to develop pulmonary arterial hypertension with a preserved diffusing capacity for carbon monoxide. The data support the importance of obtaining diffusing capacity for carbon monoxide and that a patient with a normal diffusing capacity for carbon monoxide while suspected to have systemic sclerosis-pulmonary arterial hypertension should be considered critically. Diffusing capacity for carbon monoxide >70% was present in too few patients to find significant differences in B-type natriuretic peptide and atrium size. Future research should seek to confirm abnormal B-type natriuretic peptide, increased left atrium size, and other evidence of myocardial involvement on diffusing capacity for carbon monoxide.
引用
收藏
页码:237 / 241
页数:5
相关论文
共 50 条
  • [41] Risk assessment validation in patients with pulmonary arterial hypertension: Data from a Southern Brazil registry (RESPHIRAR study)
    Spilimbergo, Fernanda Brum
    Rodrigues, Roger Pirath
    Dias-Pinto, Marcelo Credidio
    Blanco, Daniela Cavalet
    Barbieri, Glaucia Maria
    Andrade-Lima, Marina
    Fagundes, Ariovaldo Leal
    Gazzana, Marcelo Basso
    Roncato, Gabriela
    Mello, Marcelo Martins
    Watte, Guilherme
    Assmann, Tais Silveira
    Caurio, Cassia Ferreira Braz
    Souza, Rogerio
    Meyer, Gisela Martina Bohns
    PULMONARY CIRCULATION, 2023, 13 (01)
  • [42] Right ventricular-pulmonary arterial coupling ratio derived from 3-dimensional echocardiography predicts outcomes in systemic lupus erythematosus-associated pulmonary arterial hypertension patients
    Lan, Wei-Fang
    Deng, Yan
    Dai, Ping
    Wu, Dan-dan
    Hu, Jie
    Liao, Juan
    Meng, Hui
    LUPUS, 2024, 33 (02) : 155 - 165
  • [43] Exploration of the Shared Gene Signatures and Molecular Mechanisms Between Systemic Lupus Erythematosus and Pulmonary Arterial Hypertension: Evidence From Transcriptome Data
    Yao, Menghui
    Zhang, Chunyi
    Gao, Congcong
    Wang, Qianqian
    Dai, Mengmeng
    Yue, Runzhi
    Sun, Wenbo
    Liang, Wenfang
    Zheng, Zhaohui
    FRONTIERS IN IMMUNOLOGY, 2021, 12
  • [44] The inclusion of N-terminal pro-brain natriuretic peptide in a sensitive screening strategy for systemic sclerosis-related pulmonary arterial hypertension: a cohort study
    Vivek Thakkar
    Wendy Stevens
    David Prior
    Peter Youssef
    Danny Liew
    Eli Gabbay
    Janet Roddy
    Jennifer G Walker
    Jane Zochling
    Joanne Sahhar
    Peter Nash
    Susan Lester
    Maureen Rischmueller
    Susanna M Proudman
    Mandana Nikpour
    Arthritis Research & Therapy, 15
  • [45] The incidence rate of pulmonary arterial hypertension and scleroderma renal crisis in systemic sclerosis patients with digital ulcers on endothelin antagonist receptors (ERAs) and phosphodiesterase-5 inhibitors (PDE5i)
    Pestana-Fernandez, Melani
    Rubio-Rivas, Manuel
    Tolosa-Vilella, Carles
    Guillen-Del-Castillo, Alfredo
    Colunga-Arguelles, Dolores
    Argibay, Ana
    Mari-Alfonso, Begona
    Marin-Ballve, Adela
    Pla-Salas, Xavier
    Chamorro, Antonio-J
    Castro-Salomo, Antoni
    Madronero-Vuelta, Ana Belen
    Sanchez-Garcia, Maria Esther
    Saez-Comet, Luis
    Gonzalez-Echavarri, Cristina
    Ortego-Centeno, Norberto
    Vargas-Hitos, Jose Antonio
    Todoli-Parra, Jose Antonio
    Trapiella-Martinez, Luis
    Lledo, Gema Maria
    Freire, Mayka
    Fonollosa-Pla, Vicent
    Simeon-Aznar, Carmen Pilar
    RHEUMATOLOGY, 2021, 60 (02) : 872 - 880
  • [46] Incidence and long-term outcomes of pregnant women complicated with pulmonary arterial hypertension during different pregnancies: A prospective cohort study from China
    Yang, Menghui
    Wang, Jian
    Zhang, Xueming
    Zhuang, Qi
    Wang, Ruomeng
    Shen, Jieyan
    Lin, Jianhua
    INTERNATIONAL JOURNAL OF CARDIOLOGY, 2021, 326 : 178 - 183
  • [47] Association of Right Atrial Mechanics with Hemodynamics and Physical Capacity in Patients with Idiopathic Pulmonary Arterial Hypertension: Insight from a Single-Center Cohort in Northern Sweden
    Saha, Samir Kanti
    Soderberg, Stefan
    Lindqvist, Per
    ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES, 2016, 33 (01): : 46 - 56
  • [48] A Comparison of Echocardiographic Variables of Right Ventricular Function with Exercise Capacity After Bosentan Treatment in Patients with Pulmonary Arterial Hypertension: Results from a Multicenter, Prospective, Cohort Study
    Kim, Hyungseop
    Lee, Jin Bae
    Park, Jae-Hyeong
    Yoo, Byung-Su
    Son, Jang-Won
    Yang, Dong Heon
    Lee, Bong-Ryeol
    JOURNAL OF CLINICAL ULTRASOUND, 2017, 45 (01) : 28 - 34
  • [49] Echocardiographic assessment of regional right ventricular systolic function using two-dimensional strain echocardiography and evaluation of the predictive ability of longitudinal 2D-strain imaging for pulmonary arterial hypertension in systemic sclerosis patients
    Hekimsoy, Vedat
    Kaya, Ergun Baris
    Akdogan, Ali
    Sahiner, Levent
    Evranos, Banu
    Canpolat, Ugur
    Aytemir, Kudret
    Ozer, Necla
    Tokgozoglu, Lale
    INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING, 2018, 34 (06) : 883 - 892
  • [50] Echocardiographic assessment of regional right ventricular systolic function using two-dimensional strain echocardiography and evaluation of the predictive ability of longitudinal 2D-strain imaging for pulmonary arterial hypertension in systemic sclerosis patients
    Vedat Hekimsoy
    Ergun Barıs Kaya
    Ali Akdogan
    Levent Sahiner
    Banu Evranos
    Ugur Canpolat
    Kudret Aytemir
    Necla Özer
    Lale Tokgozoglu
    The International Journal of Cardiovascular Imaging, 2018, 34 : 883 - 892