Cargando…

Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients with Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry

OBJECTIVES: This study aims to investigate the outcomes and risk factors associated with the progression of systolic pulmonary artery pressure (sPAP) in patients with systemic rheumatic diseases. PATIENTS AND METHODS: A total of 532 patients (73 males, 459 females; median age 49 years; interquartile...

Descripción completa

Detalles Bibliográficos
Autores principales: SEO, Mi Ryoung, YEO, Jina, RYU, Hee Jung, CHOI, Hyo-jin, KO, Kwang-pil, BAEK, Han Joo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish League Against Rheumatism 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7945697/
https://www.ncbi.nlm.nih.gov/pubmed/33758812
http://dx.doi.org/10.46497/ArchRheumatol.2020.7812
_version_ 1783662909972283392
author SEO, Mi Ryoung
YEO, Jina
RYU, Hee Jung
CHOI, Hyo-jin
KO, Kwang-pil
BAEK, Han Joo
author_facet SEO, Mi Ryoung
YEO, Jina
RYU, Hee Jung
CHOI, Hyo-jin
KO, Kwang-pil
BAEK, Han Joo
author_sort SEO, Mi Ryoung
collection PubMed
description OBJECTIVES: This study aims to investigate the outcomes and risk factors associated with the progression of systolic pulmonary artery pressure (sPAP) in patients with systemic rheumatic diseases. PATIENTS AND METHODS: A total of 532 patients (73 males, 459 females; median age 49 years; interquartile range (IQR), 36 to 62 years) registered with the Registry of Pulmonary Hypertension Associated with Rheumatic Diseases were included. Mortality curves were constructed using the Kaplan- Meier method and comparisons were performed using the log-rank test. A paired t-test was performed to evaluate the patients with markedly elevated sPAP between baseline and follow-up. RESULTS: The average follow-up duration was 31 months (IQR, 9 to 60 months). Of the patients, 196 had follow-up echocardiographs at least one year later. We defined the sPAP over 60 mmHg as markedly elevated. Patients in the increased sPAP above 60 mmHg at follow-up and persistently markedly elevated sPAP were associated with worse outcomes in all-cause mortality and pulmonary arterial hypertension-related mortality (p<0.001). In patients with systemic sclerosis, the majority of patients remained static within their pressure group or rose progressively: the patients with markedly elevated sPAP at follow-up were higher than those at baseline (32% versus 15%, p<0.01). In patients with mixed connective tissue disease (MCTD) or rheumatoid arthritis (RA), the majority of patients remained static within their pressure group or gradually improved: the patients with markedly elevated sPAP at follow-up were lower than those at baseline (RA=14% versus 29%, MCTD=5% versus 16%, p<0.05). CONCLUSION: Persistently high sPAP or increase of sPAP over 60 mmHg at follow-up was associated with increased mortality. There were some differences in the progression of sPAP according to the underlying rheumatic diseases.
format Online
Article
Text
id pubmed-7945697
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Turkish League Against Rheumatism
record_format MEDLINE/PubMed
spelling pubmed-79456972021-03-22 Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients with Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry SEO, Mi Ryoung YEO, Jina RYU, Hee Jung CHOI, Hyo-jin KO, Kwang-pil BAEK, Han Joo Arch Rheumatol Original Article OBJECTIVES: This study aims to investigate the outcomes and risk factors associated with the progression of systolic pulmonary artery pressure (sPAP) in patients with systemic rheumatic diseases. PATIENTS AND METHODS: A total of 532 patients (73 males, 459 females; median age 49 years; interquartile range (IQR), 36 to 62 years) registered with the Registry of Pulmonary Hypertension Associated with Rheumatic Diseases were included. Mortality curves were constructed using the Kaplan- Meier method and comparisons were performed using the log-rank test. A paired t-test was performed to evaluate the patients with markedly elevated sPAP between baseline and follow-up. RESULTS: The average follow-up duration was 31 months (IQR, 9 to 60 months). Of the patients, 196 had follow-up echocardiographs at least one year later. We defined the sPAP over 60 mmHg as markedly elevated. Patients in the increased sPAP above 60 mmHg at follow-up and persistently markedly elevated sPAP were associated with worse outcomes in all-cause mortality and pulmonary arterial hypertension-related mortality (p<0.001). In patients with systemic sclerosis, the majority of patients remained static within their pressure group or rose progressively: the patients with markedly elevated sPAP at follow-up were higher than those at baseline (32% versus 15%, p<0.01). In patients with mixed connective tissue disease (MCTD) or rheumatoid arthritis (RA), the majority of patients remained static within their pressure group or gradually improved: the patients with markedly elevated sPAP at follow-up were lower than those at baseline (RA=14% versus 29%, MCTD=5% versus 16%, p<0.05). CONCLUSION: Persistently high sPAP or increase of sPAP over 60 mmHg at follow-up was associated with increased mortality. There were some differences in the progression of sPAP according to the underlying rheumatic diseases. Turkish League Against Rheumatism 2020-04-27 /pmc/articles/PMC7945697/ /pubmed/33758812 http://dx.doi.org/10.46497/ArchRheumatol.2020.7812 Text en Copyright © 2020, Turkish League Against Rheumatism http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Article
SEO, Mi Ryoung
YEO, Jina
RYU, Hee Jung
CHOI, Hyo-jin
KO, Kwang-pil
BAEK, Han Joo
Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients with Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry
title Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients with Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry
title_full Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients with Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry
title_fullStr Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients with Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry
title_full_unstemmed Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients with Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry
title_short Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients with Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry
title_sort outcomes and risk factors of systolic pulmonary artery pressure progression in patients with systemic rheumatic diseases: follow-up results from a korean registry
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7945697/
https://www.ncbi.nlm.nih.gov/pubmed/33758812
http://dx.doi.org/10.46497/ArchRheumatol.2020.7812
work_keys_str_mv AT seomiryoung outcomesandriskfactorsofsystolicpulmonaryarterypressureprogressioninpatientswithsystemicrheumaticdiseasesfollowupresultsfromakoreanregistry
AT yeojina outcomesandriskfactorsofsystolicpulmonaryarterypressureprogressioninpatientswithsystemicrheumaticdiseasesfollowupresultsfromakoreanregistry
AT ryuheejung outcomesandriskfactorsofsystolicpulmonaryarterypressureprogressioninpatientswithsystemicrheumaticdiseasesfollowupresultsfromakoreanregistry
AT choihyojin outcomesandriskfactorsofsystolicpulmonaryarterypressureprogressioninpatientswithsystemicrheumaticdiseasesfollowupresultsfromakoreanregistry
AT kokwangpil outcomesandriskfactorsofsystolicpulmonaryarterypressureprogressioninpatientswithsystemicrheumaticdiseasesfollowupresultsfromakoreanregistry
AT baekhanjoo outcomesandriskfactorsofsystolicpulmonaryarterypressureprogressioninpatientswithsystemicrheumaticdiseasesfollowupresultsfromakoreanregistry