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Prognostic significance of insulin resistance in pulmonary hypertension

AIMS: The relationship between insulin resistance (IR) and glucose intolerance with pulmonary hypertension (PH) has been suggested in recent investigations. In the present study, we aimed to show the prevalence of IR and its correlation with haemodynamic variables as well as its prognostic significa...

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Autores principales: Zare, Elahe, Kafshbani, Parvaneh, Chenaghlou, Maryam, Noori, Mehdi, Ghaemmaghami, Zahra, Amin, Ahmad, Taghavi, Sepideh, Naderi, Nasim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788000/
https://www.ncbi.nlm.nih.gov/pubmed/34904389
http://dx.doi.org/10.1002/ehf2.13752
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author Zare, Elahe
Kafshbani, Parvaneh
Chenaghlou, Maryam
Noori, Mehdi
Ghaemmaghami, Zahra
Amin, Ahmad
Taghavi, Sepideh
Naderi, Nasim
author_facet Zare, Elahe
Kafshbani, Parvaneh
Chenaghlou, Maryam
Noori, Mehdi
Ghaemmaghami, Zahra
Amin, Ahmad
Taghavi, Sepideh
Naderi, Nasim
author_sort Zare, Elahe
collection PubMed
description AIMS: The relationship between insulin resistance (IR) and glucose intolerance with pulmonary hypertension (PH) has been suggested in recent investigations. In the present study, we aimed to show the prevalence of IR and its correlation with haemodynamic variables as well as its prognostic significance in this group of patients. METHODS AND RESULTS: Among 100 new and returning patients with PH, scheduled for right heart catheterization (RHC), 59 non‐diabetic patients were enrolled. The homeostasis model assessment of insulin resistance (HOMA‐IR) was used to assess IR. The study population were followed up for a median (interquartile range) of 48 (23–48) months for all‐cause mortalities. Most of the study population [mean (standard deviation) age of 45.9 (17.3)] were classified as class I of PH classification (47.5%). Overall, 27% of our study population had IR considering the Iranian cut points of HOMA‐IR. The prevalence of IR in non‐diabetic, non‐metabolic syndrome patients with precapillary PH (PAH) was 34.2%, which was higher than the prevalence of IR in non‐diabetic, non‐metabolic syndrome Iranian population (24.1%). There was no difference between IR and insulin sensitive (IS) groups regarding demographic and clinical findings, 6 min walk test, and laboratory and haemodynamic data in univariable and multivariable analyses. The mortality rate in the follow‐up period was 44.1%. The survival of patient with IR was slightly lower than IS patients; however, IR was not an independent predictor of death. CONCLUSIONS: The glucose metabolism is dysregulated in patients with PH, and IR may increase the risk of adverse events among these patients.
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spelling pubmed-87880002022-01-31 Prognostic significance of insulin resistance in pulmonary hypertension Zare, Elahe Kafshbani, Parvaneh Chenaghlou, Maryam Noori, Mehdi Ghaemmaghami, Zahra Amin, Ahmad Taghavi, Sepideh Naderi, Nasim ESC Heart Fail Original Articles AIMS: The relationship between insulin resistance (IR) and glucose intolerance with pulmonary hypertension (PH) has been suggested in recent investigations. In the present study, we aimed to show the prevalence of IR and its correlation with haemodynamic variables as well as its prognostic significance in this group of patients. METHODS AND RESULTS: Among 100 new and returning patients with PH, scheduled for right heart catheterization (RHC), 59 non‐diabetic patients were enrolled. The homeostasis model assessment of insulin resistance (HOMA‐IR) was used to assess IR. The study population were followed up for a median (interquartile range) of 48 (23–48) months for all‐cause mortalities. Most of the study population [mean (standard deviation) age of 45.9 (17.3)] were classified as class I of PH classification (47.5%). Overall, 27% of our study population had IR considering the Iranian cut points of HOMA‐IR. The prevalence of IR in non‐diabetic, non‐metabolic syndrome patients with precapillary PH (PAH) was 34.2%, which was higher than the prevalence of IR in non‐diabetic, non‐metabolic syndrome Iranian population (24.1%). There was no difference between IR and insulin sensitive (IS) groups regarding demographic and clinical findings, 6 min walk test, and laboratory and haemodynamic data in univariable and multivariable analyses. The mortality rate in the follow‐up period was 44.1%. The survival of patient with IR was slightly lower than IS patients; however, IR was not an independent predictor of death. CONCLUSIONS: The glucose metabolism is dysregulated in patients with PH, and IR may increase the risk of adverse events among these patients. John Wiley and Sons Inc. 2021-12-13 /pmc/articles/PMC8788000/ /pubmed/34904389 http://dx.doi.org/10.1002/ehf2.13752 Text en © 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Zare, Elahe
Kafshbani, Parvaneh
Chenaghlou, Maryam
Noori, Mehdi
Ghaemmaghami, Zahra
Amin, Ahmad
Taghavi, Sepideh
Naderi, Nasim
Prognostic significance of insulin resistance in pulmonary hypertension
title Prognostic significance of insulin resistance in pulmonary hypertension
title_full Prognostic significance of insulin resistance in pulmonary hypertension
title_fullStr Prognostic significance of insulin resistance in pulmonary hypertension
title_full_unstemmed Prognostic significance of insulin resistance in pulmonary hypertension
title_short Prognostic significance of insulin resistance in pulmonary hypertension
title_sort prognostic significance of insulin resistance in pulmonary hypertension
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788000/
https://www.ncbi.nlm.nih.gov/pubmed/34904389
http://dx.doi.org/10.1002/ehf2.13752
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