Metabolic syndrome is associated with increased cardiovascular risk and disease damage in patients with Takayasu arteritis

Objective Metabolic syndrome (MetS) is one of the preventable risk factors for cardiovascular disease (CVD). The aim of this study was to investigate the effect of MetS on CVD and cumulative organ damage in a multi‐center, large cohort of patients with Takayasu arteritis (TAK). Methods This is a cro...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of rheumatic diseases 2022-07, Vol.25 (7), p.775-780
Hauptverfasser: Sağlam, Burçin, Kaymaz‐Tahra, Sema, Kenar, Gökçe, Kocaer, Sinem, Omma, Ahmet, Erden, Abdulsamet, Kara, Mete, Yazıcı, Ayten, Cefle, Ayşe, Gerçik, Önay, Akar, Servet, Aksu, Kenan, Keser, Gökhan, Yarkan Tuğsal, Handan, Önen, Fatoş, Kamalı, Sevil, Alibaz‐Öner, Fatma, Direskeneli, Haner, Alpay‐Kanıtez, Nilüfer
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Objective Metabolic syndrome (MetS) is one of the preventable risk factors for cardiovascular disease (CVD). The aim of this study was to investigate the effect of MetS on CVD and cumulative organ damage in a multi‐center, large cohort of patients with Takayasu arteritis (TAK). Methods This is a cross‐sectional study involving 192 consecutive TAK patients from seven tertiary rheumatology centers in Turkey. Clinical data of TAK patients fulfilling the 1990 American College of Rheumatology classification criteria were collected from medical records. They were evaluated for risk factors of CVD, disease activity, damage, and MetS at their last visits. Results A total of 192 consecutive TAK patients were included in this study. One hundred and fifty‐eight (82%) were female, the mean age was 43.3 ± 13 years, and mean disease duration was 13.5 ± 9.3 years. MetS was detected in 50 (26%) of the patients and CVD was detected in 28 (14.6%). The presence of MetS was detected as an independent risk factor for CVD (P 
ISSN:1756-1841
1756-185X
DOI:10.1111/1756-185X.14335