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Coexistence of Moderate-to-Severe Obstructive Sleep Apnea and Inflammation Accelerates the Risk of Progression of Arterial Stiffness: A Prospective 6-Year Study.
Kim, Jinkwan; Yoon, Dae Wui; Myoung, Sungmin; Lee, Seung Ku; Shin, Chol.
Afiliação
  • Kim J; Department of Biomedical Laboratory Science, College of Health Science, Jungwon University, Geo-San 28024, Korea.
  • Yoon DW; Department of Biomedical Laboratory Science, College of Health Science, Jungwon University, Geo-San 28024, Korea.
  • Myoung S; Department of Medical Information and Administration, College of Health Science, Jungwon University, Geo-San 28024, Korea.
  • Lee SK; Institute of Human Genomic Study, Korea University Ansan Hospital, Korea University, Ansan 15355, Korea.
  • Shin C; Institute of Human Genomic Study, Korea University Ansan Hospital, Korea University, Ansan 15355, Korea.
Life (Basel) ; 12(11)2022 Nov 08.
Article em En | MEDLINE | ID: mdl-36362978
ABSTRACT
Both obstructive sleep apnea (OSA) and inflammation have now been recognized as imposing substantial cardiometabolic risk. However, no prospective study has reported whether the coexistence of OSA and inflammation exacerbates the progressive arterial stiffening. Thus, the purpose of this study is to examine whether these conditions increase the risk of the progression of arterial stiffening. A total of 1945 participants were randomly selected for the study. Subjects with elevated inflammation were divided by high-sensitivity C-reactive protein (hsCRP) levels. A polysomnography and brachial-ankle pulse wave velocity (baPWV) were performed. The elevation of the baPWV was defined as the levels in the highest quartile of the baPWV. The percentage of the elevated baPWV and the change in the baPWV (ΔbaPWV) were higher in individuals with OSA and higher hsCRP levels. After adjusting for confounders, the participants with OSA and inflammation in the groups not treated with antihypertensive medication had a higher risk of an elevated ΔbaPWV in contrast to those with neither variable. Particularly, the alteration in the baPWV differed significantly based on the existence of moderate-to-severe OSA and inflammation at the 6-year follow-up. In combination, these conditions are associated with an accelerated risk of a future burden of the progression of the arterial stiffness, suggesting a potential important role in the increased risk of CVD.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article