6万人の米国成人を対象とした研究、炎症性タンパク質と致死的心筋梗塞などの関連を確認(Study of 60,000 U.S. adults links inflammatory protein to fatal heart attacks, other negative outcomes)

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2026-08-25 バッファロー大学(UB)

バッファロー大学の研究チームは、閉塞性睡眠時無呼吸症候群(OSA)と心血管疾患による死亡リスクとの関連を調べた。米国女性を対象とした長期追跡データを解析した結果、OSAの重症度が高いほど心血管疾患による死亡リスクが高くなる傾向が確認された。特に、閉経後女性では睡眠中の呼吸停止による低酸素状態や睡眠の分断が、血圧上昇、血管機能の悪化、心血管系への慢性的な負担につながる可能性が示唆された。研究は、OSAが単なる睡眠上の問題ではなく、心血管疾患の重要なリスク因子となり得ることを示している。また、女性ではOSAがいびきなど典型的な症状として現れにくく、見逃されやすいことから、特に中高年女性の心血管リスク評価において睡眠時無呼吸への注意が必要だと指摘している。早期の診断と治療が心血管疾患による死亡リスク低減につながる可能性がある。

<関連情報>

血清インターロイキン-6濃度による9つの心血管疾患および死亡率アウトカムの予後予測値:クロスコホートコラボレーション(CCC) The Prognostic Value of Serum Interleukin-6 Concentrations for 9 Cardiovascular and Mortality Outcomes: The Cross Cohort Collaboration (CCC)

Zhiqi Yao, Zeina A. Dardari, Michael J. LaMonte, Kunihiro Matsushita, Christie M. Ballantyne, Joao A. Lima, Ramachandran S. Vasan, … , and Michael J. Blaha
Journal of the American Chemical Society  Published:27 May 2026

Abstract

Background
Interleukin (IL)–6 has emerged as a promising target for cardiovascular disease (CVD) prevention. Better understanding IL-6’s contribution to CVD events in community-based, diverse cohorts and in clinically relevant subgroups will provide critical context about IL-6 inhibition for CVD prevention.

Objectives
The aim of this study was to evaluate the association of circulating IL-6 concentrations with incident cardiovascular events and mortality using pooled data from large multiethnic prospective cohorts.

Methods
The authors harmonized individual-level participant data from 14 cohorts with blood IL-6 measurements and follow-up data on any of 9 prespecified outcomes: myocardial infarction, stroke, atrial fibrillation, heart failure, total coronary heart disease (CHD), total CVD, all-cause mortality, CVD-specific mortality, and CHD-specific mortality. Multivariable-adjusted Cox proportional hazards models were used to estimate HRs and corresponding 95% CIs. IL-6 was analyzed by quartiles and as a log-transformed continuous variable. Associations were further examined by chronic kidney disease status, diabetes status, high-sensitivity C-reactive protein (hsCRP) concentrations, body mass index categories, as well as in secondary prevention. Discrimination was evaluated using the area under the curve across 4 models: base, base plus IL-6, base plus hsCRP, and base plus both markers.

Results
Among 59,396 participants, the median IL-6 concentration was 1.91 pg/mL. The mean age was 63.6 ± 12.4 years. 67.6% were women, and 20.6% were Black. The longest median follow-up time was 15.8 years (for CVD-specific mortality). Higher IL-6 concentrations were associated with increased risk for all 9 outcomes. The strongest association was observed for CHD-specific mortality, with an adjusted HR of 2.12 (95% CI: 1.88-2.39) in the highest compared with the lowest IL-6 quartile. The weakest association was for myocardial infarction (HR: 1.45; 95% CI: 1.28-1.64). Findings were robust and consistent in all key subgroups as well as in secondary prevention. IL-6 alone demonstrated modest additive discrimination beyond hsCRP for stroke, heart failure, CVD, CHD, and mortality.

Conclusions
In this large, harmonized, individual-level participant data analysis of prospective cohorts, higher IL-6 concentrations were strongly associated with 9 cardiovascular and mortality outcomes after controlling for clinical covariates. These associations were consistent across cardiometabolic subgroups, chronic kidney disease status, and secondary prevention populations, highlighting the broad and consistent role of IL-6-mediated inflammation in cardiovascular risk.

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