肥満治療薬の心臓への効果は体重減少だけでは説明できない(Obesity drug heart benefits not just due to weight loss)

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2026-09-24 エディンバラ大学

エディンバラ大学の研究チームは、肥満または過体重の患者を対象としたSELECT試験の17,600人超のデータを解析し、セマグルチドによる心血管疾患リスク低下は、体重減少だけでは説明できないことを示した。セマグルチド投与群では、心筋梗塞、脳卒中、心血管死などの重大な心血管イベントが約20%少なかった。体重、腹囲、血圧、コレステロール、糖尿病指標、炎症、腎機能などの変化を個別・総合的に分析したところ、これらで説明できるリスク低下は最大でも約半分だった。したがって、セマグルチドには体重減少とは別の心血管保護作用がある可能性が示された。ただし、その具体的な機序はまだ不明で、抗炎症作用や心筋・血管への直接作用などが候補として挙げられている。研究はSELECT試験のデータを用いた解析で、European Heart Journalに掲載された。

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セマグルチドと心血管リスク低減:SELECT試験の媒介分析 Semaglutide and cardiovascular risk reduction: a mediation analysis of the SELECT trial

Helen M Colhoun, A Michael Lincoff, Donna Ryan, Ildiko Lingvay, Steven E Kahn, G Kees Hovingh, Søren Hardt-Lindberg, Tugce Kalayci Oral, Peter E Weeke, Martin Linder,…
European Heart Journal  Published:23 September 2026
DOI:https://doi.org/10.1093/eurheartj/ehag524

肥満治療薬の心臓への効果は体重減少だけでは説明できない(Obesity drug heart benefits not just due to weight loss)

Abstract

Background and Aims
In SELECT, subcutaneous semaglutide (target dose 2.4 mg) weekly in adults with pre-existing cardiovascular disease and body mass index ≥27 kg/m2 without diabetes significantly reduced major adverse cardiovascular events (MACE) by 20% vs placebo. This analysis explored potential mediators of this cardiovascular benefit.

Methods
Changes from randomization to 24 months in body weight, waist circumference, plasma high-sensitivity C-reactive protein (hsCRP), glycated haemoglobin (HbA1c), lipids, blood pressure, estimated glomerular filtration rate, and urinary albumin-to-creatinine ratio were examined individually, and in combination, as potential mediators of MACE risk reduction, using the Vansteelandt repeated regression method (a counterfactual approach).

Results
Semaglutide significantly (P < .05) improved all potential mediators investigated. Point estimates for % mediation were largest for waist circumference (64.0% [95% confidence interval (CI) 27.5, 179.6]), hsCRP (42.1% [17.9, 110.5]), HbA1c (29.0% [−20.7, 120.5]), and body weight (19.5% [−33.0, 110.7]), examined separately, but all had wide CIs. Supplementary analyses suggested unreliability of estimates for body weight and waist circumference, potentially due to differing relationship of body weight and waist change to MACE between treatment arms. Multivariable analysis estimated joint mediation for all potential mediators combined to be 31.4% (95% CI −30.1, 143.6). When variables other than body weight and waist circumference were considered, % mediation was 46.0% (95% CI −6.0, 161.0).

Conclusions
Mediation analyses could not fully ascribe the effects of semaglutide on MACE to known risk factors in SELECT with any certainty. Further investigation of potential additional biomarkers and mediators of semaglutide’s cardiovascular protective effect are of interest.

医療・健康
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