Adiposity modifies the association between heart failure risk and glucose metabolic disorder in older individuals: a community-based prospective cohort study.

IF 8.5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Diabetology Pub Date : 2024-08-27 DOI:10.1186/s12933-024-02418-5
Liming Hou, Xin Wang, Peilin Li, Hua Zhang, Yanli Yao, Zhendong Liu, Juan Wang, Weike Liu
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Abstract

Background: Glucose metabolic disorder is associated with the risk of heart failure (HF). Adiposity is a comorbidity that is inextricably linked with abnormal glucose metabolism in older individuals. However, the effect of adiposity on the association between glucose metabolic disorder and HF risk, and the underlying mechanism remain unclear.

Methods: A total of 13,251 participants aged ≥ 60 years from a cohort study were categorized into euglycemia, prediabetes, uncontrolled diabetes, and well-controlled diabetes. Adiposity was assessed using body mass index (BMI), waist-to-hip ratio (WHR), and visceral fat area (VFA). Adiposity-associated metabolic activities were evaluated using adiponectin-to-leptin ratio (ALR), homeostatic model assessment of insulin resistance (HOMA-IR), and triglyceride-glucose index (TyG). The first occurrence of HF served as the outcome during the follow-up period.

Results: A total of 1,138 participants developed HF over the course of an average follow-up period of 10.9 years. The rate of incident HF occurrence was higher in prediabetes, uncontrolled diabetes, and well-controlled diabetes participants compared to that in euglycemia participants. However, the high rates were significantly attenuated by BMI, VFA, and WHR. For WHR in particular, the hazard ratio for incident HF was 1.18 (95% confidence interval (CI): 1.03, 1.35, Padj.=0.017) in prediabetes, 1.59 (95% CI: 1.34, 1.90, Padj.<0.001) in uncontrolled diabetes, and 1.10 (95% CI: 0.85, 1.43, Padj.=0.466) in well-controlled diabetes. The population attributable risk percentage for central obesity classified by WHR for incident HF was 30.3% in euglycemia, 50.0% in prediabetes, 48.5% in uncontrolled diabetes, and 54.4% in well-controlled diabetes. Adiposity measures, especially WHR, showed a significant interaction with glucose metabolic disorder in incident HF (all Padj.<0.001). ALR was negatively associated and HOMA-IR and TyG were positively associated with BMI, WHR, VFA, and incident HF (all Padj.<0.05). ALR, HOMA-IR, and TyG mediated the associations for BMI, WHR and VFA with incident HF (all Padj.<0.05).

Conclusions: Adiposity attenuated the association of glucose metabolic disorder with incident HF. The results also showed that WHR may be an appropriate indicator for evaluating adiposity in older individuals. Adiposity-associated metabolic activities may have a bridging role in the process of adiposity attenuating the association between glucose metabolic disorder and incident HF.

Trial registration: retrospectively registered number: ChiCTR-EOC-17,013,598.

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肥胖会改变老年人心力衰竭风险与葡萄糖代谢紊乱之间的关系:一项基于社区的前瞻性队列研究。
背景:糖代谢紊乱与心力衰竭(HF)风险有关。肥胖是一种与老年人糖代谢异常密不可分的合并症。然而,脂肪对糖代谢紊乱与心力衰竭风险之间关系的影响及其内在机制仍不清楚:方法:将一项队列研究中 13251 名年龄≥ 60 岁的参与者分为优生、糖尿病前期、糖尿病未控制和糖尿病控制良好四类。通过体重指数(BMI)、腰臀比(WHR)和内脏脂肪面积(VFA)来评估肥胖程度。脂肪相关代谢活动通过脂肪连素与瘦素比值(ALR)、胰岛素抵抗稳态模型评估(HOMA-IR)和甘油三酯-葡萄糖指数(TyG)进行评估。在随访期间,以首次出现高血压作为结果:结果:在平均 10.9 年的随访期内,共有 1 138 名参与者患上了心房颤动。与优生优育者相比,糖尿病前期、糖尿病未控制和糖尿病控制良好者的心房颤动发生率更高。然而,体重指数(BMI)、血管内皮脂肪含量(VFA)和体重指数(WHR)会明显降低高发率。特别是WHR,在糖尿病前期,发生高血压的危险比为1.18(95% 置信区间(CI):1.03, 1.35, Padj.=0.017),在糖尿病控制良好的人群中,发生高血压的危险比为1.59(95% CI:1.34, 1.90, Padj.adj.=0.466)。以 WHR 分类的中心性肥胖对高血脂事件的人群可归因风险百分比在优血症中为 30.3%,在糖尿病前期为 50.0%,在未控制的糖尿病中为 48.5%,在控制良好的糖尿病中为 54.4%。脂肪测量指标,尤其是 WHR,与发生 HF 的糖代谢紊乱有显著的交互作用(全部为 Padj.adj.adj.结论:脂肪减少了葡萄糖代谢紊乱与心房颤动的关联。研究结果还表明,WHR 可能是评估老年人肥胖程度的适当指标。与脂肪相关的代谢活动可能在脂肪减少葡萄糖代谢紊乱与心房颤动之间的关联过程中起到桥梁作用:ChiCTR-EOC-17,013,598.
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来源期刊
Cardiovascular Diabetology
Cardiovascular Diabetology 医学-内分泌学与代谢
CiteScore
12.30
自引率
15.10%
发文量
240
审稿时长
1 months
期刊介绍: Cardiovascular Diabetology is a journal that welcomes manuscripts exploring various aspects of the relationship between diabetes, cardiovascular health, and the metabolic syndrome. We invite submissions related to clinical studies, genetic investigations, experimental research, pharmacological studies, epidemiological analyses, and molecular biology research in this field.
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