Mahya Mehri Hajmir, Bahar Sayoldin, Ali Rahnavard, Matthew D Barberio, Rob M van Dam
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Linear regression models assessed changes in BCAA levels in relation to changes in cardiometabolic risk factors. We adjusted for multiple testing by using false discovery rate-adjusted Q values.</p><p><strong>Results: </strong>Increases in BCAA levels over 6 months (per 1 SD) were associated with increases in insulin resistance (HOMA-IR: Beta = 0.22, SE = 0.07), inflammation (GlycA: Beta = 0.03 mmol/l, SE = 0.004), ApoB (Beta = 0.02 g/l, SE = 0.006), and VLDL-cholesterol (Beta = 0.03 mmol/l, SE = 0.007) over the same period (all Q-values <0.01). Associations with HDL-cholesterol and triglycerides differed for valine versus leucine and isoleucine. No significant associations were observed with fasting glucose or blood pressure.</p><p><strong>Conclusion: </strong>Increasing levels of BCAAs were associated with insulin resistance, inflammation, and unfavorable lipid profiles, indicating their potential as targets for CVD prevention. Further research is warranted to elucidate how individual BCAAs influence lipid metabolism.</p>","PeriodicalId":520805,"journal":{"name":"The Journal of clinical endocrinology and metabolism","volume":" ","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Plasma branched-chain amino acid and cardiovascular disease risk factors: a longitudinal analysis of a lifestyle trial.\",\"authors\":\"Mahya Mehri Hajmir, Bahar Sayoldin, Ali Rahnavard, Matthew D Barberio, Rob M van Dam\",\"doi\":\"10.1210/clinem/dgaf509\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Context: </strong>Branched-chain amino acid (BCAAs) levels have been associated with a higher risk of cardiovascular diseases (CVD), but studies of the impact of BCAAs on CVD risk factors have mainly been cross-sectional.</p><p><strong>Objective: </strong>We examined the longitudinal association between changes in BCAA levels and CVD risk factors in a lifestyle trial.</p><p><strong>Method: </strong>We used data from 708 male and female participants, aged 25-78, of the U.S. PREMIER study. 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引用次数: 0
摘要
背景:支链氨基酸(BCAAs)水平与较高的心血管疾病(CVD)风险相关,但关于支链氨基酸对CVD危险因素影响的研究主要是横断面的。目的:在一项生活方式试验中,我们研究了BCAA水平变化与心血管疾病危险因素之间的纵向关联。方法:我们使用708名男性和女性参与者的数据,年龄在25-78岁,来自美国PREMIER研究。数据和生物标本来自NHLBI BioLINCC资源库。参与者接受了生活方式方面的建议,或在饮食、体育活动和减肥方面的全面咨询。生物标志物在基线和6个月随访时用核磁共振波谱测定。线性回归模型评估了与心脏代谢危险因素变化相关的BCAA水平变化。我们通过使用错误发现率调整Q值来调整多重测试。结果:BCAA水平在6个月内(每1 SD)升高与胰岛素抵抗(HOMA-IR: Beta = 0.22, SE = 0.07)、炎症(GlycA: Beta = 0.03 mmol/l, SE = 0.004)、ApoB (Beta = 0.02 g/l, SE = 0.006)和vldl -胆固醇(Beta = 0.03 mmol/l, SE = 0.007)升高相关(所有q值)BCAAs水平升高与胰岛素抵抗、炎症和不利的脂质谱相关,表明它们有可能成为心血管疾病预防的靶点。需要进一步的研究来阐明单个支链氨基酸如何影响脂质代谢。
Plasma branched-chain amino acid and cardiovascular disease risk factors: a longitudinal analysis of a lifestyle trial.
Context: Branched-chain amino acid (BCAAs) levels have been associated with a higher risk of cardiovascular diseases (CVD), but studies of the impact of BCAAs on CVD risk factors have mainly been cross-sectional.
Objective: We examined the longitudinal association between changes in BCAA levels and CVD risk factors in a lifestyle trial.
Method: We used data from 708 male and female participants, aged 25-78, of the U.S. PREMIER study. Data and biospecimens were from the NHLBI BioLINCC Repository. Participants received lifestyle advice or comprehensive counseling on diet, physical activity, and weight loss. Biomarkers were measured with NMR spectroscopy at baseline and the 6-month follow-up. Linear regression models assessed changes in BCAA levels in relation to changes in cardiometabolic risk factors. We adjusted for multiple testing by using false discovery rate-adjusted Q values.
Results: Increases in BCAA levels over 6 months (per 1 SD) were associated with increases in insulin resistance (HOMA-IR: Beta = 0.22, SE = 0.07), inflammation (GlycA: Beta = 0.03 mmol/l, SE = 0.004), ApoB (Beta = 0.02 g/l, SE = 0.006), and VLDL-cholesterol (Beta = 0.03 mmol/l, SE = 0.007) over the same period (all Q-values <0.01). Associations with HDL-cholesterol and triglycerides differed for valine versus leucine and isoleucine. No significant associations were observed with fasting glucose or blood pressure.
Conclusion: Increasing levels of BCAAs were associated with insulin resistance, inflammation, and unfavorable lipid profiles, indicating their potential as targets for CVD prevention. Further research is warranted to elucidate how individual BCAAs influence lipid metabolism.