Diet, Gut Microbiota, and Histidine Metabolism Toward Imidazole Propionate Production in Relation to Type 2 Diabetes

IF 14.8 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Diabetes Care Pub Date : 2025-05-09 DOI:10.2337/dc24-2816
Hongbo Yang, Kai Luo, Brandilyn A. Peters, Yi Wang, Yanbo Zhang, Martha Daviglus, Amber Pirzada, Christina Cordero, Bing Yu, Robert D. Burk, Robert Kaplan, Qibin Qi
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引用次数: 0

Abstract

OBJECTIVE To examine associations of serum imidazole propionate (ImP), histidine, and their ratio with incident type 2 diabetes (T2D) and related dietary and gut microbial factors in U.S. Hispanic/Latino people. RESEARCH DESIGN AND METHODS In the Hispanic Community Health Study/Study of Latinos, we evaluated serum ImP, histidine, and ImP-to-histidine ratio at baseline (2008–2011) and their cross-sectional associations with dietary intake and prospective associations with incident T2D over ∼12 years (n = 4,632). In a subsample with gut microbiota data during a follow-up visit (2016–2018), we examined gut microbial species associated with serum ImP and their potential interactions with dietary intake. RESULTS Serum ImP and ImP-to-histidine ratio were positively associated with incident T2D (hazard ratio [95% CI] = 1.17 [1.00–1.36] and 1.33 [1.14–1.55], respectively, comparing highest and lowest tertiles), whereas histidine was inversely associated with incident T2D (hazard ratio = 0.75 [95% CI 0.64–0.86]). A higher amount of fiber intake was associated with lower serum ImP level and ImP-to-histidine ratio, whereas histidine intake was not associated with serum ImP level in the overall sample. Fifty-three bacterial species, including 19 putative ImP producers, were associated with serum ImP. Histidine intake was positively associated with serum ImP and ImP-to-histidine ratio only in participants with a high ImP-associated gut microbiota score (P = 0.03 and 0.02, respectively, for interaction). The associations of fiber intake with serum ImP and ImP-to-histidine ratio were partly mediated by ImP-associated gut microbiota (proportion mediated = 31.4% and 19.8%, respectively). CONCLUSIONS This study suggested an unfavorable relationship between histidine metabolism toward ImP production, potentially regulated by dietary intake and gut microbiota, and risk of T2D in U.S. Hispanics/Latino people.
饮食、肠道菌群和组氨酸代谢与2型糖尿病相关的咪唑丙酸生成
目的研究美国西班牙裔/拉丁裔人群血清丙酸咪唑(ImP)、组氨酸及其比值与2型糖尿病(T2D)发病及相关饮食和肠道微生物因素的关系。研究设计和方法在西班牙裔社区健康研究/拉丁裔研究中,我们评估了基线(2008-2011年)时血清ImP、组氨酸和ImP /组氨酸比值,以及它们与饮食摄入的横断面相关性,以及与12年内T2D事件的前瞻性相关性(n = 4,632)。在随访期间(2016-2018年)的肠道微生物群数据亚样本中,我们检查了与血清ImP相关的肠道微生物种类及其与饮食摄入的潜在相互作用。结果血清ImP和ImP /组氨酸比值与T2D的发生呈正相关(风险比[95% CI]分别为1.17[1.00-1.36]和1.33[1.14-1.55],比较最高和最低三分位数),而组氨酸与T2D的发生呈负相关(风险比= 0.75 [95% CI 0.64-0.86])。较高的纤维摄入量与较低的血清ImP水平和ImP /组氨酸比值相关,而在整个样本中,组氨酸摄入量与血清ImP水平无关。53种细菌,包括19种推定的ImP产生者,与血清ImP相关。组氨酸摄入量与血清ImP和ImP /组氨酸比率呈正相关,仅在ImP相关肠道微生物群评分较高的参与者中(P分别= 0.03和0.02)。纤维摄入量与血清ImP和ImP /组氨酸比值的关联部分由ImP相关肠道菌群介导(比例分别为31.4%和19.8%)。结论:本研究表明,在美国西班牙裔/拉丁裔人群中,组氨酸代谢与ImP产生(可能受饮食摄入和肠道微生物群的调节)和T2D风险之间存在不利关系。
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来源期刊
Diabetes Care
Diabetes Care 医学-内分泌学与代谢
CiteScore
27.80
自引率
4.90%
发文量
449
审稿时长
1 months
期刊介绍: The journal's overarching mission can be captured by the simple word "Care," reflecting its commitment to enhancing patient well-being. Diabetes Care aims to support better patient care by addressing the comprehensive needs of healthcare professionals dedicated to managing diabetes. Diabetes Care serves as a valuable resource for healthcare practitioners, aiming to advance knowledge, foster research, and improve diabetes management. The journal publishes original research across various categories, including Clinical Care, Education, Nutrition, Psychosocial Research, Epidemiology, Health Services Research, Emerging Treatments and Technologies, Pathophysiology, Complications, and Cardiovascular and Metabolic Risk. Additionally, Diabetes Care features ADA statements, consensus reports, review articles, letters to the editor, and health/medical news, appealing to a diverse audience of physicians, researchers, psychologists, educators, and other healthcare professionals.
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