4.5 Article

Chronic inflammation role in the obesity-diabetes association: a case-cohort study

期刊

DIABETOLOGY & METABOLIC SYNDROME
卷 5, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/1758-5996-5-31

关键词

Diabetes; Obesity; Inflammation; Adipokines; Humans; Epidemiologic studies

资金

  1. National Heart, Lung, and Blood Institute [HHSN268201100005C, HHSN268201100006C, HHSN268201100007C, HHSN268201100008C, HHSN268201100009C, HHSN268201100010C, HHSN268201100011C, HHSN268201100012C]
  2. National Institute of Diabetes, Digestive and Kidney Diseases [R01-DK056918]
  3. Centers of Excellence Grant from the CNPq (Brazilian National Council for Scientific and Technological Development)

向作者/读者索取更多资源

Background: Chronic inflammation is related to both obesity and diabetes. Our aim was to investigate to what extent this inflammation contributes to the association between obesity and diabetes. Methods: Using a case-cohort design, we followed 567 middle-aged individuals who developed diabetes and 554 who did not over 9 years within the ARIC Study. Weighted Cox proportional hazards analyses permitted statistical inference to the entire cohort. Results: Obese individuals (BMI >= 30 kg/m(2)), compared to those with BMI<25 kg/m(2), presented a large increased risk of developing diabetes (HR[obesity]=6.4, 95%CI 4.5-9.2), as did those in the highest (compared to the lowest) quartile of waist circumference (HR[waist]=8.3, 95%CI 5.6-12.3), in analyses adjusted for age, gender, ethnicity, study center, and parental history of diabetes. Notably, further adjustment for adiponectin and inflammation markers halved the magnitude of these associations (HR[obesity]=3.2, 95%CI 2.1-4.7; and HR[waist]=4.2, 95%CI 2.8-6.5). In similar modeling, attenuation obtained by adding fasting insulin, instead of these markers, was only slightly more pronounced HR[obesity]=2.7, 95%CI 1.7-4.1; and HR[waist]=3.6, 95%CI 2.3-5.8). Conclusions: The marked decrease in the obesity-diabetes association after taking into account inflammation markers and adipokines indicates their major role in the pathways leading to adult onset of diabetes in obese individuals.

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