Literature DB >> 19878507

Adipocytokines and the metabolic syndrome among older persons with and without obesity: the InCHIANTI study.

Sari Stenholm1, Annemarie Koster, Dawn E Alley, Marjolein Visser, Marcello Maggio, Tamara B Harris, Josephine M Egan, Stefania Bandinelli, Jack M Guralnik, Luigi Ferrucci.   

Abstract

OBJECTIVES: Adipose tissue-derived inflammation may contribute to metabolic alterations and eventually to the metabolic syndrome (MetS). The purpose of this study was to: (1) examine the role of adipocytokines in the association between obesity and the MetS and (2) to determine whether the association is different in obese and non-obese persons.
DESIGN: Cross-sectional population-based InCHIANTI study.
SUBJECTS: A total of 944 community-dwelling adults aged 65 years and older living in Tuscany, Italy. MEASUREMENTS: Obesity was defined as body mass index > or =30 kg/m2 and MetS as > or =3 of the ATP-III criteria. Circulating levels of C-reactive protein, interleukin (IL)-6, IL-1 receptor antagonist (IL-1ra), IL-18, tumour necrosis factor (TNF)-alpha R1, adiponectin, resistin and leptin were measured. Additionally, insulin resistance was determined using the homeostasis model assessment (HOMA-IR).
RESULTS: The prevalence of the MetS was 32%. Both overall and abdominal obesity were significantly associated with the MetS after adjusting for inflammatory cytokines, adipokines and lifestyle factors. After adjusting for multiple confounders and HOMA-IR, IL-1ra, TNF-alpha R1 and adiponectin (P < 0.05) remained significantly associated with the MetS. Having multiple cytokines in the highest tertile increased the likelihood of having the MetS in both obese (P for trend 0.002) and non-obese persons (P for trend 0.001) independent of insulin resistance.
CONCLUSIONS: Non-obese and obese individuals who develop an intense pro-inflammatory state may be more prone to develop the MetS than those with lower levels of inflammation.

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Year:  2010        PMID: 19878507      PMCID: PMC2888845          DOI: 10.1111/j.1365-2265.2009.03742.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


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