4.7 Article

Association of Subclinical Inflammation With Polyneuropathy in the Older Population KORA F4 study

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DIABETES CARE
卷 36, 期 11, 页码 3663-3670

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AMER DIABETES ASSOC
DOI: 10.2337/dc13-0382

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  1. German Federal Ministry of Health (Berlin, Germany)
  2. Ministry of Innovation, Science, and Research of the State of North Rhine-Westphalia (Dusseldorf, Germany)
  3. German Research Foundation (DFG) [RA 459/3-1]
  4. German Federal Ministry of Education and Research (BMBF)
  5. Helmholtz Zentrum Munchen, German Research Center for Environmental Health
  6. German Federal Ministry of Science and Research (Berlin, Germany)
  7. State of Bavaria

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OBJECTIVEInflammatory processes have been implicated in the pathogenesis of diabetic distal sensorimotor polyneuropathy (DSPN), but their possible relationship has not been assessed at the population level.RESEARCH DESIGN AND METHODSWe determined serum concentrations of mediators of subclinical inflammation among 1,047 participants 61-82 years of age from the population-based Cooperative Health Research in the Region of Augsburg (KORA) F4 study (Germany). Logistic and linear regression models were fitted to assess associations between immune mediators (log-transformed) and the presence of clinical DSPN (dichotomous variable) or Michigan Neuropathy Screening Instrument (MNSI) examination score (continuous variable), respectively.RESULTSSerum concentrations of the anti-inflammatory interleukin (IL)-1 receptor antagonist (IL-1RA) were positively associated with the presence of DSPN and higher MNSI scores in age-adjusted and sex-adjusted analyses, whereas IL-6, IL-18, and soluble intercellular adhesion molecule-1 were positively associated with only MNSI scores. No associations were observed for adiponectin, C-reactive protein, or tumor necrosis factor-. Associations for IL-1RA and IL-6 with the MNSI score remained statistically significant after additional adjustment for waist circumference, height, hypertension, cholesterol, smoking, alcohol intake, physical activity, history of myocardial infarction or stroke, presence of neurological conditions, and use of nonsteroidal anti-inflammatory drugs.CONCLUSIONSWe conclude that DSPN is linked to proinflammatory and anti-inflammatory, possibly compensatory, processes in the older general population. Future studies should clarify the temporal sequence and causality of these associations.

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