Association of Subclinical Inflammation With Polyneuropathy in the Older Population
Aged, 80 and over
Inflammation
Male
Interleukin-6
Tumor Necrosis Factor-alpha
Anti-Inflammatory Agents, Non-Steroidal
Interleukin-18
Middle Aged
Intercellular Adhesion Molecule-1
3. Good health
Interleukin 1 Receptor Antagonist Protein
Polyneuropathies
03 medical and health sciences
C-Reactive Protein
0302 clinical medicine
Diabetic Neuropathies
Germany
Humans
Female
Inflammation Mediators
Waist Circumference
Original Research
Aged
DOI:
10.2337/dc13-0382
Publication Date:
2013-09-06T03:56:03Z
AUTHORS (10)
ABSTRACT
OBJECTIVE
Inflammatory 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 METHODS
We 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.
RESULTS
Serum 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-α. 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.
CONCLUSIONS
We 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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