4.5 Article

Markers of inflammation in prevalent and incident Parkinson's disease in the Cardiovascular Health Study

Journal

PARKINSONISM & RELATED DISORDERS
Volume 18, Issue 3, Pages 274-278

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.parkreldis.2011.11.003

Keywords

Albumins; C-reactive protein; Inflammation; Interleukin-6; Odds ratio; Parkinson's disease; Tumor necrosis factor-alpha

Funding

  1. NCATS NIH HHS [KL2 TR000146, UL1 TR000005] Funding Source: Medline
  2. NCRR NIH HHS [KL2 RR024154, KL2 RR024154-01] Funding Source: Medline
  3. NHLBI NIH HHS [N01HC85079, T32 HL007902-01, N01 HC045133, N01 HC035129, N01 HC085086, T32 HL007902, U01 HL080295-01, N01HC55222, U01 HL080295, N01 HC075150] Funding Source: Medline
  4. NIA NIH HHS [P30 AG024827, P30 AG024827-01, R01 AG015928-02] Funding Source: Medline
  5. NINDS NIH HHS [R03 NS057257, R03 NS057257-02, K23 NS070867, R03 NS057257-01A2] Funding Source: Medline

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Background: Studies demonstrate existence of inflammation in prevalent Parkinson's disease (PD). We assessed associations of baseline levels of inflammatory markers with prevalent PD at baseline (1989) and incident PD identified over 13 years of follow-up of the Cardiovascular Health Study. Methods: Blood samples at baseline were measured for fibrinogen, interleukin-6, tumor necrosis factor-alpha, C-reactive protein, albumin, and white blood cells. The analysis included 60 prevalent and 154 incident PD cases. Results: Risk of prevalent PD was significantly higher per doubling of IL-6 among women (odds ratio [OR] = 1.5, 95% confidence interval [CI]: 1.0, 2.4) and WBC among men (OR: 2.4, 95% Cl: 1.2, 4.9) in multivariate models. Risk of incident PD was not associated with higher levels of any biomarker after adjusting for age, smoking, African American race, and history of diabetes. Inverse associations with incident PD were observed per doubling of C-reactive protein (OR = 0.9; 95% Cl: 0.8, 1.0) and of fibrinogen among women (OR = 0.4; 95% Cl: 0.2, 0.8). Conclusions: Although inflammation exists in PD, it may not represent an etiologic factor. Our findings suggest the need for larger studies that measure inflammatory markers before PD onset. Published by Elsevier Ltd.

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