4.3 Article

Differential Association of Serum n-3 Polyunsaturated Fatty Acids with Various Cerebrovascular Lesions in Japanese Men

Journal

CEREBROVASCULAR DISEASES
Volume 51, Issue 6, Pages 774-780

Publisher

KARGER
DOI: 10.1159/000524243

Keywords

Fatty acids; Cerebrovascular disease; Epidemiology

Funding

  1. Ministry of Education, Culture, Sports, Science, and Technology Japan
  2. [17209023, 21249043, 23249036, 25253046, 15H02528, 18H04074, R01 HL068200]
  3. National Institutes of Health, US [13307016]
  4. GlaxoSmithKline GB
  5. Grants-in-Aid for Scientific Research [18H04074, 15H02528] Funding Source: KAKEN

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This study investigated the association between n-3 PUFAs and cerebrovascular lesions in Japanese men. The results suggest that n-3 PUFAs may have a protective effect against large-artery stenosis in the brain, but not against small vessel lesions.
Background: An association between a high intake of marine-derived n-3 polyunsaturated fatty acids (n-3 PUFAs) with a lower risk of coronary heart disease was previously reported. However, the association between n-3 PUFAs and cerebrovascular lesions remains unclear. We evaluated this association in a general-population-based sample of Japanese men. Methods: Participants were community-dwelling men (40-79 years old) living in Kusatsu City, Shiga, Japan. Serum concentrations of n-3 PUFAs, defined as the sum of eicosapentaenoic and docosahexaenoic acids, were measured via gas-liquid chromatography between 2006 and 2008. Magnetic resonance imaging was used to assess cerebrovascular lesions (including intracerebral large-artery stenosis, lacunar infarction, and microbleeds) and white matter lesions between 2012 and 2015. Logistic regression adjusting for conventional cardiovascular risk factors was used to estimate the odds ratio of prevalent cerebrovascular lesions per 1 standard deviation higher serum concentration of n-3 PUFAs. Results: Of a total of 739 men, the numbers (crude prevalence in %) of prevalent cerebral large-artery stenoses, lacunar infarctions, microbleeds, and white matter lesions were 222 (30.0), 162 (21.9), 103 (13.9), and 164 (22.2), respectively. A 1 standard deviation higher concentration of n-3 PUFAs (30.5 mu mol/L) was independently associated with lower odds of cerebral large-artery stenosis (multivariable-adjusted odds ratio, 0.80; 95% confidential interval, 0.67-0.97). There were no significant associations of n-3 PUFAs with the other types of lesions. Conclusions: n-3 PUFAs may have protective effects against large-artery stenosis, but not small vessel lesions, in the brain.

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