Associations among objectively measured physical activity, fasting plasma homocysteine concentration, and MTHFR C677T genotype View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-03-31

AUTHORS

Haruka Murakami, Motoyuki Iemitsu, Kiyoshi Sanada, Yuko Gando, Yumi Ohmori, Ryoko Kawakami, Satoshi Sasaki, Izumi Tabata, Motohiko Miyachi

ABSTRACT

Elevated fasting plasma homocysteine (Hcy) level is a vascular disease risk factor. Plasma Hcy is affected by 5,10-methylenetetrahydofolate reductase (MTHFR) genotype and dietary folate intake. This cross-sectional study in 434 Japanese adults examined the associations among objectively measured physical activity (PA), plasma Hcy adjusting for dietary folate intake, and MTHFR C677T genotype. Daily PA was measured by triaxial accelerometry and all subjects completed a questionnaire about their dietary habits. Plasma Hcy and MTHFR C677T genotype were determined. Plasma Hcy in subjects with the TT genotype was significantly higher than in those with CC or CT genotype (p < 0.001). Plasma Hcy was significantly different between ≥200 (7.6 ± 0.2 nmol/mL) and <200 µg/day (8.3 ± 0.3 nmol/mL) folate intake groups (p = 0.003). There were no differences in plasma Hcy adjusting for age, sex, and folate intake between groups according to PA category in all subjects. However, there were significant interactions between time spent in light PA (p = 0.003), vigorous PA (p = 0.001), or inactivity (p = 0.004), and MTHFR genotype. In only the TT genotype, shorter time spent in light PA was associated with higher plasma Hcy than a longer time spent in light PA (11.5 ± 3.3 nmol/mL vs. 8.5 ± 3.3 nmol/mL, p < 0.001), and longer time spent in vigorous PA and inactivity were associated with higher plasma Hcy (11.8 ± 3.3 nmol/mL vs. 8.4 ± 3.2 nmol/mL, 11.6 ± 3.3 nmol/mL vs. 8.4 ± 3.3 nmol/mL, respectively, p < 0.001). In conclusion, light and vigorous PA were associated with plasma Hcy only in the TT genotype, but there were no such associations in all genotypes. More... »

PAGES

2997-3005

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00421-011-1926-z

DOI

http://dx.doi.org/10.1007/s00421-011-1926-z

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1016067758

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/21451940


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