Please use this identifier to cite or link to this item:
Title: Association of catechol-O-methyltransferase (COMT) polymorphism and cognition, BMI, blood pressure, and uric acid in a Chinese cohort
Authors: 國立臺灣師範大學科學教育研究所
Yeh, T. K.
Chang, C. Y.
Hu, C.Y.
Lin, P. J.
Yeh, T. C.
Issue Date: 4-Sep-2010
Abstract: The catechol-O-methyltransferase (COMT) is an intracellular methylation enzyme that catalyzes degradation pathway and inactivates the function of catecholamines and estrogens, both of which are of known importance for cardiovascular risk factors such as obesity and hypertension. A single nucleotide polymorphism (SNP), a G to A transition in exon 4 of the COMT gene resulting in a valine to methionine substitution at residue 158, has been found to be associated with differential COMT activity. We hypothesized that this polymorphism might play a possible contribution for diversity physiology due to the COMT widespread over the organs and tissues. Totally, 711 volunteers, aged 16–17 years old, all physically healthy Han Chinese descendants were recruited. Subjects underwent extensive anthropometric, clinical and biochemical assessment. The result reveals that subjects with Met/Met homozygous displayed higher BMI, diastolic pressure, and uric acid significantly. This finding may suggest a possible risk factor of COMT in obesity, hypertension, and hyperuricemia.
ISSN: 0168-0102
Other Identifiers: ntnulib_tp_C0701_02_104
Appears in Collections:教師著作

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.