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Polymorphism of debrisoquine 4-hydroxylation and family studies of poor metabolizers in Chinese population

  
@article{APS5353,
	author = {Yun-long DU and Ya-qing LOU},
	title = {Polymorphism of debrisoquine 4-hydroxylation and family studies of poor metabolizers in Chinese population},
	journal = {Acta Pharmacologica Sinica},
	volume = {11},
	number = {1},
	year = {2016},
	keywords = {},
	abstract = {Debrisoquine hydroxylation capacity determined as the ratio of debrisoquine over 4-OH-debrisoquine in 8-h urine after a single dose (10 mg) was studied in 140 unrelated Chinese Han subjects and 2 families of poor metabolizers (PM) of debrisoquine. In the 140 Chinese subjects the frequency of PM was found to be 1.43% (2/140), much lower than the 5-10% in white population reported. No sex difference was shown on the hydroxylation of debrisoquine. The recoveries of debrisoquin, 4-OH-debrisoquine in 8-h urine were 16 +/- 11 and 13 +/- 6%, respectively. None of the parents in the 2 families was PMs. Phenotype distribution in each family and population was consistent with the hypothesis that debrisoquine 4-OH-hydroxylation activity is under diallelic, monogenetic control, with the PM phenotype inheriting in an autosomal recessive trait.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/5353}
}