Bathum L, Andersen-Ranberg K, Boldsen J, Brøsen K, Jeune B
Department of Clinical Biochemistry, Odense University Hospital, Denmark.
Eur J Clin Pharmacol. 1998 Jul;54(5):427-30. doi: 10.1007/s002280050487.
To test whether some genotypes for CYP2D6 or CYP2C19 could contribute to longevity, we genotyped 241 Danish nonagenarians and centenarians for CYP2D6 and CYP2C19.
For CYP2D6 we identified the alleles CYP2D61, CYP2D63 and CYP2D64 with allele-specific polymerase chain reaction (PCR). The CYP2D65 alleles were identified with a long PCR method. For CYP2C19 we identified the alleles CYP2C191, CYP2C192 and CYP2C19*3 with an oligonucleotide ligation assay.
The four alleles for CYP2D6 did not occur in Hardy-Weinberg proportions. The frequency of poor metabolism was slightly higher (10.2%) than expected [7.7%; odds ratio (OR) = 1.36 (0.75-2.40)]. The genotypes for CYP2C19 occur in Hardy-Weinberg proportions. The frequency of poor metabolism (3.8%) was not significantly different from a young control group [3.1%; OR = 1.21 (0.26-5.75)].
CYP2D6 could play a role in human longevity due to the lack of Hardy-Weinberg proportions. If CYP2D6 only plays a role in longevity by protecting the poor metabolizers from cancer, we should expect a rise in the frequency in these genotypes in Denmark from 7.7% among young adults to 10-11% among very old people. We found a frequency of poor metabolism of 10.2% in the very old group. CYP2C19 is - due to the occurrence of Hardy-Weinberg proportions and the expected number of poor metabolizers unlikely to contribute to human longevity.
为了测试细胞色素P450 2D6(CYP2D6)或细胞色素P450 2C19(CYP2C19)的某些基因型是否与长寿有关,我们对241名丹麦的九旬老人和百岁老人进行了CYP2D6和CYP2C19基因分型。
对于CYP2D6,我们采用等位基因特异性聚合酶链反应(PCR)鉴定等位基因CYP2D61、CYP2D63和CYP2D64。采用长PCR方法鉴定CYP2D65等位基因。对于CYP2C19,我们采用寡核苷酸连接测定法鉴定等位基因CYP2C191、CYP2C192和CYP2C19*3。
CYP2D6的四个等位基因不符合哈迪-温伯格比例。代谢不良的频率略高于预期(10.2%)[7.7%;优势比(OR)=1.36(0.75 - 2.40)]。CYP2C19的基因型符合哈迪-温伯格比例。代谢不良的频率(3.8%)与年轻对照组[3.1%;OR = 1.21(0.26 - 5.75)]无显著差异。
由于不符合哈迪-温伯格比例,CYP2D6可能在人类长寿中发挥作用。如果CYP2D6仅通过保护代谢不良者免受癌症影响而在长寿中发挥作用,那么我们应该预期丹麦这些基因型的频率会从年轻人中的7.7%上升到非常年长者中的10 - 11%。我们在非常年长者组中发现代谢不良的频率为10.2%。由于符合哈迪-温伯格比例以及代谢不良者的预期数量,CYP2C19不太可能对人类长寿有贡献。