Monteleone Palmiero, Tortorella Alfonso, Castaldo Eloisa, Di Filippo Carmela, Maj Mario
Department of Psychiatry, University of Naples SUN, Largo Madonna delle Grazie, 80138 Naples, Italy.
Neurosci Lett. 2006 May 8;398(3):325-7. doi: 10.1016/j.neulet.2006.01.023. Epub 2006 Feb 9.
Genetic factors likely contribute to the biological vulnerability to anorexia nervosa (AN) and bulimia nervosa (BN). We investigated whether the Arg51Gln and/or the Leu72Met gene polymorphisms of the human ghrelin, a peptide involved in the regulation of eating behavior, were associated to AN and/or BN. Two-hundred-ninety-two Caucasian women (114 with BN, 59 with AN and 119 healthy controls) participated into the study. No significant differences were found in the frequencies of the Arg51Gln and the Leu72Met ghrelin gene variants among patients with AN or BN and healthy controls. Moreover, no significant differences emerged in eating-related phenotypic variables between patients carrying the Leu72Met genotype as compared to those with the Leu72Leu genotype. These results suggest that the Arg51Gln and the Leu72Met polymorphisms of the human ghrelin gene do not contribute to the genetic susceptibility to AN and BN.
遗传因素可能导致神经性厌食症(AN)和神经性贪食症(BN)的生物学易感性。我们研究了参与饮食行为调节的肽类——人胃饥饿素的Arg51Gln和/或Leu72Met基因多态性是否与AN和/或BN相关。292名白种女性(114名患有BN,59名患有AN,119名健康对照)参与了该研究。在AN或BN患者与健康对照之间,未发现Arg51Gln和Leu72Met胃饥饿素基因变体的频率存在显著差异。此外,携带Leu72Met基因型的患者与携带Leu72Leu基因型的患者相比,在饮食相关表型变量上也未出现显著差异。这些结果表明,人胃饥饿素基因的Arg51Gln和Leu72Met多态性对AN和BN的遗传易感性没有影响。