Friedel S, Horro F Fontenla, Wermter A K, Geller F, Dempfle A, Reichwald K, Smidt J, Brönner G, Konrad K, Herpertz-Dahlmann B, Warnke A, Hemminger U, Linder M, Kiefl H, Goldschmidt H P, Siegfried W, Remschmidt H, Hinney A, Hebebrand J
Clinical Research Group, Department of Child and Adolescent Psychiatry and Psychotherapy, Philipps-University of Marburg, 35039 Marburg, Germany.
Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):96-9. doi: 10.1002/ajmg.b.30090.
Several lines of evidence indicate an involvement of brain derived neurotrophic factor (BDNF) in body weight regulation and activity: heterozygous Bdnf knockout mice (Bdnf(+/-)) are hyperphagic, obese, and hyperactive; furthermore, central infusion of BDNF leads to severe, dose-dependent appetite suppression and weight loss in rats. We searched for the role of BDNF variants in obesity, eating disorders, and attention-deficit/hyperactivity disorder (ADHD). A mutation screen (SSCP and DHPLC) of the translated region of BDNF in 183 extremely obese children and adolescents and 187 underweight students was performed. Additionally, we genotyped two common polymorphisms (rs6265: p.V66M; c.-46C > T) in 118 patients with anorexia nervosa, 80 patients with bulimia nervosa, 88 patients with ADHD, and 96 normal weight controls. Three rare variants (c.5C > T: p.T2I; c.273G > A; c.*137A > G) and the known polymorphism (p.V66M) were identified. A role of the I2 allele in the etiology of obesity cannot be excluded. We found no association between p.V66M or the additionally genotyped variant c.-46C > T and obesity, ADHD or eating disorders. This article contains supplementary material, which may be viewed at the American Journal of Medical Genetics website at http://www.interscience.wiley.com/jpages/0148-7299:1/suppmat/index.html.
多项证据表明脑源性神经营养因子(BDNF)参与体重调节和活动:杂合子Bdnf基因敲除小鼠(Bdnf(+/-))食欲亢进、肥胖且多动;此外,向大鼠脑内注射BDNF会导致严重的、剂量依赖性的食欲抑制和体重减轻。我们探究了BDNF变体在肥胖症、饮食失调和注意力缺陷多动障碍(ADHD)中的作用。对183名极度肥胖的儿童和青少年以及187名体重过轻的学生进行了BDNF编码区的突变筛查(单链构象多态性分析和变性高效液相色谱分析)。此外,我们对118例神经性厌食症患者、80例神经性贪食症患者、88例ADHD患者和96名体重正常的对照者进行了两个常见多态性位点(rs6265:p.V66M;c.-46C>T)的基因分型。鉴定出三个罕见变体(c.5C>T:p.T2I;c.273G>A;c.*137A>G)和已知的多态性位点(p.V66M)。不能排除I2等位基因在肥胖病因学中的作用。我们未发现p.V66M或另外进行基因分型的变体c.-46C>T与肥胖症、ADHD或饮食失调之间存在关联。本文包含补充材料,可在美国医学遗传学杂志网站http://www.interscience.wiley.com/jpages/0148-7299:1/suppmat/index.html上查看。