Oksanen L, Ohman M, Heiman M, Kainulainen K, Kaprio J, Mustajoki P, Koivisto V, Koskenvuo M, Jänne O A, Peltonen L, Kontula K
Department of Medicine, University of Helsinki, Finland.
Hum Genet. 1997 May;99(5):559-64. doi: 10.1007/s004390050406.
Leptin, the product of the ob gene, reduces body fat in genetically obese animals and circulates in elevated concentrations in the blood of obese patients. Polymorphic markers situated in the proximity of the human ob gene have recently been suggested to be linked to morbid obesity. We have studied the possible association between the microsatellite markers near the ob gene and morbid obesity in 252 morbidly obese patients with a mean body mass index (BMI) of 43 +/- 7 kg/m2, and 151 lean controls with a mean BMI of 22 +/- 2 kg/m2, and searched for linkage of these gene markers to obesity in 76 affected sib-pairs (BMI > or = 32). No significant association was observed between any of the eight microsatellite markers and morbid obesity, and affected-sib-pair analysis failed to show linkage of three selected ob gene markers to obesity in the sibships. There was a strong positive correlation between serum leptin levels and BMI in morbidly obese patients; a carrier status for either of the two most prevalent alleles of the microsatellite marker D7S530 in the vicinity of the ob gene was associated with serum leptin levels in the obese subjects. Two of the markers (D7S2519, D7S649) showed a significant relation to the weight-losing response to a 16-week very-low-calorie dietary intervention. We have thus been able to confirm a tight relationship between serum leptin and body mass but have found no evidence for genetic linkage of the ob gene markers to morbid obesity in a population considered to represent a genetic isolate and to be an ideal model for studies of complex disorders.
瘦素是ob基因的产物,可减少遗传性肥胖动物的体脂,且在肥胖患者血液中的浓度升高。最近有人提出,位于人类ob基因附近的多态性标记与病态肥胖有关。我们研究了ob基因附近的微卫星标记与病态肥胖之间的可能关联,研究对象为252例病态肥胖患者(平均体重指数[BMI]为43±7kg/m²)和151例瘦人对照(平均BMI为22±2kg/m²),并在76对患病同胞对(BMI≥32)中寻找这些基因标记与肥胖的连锁关系。在八个微卫星标记中,未观察到任何一个与病态肥胖有显著关联,且患病同胞对分析未能显示在同胞关系中三个选定的ob基因标记与肥胖有连锁关系。病态肥胖患者的血清瘦素水平与BMI之间存在很强的正相关;ob基因附近微卫星标记D7S530的两个最常见等位基因中的任何一个的携带状态与肥胖受试者的血清瘦素水平有关。其中两个标记(D7S2519、D7S649)显示出与16周极低热量饮食干预的减肥反应有显著关系。因此,我们能够证实血清瘦素与体重之间存在紧密关系,但在一个被认为是遗传隔离群体且是复杂疾病研究理想模型的人群中,没有发现ob基因标记与病态肥胖存在遗传连锁的证据。