Genetic and hereditary aspects of childhood obesity

被引:72
作者
Farooqi, IS
机构
[1] Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, England
[2] Univ Cambridge, Addenbrookes Hosp, Dept Clin Med, Cambridge CB2 2QQ, England
基金
英国惠康基金;
关键词
genes; leptin; melanocortin;
D O I
10.1016/j.beem.2005.04.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genetic factors are involved in the regulation of body weight and in determining individual responses to environmental factors such as diet and exercise. The identification and characterization of monogenic obesity syndromes have led to an improved understanding of the precise nature of the inherited component of severe obesity and has had undoubted medical benefits, whilst helping to dispel the notion that obesity represents an individual defect in behaviour with no biological basis. For individuals at highest risk of the complications of severe obesity, such findings provide a starting point for providing more rational mechanism-based therapies, as has successfully been achieved for one disorder, congenital leptin deficiency.
引用
收藏
页码:359 / 374
页数:16
相关论文
共 58 条
  • [1] AHIRNA RS, 1996, NATURE, V382, P250
  • [2] Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
    Ansley, SJ
    Badano, JL
    Blacque, OE
    Hill, J
    Hoskins, BE
    Leitch, CC
    Kim, JC
    Ross, AJ
    Eichers, ER
    Teslovich, TM
    Mah, AK
    Johnsen, RC
    Cavender, JC
    Lewis, RA
    Leroux, MR
    Beales, PL
    Katsanis, N
    [J]. NATURE, 2003, 425 (6958) : 628 - 633
  • [3] Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2
    Badano, JL
    Ansley, SJ
    Leitch, CC
    Lewis, RA
    Lupski, JR
    Katsanis, N
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (03) : 650 - 658
  • [4] Genetics of body-weight regulation
    Barsh, GS
    Farooqi, IS
    O'Rahilly, S
    [J]. NATURE, 2000, 404 (6778) : 644 - 651
  • [5] BOUCHARD C, 1990, INT J OBESITY, V14, P55
  • [6] PRADER-WILLI SYNDROME - CURRENT UNDERSTANDING OF CAUSE AND DIAGNOSIS
    BUTLER, MG
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 35 (03): : 319 - 332
  • [7] A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism
    Challis, BG
    Pritchard, LE
    Creemers, JWM
    Delplanque, J
    Keogh, JM
    Luan, J
    Wareham, NJ
    Yeo, GSH
    Bhattacharyya, S
    Froguel, P
    White, A
    Farooqi, IS
    O'Rahilly, S
    [J]. HUMAN MOLECULAR GENETICS, 2002, 11 (17) : 1997 - 2004
  • [8] Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome
    Chandler, KE
    Kidd, A
    Al-Gazali, L
    Kolehmainen, J
    Lehesjoki, AE
    Black, GCM
    Clayton-Smith, J
    [J]. JOURNAL OF MEDICAL GENETICS, 2003, 40 (04) : 233 - 241
  • [9] A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
    Clément, K
    Vaisse, C
    Lahlou, N
    Cabrol, S
    Pelloux, V
    Cassuto, D
    Gourmelen, M
    Dina, C
    Chambaz, J
    Lacorte, JM
    Basdevant, A
    Bougneres, P
    Lebouc, Y
    Froguel, P
    Guy-Grand, B
    [J]. NATURE, 1998, 392 (6674) : 398 - 401
  • [10] COHEN MM, 1973, J PEDIATR-US, V83, P280