The dysmetabolic syndrome

被引:163
作者
Groop, L [1 ]
Orho-Melander, M [1 ]
机构
[1] Lund Univ, Wallenberg Lab, Dept Endocrinol, Malmo, Sweden
关键词
abdominal obesity; dyslipidaemia; hypertension; insulin resistance; thrifty genes; type; 2; diabetes;
D O I
10.1046/j.1365-2796.2001.00864.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The first unifying definition for the metabolic syndrome was proposed by WHO in 1998. In accordance to this, patients with type 2 diabetes mellitus or impaired glucose tolerane have the syndrome if they fulfil two of the criteria: hypertension, dyslipidaemia. obesity/abdominal obesity and microalbuminuria. Persons with normal glucose tolerance (NGT) should also be insulin resistant. About 40% of persons with impaired glucose tolerance (IGT) and 70% of patients with type 2 diabetes have features of the syndrome. Importantly, presence of the dysmetabolic syndrome is associated with reduced survival, particularly because of increased cardiovascular mortality. The dysmetabolic syndrome most likely results from interplay between several genes and an affluent environment. Compatible with the thrifty gene theory, common variants in genes regulating lipolysis, thermogenesis and glucose uptake in skeletal muscle account for a large part of such thrift-v genes. However, hitherto unknown genes may still be identified by random gene approaches.
引用
收藏
页码:105 / 120
页数:16
相关论文
共 159 条
[1]   Postprandial lipemic response is modified by the polymorphism at codon 54 of the fatty acid-binding protein 2 gene [J].
Ågren, JJ ;
Valve, R ;
Vidgren, H ;
Laakso, M ;
Uusitupa, M .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (10) :1606-1610
[2]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[3]  
2-S
[4]   AMINO-ACID POLYMORPHISMS OF INSULIN-RECEPTOR SUBSTRATE-1 IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
ALMIND, K ;
BJORBAEK, C ;
VESTERGAARD, H ;
HANSEN, T ;
ECHWALD, S ;
PEDERSEN, O .
LANCET, 1993, 342 (8875) :828-832
[5]   Genetic polymorphisms and disease [J].
Altshuler, D ;
Kruglyak, L ;
Lander, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (22) :1626-1626
[6]   The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes [J].
Altshuler, D ;
Hirschhorn, JN ;
Klannemark, M ;
Lindgren, CM ;
Vohl, MC ;
Nemesh, J ;
Lane, CR ;
Schaffner, SF ;
Bolk, S ;
Brewer, C ;
Tuomi, T ;
Gaudet, D ;
Hudson, TJ ;
Daly, M ;
Groop, L ;
Lander, ES .
NATURE GENETICS, 2000, 26 (01) :76-80
[7]  
[Anonymous], PROGR OBESITY RES
[8]   Effects of mutations in the human uncoupling protein 3 gene on the respiratory quotient and fat oxidation in severe obesity and type 2 diabetes [J].
Argyropoulos, G ;
Brown, AM ;
Willi, SM ;
Zhu, JG ;
He, YF ;
Reitman, M ;
Gevao, SM ;
Spruill, I ;
Garvey, WT .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (07) :1345-1351
[9]   Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production [J].
Arsenijevic, D ;
Onuma, H ;
Pecqueur, C ;
Raimbault, S ;
Manning, BS ;
Miroux, B ;
Couplan, E ;
Alves-Guerra, MC ;
Goubern, M ;
Surwit, R ;
Bouillaud, F ;
Richard, D ;
Collins, S ;
Ricquier, D .
NATURE GENETICS, 2000, 26 (04) :435-439
[10]   PPARγ, the ultimate thrifty gene [J].
Auwerx, J .
DIABETOLOGIA, 1999, 42 (09) :1033-1049