Type 2 diabetes mellitus

被引:1102
作者
DeFronzo, Ralph A. [1 ,2 ]
Ferrannini, Ele [3 ]
Groop, Leif [4 ]
Henry, Robert R. [5 ]
Herman, William H. [6 ]
Holst, Jens Juul [7 ]
Hu, Frank B. [8 ,9 ,10 ]
Kahn, C. Ronald [11 ,12 ]
Raz, Itamar [13 ]
Shulman, Gerald I. [14 ,15 ,16 ]
Simonson, Donald C. [17 ]
Testa, Marcia A. [18 ]
Weiss, Ram [19 ]
机构
[1] Univ Texas Hlth Sci Ctr, South Texas Vet Hlth Care Syst, Dept Med, Diabet Div, 701 S Zarzamoro, San Antonio, TX 78207 USA
[2] Texas Diabet Inst, San Antonio, TX 78207 USA
[3] CNR Inst Clin Physiol, Pisa, Italy
[4] Lund Univ, Ctr Diabet, Dept Clin Sci Malmoe Diabet & Endocrinol, Lund, Sweden
[5] Univ Calif San Diego, VA San Diego Healthcare Syst, Ctr Metab Res, Sect Diabet Endocrinol & Metab, San Diego, CA USA
[6] Univ Michigan, Ann Arbor, MI USA
[7] Univ Copenhagen, Copenhagen, Denmark
[8] Harvard Med Sch, Brigham & Womens Hosp, Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA USA
[9] Harvard Med Sch, Brigham & Womens Hosp, Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[10] Harvard Med Sch, Brigham & Womens Hosp, Channing Div Network Med, Boston, MA USA
[11] Harvard Med Sch, Boston, MA USA
[12] Joslin Diabet Ctr, Boston, MA USA
[13] Hadassah Hebrew Univ Hosp, Div Internal Med, Diabet Unit, Jerusalem, Israel
[14] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT USA
[15] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT USA
[16] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT USA
[17] Harvard Med Sch, Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, Boston, MA USA
[18] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA USA
[19] Hebrew Univ Jerusalem, Braun Sch Publ Hlth, Dept Human Metab & Nutr, Jerusalem, Israel
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
BETA-CELL FUNCTION; IMPAIRED GLUCOSE-TOLERANCE; HEPATIC INSULIN-RESISTANCE; ENDOPLASMIC-RETICULUM STRESS; LIFE-STYLE INTERVENTIONS; QUALITY-OF-LIFE; DIPEPTIDYL PEPTIDASE-4 INHIBITORS; IRS-1 SERINE PHOSPHORYLATION; ADIPOSE-TISSUE INFLAMMATION; CARDIOVASCULAR RISK-FACTORS;
D O I
10.1038/nrdp.2015.19
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Type 2 diabetes mellitus (T2DM) is an expanding global health problem, closely linked to the epidemic of obesity. Individuals with T2DM are at high risk for both microvascular complications (including retinopathy, nephropathy and neuropathy) and macrovascular complications (such as cardiovascular comorbidities), owing to hyperglycaemia and individual components of the insulin resistance (metabolic) syndrome. Environmental factors (for example, obesity, an unhealthy diet and physical inactivity) and genetic factors contribute to the multiple pathophysiological disturbances that are responsible for impaired glucose homeostasis in T2DM. Insulin resistance and impaired insulin secretion remain the core defects in T2DM, but at least six other pathophysiological abnormalities contribute to the dysregulation of glucose metabolism. The multiple pathogenetic disturbances present in T2DM dictate that multiple antidiabetic agents, used in combination, will be required to maintain normoglycaemia. The treatment must not only be effective and safe but also improve the quality of life. Several novel medications are in development, but the greatest need is for agents that enhance insulin sensitivity, halt the progressive pancreatic beta-cell failure that is characteristic of T2DM and prevent or reverse the microvascular complications. For an illustrated summary of this Primer,
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页数:22
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