New insights into the mechanisms of diabetic complications: role of lipids and lipid metabolism

被引:310
|
作者
Eid, Stephanie [1 ]
Sas, Kelli M. [2 ]
Abcouwer, Steven F. [3 ]
Feldman, Eva L. [1 ]
Gardner, Thomas W. [3 ,4 ]
Pennathur, Subramaniam [2 ,4 ]
Fort, Patrice E. [3 ,4 ]
机构
[1] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
[2] Univ Michigan, Dept Internal Med, Div Nephrol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Kellogg Eye Ctr, Dept Ophthalmol & Visual Sci, 1000 Wall St, Ann Arbor, MI 48105 USA
[4] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
Diabetes; Diabetic complications; Lipid metabolism; Omics; Review; Specific mechanisms; KIDNEY-DISEASE; CARDIOVASCULAR-DISEASE; OXIDATIVE STRESS; GLUCOSE CONTROL; OXIDIZED LDL; RISK-FACTORS; KEY ROLE; RETINOPATHY; TYPE-1; PROGRESSION;
D O I
10.1007/s00125-019-4959-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes adversely affects multiple organs, including the kidney, eye and nerve, leading to diabetic kidney disease, diabetic retinopathy and diabetic neuropathy, respectively. In both type 1 and type 2 diabetes, tissue damage is organ specific and is secondary to a combination of multiple metabolic insults. Hyperglycaemia, dyslipidaemia and hypertension combine with the duration and type of diabetes to define the distinct pathophysiology underlying diabetic kidney disease, diabetic retinopathy and diabetic neuropathy. Only recently have the commonalities and differences in the metabolic basis of these tissue-specific complications, particularly those involving local and systemic lipids, been systematically examined. This review focuses on recent progress made using preclinical models and human-based approaches towards understanding how bioenergetics and metabolomic profiles contribute to diabetic kidney disease, diabetic retinopathy and diabetic neuropathy. This new understanding of the biology of complication-prone tissues highlights the need for organ-specific interventions in the treatment of diabetic complications.
引用
收藏
页码:1539 / 1549
页数:11
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