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Diabetic Microvascular Disease: An Endocrine Society Scientific Statement.糖尿病微血管病变:内分泌学会科学声明
J Clin Endocrinol Metab. 2017 Dec 1;102(12):4343-4410. doi: 10.1210/jc.2017-01922.
2
Review of the relationship between renal and retinal microangiopathy in diabetes mellitus patients.糖尿病患者肾微血管病变与视网膜微血管病变关系的综述。
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3
Cross-sectional analysis of adult diabetes type 1 and type 2 patients with diabetic microvascular complications from a German retrospective observational study.一项来自德国的回顾性观察研究中,对患有糖尿病微血管并发症的1型和2型成年糖尿病患者进行横断面分析。
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4
Skin advanced glycation end products glucosepane and methylglyoxal hydroimidazolone are independently associated with long-term microvascular complication progression of type 1 diabetes.皮肤晚期糖基化终产物葡糖胺和甲基乙二醛氢化咪唑酮与1型糖尿病的长期微血管并发症进展独立相关。
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[Microangiopathies of diabetics (epidemiologic and clinical observations].糖尿病微血管病变(流行病学及临床观察)
Orv Hetil. 1987 Jan 18;128(3):137-40, 143-4.
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Research digest: progress in microvascular complications.研究摘要:微血管并发症的进展
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Relation of diabetic control to development of microvascular complications.糖尿病控制与微血管并发症发生的关系。
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ISPAD Clinical Practice Consensus Guidelines 2014. Microvascular and macrovascular complications in children and adolescents.《2014年国际儿童青少年糖尿病研究学会临床实践共识指南:儿童和青少年的微血管和大血管并发症》
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本文引用的文献

1
Sensory and motor peripheral nerve function and incident mobility disability.感觉和运动外周神经功能与新发行动障碍
J Am Geriatr Soc. 2014 Dec;62(12):2273-9. doi: 10.1111/jgs.13152. Epub 2014 Dec 8.
2
Diabetic neuropathy.糖尿病性神经病。
Endocrinol Metab Clin North Am. 2013 Dec;42(4):747-87. doi: 10.1016/j.ecl.2013.06.001.
3
CHOP/ORP150 ratio in endoplasmic reticulum stress: a new mechanism for diabetic peripheral neuropathy.内质网应激中的CHOP/ORP150比率:糖尿病周围神经病变的一种新机制
Cell Physiol Biochem. 2013;32(2):367-79. doi: 10.1159/000354444. Epub 2013 Aug 15.
4
Synergistic vasculogenic effects of AMD3100 and stromal-cell-derived factor-1α in vasa nervorum of the sciatic nerve of mice with diabetic peripheral neuropathy.AMD3100 和基质细胞衍生因子-1α 对糖尿病周围神经病变小鼠坐骨神经神经血管的协同血管生成作用。
Cell Tissue Res. 2013 Nov;354(2):395-407. doi: 10.1007/s00441-013-1689-4. Epub 2013 Aug 15.
5
Inhibition of Src kinase blocks high glucose-induced EGFR transactivation and collagen synthesis in mesangial cells and prevents diabetic nephropathy in mice.Src 激酶抑制阻断高糖诱导的系膜细胞中表皮生长因子受体的转激活和胶原合成,并预防小鼠糖尿病肾病。
Diabetes. 2013 Nov;62(11):3874-86. doi: 10.2337/db12-1010. Epub 2013 Aug 13.
6
Glucose levels and risk of dementia.血糖水平与痴呆风险。
N Engl J Med. 2013 Aug 8;369(6):540-8. doi: 10.1056/NEJMoa1215740.
7
Alterations in circulating angiogenic and anti-angiogenic factors in type 2 diabetic patients with neuropathy.2型糖尿病神经病变患者循环血管生成和抗血管生成因子的改变。
Cell Biochem Funct. 2014 Mar;32(2):155-63. doi: 10.1002/cbf.2987. Epub 2013 Jul 3.
8
Glucose intolerance, insulin resistance, and pathological features of Alzheimer disease in the Baltimore Longitudinal Study of Aging.在巴尔的摩纵向衰老研究中,葡萄糖耐量不良、胰岛素抵抗与阿尔茨海默病的病理特征。
JAMA Neurol. 2013 Sep 1;70(9):1167-72. doi: 10.1001/jamaneurol.2013.284.
9
Association of chronic kidney disease and cerebral small vessel disease with cognitive impairment in elderly patients with type 2 diabetes.老年2型糖尿病患者慢性肾脏病和脑小血管病与认知障碍的关联
Dement Geriatr Cogn Dis Extra. 2013 Jul 2;3(1):212-22. doi: 10.1159/000351424. Print 2013 Jan.
10
Pathogenesis of diabetic neuropathy: focus on neurovascular mechanisms.糖尿病性神经病的发病机制:关注神经血管机制。
Eur J Pharmacol. 2013 Nov 5;719(1-3):180-186. doi: 10.1016/j.ejphar.2013.07.017. Epub 2013 Jul 17.

糖尿病微血管病变:内分泌学会科学声明

Diabetic Microvascular Disease: An Endocrine Society Scientific Statement.

作者信息

Barrett Eugene J, Liu Zhenqi, Khamaisi Mogher, King George L, Klein Ronald, Klein Barbara E K, Hughes Timothy M, Craft Suzanne, Freedman Barry I, Bowden Donald W, Vinik Aaron I, Casellini Carolina M

机构信息

Division of Endocrinology, Department of Medicine, University of Virginia.

Section of Vascular Cell Biology, Joslin Diabetes Center, Harvard Medical School.

出版信息

J Clin Endocrinol Metab. 2017 Dec 1;102(12):4343-4410. doi: 10.1210/jc.2017-01922.

DOI:10.1210/jc.2017-01922
PMID:29126250
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5718697/
Abstract

Both type 1 and type 2 diabetes adversely affect the microvasculature in multiple organs. Our understanding of the genesis of this injury and of potential interventions to prevent, limit, or reverse injury/dysfunction is continuously evolving. This statement reviews biochemical/cellular pathways involved in facilitating and abrogating microvascular injury. The statement summarizes the types of injury/dysfunction that occur in the three classical diabetes microvascular target tissues, the eye, the kidney, and the peripheral nervous system; the statement also reviews information on the effects of diabetes and insulin resistance on the microvasculature of skin, brain, adipose tissue, and cardiac and skeletal muscle. Despite extensive and intensive research, it is disappointing that microvascular complications of diabetes continue to compromise the quantity and quality of life for patients with diabetes. Hopefully, by understanding and building on current research findings, we will discover new approaches for prevention and treatment that will be effective for future generations.

摘要

1型和2型糖尿病均会对多个器官的微血管产生不利影响。我们对这种损伤的发生机制以及预防、限制或逆转损伤/功能障碍的潜在干预措施的理解在不断发展。本声明回顾了促进和消除微血管损伤所涉及的生化/细胞途径。该声明总结了在三种典型的糖尿病微血管靶组织(眼睛、肾脏和周围神经系统)中发生的损伤/功能障碍类型;该声明还回顾了有关糖尿病和胰岛素抵抗对皮肤、大脑、脂肪组织以及心脏和骨骼肌微血管影响的信息。尽管进行了广泛而深入的研究,但令人失望的是,糖尿病微血管并发症仍然影响糖尿病患者的生活质量和数量。希望通过理解并基于当前的研究结果,我们将发现新的预防和治疗方法,这些方法将对子孙后代有效。