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糖尿病中的肾脏保护:血糖控制的作用。

Renal protection in diabetes: role of glycemic control.

作者信息

Fioretto Paola, Bruseghin Marino, Berto Ilaria, Gallina Pietro, Manzato Enzo, Mussap Michele

机构信息

Department of Medical and Surgical Sciences, University of Padova, Via Giustiniani 2, 35128 Padova, Italy.

出版信息

J Am Soc Nephrol. 2006 Apr;17(4 Suppl 2):S86-9. doi: 10.1681/ASN.2005121343.

DOI:10.1681/ASN.2005121343
PMID:16565255
Abstract

Diabetes is the most common cause of ESRD in Western countries. This article describes the impact of glycemic control in the various stages of the disease and considers the impact of tight glycemic control on the development and progression of diabetic nephropathy (DN). The Diabetes Control and Complications Trial and the United Kingdom Prospective Diabetic Study have demonstrated in type 1 and type 2 diabetes that intensive glycemic control significantly reduces the risk for development of microalbuminuria. Although observational studies suggest an impact of glycemia also on the progression of DN, fewer data are available on the impact of improved metabolic control in secondary prevention. The long-term follow-up of the patients who participated in the Diabetes Control and Complications Trial (Epidemiology of Diabetes Interventions and Complications Study) demonstrated a sustained effect of previous tight glycemic control on both development and progression of DN. Finally, long-term normoglycemia, achieved by pancreas transplantation, is able not only to prevent the development of early diabetic glomerulopathy in kidney transplant recipients but also to halt progression and induce regression of the established diabetic renal lesions in nonuremic patients. Taken together, these studies strongly demonstrate that improvement in glucose control is the most important therapeutic approach in primary prevention. Tight glycemic control also is important in slowing progression of DN, and if blood glucose is normalized, then regression of DN can be achieved. Therefore, a target of glycated hemoglobin levels <7% should be recommended in all patients with diabetes.

摘要

在西方国家,糖尿病是终末期肾病(ESRD)最常见的病因。本文描述了血糖控制在该疾病各个阶段的影响,并探讨了严格血糖控制对糖尿病肾病(DN)发生和进展的影响。糖尿病控制与并发症试验(DCCT)和英国前瞻性糖尿病研究(UKPDS)已在1型和2型糖尿病患者中证实,强化血糖控制可显著降低微量白蛋白尿的发生风险。尽管观察性研究表明血糖水平对DN的进展也有影响,但关于二级预防中改善代谢控制的影响的数据较少。参与糖尿病控制与并发症试验的患者的长期随访(糖尿病干预与并发症流行病学研究)表明,既往严格的血糖控制对DN的发生和进展均有持续影响。最后,通过胰腺移植实现的长期血糖正常不仅能够预防肾移植受者早期糖尿病肾小球病变的发生,还能阻止非尿毒症患者已有的糖尿病肾脏病变进展并使其逆转。综上所述,这些研究有力地证明,改善血糖控制是一级预防中最重要的治疗方法。严格的血糖控制对于减缓DN的进展也很重要,并且如果血糖恢复正常,则可以实现DN的逆转。因此,应建议所有糖尿病患者将糖化血红蛋白水平目标设定为<7%。

相似文献

1
Renal protection in diabetes: role of glycemic control.糖尿病中的肾脏保护:血糖控制的作用。
J Am Soc Nephrol. 2006 Apr;17(4 Suppl 2):S86-9. doi: 10.1681/ASN.2005121343.
2
Lessons learned from studies of the natural history of diabetic nephropathy in young type 1 diabetic patients.从年轻1型糖尿病患者糖尿病肾病自然史研究中吸取的经验教训。
Pediatr Endocrinol Rev. 2008 Aug;5 Suppl 4:958-63.
3
Glycemic control and the initiation and progression of the complications of diabetes mellitus.血糖控制与糖尿病并发症的发生及进展
Kidney Int Suppl. 1997 Dec;63:S36-9.
4
The relationship between glucose control and the development of diabetic nephropathy in type I diabetes.1型糖尿病中血糖控制与糖尿病肾病发生之间的关系。
Semin Nephrol. 1997 Mar;17(2):101-13.
5
Diabetic nephropathy.糖尿病肾病
Saudi J Kidney Dis Transpl. 2006 Dec;17(4):481-90.
6
[Pancreas transplantation: who and when?].[胰腺移植:哪些人适合以及何时进行?]
Cas Lek Cesk. 2001 Apr 12;140(7):195-9.
7
The effects of pancreas transplantation on the glomerular structure of renal allografts in patients with insulin-dependent diabetes.胰腺移植对胰岛素依赖型糖尿病患者同种异体肾移植肾小球结构的影响。
N Engl J Med. 1989 Jul 13;321(2):80-5. doi: 10.1056/NEJM198907133210204.
8
Glycemic control in diabetic CKD patients: where do we stand?糖尿病合并慢性肾脏病患者的血糖控制:我们目前的状况如何?
Am J Kidney Dis. 2008 Oct;52(4):766-77. doi: 10.1053/j.ajkd.2008.04.011. Epub 2008 Jun 24.
9
Diabetic nephropathy -- a multifaceted target of new therapies.糖尿病肾病——新疗法的多方面靶点。
Discov Med. 2010 Nov;10(54):406-15.
10
[Physiopathology of diabetic nephropathy: what we learn from transplantation].[糖尿病肾病的病理生理学:我们从移植中学到了什么]
Nephrologie. 1998;19(3):105-9.

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