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遗传性糖尿病的发病机制。

Pathogenetic mechanisms of hereditary diabetes mellitus.

作者信息

Rüdiger H W, Dreyer M

出版信息

Hum Genet. 1983;63(2):100-6. doi: 10.1007/BF00291526.

DOI:10.1007/BF00291526
PMID:6341209
Abstract

Novel laboratory techniques such as the determination of proinsulin, insulin, C-peptide and insulin receptors have allowed further subclassification of diabetes mellitus today as representing a symptom rather than a disease. Numerous pathogenetic mechanisms of diabetes have been identified, many of these being genetically determined and this may extend possibilities for genetic counselling. As a geneticist's view, the pathogenetic concept of diabetes presented here is mostly confined to genetic mechanisms, leaving aside other influences on the development of diabetes such as hormones, viruses, nutrition and drugs. Mendelian inherited diabetic disorders are related to different pathogenetic principles where possible, being speculative in some cases.

摘要

诸如测定胰岛素原、胰岛素、C肽和胰岛素受体等新型实验室技术,使得如今糖尿病能够进一步细分,它现在被视为一种症状而非一种疾病。已经确定了糖尿病的多种发病机制,其中许多是由基因决定的,这可能会增加遗传咨询的可能性。从遗传学家的角度来看,这里提出的糖尿病发病机制概念主要局限于遗传机制,而忽略了其他对糖尿病发展的影响因素,如激素、病毒、营养和药物。孟德尔遗传糖尿病紊乱尽可能与不同的发病机制相关,在某些情况下具有推测性。

相似文献

1
Pathogenetic mechanisms of hereditary diabetes mellitus.遗传性糖尿病的发病机制。
Hum Genet. 1983;63(2):100-6. doi: 10.1007/BF00291526.
2
Pathogenetic mechanisms of hereditary diabetes mellitus.遗传性糖尿病的发病机制。
Biomed Biochim Acta. 1985;44(1):5-13.
3
Genetics of diabetes.
Prog Clin Biol Res. 1985;200:257-67.
4
Pathophysiology of diabetes mellitus.糖尿病的病理生理学
Med Clin North Am. 1971 Jul;55(4):821-34. doi: 10.1016/s0025-7125(16)32478-6.
5
Insulin resistance in non-insulin dependent (type II) and insulin dependent (type I) diabetes mellitus.非胰岛素依赖型(II型)和胰岛素依赖型(I型)糖尿病中的胰岛素抵抗。
Adv Exp Med Biol. 1985;189:176-205.
6
Beta-cell behavior, evaluated as basal and mixed meal-stimulated insulin, and proinsulin secretion, in elderly diabetic patients with "secondary failure".对患有“继发性失效”的老年糖尿病患者的β细胞行为进行评估,评估指标为基础胰岛素和混合餐刺激后的胰岛素以及胰岛素原分泌。
J Endocrinol Invest. 1999;22(10 Suppl):86-7.
7
Human type 2 diabetes: morphological evidence for abnormal beta-cell function.人类2型糖尿病:β细胞功能异常的形态学证据。
Diabetes. 2001 Feb;50 Suppl 1:S172-7. doi: 10.2337/diabetes.50.2007.s172.
8
Etiologic, pathophysiologic and clinical interrelationships in diabetes.糖尿病的病因、病理生理及临床相互关系
Johns Hopkins Med J. 1975 Jan;136(1):25-37.
9
[Molecular aspects of diabetes mellitus: the regulation of insulin biosynthesis].[糖尿病的分子层面:胰岛素生物合成的调节]
Probl Endokrinol (Mosk). 1982 May-Jun;28(3):79-89.
10
[Pathogenesis and the basic principles of treating diabetes mellitus].[糖尿病的发病机制及治疗基本原则]
Vestn Akad Med Nauk SSSR. 1980(7):10-8.

引用本文的文献

1
Genetic disorders presenting as "schizophrenia". Karl Bonhoeffer's early view of the psychoses in the light of medical genetics.表现为“精神分裂症”的遗传疾病。卡尔·博恩霍费尔根据医学遗传学对精神病的早期观点。
Hum Genet. 1983;65(1):1-10. doi: 10.1007/BF00285021.
2
Genetic control of adrenergic receptors on human platelets. A twin study.人类血小板肾上腺素能受体的遗传控制。一项双胞胎研究。
Hum Genet. 1983;64(2):105-9. doi: 10.1007/BF00327103.
3
Impaired insulin-induced RNA synthesis secondary to a genetically defective insulin receptor.继发于遗传性胰岛素受体缺陷的胰岛素诱导的RNA合成受损。

本文引用的文献

1
HLA genotype studies in juvenile insulin-dependent diabetes.青少年胰岛素依赖型糖尿病的人类白细胞抗原基因型研究。
Diabetologia. 1980 Sep;19(3):189-93. doi: 10.1007/BF00275267.
2
Diabetes due to secretion of an abnormal insulin.
N Engl J Med. 1980 Jan 17;302(3):129-35. doi: 10.1056/NEJM198001173020301.
3
A human proinsulin variant at arginine 65.一种在精氨酸65处的人胰岛素原变体。
Nature. 1981 Jun 25;291(5817):679-81. doi: 10.1038/291679a0.
Hum Genet. 1985;69(1):76-8. doi: 10.1007/BF00295533.
4
A new familial syndrome with impaired function of three related peptide growth factors.一种伴有三种相关肽生长因子功能受损的新型家族综合征。
Hum Genet. 1989 Oct;83(3):209-16. doi: 10.1007/BF00285157.
5
Risk calculations for hereditary effects of ionizing radiation in humans.人类电离辐射遗传效应的风险计算。
Hum Genet. 1992 May;89(2):127-46. doi: 10.1007/BF00217113.
4
Diabetes in identical twins. A study of 200 pairs.同卵双胞胎中的糖尿病。一项对200对双胞胎的研究。
Diabetologia. 1981 Feb;20(2):87-93. doi: 10.1007/BF00262007.
5
Hypoglycemia associated with antibodies to the insulin receptor.与胰岛素受体抗体相关的低血糖症。
N Engl J Med. 1982 Dec 2;307(23):1422-6. doi: 10.1056/NEJM198212023072303.
6
Cell culture studies on patients with extreme insulin resistance. I. Receptor defects on cultured fibroblasts.极端胰岛素抵抗患者的细胞培养研究。I. 培养成纤维细胞的受体缺陷。
J Clin Endocrinol Metab. 1982 Feb;54(2):261-8. doi: 10.1210/jcem-54-2-261.
7
Structure of the insulin receptor of the cultured human lymphoblastoid cell IM-9. Evidence suggesting that two subunits are required for insulin binding.培养的人淋巴母细胞IM-9胰岛素受体的结构。有证据表明胰岛素结合需要两个亚基。
J Biol Chem. 1982 Jan 25;257(2):894-8.
8
Qualitative abnormalities in insulin binding in a patient with extreme insulin resistance: decreased sensitivity to alterations in temperature and pH.一名极端胰岛素抵抗患者胰岛素结合的定性异常:对温度和pH值变化的敏感性降低。
Proc Natl Acad Sci U S A. 1981 Nov;78(11):7157-61. doi: 10.1073/pnas.78.11.7157.
9
Insulin binding and insulin action in fibroblasts from patients with maturity-onset diabetes of the young.青年发病的成年型糖尿病患者成纤维细胞中的胰岛素结合与胰岛素作用
Diabetes. 1981 Nov;30(11):940-6. doi: 10.2337/diab.30.11.940.
10
Erythrocyte and monocyte insulin binding in man: a comparative analysis in normal and disease states.人体红细胞和单核细胞的胰岛素结合:正常和疾病状态下的比较分析。
Diabetes. 1981 Nov;30(11):896-902. doi: 10.2337/diab.30.11.896.