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酮症起病型日本非胰岛素依赖型糖尿病患者的分析及长期随访

Analysis and a long-term follow up of ketosis-onset Japanese NIDDM patients.

作者信息

Tanaka K, Moriya T, Kanamori A, Yajima Y

机构信息

Department of Internal Medicine, Kitasato, University School of Medicine, Sagamihara, Kanagawa, Japan.

出版信息

Diabetes Res Clin Pract. 1999 May;44(2):137-46. doi: 10.1016/s0168-8227(99)00023-6.

DOI:10.1016/s0168-8227(99)00023-6
PMID:10414933
Abstract

It has been reported that excessive intake of sugar-containing soft drinks results in diabetic ketoacidosis (DKA) or ketosis (DK) in obese patients with non-insulin dependent diabetes mellitus (NIDDM). We describe the clinical characteristics and results of long-term follow-up for 24 newly-diagnosed patients with acute-onset NIDDM presenting with DKA or DK. A history of excessive intake of sugar-containing soft drinks was found in 19 (Group A); serious non-diabetic illnesses were found in 5 (Group B). The range of patient ages in Group A was 16 to 57 years while all patients in Group B were 60 years or older. In Group A, no patient was positive for autoantibodies, specific HLAs for Japanese insulin dependent diabetes mellitus, or mutation of the beta-3-adrenergic receptor gene. The body mass indices (BMIs) at onset and admission and serum C-peptide immunoreactivities at admission and discharge were significantly higher in patients in Group A than in patients Group B. In conclusion, we reconfirmed that excessive intake of sugar-containing soft drinks is one of the contributing factors in DKA or DK-onset NIDDM patients. We found no autoimmune mechanism involved in the pathogenesis and that a polymorphism in the beta-3-adrenergic receptor gene could be associated with the development of soft-drink ketosis.

摘要

据报道,摄入过量含糖软饮料会导致非胰岛素依赖型糖尿病(NIDDM)肥胖患者发生糖尿病酮症酸中毒(DKA)或酮症(DK)。我们描述了24例以DKA或DK急性起病的新诊断NIDDM患者的临床特征及长期随访结果。19例患者(A组)有摄入过量含糖软饮料史;5例患者(B组)有严重非糖尿病性疾病。A组患者年龄范围为16至57岁,而B组所有患者均为60岁及以上。A组中,无患者自身抗体、日本胰岛素依赖型糖尿病特异性HLA或β-3肾上腺素能受体基因突变呈阳性。A组患者起病时及入院时的体重指数(BMI)以及入院时和出院时的血清C肽免疫反应性均显著高于B组患者。总之,我们再次证实,摄入过量含糖软饮料是DKA或DK起病的NIDDM患者的致病因素之一。我们发现发病机制中无自身免疫机制参与,且β-3肾上腺素能受体基因多态性可能与软饮料性酮症的发生有关。

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