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[单克隆丙种球蛋白病患者的低血糖综合征]

[Hypoglycemic syndrome in patients with monoclonal gammopathy].

作者信息

Solovyev Maxim V, Yukina Marina Yu, Troshina Ekaterina A

机构信息

Endocrinology Research Centre.

出版信息

Probl Endokrinol (Mosk). 2020 Jun 10;65(6):474-480. doi: 10.14341/probl12266.

DOI:10.14341/probl12266
PMID:33351331
Abstract

One of the reasons for the development of hypoglycemia is the synthesis of autoimmune antibodies to insulin or its receptor – insulin autoimmune syndrome (IAS). The largest number of cases of this syndrome is described in the Japanese population. The antibodies to insulin are most often polyclonal immunoglobulins. In monoclonal gammopathy of undetermined significance and multiple myeloma secreted pathological monoclonal immunoglobulin may have an affinity for human insulin, which induces the development of IAS. The prolonged persistence of episodes of hypoglycemia of unknown origin requires the exclusion of the monoclonal nature of secreted antibodies to insulin. Often the presence of pathological secretion for a long time is not recognized due to the absence of other manifestations of the disease. The manifestation of gammopathy is represented by a wide range of symptoms and syndromes requiring the collaboration of doctors of various specialties. This review summarizes the literature on IAS in patients with monoclonal gammopathy, whose disease debuted from episodes of spontaneous hypoglycemia. When hemoblastosis remission is achieved (when the secretion of the pathological protein is minimal or not determined), the glucose, insulin, and antibodies levels of insulin normalize, and when multiple myeloma recurs, episodes of hypoglycemia resume. The onset of the disease from the IAS can be considered as a new criterion for symptomatic multiple myeloma, dictating the need for the initiation of specific therapy.

摘要

低血糖发生的原因之一是机体合成了针对胰岛素或其受体的自身免疫抗体——胰岛素自身免疫综合征(IAS)。该综合征的病例数在日本人群中描述最多。胰岛素抗体最常见的是多克隆免疫球蛋白。在意义未明的单克隆丙种球蛋白病和多发性骨髓瘤中,分泌的病理性单克隆免疫球蛋白可能对人胰岛素具有亲和力,从而诱发IAS的发生。不明原因低血糖发作的长期持续存在需要排除分泌的胰岛素抗体的单克隆性质。由于缺乏疾病的其他表现,病理性分泌长期存在的情况往往未被识别。丙种球蛋白病的表现由广泛的症状和综合征组成,需要各专科医生的协作。本综述总结了关于单克隆丙种球蛋白病患者中IAS的文献,这些患者的疾病始于自发性低血糖发作。当血液系统疾病缓解时(病理性蛋白分泌极少或未检测到),血糖、胰岛素及胰岛素抗体水平恢复正常,而当多发性骨髓瘤复发时,低血糖发作又会再次出现。IAS导致的疾病发作可被视为有症状多发性骨髓瘤的一个新的标准,这表明需要启动特异性治疗。

相似文献

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[Hypoglycemic syndrome in patients with monoclonal gammopathy].[单克隆丙种球蛋白病患者的低血糖综合征]
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Resolution of dysglycaemia after treatment of monoclonal gammopathy of endocrine significance.内分泌相关意义单克隆丙种球蛋白血症治疗后血糖异常的缓解。
Eur J Endocrinol. 2023 Dec 6;189(6):K25-K29. doi: 10.1093/ejendo/lvad138.
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[Monoclonal gammopathy of undetermined significance and multiple myeloma].意义未明的单克隆丙种球蛋白病和多发性骨髓瘤
Z Rheumatol. 2017 Oct;76(Suppl 2):33-37. doi: 10.1007/s00393-017-0335-z.
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Relapsing and remitting severe hypoglycemia due to a monoclonal anti-insulin antibody heralding a case of multiple myeloma.由于单克隆抗胰岛素抗体导致反复发作和缓解的严重低血糖,预示着多发性骨髓瘤病例的发生。
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Unusual Manifestations of Essential Monoclonal Gammopathy. II. Simulation of the Insulin Autoimmune Syndrome.原发性单克隆丙种球蛋白病的不寻常表现。II. 胰岛素自身免疫综合征的模拟
Rambam Maimonides Med J. 2015 Jul 30;6(3):e0027. doi: 10.5041/RMMJ.10212.
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Monoclonal gammopathy of renal significance: when MGUS is no longer undetermined or insignificant.肾脏相关意义的单克隆丙种球蛋白病:当 MGUS 不再是不确定或无意义的时候。
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Recurrent Hypoglycaemia due to Insulin Autoimmune Disease (Hirata Disease) Associated with Monoclonal Gammopathy of Unknown Significance.胰岛素自身免疫性疾病(平田病)伴意义未明的单克隆丙种球蛋白病所致复发性低血糖症
J Assoc Physicians India. 2015 Oct;63(10):68-9.

引用本文的文献

1
Insulin Autoimmune Syndrome: A Chinese Expert Consensus Statement.胰岛素自身免疫综合征:中国专家共识声明
Aging Med (Milton). 2025 Feb 22;8(1):e70007. doi: 10.1002/agm2.70007. eCollection 2025 Feb.
2
Insulin Autoimmune Syndrome: A Systematic Review.胰岛素自身免疫综合征:一项系统评价
Int J Endocrinol. 2023 Feb 15;2023:1225676. doi: 10.1155/2023/1225676. eCollection 2023.