• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

6号染色体q24相关的糖尿病

Chromosome 6q24-related diabetes mellitus.

作者信息

Yorifuji Tohru, Higuchi Shinji, Hosokawa Yuki, Kawakita Rie

机构信息

Division of Pediatric Endocrinology and Metabolism, Children's Medical Center, Osaka City General Hospital, Osaka, Japan.

Department of Genetic Medicine, Osaka City General Hospital, Osaka, Japan.

出版信息

Clin Pediatr Endocrinol. 2018;27(2):59-65. doi: 10.1297/cpe.27.59. Epub 2018 Apr 13.

DOI:10.1297/cpe.27.59
PMID:29662264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5897580/
Abstract

Chromosome 6q24-related diabetes mellitus is the most common cause of transient neonatal diabetes (TNDM), accounting for approximately two-thirds of all TNDM cases. Patients with 6q24-TNDM develop insulin-requiring diabetes soon after birth, followed by the gradual improvement and eventual remission of the disorder by 18 mo of age. The most important clinical feature of affected patients is a small-for-gestational age (SGA) birth weight, which reflects the lack of insulin in utero. It is believed that 6q24-TNDM is caused by the overexpression of the paternal allele of the imprinted locus in chromosome 6q24, which contains only two expressed genes, and Identified mechanisms include: (1) duplication of the paternal allele, (2) paternal uniparental disomy, and (3) hypomethylation of the maternal allele. Many patients with TNDM relapse after puberty. Relapsed 6q24-related diabetes is no longer transient and typically occurs in non-obese patients who are autoantibody negative. Thus, these patients possess features indistinguishable from those of maturity-onset diabetes of the young (MODY). Conversely, it has been shown that not all patients with 6q24-related diabetes have a history of TNDM. 6q24-related diabetes should therefore be considered as one of the differential diagnoses for patients with MODY-like diabetes, especially when they are SGA at birth.

摘要

6号染色体q24相关的糖尿病是短暂性新生儿糖尿病(TNDM)最常见的病因,约占所有TNDM病例的三分之二。6q24-TNDM患者在出生后不久就会发展为需要胰岛素治疗的糖尿病,随后病情逐渐改善,并在18个月龄时最终缓解。受影响患者最重要的临床特征是小于胎龄(SGA)出生体重,这反映了子宫内胰岛素的缺乏。据信,6q24-TNDM是由6号染色体q24印记位点的父本等位基因过度表达引起的,该位点仅包含两个表达基因,已确定的机制包括:(1)父本等位基因重复,(2)父本单亲二体,以及(3)母本等位基因低甲基化。许多TNDM患者在青春期后复发。复发的6q24相关糖尿病不再是短暂性的,通常发生在自身抗体阴性的非肥胖患者中。因此,这些患者具有与青年成年发病型糖尿病(MODY)难以区分的特征。相反,研究表明并非所有6q24相关糖尿病患者都有TNDM病史。因此,6q24相关糖尿病应被视为MODY样糖尿病患者的鉴别诊断之一,尤其是当他们出生时为SGA时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2004/5897580/24c49d886a69/cpe-27-059-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2004/5897580/24c49d886a69/cpe-27-059-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2004/5897580/24c49d886a69/cpe-27-059-g001.jpg

相似文献

1
Chromosome 6q24-related diabetes mellitus.6号染色体q24相关的糖尿病
Clin Pediatr Endocrinol. 2018;27(2):59-65. doi: 10.1297/cpe.27.59. Epub 2018 Apr 13.
2
Diabetes Mellitus, 6q24-Related Transient Neonatal与6q24相关的短暂性新生儿糖尿病
3
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patients.6q24 暂时性新生儿糖尿病(6q24 TNDM)的临床表现及国际患者队列中的基因型-表型相关性。
Diabetologia. 2013 Apr;56(4):758-62. doi: 10.1007/s00125-013-2832-1. Epub 2013 Feb 6.
4
Relapsing 6q24-related transient neonatal diabetes mellitus with insulin resistance: A case report.伴有胰岛素抵抗的复发性6q24相关短暂性新生儿糖尿病:一例报告
Clin Pediatr Endocrinol. 2020;29(4):179-182. doi: 10.1297/cpe.29.179. Epub 2020 Oct 3.
5
Abnormalities in chromosome 6q24 as a cause of early-onset, non-obese, non-autoimmune diabetes mellitus without history of neonatal diabetes.6q24染色体异常作为早发、非肥胖、非自身免疫性糖尿病且无新生儿糖尿病病史的病因
Diabet Med. 2015 Jul;32(7):963-7. doi: 10.1111/dme.12758. Epub 2015 Apr 11.
6
Bisulphite sequencing of the transient neonatal diabetes mellitus DMR facilitates a novel diagnostic test but reveals no methylation anomalies in patients of unknown aetiology.短暂性新生儿糖尿病甲基化区域的亚硫酸氢盐测序有助于开展一项新的诊断测试,但在病因不明的患者中未发现甲基化异常。
Hum Genet. 2005 Mar;116(4):255-61. doi: 10.1007/s00439-004-1236-1. Epub 2005 Jan 6.
7
Transient Neonatal Diabetes Mellitus with the Rare Association of Nonsuppurative Sialadenitis and Genetic Defects in 6q24.伴有非化脓性涎腺炎和6q24基因缺陷罕见关联的短暂性新生儿糖尿病
Case Rep Pediatr. 2021 Aug 11;2021:5901898. doi: 10.1155/2021/5901898. eCollection 2021.
8
Transient neonatal diabetes mellitus and hypomethylation at additional imprinted loci: novel ZFP57 mutation and review on the literature.一过性新生儿糖尿病和额外印记基因座的低甲基化:新型 ZFP57 突变及文献复习。
Acta Diabetol. 2019 Mar;56(3):301-307. doi: 10.1007/s00592-018-1239-3. Epub 2018 Oct 13.
9
Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy.暂时性新生儿糖尿病各亚型之间存在差异,可指导诊断和治疗。
Eur J Endocrinol. 2021 Apr;184(4):575-585. doi: 10.1530/EJE-20-1030.
10
A novel imprinted gene, HYMAI, is located within an imprinted domain on human chromosome 6 containing ZAC.一种新的印记基因HYMAI位于人类6号染色体上包含ZAC的一个印记区域内。
Genomics. 2000 Aug 1;67(3):248-55. doi: 10.1006/geno.2000.6266.

引用本文的文献

1
Biparental and Androgenetic Somatic Mosaicism with Presentation of Non-Syndromic Severe Neonatal Hyperinsulinemia.双亲和雄激素体细胞嵌合现象伴非综合征性严重新生儿高胰岛素血症表现
Int J Mol Sci. 2025 Aug 19;26(16):7985. doi: 10.3390/ijms26167985.
2
Insulin resistant diabetes mellitus in a girl with mild Rabson-Mendenhall syndrome: efficacy of sodium glucose co-transporter 2 inhibitor.一名患有轻度拉布森 - 门登霍尔综合征女孩的胰岛素抵抗型糖尿病:钠 - 葡萄糖协同转运蛋白2抑制剂的疗效
Diabetol Int. 2024 Nov 15;16(1):182-187. doi: 10.1007/s13340-024-00773-y. eCollection 2025 Jan.
3
PLAGL1 overexpression induces cytoplasmic DNA accumulation that triggers cGAS/STING activation.

本文引用的文献

1
Role of ZAC1 in transient neonatal diabetes mellitus and glucose metabolism.ZAC1在短暂性新生儿糖尿病和葡萄糖代谢中的作用。
World J Biol Chem. 2015 Aug 26;6(3):95-109. doi: 10.4331/wjbc.v6.i3.95.
2
Role of noninsulin therapies alone or in combination in chromosome 6q24-related transient neonatal diabetes: sulfonylurea improves but does not always normalize insulin secretion.非胰岛素治疗单独或联合应用在6q24相关短暂性新生儿糖尿病中的作用:磺脲类药物可改善胰岛素分泌,但并不总能使其恢复正常。
Diabetes Care. 2015 Jun;38(6):e86-7. doi: 10.2337/dc14-3056.
3
Abnormalities in chromosome 6q24 as a cause of early-onset, non-obese, non-autoimmune diabetes mellitus without history of neonatal diabetes.
PLAGL1 过表达诱导细胞质 DNA 积累,从而触发 cGAS/STING 激活。
J Cell Mol Med. 2024 Oct;28(19):e70130. doi: 10.1111/jcmm.70130.
4
Exploring early DNA methylation alterations in type 1 diabetes: implications of glycemic control.探讨 1 型糖尿病中早期 DNA 甲基化改变:血糖控制的影响。
Front Endocrinol (Lausanne). 2024 Jun 5;15:1416433. doi: 10.3389/fendo.2024.1416433. eCollection 2024.
5
Continuous Glucose Monitoring in Transient Neonatal Diabetes Mellitus-2 Case Reports and Literature Review.短暂性新生儿糖尿病的连续血糖监测——2例病例报告及文献综述
Diagnostics (Basel). 2023 Jul 4;13(13):2271. doi: 10.3390/diagnostics13132271.
6
Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis.对临床疑似青年起病的成年型糖尿病(MODY)且基因诊断阴性的患者进行转录组分析。
Orphanet J Rare Dis. 2022 Mar 4;17(1):105. doi: 10.1186/s13023-022-02263-3.
7
A Case of Type 2 Diabetes Mellitus With t(6;7)(q24;q31.2) Balanced Translocation.一例伴有t(6;7)(q24;q31.2)平衡易位的2型糖尿病病例。
J Med Cases. 2022 Jan;13(1):21-25. doi: 10.14740/jmc3843. Epub 2022 Jan 17.
8
Imprinting disorders in humans: a review.人类印迹紊乱:综述。
Curr Opin Pediatr. 2020 Dec;32(6):719-729. doi: 10.1097/MOP.0000000000000965.
9
Relapsing 6q24-related transient neonatal diabetes mellitus with insulin resistance: A case report.伴有胰岛素抵抗的复发性6q24相关短暂性新生儿糖尿病:一例报告
Clin Pediatr Endocrinol. 2020;29(4):179-182. doi: 10.1297/cpe.29.179. Epub 2020 Oct 3.
10
Molecular and clinical characteristics of monogenic diabetes mellitus in southern Chinese children with onset before 3 years of age.中国南方3岁前发病的儿童单基因糖尿病的分子和临床特征
BMJ Open Diabetes Res Care. 2020 Aug;8(1). doi: 10.1136/bmjdrc-2020-001345.
6q24染色体异常作为早发、非肥胖、非自身免疫性糖尿病且无新生儿糖尿病病史的病因
Diabet Med. 2015 Jul;32(7):963-7. doi: 10.1111/dme.12758. Epub 2015 Apr 11.
4
ISPAD Clinical Practice Consensus Guidelines 2014. The diagnosis and management of monogenic diabetes in children and adolescents.国际儿童青少年糖尿病研究学会(ISPAD)2014年临床实践共识指南。儿童和青少年单基因糖尿病的诊断与管理。
Pediatr Diabetes. 2014 Sep;15 Suppl 20:47-64. doi: 10.1111/pedi.12192.
5
Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study [corrected].与新生儿糖尿病患儿遗传变化相关的神经心理功能障碍和发育缺陷:一项前瞻性队列研究[更正]。
Lancet Diabetes Endocrinol. 2013 Nov;1(3):199-207. doi: 10.1016/S2213-8587(13)70059-7. Epub 2013 Sep 6.
6
Clinical utility gene card for: Transient Neonatal Diabetes Mellitus, 6q24-related.6q24相关的短暂性新生儿糖尿病临床实用基因卡片
Eur J Hum Genet. 2014 Sep;22(9). doi: 10.1038/ejhg.2014.27. Epub 2014 Feb 26.
7
Relapsing 6q24-related transient neonatal diabetes mellitus successfully treated with a dipeptidyl peptidase-4 inhibitor: a case report.用二肽基肽酶-4抑制剂成功治疗复发性6q24相关短暂性新生儿糖尿病:一例报告
Pediatr Diabetes. 2014 Dec;15(8):606-10. doi: 10.1111/pedi.12123. Epub 2014 Feb 19.
8
De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed.GCK、HNF1A 和 HNF4A 的新生突变在 MODY 中可能比之前认为的更为常见。
Diabetologia. 2014 Mar;57(3):480-4. doi: 10.1007/s00125-013-3119-2. Epub 2013 Dec 10.
9
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patients.6q24 暂时性新生儿糖尿病(6q24 TNDM)的临床表现及国际患者队列中的基因型-表型相关性。
Diabetologia. 2013 Apr;56(4):758-62. doi: 10.1007/s00125-013-2832-1. Epub 2013 Feb 6.
10
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop.印迹在 PLAGL1 结构域内的是一个由 70kb 的 CTCF/黏合蛋白介导的非等位染色质环。
Nucleic Acids Res. 2013 Feb 1;41(4):2171-9. doi: 10.1093/nar/gks1355. Epub 2013 Jan 7.