Suppr超能文献

Williams 综合征成人中糖尿病和糖尿病前期的高发率。

High prevalence of diabetes and pre-diabetes in adults with Williams syndrome.

机构信息

Center for Human Genetics, Simches Research Building, 185 Cambridge Street, Rm 222, Boston, MA 02115, USA.

出版信息

Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):291-8. doi: 10.1002/ajmg.c.30261.

Abstract

A standard oral glucose tolerance test (OGTT) was administered to 28 adults with Williams syndrome (WS). Three quarters of the WS subjects showed abnormal glucose curves, meeting diagnostic criteria for either diabetes or the pre-diabetic state of impaired glucose tolerance. Fasting mean glucose and median insulin levels did not differ significantly in the total WS cohort versus age-gender-BMI matched controls, though the glucose area under the curve was greater in the WS subjects. HbA1c levels were not as reliable as the OGTT in diagnosing the presence of diabetes. Given the high prevalence of impaired glucose regulation, adults with WS should be screened for diabetes, and when present should be treated in accordance with standard medical practice. Hemizygosity for a gene mapping to the Williams syndrome chromosome region (WSCR) is likely the major factor responsible for the high frequency of diabetes in WS. Syntaxin-1A is a prime candidate gene based on its location in the WSCR, its role in insulin release, and the presence of abnormal glucose metabolism in mouse models with aberrantly expressed Stx-1a.

摘要

对 28 名患有威廉姆斯综合征(WS)的成年人进行了标准口服葡萄糖耐量试验(OGTT)。四分之三的 WS 患者表现出异常的葡萄糖曲线,符合糖尿病或葡萄糖耐量受损的糖尿病前期状态的诊断标准。尽管 WS 患者的葡萄糖曲线下面积较大,但总 WS 队列与年龄、性别、BMI 匹配的对照组相比,空腹平均血糖和中位数胰岛素水平没有显著差异。HbA1c 水平在诊断糖尿病方面不如 OGTT 可靠。鉴于葡萄糖调节受损的高患病率,WS 成年人应进行糖尿病筛查,一旦确诊,应按照标准医疗实践进行治疗。映射到威廉姆斯综合征染色体区域(WSCR)的基因的半合性可能是 WS 中糖尿病高发的主要因素。突触融合蛋白 1A 是一个主要的候选基因,基于其在 WSCR 中的位置、在胰岛素释放中的作用以及在表达异常的 Stx-1a 的小鼠模型中存在异常的葡萄糖代谢。

相似文献

1
High prevalence of diabetes and pre-diabetes in adults with Williams syndrome.
Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):291-8. doi: 10.1002/ajmg.c.30261.
2
Prevalence of diabetes and pre-diabetes in a cohort of Italian young adults with Williams syndrome.
Am J Med Genet A. 2013 Apr;161A(4):817-21. doi: 10.1002/ajmg.a.35655. Epub 2013 Mar 12.
3
Glucose and lipid metabolism, bone density, and body composition in individuals with Williams syndrome.
Clin Endocrinol (Oxf). 2018 Nov;89(5):596-604. doi: 10.1111/cen.13829. Epub 2018 Sep 18.
5
Not performing an OGTT results in significant underdiagnosis of (pre)diabetes in a high risk adult Caucasian population.
Int J Obes (Lond). 2017 Nov;41(11):1615-1620. doi: 10.1038/ijo.2017.165. Epub 2017 Jul 19.
7
Impaired glucose metabolism in subjects with the Williams-Beuren syndrome: A five-year follow-up cohort study.
PLoS One. 2017 Oct 20;12(10):e0185371. doi: 10.1371/journal.pone.0185371. eCollection 2017.
8
Prevalence of Prediabetes Among Adolescents and Young Adults in the United States, 2005-2016.
JAMA Pediatr. 2020 Feb 1;174(2):e194498. doi: 10.1001/jamapediatrics.2019.4498. Epub 2020 Feb 3.
9
Low circulating vitamin D levels are associated with increased arterial stiffness in prediabetic subjects identified according to HbA1c.
Atherosclerosis. 2015 Dec;243(2):395-401. doi: 10.1016/j.atherosclerosis.2015.09.038. Epub 2015 Oct 9.

引用本文的文献

1
Metabolomic profiles in serum uncover novel biomarkers in children with Williams-Beuren syndrome.
Sci Rep. 2025 Mar 19;15(1):9437. doi: 10.1038/s41598-025-94018-w.
4
A case report of interventricular hemorrhage in William-Beuren syndrome.
Ann Med Surg (Lond). 2022 Aug 5;80:104305. doi: 10.1016/j.amsu.2022.104305. eCollection 2022 Aug.
5
Psychotic Symptoms and Malignant Neuroleptic Syndrome in Williams Syndrome: A Case Report.
Front Psychiatry. 2022 May 31;13:891757. doi: 10.3389/fpsyt.2022.891757. eCollection 2022.
6
Williams syndrome.
Nat Rev Dis Primers. 2021 Jun 17;7(1):42. doi: 10.1038/s41572-021-00276-z.
8
Williams Syndrome, Human Self-Domestication, and Language Evolution.
Front Psychol. 2019 Mar 18;10:521. doi: 10.3389/fpsyg.2019.00521. eCollection 2019.
9
Integrative network analysis reveals biological pathways associated with Williams syndrome.
J Child Psychol Psychiatry. 2019 May;60(5):585-598. doi: 10.1111/jcpp.12999. Epub 2018 Oct 25.
10
The 7q11.23 Protein DNAJC30 Interacts with ATP Synthase and Links Mitochondria to Brain Development.
Cell. 2018 Nov 1;175(4):1088-1104.e23. doi: 10.1016/j.cell.2018.09.014.

本文引用的文献

1
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.
Nat Genet. 2008 Feb;40(2):149-51. doi: 10.1038/ng.2007.61. Epub 2008 Jan 13.
3
Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
Nat Genet. 2008 Feb;40(2):161-9. doi: 10.1038/ng.76. Epub 2008 Jan 13.
5
Imaging analysis reveals mechanistic differences between first- and second-phase insulin exocytosis.
J Cell Biol. 2007 May 21;177(4):695-705. doi: 10.1083/jcb.200608132. Epub 2007 May 14.
6
Antihypertensive medications and the risk of incident type 2 diabetes.
Diabetes Care. 2006 May;29(5):1065-70. doi: 10.2337/diacare.2951065.
7
New-onset type-2 diabetes associated with atypical antipsychotic medications.
Prog Neuropsychopharmacol Biol Psychiatry. 2006 Jul;30(5):919-23. doi: 10.1016/j.pnpbp.2006.02.007. Epub 2006 Apr 3.
8
GTF2IRD1 in craniofacial development of humans and mice.
Science. 2005 Nov 18;310(5751):1184-7. doi: 10.1126/science.1116142. Epub 2005 Nov 3.
10
Transgenic mouse overexpressing syntaxin-1A as a diabetes model.
Diabetes. 2005 Sep;54(9):2744-54. doi: 10.2337/diabetes.54.9.2744.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验