Center for Human Genetics, Simches Research Building, 185 Cambridge Street, Rm 222, Boston, MA 02115, USA.
Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):291-8. doi: 10.1002/ajmg.c.30261.
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.
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。