Suppr超能文献

普拉德-威利综合征与对照个体中瘦素蛋白水平的比较。

Comparison of leptin protein levels in Prader-Willi syndrome and control individuals.

作者信息

Butler M G, Moore J, Morawiecki A, Nicolson M

机构信息

Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA.

出版信息

Am J Med Genet. 1998 Jan 6;75(1):7-12.

Abstract

Prader-Willi syndrome (PWS) is characterized by early childhood obesity, mental deficiency, hypogonadism, hypotonia, hypopigmentation, short stature, small hands and feet, and a characteristic face. It is the most common genetic cause of obesity and obesity is the most significant health problem for PWS patients. Ob protein (leptin), which is produced by adipose tissue, is thought to play a significant role in obesity; thus, unusually low plasma leptin levels, or relative loss of sensitivity to leptin in PWS subjects, could be an important factor in their obesity. We measured plasma leptin levels in 19 obese and 14 non-obese PWS patients [mean body mass index (BMI) 37.2 and 22.0, respectively] and compared these levels to those of 28 obese controls (mean BMI 35.5) and 16 non-obese control individuals (mean BMI 21.6). The mean plasma leptin concentration (ng/ml) for obese PWS subjects was 33.4 and 23.6 for non-obese PWS subjects. Obese control leptin was 36.2 ng/ml and non-obese control was 9.9. Among the control groups, leptin levels in females were significantly higher than those in males; the obese males and females had significantly higher leptin than their respective non-obese counterparts. These differences did not hold true for the PWS subjects. Leptin levels in obese PWS males and females were similar, and the same was true of the non-obese PWS males and females. The differences between obese and non-obese PWS subjects of both sexes were small and not significant. Comparing control groups with their PWS counterparts revealed no significant differences, with one exception: circulating plasma leptin levels in non-obese PWS males were nearly five times higher than in non-obese control males with similar BMI. This difference may reflect a more female pattern of fat distribution and hypogonadism, which are characteristic of PWS males. Leptin levels in PWS patients were not obviously correlated with the chromosome 15 finding seen in the patients.

摘要

普拉德-威利综合征(PWS)的特征包括儿童期早期肥胖、智力缺陷、性腺功能减退、肌张力减退、色素沉着减退、身材矮小、手脚小以及具有特征性面容。它是肥胖最常见的遗传病因,而肥胖是PWS患者最严重的健康问题。由脂肪组织产生的Ob蛋白(瘦素)被认为在肥胖中起重要作用;因此,PWS患者血浆瘦素水平异常低,或对瘦素的敏感性相对丧失,可能是其肥胖的一个重要因素。我们测量了19名肥胖和14名非肥胖PWS患者的血浆瘦素水平[平均体重指数(BMI)分别为37.2和22.0],并将这些水平与28名肥胖对照者(平均BMI 35.5)和16名非肥胖对照个体(平均BMI 21.6)的水平进行比较。肥胖PWS受试者的平均血浆瘦素浓度(ng/ml)为33.4,非肥胖PWS受试者为23.6。肥胖对照者的瘦素为36.2 ng/ml,非肥胖对照者为9.9。在对照组中,女性的瘦素水平显著高于男性;肥胖男性和女性的瘦素水平显著高于各自的非肥胖对应者。这些差异在PWS受试者中并不成立。肥胖PWS男性和女性的瘦素水平相似,非肥胖PWS男性和女性也是如此。肥胖和非肥胖PWS两性受试者之间的差异很小且不显著。将对照组与其PWS对应者进行比较,除了一个例外,没有发现显著差异:非肥胖PWS男性的循环血浆瘦素水平几乎是BMI相似的非肥胖对照男性的五倍。这种差异可能反映了PWS男性更具女性特征的脂肪分布模式和性腺功能减退。PWS患者的瘦素水平与患者中观察到的15号染色体发现没有明显相关性。

相似文献

引用本文的文献

5
Prader-Willi syndrome: an update on obesity and endocrine problems.普拉德-威利综合征:肥胖与内分泌问题的最新进展
Ann Pediatr Endocrinol Metab. 2021 Dec;26(4):227-236. doi: 10.6065/apem.2142164.082. Epub 2021 Dec 31.

本文引用的文献

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