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男孩中FRAXE重复序列数量与其母亲及外祖母患糖尿病证据之间的意外关联。

Unexpected Associations between the Number of FRAXE Repeats in Boys and Evidence of Diabetes in Their Mothers and Maternal Grandmothers.

作者信息

Golding Jean, Clark Rosie, Gregory Steven, Ellis Genette, Suderman Matthew, Iles-Caven Yasmin, Pembrey Marcus E

机构信息

Centre for Academic Child Health, Bristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, U.K.

MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol BS8 2BN, U.K.

出版信息

OBM Genet. 2021 Oct 29;5(4):15. doi: 10.21926/obm.genet.2104141.

Abstract

The FRAXE section of the FMR2 gene, located on the X chromosome, contains varying numbers of trinucleotide repeats; boys with over 200 repeats tend to have mild cognitive impairments, though this is rare. Little is known, however, concerning the phenotypes of individuals with smaller numbers of repeats. Here we answer the research question as to whether the health of ancestors of boys from whom the relevant X chromosome was inherited differed in any way according to the number of FRAXE repeats. Numbers of FRAXE repeats in 5057 boys from the Avon Longitudinal Study of Parents and Children (ALSPAC) were assessed. The distribution was bimodal, with the second smaller distribution starting at 22 repeats. We tested whether possession of 22+ repeats was associated with differences in the health of mothers (who share the X chromosome) and maternal grandmothers (half of whom share it). Female ancestors of boys with >21 repeats compared with <22 showed that maternal grandmothers (MGM) and mothers (M) had an increased risk of diabetes: MGM Type I odds ratio (OR) 2.40 [95%CI: 1.07,5.38]; MGM Type II OR 1.61 [0.96,2.70]; M OR 1.95 [0.96,3.94] using self-reported questionnaire measures. These results were confirmed from maternal medical records which revealed an increased level of diabetes [OR 2.40 (1.16,4.96)] and an increased risk of repeated glycosuria during pregnancy [OR 1.60 (1.08,2.36)]. We tested numbers of FRAXA repeats and showed no such associations, indicating that the findings were not associated with triploid repeats in general. If these findings are replicated elsewhere, there are at least three possible interpretations: (i) maternal diabetes/prediabetes results in an increased number of FRAXE repeats; (ii) women with high numbers of FRAXE repeats are at increased risk of diabetes; or (iii) some common factor, e.g. genomic instability, results in both diabetes and increased repeats.

摘要

位于X染色体上的FMR2基因的FRAXE区域含有数量不等的三核苷酸重复序列;重复序列超过200次的男孩往往有轻度认知障碍,不过这种情况很罕见。然而,对于重复序列数量较少的个体的表型,人们了解得很少。在这里,我们回答一个研究问题,即根据FRAXE重复序列的数量,继承相关X染色体的男孩的祖先的健康状况是否存在任何差异。对埃文亲子纵向研究(ALSPAC)中5057名男孩的FRAXE重复序列数量进行了评估。分布呈双峰型,第二个较小的分布从22次重复开始。我们测试了拥有22次及以上重复序列是否与母亲(共享X染色体)和外祖母(其中一半共享)的健康差异有关。与重复序列少于22次的男孩相比,重复序列多于21次的男孩的女性祖先中,外祖母(MGM)和母亲(M)患糖尿病的风险增加:使用自我报告问卷测量,MGM患I型糖尿病的比值比(OR)为2.40 [95%置信区间:1.07,5.38];MGM患II型糖尿病的OR为1.61 [0.96,2.70];M患糖尿病的OR为1.95 [0.96,3.94]。这些结果从母亲的医疗记录中得到证实,记录显示糖尿病水平升高[OR 2.40(1.16,4.96)]以及孕期反复出现糖尿的风险增加[OR 1.60(1.08,2.36)]。我们测试了FRAXA重复序列的数量,未发现此类关联,这表明这些发现一般与三倍体重复序列无关。如果这些发现在其他地方得到重复验证,至少有三种可能的解释:(i)母亲患糖尿病/糖尿病前期导致FRAXE重复序列数量增加;(ii)FRAXE重复序列数量多的女性患糖尿病的风险增加;或者(iii)某些共同因素,例如基因组不稳定,导致糖尿病和重复序列增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/7612666/b67a95ab9113/EMS144007-f001.jpg

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