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Y 染色体嵌合体丢失的预测因子及其与英国生物库死亡率的相关性。

Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank.

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA.

Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, Maryland, USA.

出版信息

Sci Rep. 2018 Aug 17;8(1):12316. doi: 10.1038/s41598-018-30759-1.

Abstract

Mosaic loss of the Y chromosome (mLOY) is the most commonly reported large structural somatic event. Previous studies have indicated age and cigarette smoking increase the risk of mLOY, but the relationship of other exposures with mLOY and mLOY with disease has not been adequately investigated. We characterized mLOY in a large cohort of 223,338 men from the UK Biobank by scanning for deviations in genotyping array median log intensity ratios (mLRR) of the Y chromosome using a standard algorithm. A total of 3,789 (1.7%) men showed evidence for mLOY (mLRR < -0.15). In multivariable-adjusted logistic regression models, we found that mLOY increases exponentially with age (overall P-value < 4.9 × 10; p-value for the quadratic term = 2.1 × 10), and observed a strong association with current smoking (P-value = 7.8 × 10). We observed less mLOY in men of African ancestry (0.4%) compared to men of European ancestry (1.8%, P-value = 0.003). Although mLOY was not associated with prevalent cancer (P-value = 0.61), associations were observed for diabetes (P-value = 0.003) and cardiovascular disease (P-value = 0.01). Using Cox proportional hazards regression models, mLOY was associated with all-cause mortality among men with a high proportion of cells affected (mLRR < -0.40; HR = 1.35, 95% CI = 1.08-1.70, P-value = 0.009). In conclusion, mLOY was associated with several health-related factors as well as with all-cause mortality. Further functional studies are warranted to understand how and in what way mLOY could influence adult male health.

摘要

Y 染色体的镶嵌性缺失(mLOY)是最常报道的大型结构体细胞事件。先前的研究表明,年龄和吸烟会增加 mLOY 的风险,但其他暴露因素与 mLOY 以及 mLOY 与疾病之间的关系尚未得到充分研究。我们通过使用标准算法扫描 Y 染色体基因分型阵列中位数对数比(mLRR)的偏差,在来自英国生物库的 223,338 名男性的大型队列中对 mLOY 进行了特征描述。共有 3,789 名(1.7%)男性表现出 mLOY 的证据(mLRR < -0.15)。在多变量调整的逻辑回归模型中,我们发现 mLOY 随年龄呈指数增长(总体 P 值 < 4.9×10;二次项 P 值 = 2.1×10),并且与当前吸烟有很强的关联(P 值 = 7.8×10)。我们观察到非洲裔男性的 mLOY 较少(0.4%),而欧洲裔男性的 mLOY 较多(1.8%,P 值 = 0.003)。尽管 mLOY 与现患癌症无关(P 值 = 0.61),但与糖尿病(P 值 = 0.003)和心血管疾病(P 值 = 0.01)有关。使用 Cox 比例风险回归模型,mLOY 与受影响细胞比例较高的男性的全因死亡率相关(mLRR < -0.40;HR = 1.35,95%CI = 1.08-1.70,P 值 = 0.009)。总之,mLOY 与多种与健康相关的因素以及全因死亡率相关。需要进一步的功能研究来了解 mLOY 如何以及以何种方式影响成年男性的健康。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4669/6098142/8a6380c78b16/41598_2018_30759_Fig1_HTML.jpg

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