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Association of maternal hypertensive disorders in pregnancy with infant neurodevelopment
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作者 Bo Huang Yifan Wang +7 位作者 Yangqian Jiang Hong Lv Tao Jiang Yun Qiu Qun Lu Jiangbo Du Yuan Lin Hongxia Ma 《The Journal of Biomedical Research》 CAS CSCD 2023年第6期479-491,共13页
Inconsistent findings have been reported regarding the associations between hypertensive disorders in pregnancy (HDP) and infant neurodevelopment. Leveraging data from the Jiangsu Birth Cohort, in the present study, w... Inconsistent findings have been reported regarding the associations between hypertensive disorders in pregnancy (HDP) and infant neurodevelopment. Leveraging data from the Jiangsu Birth Cohort, in the present study, we re-visited such associations in one-year-old infants from 2 576 singleton pregnancies and 261 twin pregnancies. We first assessed infant neurodevelopment by the Bayley Scales of Infant and Toddler Development Screening Test (the Third Edition), and then estimated its association with maternal HDP using general linear regression models and Poisson regression models. In singleton pregnancies, compared with mothers unexposed to HDP, infants born to mothers with chronic hypertension exhibited a lower score (β, −0.67;95% confidence interval [CI], −1.19-−0.15) and a higher risk of "non-optimal" gross motor development (risk ratio [RR], 2.21;95% CI, 1.02-4.79);in twin pregnancies, infants born to mothers with HDP exhibited lower scores in cognition (β, −0.49;95% CI, −0.96-−0.01), receptive communication (β, −0.55;95% CI, −1.03-−0.06), and gross motor (β, −0.44;95% CI, −0.86-−0.03), and at a higher risk of "non-optimal" gross motor development (RR, 2.12;95% CI, 1.16-3.88). These findings indicate that infants born to mothers with HDP may have inferior neurodevelopment outcomes at the age of one year. 展开更多
关键词 hypertensive disorders in pregnancy infant neurodevelopment prospective birth cohort study
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Polygenic score: An anchor holding the whole life course
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作者 Guangfu Jin Hongxia Ma +1 位作者 Hongbing Shen Zhibin Hu 《Chinese Medical Journal》 SCIE CAS CSCD 2023年第8期883-885,共3页
In 2001,the draft sequence of the first human genome was reported,followed by a near-complete sequence published in 2004.One promise of the trove of genomes was to allow scientists to uncover the genetic basis of huma... In 2001,the draft sequence of the first human genome was reported,followed by a near-complete sequence published in 2004.One promise of the trove of genomes was to allow scientists to uncover the genetic basis of human diseases,and thereby to facilitate the design of rational diagnostics and therapeutics. 展开更多
关键词 DISEASES thereby RATIONAL
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