Search results for "Prenatal development"

showing 3 items of 3 documents

Early Life Origins of All-Cause and Cause-Specific Disability Pension: Findings from the Helsinki Birth Cohort Study

2015

BackgroundThere is some evidence linking sub-optimal prenatal development to an increased risk of disability pension (DP). Our aim was to investigate whether body size at birth was associated with transitioning into all-cause and cause-specific DP during the adult work career.Methods10 682 people born in 1934-44 belonging to the Helsinki Birth Cohort Study had data on birth weight extracted from birth records, and on time, type and reason of retirement between 1971 and 2011 extracted from the Finnish Centre for Pensions.ResultsAltogether 21.3% transitioned into DP during the 40-year follow-up, mainly due to mental disorders, musculoskeletal disorders and cardiovascular disease. Average age …

MalePediatricsSTRESSCHILDHOODDETERMINANTSCohort StudiesDisability Evaluation3123 Gynaecology and paediatricsBody SizeMusculoskeletal Diseasesdisability pensionRetirementMultidisciplinaryMental DisordersQHazard ratioRta3141ta3142Middle AgedAGE 60Prenatal development3. Good healthCardiovascular DiseasesCohortMedicineFemaleResearch ArticleCohort studyRiskmedicine.medical_specialtyScienceBirth weightprenatal developmentmedicineHumansCORONARY-HEART-DISEASEDisabled PersonssyntymäpainoAgedDemographyProportional Hazards Modelsbusiness.industryProportional hazards modelbirth weightDisability pensionMental healthSIZEFETAL-GROWTHWEIGHTFOLLOW-UPbusinessFollow-Up StudiesDemographyPLoS ONE
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Influence of fetal glutathione S-transferase copy number variants on adverse reproductive outcomes

2012

A nested case-control association study was designed to investigate the influence of maternal and fetal copy number variants (CNVs) on reproductive outcomes. Genotypes of ten CNVs encompassing GST and CYP genes were assessed. Significant associations were only found for child CNV genotypes. In particular, the child GSTM1 insertion allele was associated with prematurity protection (odds ratio, 95% CI: 0.67, 0.51-0.89; P < 0.01), whereas the child GSTT2B insertion allele was associated with an increased risk of being small for gestational age (odds ratio, 95% CI: 1.33, 1.07-1.67; P = 0.01). The study highlights the role of the fetal genome in prenatal development and also the need to analyse …

0303 health sciencesFetus030219 obstetrics & reproductive medicinebiologybusiness.industryObstetrics and GynecologyOdds ratioBioinformaticsmedicine.diseasePrenatal development03 medical and health sciences0302 clinical medicineGlutathione S-transferasemental disordersGenotypebiology.proteinMedicineSmall for gestational ageCopy-number variationAllelebusiness030304 developmental biologyBJOG: An International Journal of Obstetrics &amp; Gynaecology
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The development of anticipation in the fetus: A longitudinal account of human fetal mouth movements in reaction to and anticipation of touch

2013

Research suggests that fetuses open or close their mouth in relation to directed movements but it is unclear whether mouth opening anticipates the touch or is a reaction to touch, as there has been no analysis so far of (1) the facial area of touch and (2) the sequential ordering of touch and mouth movements. If there is prenatal development of the anticipation of touch we would expect the frequency of fetal mouth opening immediately preceding the arriving hand at the mouth area to increase with fetal age. Fifteen healthy fetuses, eight girls and seven boys, underwent four additional 4-D scans at 24, 28, 32, and 36 weeks gestation. Changes in the frequency of touch for different facial regi…

Fetusmedicine.medical_specialtyGestational ageAnatomyFetal ageAudiologyAnticipationPrenatal developmentBehavioral NeuroscienceMouth openingDevelopmental NeuroscienceHuman fetalDevelopmental and Educational PsychologymedicinePsychologyMouth movementsDevelopmental BiologyDevelopmental Psychobiology
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