Search results for "twin"

showing 10 items of 435 documents

Genetic and Environmental Influences on BMI From Late Childhood to Adolescence are Modified by Parental Education

2011

To investigate how parental education modifies genetic and environmental influences on variation in BMI during adolescence, self-reported BMI at 11-12, 14, and 17 years of age was collected from a population sample of 2,432 complete Finnish twin pairs born in 1983-1987. Based on parental report, twins were divided to those with high (both parents high school graduates), mixed level (one parent a graduate, the other not), and limited (neither parent a graduate) parental education. Genetic and environmental influences on variation in BMI in different education classes were modeled using twin analysis. Heritability of BMI among 11-12-year-olds with high parental education was 85-87% whereas it…

MaleParentsPediatricsmedicine.medical_specialtyAdolescentEndocrinology Diabetes and MetabolismTwinsMedicine (miscellaneous)Social EnvironmentAffect (psychology)Body Mass Index03 medical and health sciences0302 clinical medicineEndocrinologyParental educationGenetic variationmedicineHumansObesityProspective Studies030212 general & internal medicineChildSocioeconomic statusFinlandta515030304 developmental biology0303 health sciencesNutrition and DieteticsParentingGenetic VariationSocial environmentHeritabilityTwin studyEducational StatusFemaleSelf ReportPsychologyBody mass indexDemographyObesity
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Externalizing Problem Behaviors and Headache: A Follow-up Study of Adolescent Finnish Twins

2004

Objective.To examine the association of teacher- and parent-rated behavior with headache in a prospective follow-up study of adolescent Finnish twins.Methods.Questionnaire data were collected during 1995–2001 from a nationwide sample of Finnish families of 11-year-old twins who were born 1983–1987 (n = 5393) and again at age of 14. Psychological factors were measured by using parents’ and teachers’ ratings of a 37-item multidimensional rating instrument at the ages of 11 and 14.Results.At age 11, headache frequency (5 categories) was associated with total scales of externalizing and internalizing problem behaviors and adaptive behaviors, assessed by parents, but only with externalizing prob…

MaleParentsmedicine.medical_specialtyAdolescentPoor complianceChild BehaviorChild Behavior Disorders03 medical and health sciences0302 clinical medicineSurveys and QuestionnairesTwins DizygoticHumansMedicine030212 general & internal medicineChildPsychiatryAssociation (psychology)Internal-External Controlbusiness.industryTeachingIncidence (epidemiology)HeadacheFollow up studiesTwins MonozygoticQuestionnaire dataCross-Sectional StudiesLogistic ModelsPediatrics Perinatology and Child HealthFemalebusiness030217 neurology & neurosurgeryFollow-Up StudiesClinical psychologyPediatrics
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Heterozygous nonsense SCN5A mutation W822X explains a simultaneous sudden infant death syndrome.

2008

The sudden, unexpected, and unexplained death of both members of a set of healthy twins (simultaneous sudden infant death syndrome (SSIDS)) is defined as a case in which both infants meet the definition of sudden infant death syndrome individually. A search of the world medical literature resulted in only 42 reported cases of SSIDS. We report the case of a pair of identical, male, monozygotic twins, 138 days old, who suddenly died, meeting the full criteria of SSIDS and where a genetic screen was performed, resulting in a heterozygous nonsense SCN5A mutation (W822X) in both twins. Immunohistochemistry was performed on cardiac tissue samples utilizing polyclonal antibodies anti-Na+ CP type V…

MalePathologymedicine.medical_specialtyNav1.5 protein functionv1.5 protein functionmedia_common.quotation_subject2734Nonsense mutationNonsenseNa+ channel functionMuscle ProteinsSocio-culturaleBiology+Nav1.5 protein function; Na+ channel function; SCN5A gene mutation; Simultaneous sudden infant death syndrome; W822X mutation; Codon Nonsense; Diseases in Twins; Humans; Infant; Male; Muscle Proteins; NAV1.5 Voltage-Gated Sodium Channel; Sodium Channels; Sudden Infant Death; 2734Sudden deathSodium ChannelsNAV1.5 Voltage-Gated Sodium ChannelPathology and Forensic MedicinePathogenesisSCN5A gene mutationDiseases in TwinsmedicineHumansSimultaneous sudden infant death syndromeSCN5A gene mutationW822X mutationNa+ channel functionNav1.5 protein functionNaSimultaneous sudden infant death syndrome SCN5A gene mutation W822X mutation Na+ channel function Nav1.5 protein function CodonMolecular BiologyCellular localizationmedia_commonSimultaneous sudden infant death syndromeSettore BIO/16 - Anatomia UmanaSimultaneous sudden infant death syndrome SCN5A gene mutation W822X mutation Na+ channel function Nav1.5 protein functionW822X mutationInfantCell BiologyGeneral MedicineSudden infant death syndromeNonsenseTerminal deoxynucleotidyl transferaseCodon NonsenseImmunohistochemistryNa; v; 1.5 protein function; Na; +; channel function; SCN5A gene mutation; Simultaneous sudden infant death syndrome; W822X mutationchannel functionSudden Infant Death
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Intrauterine growth pattern and birthweight discordance in twin pregnancies: a retrospective study

2013

Background: Twins, compared to singletons, have an increased risk of perinatal mortality and morbidity, due mainly to a higher prevalence of preterm birth and low birthweight. Intrauterine growth restriction (IUGR) is also common and can affect one or both fetuses. In some cases, however, one twin is much smaller than the other (growth discordance). Usually, high birthweight discordance is associated with increased perinatal morbidity. The aim of this study is to describe the epidemiological features of a population of twins at birth, with particular reference to the interpretation and clinical effects of birthweight discordance. Methods: We evaluated retrospectively the clinical features o…

MalePediatricsmedicine.medical_specialtyBirth weightPopulationTwinsNeonatal anemiaIntrauterine growth restrictionGestational AgeInfant Newborn DiseasesWeight percentileSettore MED/38 - Pediatria Generale E SpecialisticaPregnancyRisk FactorsInfant MortalityDiseases in TwinsBirth WeightHumansMedicineeducationreproductive and urinary physiologyTwin PregnancyRetrospective StudiesSGAPregnancyeducation.field_of_studyFetal Growth Retardationbusiness.industryObstetricsResearchInfant NewbornTwinGestational ageBirthweight discordancemedicine.diseaseTwin studyItalyPremature birthPregnancy TwinPremature BirthFemaleMorbiditybusinessFollow-Up StudiesItalian Journal of Pediatrics
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Neonatal screening for congenital hypothyroidism in an Italian Centre: a 5-years real-life retrospective study

2021

Abstract Introduction Congenital hypothyroidism is an endocrine disease with a significant incidence in the general population (1:2000–1:3000 newborns in Italy) and a different geographical distribution, partially explained by endemic iodine deficiency, genetic traits and autoimmune thyroid diseases. Objectives Aims of this study are: to evaluate the incidence of positive neonatal blood spot screening for CH in western Sicily, identified by the screening centre of the Children Hospital “G. Di Cristina”, ARNAS, Palermo; to evaluate the impact of a lower TSH cutoff in the neonatal blood spot screening for CH. Materials and methods The TSH threshold of the neonatal screening was established as…

MalePediatricsmedicine.medical_specialtyendocrine systemendocrine system diseasesPopulationIodine deficiencyNeonatal screening TSH Twins Congenital Hypothyroidism Female Humans Incidence Infant Newborn Male Retrospective Studies Risk Factors SicilyTwins030209 endocrinology & metabolismPediatricsRJ1-57003 medical and health sciences0302 clinical medicineNeonatal ScreeningRisk Factors030225 pediatricsMedicineHumanseducationSicilyWhole bloodRetrospective Studieseducation.field_of_studyEndocrine diseasebusiness.industryTSHIncidence (epidemiology)ResearchIncidenceThyroidInfant NewbornRetrospective cohort studymedicine.diseaseIodine deficiencyCongenital hypothyroidismCongenital hypothyroidismmedicine.anatomical_structureFemalebusinessIodine deficiencyItalian Journal of Pediatrics
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Motives for physical activity in older men and women : A twin study using accelerometer-measured physical activity

2019

Motives for physical activity may vary considerably by age, sex, and the level of physical activity. We aimed to examine motives for physical activity in older men and women with different physical activity levels as well as whether genetic and/or environmental factors explain those motives. Finnish twins (mean age 72.9 years, 262 full twin pairs) self-reported their motives for physical activity. Time spent on moderate-to-vigorous physical activity was monitored using a hip-worn accelerometer. Comparisons between the different physical activity groups of older twins (n = 764-791/motive dimension) were analyzed using the Wald test, and effect sizes were calculated as Cohen's d. Quantitative…

MalePhysical fitnessPhysical activityPsychological interventionPhysical Therapy Sports Therapy and Rehabilitation030204 cardiovascular system & hematology03 medical and health sciencesSex Factors0302 clinical medicineAGEmotivationPEOPLEaged individualsAccelerometryGenetic modelingHumansOrthopedics and Sports Medicine315 Sport and fitness sciencesAgedmotivaatiokaksostutkimusdevice‐measured physical activityexerciseBARRIERSkuntoliikuntabusiness.industrykiihtyvyysmittaritMean ageexercise motivation030229 sport sciencestwinsTwin study3142 Public health care science environmental and occupational healthdevice-measured physical activity3141 Health care scienceMOTIVATORSHealth maintenanceFemalebusinessPsychologyikääntyneetfyysinen aktiivisuusClinical psychology
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Multiple sclerosis in twins from continental Italy and Sardinia: a nationwide study.

2005

Knowledge about the balance between heritable and nonheritable risk in multiple sclerosis (MS) is based on twin studies in high-prevalence areas. In a study that avoided ascertainment limitations and directly compared continental Italy (medium-prevalence) and Sardinia (high-prevalence), we ascertained 216 pairs from 34,549 patients. This gives a twinning rate of 0.62% among MS patients, significantly less than that of the general population. In continental Italy, probandwise concordance was 14.5% (95% confidence interval, 5.1-23.8) for monozygotic and 4.0% (95% confidence interval, 0.8-7.1) for dizygotic twins. Results in Sardinia resemble those in northern populations but in limited number…

MaleQuestionnairesMultiple SclerosisConcordancePopulationTwinsDizygotic twinsDisease causeMultiple Sclerosis Epidemiology TwinsCohort StudiesCohort Studies Disease Susceptibility Female Genetic Predisposition to Disease Humans Italy; epidemiology Male Multiple Sclerosis; epidemiology/genetics Questionnaires Regression Analysis TwinsSurveys and QuestionnairesmedicineHumansGenetic Predisposition to Diseaseeducationeducation.field_of_studyepidemiology/geneticsbusiness.industryMultiple sclerosismedicine.diseasePenetranceTwin studyConfidence intervalNeurologyItalyRegression AnalysisSettore MED/26 - NeurologiaFemaleepidemiologyNeurology (clinical)Disease SusceptibilitybusinessDemography
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Genetic variation in neuromuscular performance.

1973

Using a simple cumulative model of heredity plus environment, based on intrapair differences observed in monozygous (MZ) and dizygous (DZ) twins, the relative contribution of heredity to the interindividual variance in several neuromuscular parameters was determined with 15 pairs of male (8 MZ and 7 DZ) and 14 pairs of female (7 MZ and 7 DZ) twins ranging in age from 10 to 14 years. The data disclosed that in boys the variability in maximal mechanical (anaerobic) power was 99.2% genetically determined under the environmental conditions of the study. The corresponding heritability estimate values for the patellar reflex time and reaction time were 97.5% and 85.7%, respectively. In girls the …

MaleReflex StretchAdolescentPhysiologyPhysical ExertionNeuromuscular JunctionTwinsPhysiologyBiologymedicine.disease_causePregnancyPhysiology (medical)Genetic variationHereditymedicineReaction TimeHumansOrthopedics and Sports MedicineGenetic variabilityChildGeneticsmedicine.diagnostic_testBody WeightPublic Health Environmental and Occupational HealthPatellar reflexGeneral MedicineHuman physiologyPatellaHeritabilityBody HeightGenetic TechniquesGenetic CodeFemaleInternationale Zeitschrift fur angewandte Physiologie, einschliesslich Arbeitsphysiologie
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Differences in muscle and adipose tissue gene expression and cardio-metabolic risk factors in the members of physical activity discordant twin pairs

2010

High physical activity/aerobic fitness predicts low morbidity and mortality. Our aim was to identify the most up-regulated gene sets related to long-term physical activity vs. inactivity in skeletal muscle and adipose tissues and to obtain further information about their link with cardio-metabolic risk factors. We studied ten same-sex twin pairs (age range 50-74 years) who had been discordant for leisure-time physical activity for 30 years. The examinations included biopsies from m. vastus lateralis and abdominal subcutaneous adipose tissue. RNA was analyzed with the genome-wide Illumina Human WG-6 v3.0 Expression BeadChip. For pathway analysis we used Gene Set Enrichment Analysis utilizing…

MaleSELECTIONFITNESSTwinsAdipose tissuephysical activityliikuntaPhysiology/Muscle and Connective TissueDiabetes and Endocrinology/ObesityCohort Studieschemistry.chemical_compound0302 clinical medicineRisk FactorsAdipocyte311 Basic medicinegeeniekspressioFinlandRegulation of gene expression0303 health sciencesINSULIN-RESISTANCEMultidisciplinaryQRGenetics and Genomics/Gene ExpressionMiddle Agedgeenien ilmentyminen3. Good healthmedicine.anatomical_structureTRIACYLGLYCEROLAdipose Tissue/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingMedicineSKELETAL-MUSCLEFemalePublic Health and Epidemiology/Exercise and SportsResearch ArticleMuscle tissuemedicine.medical_specialtyHeart DiseasesCardiovascular DisordersScience030209 endocrinology & metabolismEXERCISEMotor ActivityBiologyCAPACITY03 medical and health sciencesInsulin resistanceSDG 3 - Good Health and Well-beingInternal medicinemetaboliamedicineHumansAerobic exerciseMuscle SkeletalCell Biology/Gene ExpressionAged030304 developmental biologymatebolismMORTALITYCholesterol HDLSkeletal muscleLipid metabolismLipid Metabolismmedicine.diseasekaksosetEndocrinologyGene Expression RegulationchemistryADAPTATIONSCHRONIC DISEASEEnergy MetabolismPLoS ONE
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Teacher-rated aggression and co-occurring behaviors and emotional problems among schoolchildren in four population-based European cohorts

2021

Aggressive behavior in school is an ongoing concern. The current focus is on specific manifestations such as bullying, but the behavior is broad and heterogenous. Children spend a substantial amount of time in school, but their behaviors in the school setting tend to be less well characterized than at home. Because aggression may index multiple behavioral problems, we used three validated instruments to assess means, correlations and gender differences of teacher-rated aggressive behavior with co-occurring externalizing/internalizing problems and social behavior in 39,936 schoolchildren aged 7-14 from 4 population-based cohorts from Finland, the Netherlands, and the UK. Correlations of aggr…

MaleSocial CognitionQuestionnairesBOYSaggressiivisuusEmotionsTwinsCHILDHOODChild BehaviorSocial ScienceskoululaisetCHILDRENADOLESCENT/dk/atira/pure/sustainabledevelopmentgoals/gender_equalityFamiliesSociologyRATINGSPARENTSPsychologyaggressiotChildkohorttitutkimusFinlandNetherlandsSchoolsSDG 5 - Gender EqualityQRPSYCHOPATHOLOGYopettajatAggressionProfessionsResearch DesignMedicineFemaleResearch ArticleSocial PsychologyScienceeducationlapset (ikäryhmät)Research and Analysis MethodsprososiaalisuusEducationtunteetHumansSocial BehaviorBehaviorSurvey ResearchCognitive PsychologyBiology and Life SciencesTeachersELEMENTARY-SCHOOLUnited KingdomongelmakäyttäytyminenProsocial BehaviorAge GroupsCONDUCT DISORDERPeople and PlacesCognitive SciencePopulation Groupings516 Educational sciencesSchool TeachersCOMORBIDITYNeuroscienceDevelopmental Biology
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