Search results for "First-degree relatives"

showing 10 items of 28 documents

C4BQ0: a genetic marker of familial HCV-related liver cirrhosis

2004

Source Department of Medicine and Pneumology, V Cervello Hospital, Via Trabucco 180, 90146 Palermo, Italy. lindpas@yahoo.it Abstract BACKGROUND AND METHODS: Host may have a role in the evolution of chronic HCV liver disease. We performed two cross-sectional prospective studies to evaluate the prevalence of cirrhosis in first degree relatives of patients with cirrhosis and the role of two major histocompatibility complex class III alleles BF and C4 versus HCV as risk factors for familial clustering. FINDINGS: Ninety-three (18.6%) of 500 patients with cirrhosis had at least one cirrhotic first degree relative as compared to 13 (2.6%) of 500 controls, (OR 7.38; CI 4.21-12.9). C4BQ0 was signifi…

AdultGenetic MarkersLiver Cirrhosismedicine.medical_specialtyCirrhosisAdolescentFamilial clusteringFamilial clusteringGastroenterologyLiver cirrhosiC4BQ0Liver diseaseInternal medicineHCV diffusionComplement C4bPrevalencemedicineHumansProspective StudiesAlleleFamily historyFirst-degree relativesMHC class III allelesChildProspective cohort studyAllelesAgedAged 80 and overHepatologybusiness.industryGastroenterologyHepatitis C ChronicMiddle Agedmedicine.diseaseCross-Sectional StudiesGenetic markerbusinessC4BQ0; Familial clustering; HCV diffusion; Liver cirrhosis; MHC class III allelesDigestive and Liver Disease
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Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no eviden…

2013

BACKGROUND Esophageal atresia with/without trachea-esophageal fistula (EA/TEF) denotes a spectrum of severe congenital malformations. The aim of this systematic study was to determine both the recurrence risk for EA/TEF, and the risk for malformations of the VATER/VACTERL association spectrum, in first-degree relatives of patients with isolated EA/TEF. METHODS A total of 108 unrelated patients with isolated EA/TEF were included. These individuals had 410 first-degree relatives including 194 siblings. The presence of EA/TEF and malformations of the VATER/VACTERL association spectrum in relatives was systematically assessed. Data from the EUROCAT network were used for comparison. RESULTS None…

AdultHeart Defects CongenitalMaleRiskEmbryologymedicine.medical_specialtyAdolescentFistulaInheritance PatternsLimb Deformities CongenitalAnal CanalKidneyGastroenterologyRecurrence riskAnus ImperforateEsophagusInternal medicinemedicineHumansEsophageal FistulaFirst-degree relativesChildEsophageal Atresiabusiness.industrySiblingsVATER/VACTERL ASSOCIATIONGeneral Medicinemedicine.diseaseVACTERL associationSpinePedigreeTracheaRadiusAtresiaCase-Control Studiesembryonic structuresPediatrics Perinatology and Child HealthCohortFemalebusinessDevelopmental BiologyTracheoesophageal FistulaBirth defects research. Part A, Clinical and molecular teratology
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Increased prevalence of autoimmune diseases in first-degree relatives of patients with celiac disease.

2003

The prevalence of autoimmune disorders is increased in patients with celiac disease (CD), and it is unknown whether their first-degree relatives also have a high risk of autoimmune disorders.To assess the prevalence of autoimmune diseases in first-degree relatives of CD patients, the authors looked for autoimmune disorders in 225 first-degree relatives of 66 children with CD (group A) and in 232 first-degree relatives of 68 healthy children (group B). For both groups, serologic screening for CD was performed through antiendomysium (EMA) and tissue transglutaminase autoantibodies (tTGAA). EMA- and tTGAA-positive subjects were offered an intestinal biopsy. The age at onset of autoimmune disea…

AdultMaleAdolescentBiopsyDiseaseGenetic determinismCoeliac diseaseAutoimmune DiseasesImmunopathologyOdds RatioMedicineHumansFamilyFirst-degree relativesRisk factorIntestinal MucosaChildAutoimmune diseaseHyperplasiabusiness.industryGastroenterologyInfantmedicine.diseaseIntestinesCeliac DiseaseEl NiñoChild PreschoolPediatrics Perinatology and Child HealthImmunologyFemaleAtrophybusinessJournal of pediatric gastroenterology and nutrition
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Intestinal permeability and genetic determinants in patients, first-degree relatives, and controls in a high-incidence area of Crohn's disease in Sou…

2005

1. Am J Gastroenterol. 2005 Dec;100(12):2730-6. Intestinal permeability and genetic determinants in patients, first-degree relatives, and controls in a high-incidence area of Crohn's disease in Southern Italy. Fries W, Renda MC, Lo Presti MA, Raso A, Orlando A, Oliva L, Giofré MR, Maggio A, Mattaliano A, Macaluso A, Cottone M. Dipartimento di Medicina Interna e Terapia Medica, Università di Messina, Messina, Italy. OBJECTIVE: A defect of gastrointestinal barrier function is considered to represent an important step in the pathogenesis of Crohn's disease (CD) but the mechanisms leading to an increased intestinal permeability (IP) are poorly understood. Since IP is influenced by pro-inflammat…

AdultMaleEndemic DiseasesRisk AssessmentStatistics NonparametricPathogenesisCapillary PermeabilityCohort StudiesIntestinal mucosaCrohn DiseaseReference ValuesMedicineHumansGenetic Predisposition to DiseaseFirst-degree relativesIntestinal Mucosapermeability.crohn's disease.NOD2Allele frequencyProbabilityCrohn's diseaseIntestinal permeabilityHepatologybusiness.industryIncidenceGastroenterologyCase-control studyMiddle Agedmedicine.diseasedigestive system diseasesPedigreeToll-Like Receptor 4Genetics PopulationItalyGenetic markerCase-Control StudiesImmunologyMutationFemalebusiness
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Bipolar II disorders in six first-degree relatives

1993

As proposed by Dunner et al (1976), the distinction of bipolar !! disorder from other effective disorders has been included in Research Diagnostic Criteria (RDC) (Spitzer et al 1978) but not in DSM-IiI-R or ICD 10 (APA 1987, WHO 1991). Family studies indicate that bipolar 1I disorder might represent a distinct diagnostic entity with a common genetic background (Gershon et al 1982; Dunner 1983; Endicott et al 1985; Andreasen et al 1987). Familial aggregation, diagnostic stability, and course of illness represent external validators for nosologic classifications (Kendler 1990). Therefore, pedigrees with multiple cases of diagnostically stable bipolar Ii disorder without cases of bipolar 1 dis…

AdultMaleNosologymedicine.medical_specialtyBipolar DisorderResearch Diagnostic CriteriaPedigree chartAntidepressive Agents TricyclicBipolar II disordermental disordersmedicineHumansFamilyBipolar disorderFirst-degree relativesPsychiatryBiological PsychiatryAgedPsychiatric Status Rating ScalesFamily aggregationICD-10Middle Agedmedicine.diseasePedigreeFemalePsychologyBiological Psychiatry
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Specific executive/attentional deficits in patients with schizophrenia or bipolar disorder who have a positive family history of psychosis

2003

Neurocognitive impairments are well documented in patients with schizophrenia and their healthy first-degree biological relatives. Less is known about neuropsychological performance in bipolar disorders, but some studies indicate that, compared to schizophrenia, bipolar disorder displays a similar profile pattern with less severe deficits. The genetic and environmental contributions to the development of neurocognitive deficits are also unclear. This study explored the effect of a family history (FH) of psychotic disorders in first-degree relatives on a variety of cognitive domains (abstraction and flexibility, verbal fluency, verbal memory, motor activity and visual-motor processing/attent…

AdultMalePsychosismedicine.medical_specialtyBipolar DisorderAdolescentNeuropsychological TestsSeverity of Illness Indexmental disordersmedicineHumansVerbal fluency testAttentionBipolar disorderFirst-degree relativesPsychiatryBiological PsychiatryAgedNeuropsychologyMiddle Agedmedicine.diseaseDiagnostic and Statistical Manual of Mental DisordersPsychiatry and Mental healthPsychotic DisordersSchizophreniaSchizophreniaFemaleVerbal memoryCognition DisordersPsychologyNeurocognitiveJournal of Psychiatric Research
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Subclinical thought disorder in first-degree relatives of schizophrenic patients. Results from a matched-pairs study with the Thought Disorder Index

1995

To assess the frequency and quality of formal thought disorder in schizophrenic patients and their first-degree relatives, a consecutive series of 36 unmedicated patients, 20 siblings of these patients and 37 normal control subjects were examined with Holzman's Thought Disorder Index (TDI). As a proof of the internal validity of this tool, the patients demonstrated significantly more thought disorder than the controls as measured by the TDI total score and various subscores, which proved the internal validity of this tool in a German-speaking sample. In addition, in a pairwise comparison with controls who were individually matched by age and sex the patients' siblings had a significantly hi…

AdultMalePsychosismedicine.medical_specialtySeverity of Illness IndexThinkingmedicineHumansFamilyInternal validitySiblingFirst-degree relativesPsychiatrySubclinical infectionPsychiatric Status Rating ScalesThought disorderCognitive disorderMiddle Agedmedicine.diseasePsychiatry and Mental healthSchizophreniaSchizophreniaFemalemedicine.symptomPsychologyClinical psychologyActa Psychiatrica Scandinavica
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A SCAN-SADS comparison study of psychotic subjects and their first-degree relatives

1993

Two diagnostic interviews, the Schedule for Affective Disorders and Schizophrenia (lifetime version) (SADS-LA) and the Schedule for the Clinical Assessment of Neuropsychiatry (SCAN) were compared for main diagnoses and for their acceptibility to psychotic subjects and their psychiatrically well relatives. Broad agreement for DSM-III, DSM-III-R and draft ICD-10 diagnoses was good, although there were areas of disagreement between the two interviews which are discussed.

AdultMalemedicine.medical_specialtyAdolescentPsychometricsNeuropsychiatrybehavioral disciplines and activitiesTerminology as Topicmental disordersmedicineHumansFamilyPharmacology (medical)First-degree relativesMedical diagnosisPsychiatryBiological PsychiatryAgedPsychiatric Status Rating ScalesReproducibility of ResultsSchedule for Affective Disorders and SchizophreniaGeneral MedicineMiddle AgedPsychiatry and Mental healthPsychotic DisordersComparison studyFemalePsychologyClinical psychologyEuropean Archives of Psychiatry and Clinical Neuroscience
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Reward anticipation revisited- evidence from an fMRI study in euthymic bipolar I patients and healthy first-degree relatives.

2017

Abstract Background Symptomatic phases in bipolar disorder (BD) are hypothesized to result from a hypersensitive behavioral activation system (BAS) being sensitive to potential rewards. However, studies on the neuronal underpinnings of reward anticipation in BD are scarce with contradictory findings and possibly confounded by effects of dopaminergic medication, necessitating further research on dysfunctional motivation in BD. Moreover, its role as vulnerability marker for BD is unclear. Methods Functional imaging was conducted in 16 euthymic BD-I patients free from dopaminergic medication and 19 healthy first-degree relatives using a monetary incentive delay task and compared to parallelize…

AdultMalemedicine.medical_specialtyBipolar DisorderGyrus Cinguli03 medical and health sciences0302 clinical medicineRewardmedicineHumansFamilyBipolar disorderFirst-degree relativesPsychiatryAnterior cingulate cortexMotivationVentral striatumDopaminergicBehavioral activationmedicine.diseaseAnticipationMagnetic Resonance Imaging030227 psychiatryFunctional imagingPsychiatry and Mental healthClinical Psychologymedicine.anatomical_structureFemalePsychologypsychological phenomena and processes030217 neurology & neurosurgeryClinical psychologyJournal of affective disorders
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Increased impulsivity as a vulnerability marker for bipolar disorder: Evidence from self-report and experimental measures in two high-risk populations

2015

Abstract Background Heightened impulsivity has been suggested as a possible risk factor for bipolar disorder (BD). However, studies on high-risk populations are scarce and have mainly focused on individuals with a genetic risk. The present study investigated two high-risk samples for BD with regard to several aspects of the impulsivity construct. Methods Unaffected relatives of BD patients (genetically defined high-risk group, N=29) and participants scoring high on the Hypomanic Personality Scale (psychometrically defined high-risk sample, N=25) were being compared to respective control groups (N=27 and N=25) using a multi-method approach. Participants were accessed on the Barratt Impulsive…

AdultMalemedicine.medical_specialtyBipolar DisorderPersonality InventoryEndophenotypesVulnerabilityStop signalImpulsivityYoung AdultRisk FactorsmedicineHumansFamilyBipolar disorderFirst-degree relativesRisk factorPsychiatrymedicine.diseasePsychiatry and Mental healthClinical PsychologyCross-Sectional StudiesCase-Control StudiesEndophenotypeImpulsive BehaviorTraitFemaleSelf Reportmedicine.symptomPsychologyPersonalityJournal of Affective Disorders
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