Search results for "case-control studies"

showing 10 items of 1567 documents

Deficit of Interleukin-7 in Serum of Patients with Crohn's Disease

2013

medicine.medical_specialtyCrohn's diseasebusiness.industryInterleukin-7GastroenterologyInterleukinmedicine.diseaseGastroenterologyCrohn DiseaseInternal medicineCase-Control StudiesmedicineImmunology and AllergyHumansbusinessBiomarkers
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The STROCSS statement: Strengthening the Reporting of Cohort Studies in Surgery

2017

Abstract Introduction The development of reporting guidelines over the past 20 years represents a major advance in scholarly publishing with recent evidence showing positive impacts. Whilst over 350 reporting guidelines exist, there are few that are specific to surgery. Here we describe the development of the STROCSS guideline ( St rengthening the R eporting o f C ohort S tudies in S urgery). Methods and analysis We published our protocol apriori . Current guidelines for case series (PROCESS), cohort studies (STROBE) and randomised controlled trials (CONSORT) were analysed to compile a list of items which were used as baseline material for developing a suitable checklist for surgical cohort…

medicine.medical_specialtyDelphi TechniqueCross-sectional studyDelphi methodGuidelines as TopicCase-control studiesArticleCohort Studies03 medical and health sciencesCase-control studies; Cohort studies; Cross-sectional; Reporting guideline; Cross-Sectional Studies; Delphi Technique; Humans; Cohort Studies; General Surgery; Guidelines as Topic0302 clinical medicineCross-sectionalHumansMedicinecomputer.programming_languageProtocol (science)business.industryReporting guidelineGeneral MedicineGuidelineChecklistSurgeryCross-Sectional StudiesGeneral Surgery030220 oncology & carcinogenesisCohort030211 gastroenterology & hepatologySurgerybusinesscomputerDelphiCohort studyInternational Journal of Surgery
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Increased risk for cervical disease progression of French women infected with the human papillomavirus type 16 E6-350G variant.

2006

Abstract To test the significance of human papillomavirus (HPV) type 16 and HPV16 E6 variants as risk factors for viral persistence and progression to high-grade lesion, we did a nested case-control study within a cohort study of >15,000 Caucasian French women. Three groups infected with high-risk HPV were compared: (a) women with cleared infection (controls, n = 201), (b) women with persistent infection (cases, n = 87), and (c) women who progressed into high-grade lesion (cases, n = 58). Women with persistent HPV infection and those that progressed into high-grade lesions were likelier to harbor HPV16 than other high-risk HPV types [odds ratio (OR), 2.4; 95% confidence interval (95%…

medicine.medical_specialtyEpidemiologyUterine Cervical NeoplasmsCervical intraepithelial neoplasiaLesionCohort StudiesRisk FactorsInternal medicineEpidemiologymedicineOdds RatioHumansRisk factorbusiness.industryPapillomavirus InfectionsHPV infectionvirus diseasesOdds ratioOncogene Proteins Viralmedicine.diseaseUterine Cervical DysplasiaRepressor ProteinsOncologyCase-Control StudiesImmunologyDisease ProgressionFemaleViral diseaseFrancemedicine.symptombusinessCohort studyCancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
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Gastroesophageal reflux in young children treated for esophageal atresia: evaluation with pH-multichannel intraluminal impedance

2011

Objectives: Gastroesophageal reflux (GER) and dismotility occur frequently after repair of esophageal atresia (EA). GER-associated complications can manifest either early or later; then precocious diagnosis and treatment are essential. The aim of the study was to evaluate characteristics of GER and esophageal clearance in children treated for EA with distal tracheoesophageal fistula, using pH-multichannel intraluminal impedance (pH-MII). Patients and Methods: Twenty-two children (ages 3‐40 months) treated for EA at birth, and 20 normal children of similar age with suspected GER disease were included in the study. Impedance parameters were analyzed according to age and symptoms. Results: Ref…

medicine.medical_specialtyEsophageal pH MonitoringTracheoesophageal fistulaSettore MED/42 - Igiene Generale E ApplicataGastroenterologyGastric AcidEsophagusPostoperative ComplicationsBolus (medicine)Internal medicinemedicineHumansEsophagusGastrointestinal TransitEsophageal Atresiaesophageal atresia esophageal dismotility gastroesophageal reflux disease multichannel intraluminal impedance ph-metryEsophageal diseasebusiness.industryfungiSignificant differenceSettore MED/20 - Chirurgia Pediatrica E InfantileGastroenterologyRefluxInfantHydrogen-Ion Concentrationmedicine.diseasemedicine.anatomical_structureEl NiñoCase-Control StudiesChild PreschoolAtresiaPediatrics Perinatology and Child HealthGastroesophageal RefluxbusinessTracheoesophageal Fistula
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Influence of foot pain on frailty symptoms in an elderly population: a case-control study.

2021

[Abstract] BACKGROUND: Frailty is a condition that can increase the risk of falls. In addition, foot disorders can negatively influence elderly people, thus affecting their condition of frailty. OBJECTIVE: To determine whether foot pain can influence a greater degree of frailty. DESIGN AND SETTING: Cross-sectional descriptive study conducted at the University of Valencia, Valencia, Spain. METHODS: A sample older than 60 years (n = 52), including 26 healthy subjects and 26 foot pain patients, was recruited. Frailty disability was measured using the 5-Frailty scale and the Edmonton Frailty scale (EFS). RESULTS: There were statistically significant differences in the total EFS score and in mos…

medicine.medical_specialtyFrail ElderlyFrailty syndromePainFoot deformitiesSurveys03 medical and health sciencesElderly0302 clinical medicineInfermeriaFoot diseasesFoot disordersElderly populationmedicineElderly peopleHumansSurveys and questionnaireFrail elderly030212 general & internal medicineDeformidades del pieAgedEnfermedades del pieFrailtyQuestionnairebusiness.industryRHealthy subjectsCase-control studyGeneral Medicinemedicine.diseaseFrail elderlyEncuestasCross-Sectional StudiesCase-Control StudiesPhysical therapyMann–Whitney U testMedicinebusinessVulnerabilidadAncianosPersonas mayores vulnerables030217 neurology & neurosurgeryFoot (unit)Sao Paulo medical journal = Revista paulista de medicina
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Alleles and haplotypes of the estrogen receptor alpha gene are associated with an increased risk of spontaneous abortion.

2010

Objective To investigate whether polymorphisms in estrogen receptor alpha (ERα) or beta (ERβ) genes are associated with a risk of miscarriage. Design A retrospectively analyzed, prospectively obtained database of cases and controls. Setting University hospital menopause unit. Patient(s) 177 women with at least one spontaneous abortion and 442 controls with at least one live birth and no history of miscarriage. Intervention(s) None. Main Outcome Measure(s) Genotype frequencies and odd ratios for abortion risk in cases and controls for four single nucleotide polymorphisms (SNPs) located in intron 1 (C>T and A>G), intron 4 (A>T), and exon 8 (T>C) for the ERα gene, and two SNPs located in intro…

medicine.medical_specialtyGenetic LinkageSingle-nucleotide polymorphismAbortionBiologyPolymorphism Single NucleotideGene FrequencyPolymorphism (computer science)PregnancyRisk FactorsInternal medicineGenotypemedicineEstrogen Receptor betaHumansGenetic Predisposition to DiseaseRisk factorAllelesRetrospective StudiesHaplotypeEstrogen Receptor alphaObstetrics and GynecologyMiddle AgedGenotype frequencyAbortion SpontaneousEndocrinologyReproductive MedicineHaplotypesCase-Control StudiesFemaleEstrogen receptor alphaFertility and sterility
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Association analysis between gene variants of the tyrosine hydroxylase and the serotonin transporter in borderline personality disorder.

2010

For patients with borderline personality disorder (BPD), we previously reported an independent effect of the catechol-o-methyl-transferase (COMT) low-activity (Met(158)) allele and an interaction with the low-expression allele of the deletion/insertion (short/long or S/L, resp.) polymorphism in the serotonin transporter-linked promoter region (5-HTTLPR). The purpose of the present study was to extend these findings to the tyrosine hydroxylase (TH) Val(81)Met single nucleotide polymorphism (SNP), the 5-HTTLPR S/L polymorphism incorporating the recently described functional A/G SNP within the long allele of the 5-HTTLPR (rs25531) as well as the variable number of tandem repeat (VNTR) polymorp…

medicine.medical_specialtyGenotypeTyrosine 3-MonooxygenaseGenome-wide association studySingle-nucleotide polymorphismCatechol O-MethyltransferasePolymorphism Single NucleotidePolymorphism (computer science)Borderline Personality DisorderInternal medicinemental disordersGenotypemedicineSNPHumansAlleleBiological PsychiatrySerotonin transporterAllelesGenetic associationGeneticsSerotonin Plasma Membrane Transport ProteinsbiologyGenetic VariationDiagnostic and Statistical Manual of Mental DisordersPsychiatry and Mental healthEndocrinologyCase-Control Studiesbiology.proteinPsychologyGenome-Wide Association StudyThe world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry
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Social functioning as a significant factor in women's help-seeking behaviour during the climacteric period.

1993

In order to identify the psychosocial factors that lead to the demand for medical care related to the menopause, we carried out a case/control study. A case was defined as a woman who sought gynaecological care due to "menopausal complaints" (n = 85) and a control referred to a woman drawn at random from the general population. The cases showed greater psychiatric morbidity and social dissatisfaction, a lower level of diffused social support and a higher frequency of severe life events and the controls showed greater social maladjustment in objective conditions. The multivariate analysis (logistic regression) carried out after adjusting all the relevant variables, indicated that the demand …

medicine.medical_specialtyHealth (social science)Multivariate analysisSocial PsychologyEpidemiologyPopulationLogistic regressionLife Change EventsSocial supportRisk FactorsEpidemiologymedicineHumansWomenPsychiatryeducationeducation.field_of_studySocializationSocial SupportMiddle AgedPatient Acceptance of Health Caremedicine.diseaseHelp-seekingMenopausePsychiatry and Mental healthMental HealthCase-Control StudiesWomen's HealthFemaleMenopausePsychologyPsychosocialSocial AdjustmentSocial psychiatry and psychiatric epidemiology
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Intra- and inter-foot coordination in quiet standing: footwear and posture effects.

2012

Intra-foot coordination between center of pressure (COP) of the ball and heel of the foot in single leg standing and inter-foot coordination of the right and left foot during bipedal stance was examined as a function of postural stance (two legs, one leg, and toe postures), footwear (barefoot, different area based high heel shoes) and postural training (ballet group and regular exercising group). Young adult females performed three 20s trials in each postural condition. In general, the traditional variability measures of COPnet motion increased under the less stable postural support conditions and ballet dancers had better balance in single leg standing. Regularity analysis revealed a negat…

medicine.medical_specialtyHeelBalletPostureBiophysicsBarefootYoung AdultCenter of pressure (terrestrial locomotion)Reference ValuesTask Performance and AnalysismedicineHumansOrthopedics and Sports MedicineDancingPostural BalanceAnalysis of VarianceFootRehabilitationHigh heelShoesbody regionsmedicine.anatomical_structureReference valuesCase-Control StudiesPhysical therapyFemaleHeelBallet dancerPsychologyPsychomotor PerformanceQuiet standingGaitposture
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Genetic variants in the MTHFR are not associated with fatty liver disease.

2020

The common missense sequence variants of methylenetetrahydrofolate reductase (MTHFR), rs1801131 (c.A1298C) and rs1801133 (c.C677T), favour the development of hyperhomocysteinemia and diminished DNA methylation. Previous studies, carried out in small series and with suboptimal characterization of the hepatic phenotype, tested the association of these genetic variants with fatty liver disease (FLD), with conflicting results. Here, we assessed the association of rs1801131 and rs1801133 with hepatic phenotype in the Liver Biopsy Cross-Sectional Cohort, a large cohort (n=1375 from Italy and 411 from Finland) of European individuals with suspect FLD associated with dysmetabolism. A total of 1786 …

medicine.medical_specialtyHyperhomocysteinemiaGenotypeGastroenterologyPolymorphism Single Nucleotide03 medical and health sciences0302 clinical medicineNAFLDInternal medicinesteatosisMedicineMissense mutationHumansGenetic Predisposition to DiseaseFinlandMethylenetetrahydrofolate Reductase (NADPH2)Hepatologymedicine.diagnostic_testbiologybusiness.industryFatty liverNASHmedicine.diseaseFatty LiverCross-Sectional StudiesItaly030220 oncology & carcinogenesisLiver biopsyMethylenetetrahydrofolate reductaseCase-Control StudiesMTHFRDNA methylationCohortbiology.proteinfatty liver disease030211 gastroenterology & hepatologySteatosisfibrosibusinessLiver international : official journal of the International Association for the Study of the LiverREFERENCES
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