Search results for "FREQUENCY"

showing 10 items of 2158 documents

SELPLG Gene Polymorphisms in Relation to Plasma SELPLG Levels and Coronary Artery Disease

2003

P-selectin and P-selectin glycoprotein ligand (SELPLG, selectin P ligand) constitute a receptor/ligand complex that is likely to be involved in the development of atherosclerosis and its complications. While the genetic variability of P-selectin has already been investigated in depth, that of the SELPLG gene has not yet been extensively explored. The coding and regulatory sequences of the SELPLG were screened and nine polymorphisms were identified. The identified polymorphisms were genotyped in the AtheroGene study, a case-control study of coronary artery disease (CAD). Haplotype analysis revealed that two polymorphisms of SELPLG, the M62I and the VNTR, independently influenced plasma SELPL…

AdultMalemedicine.medical_specialtyP-selectinEnzyme-Linked Immunosorbent AssayCoronary Artery DiseaseBiologyLigandsPolymerase Chain ReactionCoronary artery diseaseGene FrequencySELPLG GeneInternal medicineGeneticsmedicineHumansGenetic variabilityReceptorGenePolymorphism Single-Stranded ConformationalTriglyceridesGenetics (clinical)GeneticsMembrane GlycoproteinsPolymorphism GeneticHaplotypemedicine.diseaseP-SelectinCholesterolEndocrinologyHaplotypesRegulatory sequenceFemaleAnnals of Human Genetics
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Incidence of Crohn's disease and CARD15 mutation in a small township in Sicily.

2006

Background: The incidence of Crohn's disease (CD) has been shown to be lower in Southern than in Northern Europe. Data on the frequency of the NOD2/CARD15 mutations for Mediterranean area are very scant. Aim: To determine the incidence of CD from 1979 to 2002 in a township in Sicily together with the allele frequency of NOD2/CARD15 mutations in patients, family members and controls, and to determine the allele frequency of these mutations in sporadic CD from other areas of Sicily in comparison with a control population. Methods: Casteltermini is a small town close to Agrigento (Sicily) with a population of 9,130 inhabitants. All the diagnoses of inflammatory bowel disease (IBD) made from 19…

AdultMalemedicine.medical_specialtyPathologyAdolescentEpidemiologyPopulationNod2 Signaling Adaptor ProteinInflammatory bowel diseaseGastroenterologyCrohn DiseaseGene FrequencyInternal medicineEpidemiologyPrevalencemedicineHumansGenetic Predisposition to DiseaseRisk factoreducationAllele frequencySicilyNOD2/CARD15Crohn's diseaseeducation.field_of_studybusiness.industryIncidence (epidemiology)IncidenceMiddle Agedmedicine.diseaseUlcerative colitisdigestive system diseasesCrohn's diseaseMutationColitis UlcerativeFemalebusinessEuropean journal of epidemiology
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Frequency of NOD2/CARD15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian Group for Inflammatory Bowel Diseas…

2004

Abstract Background. Three variants of the NOD 2 /CARD 15 gene are strongly associated with susceptibility to Crohn’s disease; however, striking racial and geographic differences of their frequency have been described. Aims. We have compared the allele frequencies of familial cases of Crohn’s disease recruited in a multicentre study across Italy, in order to disclose possible geographic heterogeneity. Moreover, we also compared the allele frequencies in sporadic cases of Crohn’s disease and healthy controls from Southern Italy with those reported in other two populations from Central and Northern Italy. Subjects and Methods. A total of 731 subjects were genotyped for the polymorphism of thr…

AdultMalemedicine.medical_specialtyPathologyGenotypeNod2 Signaling Adaptor ProteinDiseaseInflammatory bowel diseaseGastroenterologyInflammatory bowel diseaseNOD2Frameshift mutationGeneticCrohn DiseaseGene FrequencyPolymorphism (computer science)NOD2Internal medicineMedicineHumansGenetic Predisposition to DiseaseCARD15Frameshift MutationAllele frequencyAgedCrohn's diseasePolymorphism GeneticHepatologybusiness.industrySignificant differenceGastroenterologyIntracellular Signaling Peptides and ProteinsMiddle Agedmedicine.diseaseCrohn's diseaseItalyFemalebusinessCarrier Proteins
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Association of -1082 interleukin-10 gene polymorphism in Peruvian adults with chronic periodontitis

2014

Objectives: The aim of this study was to assess association of the -1082 IL-10 gene polymorphism with chronic periodontitis CP in a Peruvian population. Study Design: Samples of venous blood and DNA were obtained from 106 Peruvian subjects: a) 53 periodontally healthy; and b) 53 with CP. The association of the -1082 IL-10 promoter sequences was assessed by Polymerase chain reaction-restriction fragment length polymorfism (PCR-RFLP). Student’s t test were used to assess the clinical parameters, as well as the χ2 test and the odds ratio (OR), with 95% confidence intervals (CI) used performed for estimates regarding genotype and allele frequencies. Results: There were statistically significant…

AdultMalemedicine.medical_specialtyPathologyPopulationOdontologíaGastroenterologyYoung AdultInternal medicineGenotypePerumedicineHumansAlleleeducationGeneral DentistryAllele frequencyAgededucation.field_of_studyOral Medicine and PathologyPolymorphism Geneticbusiness.industryResearchOdds ratioMiddle Aged:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludChronic periodontitisConfidence intervalInterleukin-10Cross-Sectional StudiesOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASChronic PeriodontitisSurgeryFemaleGene polymorphismbusinessMedicina Oral, Patología Oral y Cirugía Bucal
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Neuromuscular fatigue during dynamic maximal strength and hypertrophic resistance loadings

2011

The purpose of this study was to compare the acute neuromuscular fatigue during dynamic maximal strength and hypertrophic loadings, known to cause different adaptations underlying strength gain during training. Thirteen healthy, untrained males performed two leg press loadings, one week apart, consisting of 15 sets of 1 repetition maximum (MAX) and 5 sets of 10 repetition maximums (HYP). Concentric load and muscle activity, electromyography (EMG) amplitude and median frequency, was assessed throughout each set. Additionally, maximal bilateral isometric force and muscle activity was assessed pre-, mid-, and up to 30 min post-loading. Concentric load during MAX was decreased after set 10 (P<0…

AdultMalemedicine.medical_specialtyPhysical ExertionNeural ConductionNeuromuscular JunctionBiophysicsNeuroscience (miscellaneous)Isometric exerciseElectromyographyConcentricWeight-BearingMedian frequencyIsometric ContractionInternal medicineMaximal strengthmedicineHumansta315Muscle SkeletalLeg pressSimulationMathematicsmedicine.diagnostic_testResistance TrainingEMG amplitudeNeuromuscular fatigueMuscle FatiguePhysical EnduranceCardiologyNeurology (clinical)Journal of Electromyography and Kinesiology
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Influence of lactate accumulation of EMG frequency spectrum during repeated concentric contractions

1983

One hundred and twenty consecutive maximal leg extensions at a constant angular velocity of 1.5 radians . s-1 were performed by nine physical education students. Integrated electromyographic (IEMG) activity and power spectrum density function (PSDF) of the EMG were recorded from m. vastus lateralis, vastus medialis and m. rectus femoris using bipolar surface electrodes. Muscle biopsies were obtained from m. vastus lateralis before and after exercise. Tissue samples were analyzed for muscle fiber type distribution and lactate and glycogen concentration. Muscle force and IEMG decreased in parallel over the exercise period. Thus, the IEMG/force ratio was unchanged. Mean power frequency (MPF) o…

AdultMalemedicine.medical_specialtyPhysiologyVastus medialisAction PotentialsElectromyographyIsometric exerciseConcentricchemistry.chemical_compoundIsometric ContractionInternal medicinemedicineHumansmedicine.diagnostic_testGlycogenElectromyographyMusclesMotor neuronMean frequencyEndocrinologymedicine.anatomical_structurechemistryLactatesmedicine.symptomEnergy MetabolismGlycogenMuscle ContractionMuscle contractionActa Physiologica Scandinavica
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Torque decrease during submaximal evoked contractions of the quadriceps muscle is linked not only to muscle fatigue.

2015

International audience; The aim of this study was to analyze the neuromuscular mechanisms involved in the torque decrease induced by submaximal electromyostimulation (EMS) of the quadriceps muscle. It was hypothesized that torque decrease after EMS would reflect the fatigability of the activated motor units (MUs), but also a reduction in the number of MUs recruited as a result of changes in axonal excitability threshold. Two experiments were performed on 20 men to analyze 1) the supramaximal twitch superimposed and evoked at rest during EMS (Experiment 1, n = 9) and 2) the twitch response and torque-frequency relation of the MUs activated by EMS (Experiment 2, n = 11). Torque loss was asses…

AdultMalemedicine.medical_specialtyPhysiology[ SDV.MHEP.AHA ] Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO]recruitment ordermotor unit activationhuman skeletal-muscleperipheral fatigueIsometric exercisenerveisometric contractionQuadriceps MusclePhysiology (medical)Internal medicinemedicineTorqueHumansvoluntaryelectrical stimulationMotor NeuronsMuscle fatiguebusiness.industryElectromyographyQuadriceps muscletorque-frequency relationfemorisAnatomyneuromuscular electrical-stimulationtwitch interpolationElectric StimulationTorquefrequency[ SDV.NEU ] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]Muscle FatigueCardiologyfemoral nerve stimulationbusinessFemoral NerveMuscle ContractionJournal of applied physiology (Bethesda, Md. : 1985)
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Association between +1059G/C CRP polymorphism and acute myocardial infarction in a cohort of patients from Sicily: a pilot study.

2006

Inflammation plays a role in all the phases of atherosclerosis, and increased production of the acute-phase reactant, C-reactive protein (CRP), predicts future cardiovascular events. Furthermore, CRP has been claimed to play a role in the pathogenesis of atherosclerosis; therefore, CRP polymorphisms might be associated with acute myocardial infarction (AMI). We have analyzed male patients affected by AMI and healthy age-related male controls from Sicily for +1059G/C CRP single-nucleotide polymorphism (SNP). There was a significantly higher frequency of +1059C SNP (P = 0.0008; OR 3.86) in patients compared to controls. CRP serum levels were significantly higher in C+ healthy subjects rather …

AdultMalemedicine.medical_specialtyPopulationMyocardial InfarctionPilot ProjectsGastroenterologyPolymorphism Single NucleotideGeneral Biochemistry Genetics and Molecular BiologyPathogenesisCohort StudiesHistory and Philosophy of ScienceGene FrequencyInternal medicinemedicineImmunogeneticsOdds RatioSNPHumansMyocardial infarctioneducationSicilyInflammationeducation.field_of_studyPolymorphism Geneticbusiness.industryGeneral NeuroscienceCase-control studyOdds ratioMiddle Agedmedicine.diseaseSurgeryC-Reactive ProteinCase-Control StudiesCohortAcute DiseasebusinessCohort studyAnnals of the New York Academy of Sciences
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A possible association between the CCK-AR gene and persistent auditory hallucinations in schizophrenia.

2004

AbstractRecent studies have suggested that DNA variations in the CCK-AR gene might predispose individuals to schizophrenia and particularly to auditory hallucinations (AH). The aim of this study is to assess the association between AH, using a specific scale for AH in schizophrenia (PSYRATS), and the CCK-AR polymorphism at 779 in a Spanish sample. A total of 105 DSM-IV schizophrenic patients with AH and 93 unrelated controls were studied. Twenty-two patients were considered as persistent auditory hallucinators, which showed similar clinical and demographic characteristic than patients with episodic AH, but with the exception of the PSYRATS values. The persistent AH group showed an excess of…

AdultMalemedicine.medical_specialtyPsychosisPeriodicityGenotypeHallucinationsSeverity of Illness IndexGenetic determinismLinkage Disequilibrium03 medical and health sciences0302 clinical medicineGene FrequencyInternal medicineSurveys and QuestionnairesSeverity of illnessmedicineHumansAlleleSex DistributionPsychiatryAllele frequencyGenetic associationDNA PrimersDemographyAuditory hallucinationPolymorphism Geneticmedicine.diseaseIntrons030227 psychiatryReceptor Cholecystokinin ADiagnostic and Statistical Manual of Mental DisordersPsychiatry and Mental healthEndocrinologySchizophreniaSchizophreniaFemalemedicine.symptomPsychology030217 neurology & neurosurgeryEuropean psychiatry : the journal of the Association of European Psychiatrists
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Vitamin D receptor gene polymorphisms and plasma renin activity in essential hypertensive individuals.

2014

Several studies analyzed 25-hydroxyvitamin D (25[OH]D) and blood pressure (BP) relationship with mixed results. Moreover, a relationship between the risk of hypertension and vitamin D receptor (VDR) gene polymorphisms, FokI and BsmI, was reported. This study was aimed to analyze these relationships in essential hypertensive (EH) patients. Seventy-one EH patients, 18-75 years old, were enrolled. Patients underwent clinical BP, 24-h ambulatory BP monitoring, 25[OH]D and plasma renin activity (PRA) evaluations. FokI and BsmI VDR polymorphisms were analyzed and compared with those of 72 healthy controls. In EH patients, the median 25[OH]D levels were lower than 30 ng ml(-1). We found a signific…

AdultMalemedicine.medical_specialtySettore MED/09 - Medicina InternaAmbulatory blood pressureAdolescentGenotypeRenal functionBlood PressureCalcitriol receptorPlasma renin activityBody Mass IndexPlasma renin activityGene FrequencyPolymorphism (computer science)Internal medicineReninInternal MedicineMedicineHumansVitamin DAgedSettore MED/14 - NefrologiaPolymorphism Geneticbiologybusiness.industryGene polymorphismMiddle AgedFokIBlood pressureEndocrinologyHypertensionMultivariate Analysisbiology.proteinReceptors CalcitriolFemaleEssential hypertenionbusinessBody mass indexJournal of human hypertension
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