Search results for "Muscle Weakness"

showing 10 items of 68 documents

Ultrastructural pathology in emetine-induced myopathy

1988

Progressive myopathy developed in two women who consumed ipecac syrup containing emetine hydrochloride to induce vomiting as part of their anorexia nervosa. Muscle biopsy specimens were characterized by severe disruption of the sarcomeres. The ultrastructural spectrum extended from "Z-band streaming" to the formation of cytoplasmic bodies and also comprised abnormalities of the sarcotubular system, thus suggesting that muscle weakness may be related to both sarcomeric and sarcotubular lesions in this self-inflicted myopathy. It is tempting to suggest that muscle weakness may be correlated with or based on the pathology in sarcomeres and the sarcotubular system. As the myopathy is clinically…

AdultSarcomeresPathologymedicine.medical_specialtyAnorexia NervosaSubstance-Related DisordersEmetineEmetine HydrochlorideEmetineBiologySarcomereUltrastructural PathologyPathology and Forensic MedicineCellular and Molecular NeuroscienceMuscular DiseasesmedicineHumansMyopathyMuscle biopsymedicine.diagnostic_testMusclesMuscle weaknessMitochondriaSarcoplasmic ReticulumAnorexia nervosa (differential diagnoses)FemaleNeurology (clinical)medicine.symptommedicine.drugActa Neuropathologica
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Power training and postmenopausal hormone therapy affect transcriptional control of specific co-regulated gene clusters in skeletal muscle

2010

At the moment, there is no clear molecular explanation for the steeper decline in muscle performance after menopause or the mechanisms of counteractive treatments. The goal of this genome-wide study was to identify the genes and gene clusters through which power training (PT) comprising jumping activities or estrogen containing hormone replacement therapy (HRT) may affect skeletal muscle properties after menopause. We used musculus vastus lateralis samples from early stage postmenopausal (50–57 years old) women participating in a yearlong randomized double-blind placebo-controlled trial with PT and HRT interventions. Using microarray platform with over 24,000 probes, we identified 665 diffe…

AgingCandidate geneTranscription GeneticvaihdevuodetmenopaussiBioinformaticsEstrogen deprivation0302 clinical medicineGene expressionestrogenTranscriptional regulation0303 health sciencesEstrogen Replacement TherapyGeneral MedicineMiddle AgedestrogeeniPostmenopausemedicine.anatomical_structureFemalevoimaharjoitteluMenopausemedicine.symptomTranscriptome-wide studymedicine.medical_specialtyPlyometric trainingmedicine.drug_classBiologyArticletranskriptomin laajuuinen tutkimus03 medical and health sciencesplyometrinen harjoitteluInternal medicinemedicineHumansSkeletal muscle characteristicsKEGGMuscle SkeletalExerciseGene030304 developmental biologyhormonikorvaushoitoSkeletal muscleMuscle weaknessdeprivaatioPower trainingAgeingEndocrinologyluurankolihaksetHormone replacement therapyEstrogenGeriatrics and Gerontology030217 neurology & neurosurgeryAGE
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The involvement of ankle muscles in maintaining balance in the upright posture is higher in elderly fallers

2016

International audience; The purpose of this study was to determine whether the mechanical contribution of ankle muscles in the upright stance differed among young adults (YA) (n = 10, age: similar to 24.3), elderly non-fallers (ENF) (n = 12, age: similar to 77.3) and elderly fallers (EF) (n = 20, age: similar to 80.7). Torque and electromyographic (EMG) activity were recorded on the triceps surae and tibialis anterior during maximum and submaximum contractions in the seated position. EMG activity was also recorded in subjects standing still. Plantar flexor (PF) and dorsal flexor (DF) torques generated in the upright posture were estimated from the torque-EMG relationship obtained during sub…

AgingPoison controltorqueBiochemistryPlantar flexionAnkle muscles0302 clinical medicineEndocrinologyCenter of pressure (terrestrial locomotion)jointFallMedicineolder-adultsPostural BalanceriskAged 80 and overMuscle Weaknessswaymedicine.anatomical_structurePostural stabilitymedicine.symptomDorsumBalancemedicine.medical_specialtyIsometric torque[ SDV.MHEP.GEG ] Life Sciences [q-bio]/Human health and pathology/Geriatry and gerontologyYoung Adult03 medical and health sciencesPhysical medicine and rehabilitationGeneticsHumansskeletal-muscleMuscle SkeletalMolecular BiologyAgedsoleusElectromyographybusiness.industryyoungMuscle weakness030229 sport sciencesCell BiologyIsometric torquebody regionsagePhysical therapyAccidental FallsfatigueAnklebusinessAnkle Joint030217 neurology & neurosurgery
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The value of neutrophil and lymphocyte count in frail older women.

2013

Increasing evidence suggests that systemic inflammation is associated with many pathophysiological processes including frailty in older adults. We evaluated the relationships between white blood cell subtypes, geriatric assessment, and frailty syndrome and in particular, how they correlate with individual frailty criteria (involuntary loss of weight, low energy or exhaustion, slow mobility, muscle weakness, and low physical activity) in frail older women. There was a significant and positive correlation between the frailty score and neutrophil count, but a significantly negative correlation was found when this score was compared to the lymphocyte count. These associations were significant o…

Agingmedicine.medical_specialtyNeutrophilsLymphocyteFrail ElderlyFrailty syndromePilot ProjectsSystemic inflammationPhysical strengthBiochemistryLeukocyte CountEndocrinologyWeight lossWhite blood cellInternal medicineWeight LossGeneticsmedicineHumansLymphocyte CountLymphocytesMuscle StrengthMolecular BiologyExerciseGeriatric AssessmentAged 80 and overHand Strengthbusiness.industryMuscle weaknessCell Biologymedicine.diseasemedicine.anatomical_structureCross-Sectional StudiesImmune System DiseasesPhysical FitnessPhysical therapyAbsolute neutrophil countFemalemedicine.symptombusinessExperimental gerontology
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Intermediate Filament Diseases: Desminopathy

2008

Desminopathy is one of the most common intermediate filament human disorders associated with mutations in closely interacting proteins, desmin and alphaB-crystallin. The inheritance pattern in familial desminopathy is characterized as autosomal dominant or autosomal recessive, but many cases have no family history. At least some and likely most sporadic desminopathy cases are associated with de novo DES mutations. The age of disease onset and rate of progression may vary depending on the type of inheritance and location of the causative mutation. Typically, the illness presents with lower and later upper limb muscle weakness slowly spreading to involve truncal, neck-flexor, facial and bulba…

GeneticsPathologymedicine.medical_specialtyPoint mutationMutantCardiomyopathyIntermediate Filamentsalpha-Crystallin B ChainGene mutationBiologymedicine.diseaseSudden deathPolymorphism Single NucleotideArticleUpper limb muscle weaknessDesminMuscular DiseasesmedicineDisease ProgressionAnimalsHumansDesminIntermediate filament
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Clinical features of prefrail older individuals and emerging peripheral biomarkers: A systematic review

2013

Frailty is a geriatric syndrome characterized by the clinical presentation of identifiable physical alterations such as loss of muscle mass and strength, energy and exercise tolerance, and decreased physiological reserve. Individuals with one or two of these alterations are defined as prefrail. The clinical features of prefrail older individuals have been investigated to a lesser extent compared to the frail population, even though this intermediate stage may provide insights into the mechanisms involved in the physical decline associated with aging and it is considered to be potentially reversible. We performed searches in the Medline, Embase, Scopus, Cinahl, and Cochrane databases from Ja…

GerontologyAgingWeaknessHealth (social science)Frail ElderlyPopulationScopusMEDLINEComorbidityCINAHLMuscle massSex FactorsRisk FactorsPrevalenceHumansMedicineeducationGeriatric AssessmentAgedAged 80 and overeducation.field_of_studyMuscle Weaknessbusiness.industryMuscle weaknessmedicine.diseaseComorbidityAccidental FallsGeriatrics and Gerontologymedicine.symptombusinessGerontologyBiomarkersArchives of Gerontology and Geriatrics
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Handgrip strength and depression among 34,129 adults aged 50 years and older in six low- and middle-income countries

2019

Introduction: Handgrip strength is a simple and inexpensive marker of health and mortality risk. It presents an ideal risk-stratifying method for use in low and middle-income countries (LMICs). There are, however, no population-based studies investigating the associations between handgrip strength and depression in LMICs. We aimed to assess these associations among community-dwelling middle-aged and older adults using nationally representative data from six LMICs. Method: Cross-sectional data on individuals aged ≥ 50 years from the World Health Organization's Study on Global Ageing and Adult Health were analyzed. Depression was based on the Composite International Diagnostic Interview. Weak…

GerontologyMalePsychological interventionPhysical strengthGhanaRussiaSouth Africa0302 clinical medicine*Hand grip strengthPrevalenceMedicineDepression (differential diagnoses)*Older adultseducation.field_of_studyMuscle WeaknessHand StrengthDepressionAge FactorsMiddle AgedPredictive valuePsychiatry and Mental healthClinical PsychologyHealthOlder adultsIncomeFemaleMental health*Mental healthAdultChinaAdolescentPopulationIndia*HealthHandgrip strengthOdds03 medical and health sciencesmarker of health and mortality riskYoung AdultSex FactorsHand grip strengthHumanseducationMexicoPovertyAgedbusiness.industry*DepressionMental health030227 psychiatryCross-Sectional StudiesLow and middle income countriesbusinesshuman activities030217 neurology & neurosurgery
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Speech treatment in nemaline myopathy: A single-subject experimental study

2020

Abstract Purpose The objective of this work was to verify the efficacy of a treatment based on myofunctional therapy techniques which aimed to improve the tongue strength, precision, and speed of a ten-year-old girl with nemaline myopathy (NM) and the repercussions of this therapy on her speech intelligibility. NM is a rare congenital muscle disorder that causes extreme muscle weakness, especially in the face and neck, as well as severe dysarthria and dysphagia, although this does not affect the nervous system or cognitive development. Method This was a single-subject experimental study which used an interrupted pre- and post-treatment time-series design, and which applied autoregressive in…

Linguistics and Languagemedicine.medical_specialtyCognitive NeuroscienceExperimental and Cognitive PsychologySpeech TherapyIntelligibility (communication)Muscle disorderAudiologyMyopathies NemalineSpeech and HearingDysarthriaNemaline myopathySpeech Production MeasurementTongueTonguemedicineHumansChildDysarthriaSpeech IntelligibilityDiadochokinesiaMuscle weaknessLPN and LVNmedicine.diseasemedicine.anatomical_structureCongenital muscle disorderFemalemedicine.symptomPsychologyJournal of Communication Disorders
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The healthy Nordic diet predicts muscle strength 10 years later in old women, but not old men

2017

Background a number of nutrients have been found to be associated with better muscle strength and mass; however, the role of the whole diet on muscle strength and mass remains still unknown. Objective to examine whether the healthy Nordic diet predicts muscle strength, and mass 10 years later among men and women. Methods about 1,072 participants belong to the Helsinki Birth Cohort Study, born 1934–44. Diet was assessed with a validated food-frequency questionnaire during 2001–04. The Nordic diet score (NDS) was calculated. The score included Nordic fruits, vegetables, cereals, ratio of polyunsaturated to saturated fatty acids, low-fat milk, fish, red meat, total fat and alcohol. Higher scor…

Male0301 basic medicineAgingTime FactorsMediterranean dietolder peopleGrip strength0302 clinical medicineSurveys and QuestionnairesElectric Impedance030212 general & internal medicine2. Zero hungerMuscle WeaknessHand StrengthAge Factorsta3141General Medicineta3142Middle Agedmedicine.anatomical_structureQuartilemuscle massBody CompositionRed meatpopulation characteristicsFemaleDiet Healthymedicine.symptommedicine.medical_specialtyNutritional Status03 medical and health sciencesSex FactorsInternal medicineHand strengthmedicineHumansMuscle Skeletal030109 nutrition & dieteticsbusiness.industryNordic dietMuscle weaknessSkeletal muscleFeeding BehaviorConfidence intervallihasmassaPhysical therapymuscle strengthGeriatrics and Gerontologybusinesslihasvoima
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Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

2020

Mice lacking GAD1 show neonatal mortality, but the human phenotype associated with GAD1 disruption is poorly characterized. Neuray et al. describe six patients with biallelic GAD1 mutations, presenting with early-infantile onset epilepsy, neurodevelopmental delay, muscle weakness and non-CNS manifestations.

Male0301 basic medicineGlutamate decarboxylaseMalalties cerebralsNeurotransmissorsNeurodevelopmental delayEpilepsy0302 clinical medicineMESH: ChildAge of OnsetChildcleft palateGAD1AcademicSubjects/SCI01870Glutamate DecarboxylaseGlutamate receptorMuscle weakness//purl.org/becyt/ford/3.1 [https]NeurotransmittersMESH: InfantHypotoniamuscle weakneCleft palateMESH: EpilepsyChild PreschoolMuscle Hypotonia[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]//purl.org/becyt/ford/3 [https]FemaleBrain diseasesAbnormalitiesmedicine.symptomMultiplemedicine.drugcleft palate; epilepsy; GAD1; muscle weakness; neurodevelopmental delayMESH: Glutamate Decarboxylasemedicine.medical_specialtyMESH: Abnormalities MultipleMESH: MutationMESH: Age of OnsetBiologyInhibitory postsynaptic potentialGAD1 cleft palate epilepsy muscle weakness neurodevelopmental delay.gamma-Aminobutyric acidGAD1neurodevelopmental delay03 medical and health sciencesExcitatory synapseInternal medicinemedicineHumansAbnormalities MultiplePreschoolAllelesMESH: Neurodevelopmental Disordersmuscle weaknessMESH: HumansEpilepsyMESH: Muscle HypotoniaMESH: AllelesMESH: Child PreschoolInfantmedicine.diseaseMESH: MaleEpilèpsiaEditor's Choice030104 developmental biologyEndocrinologyNeurodevelopmental DisordersMutationepilepsyAcademicSubjects/MED00310Neurology (clinical)Cleft palate; Epilepsy; GAD1; Muscle weakness; Neurodevelopmental delay; Abnormalities Multiple; Age of Onset; Alleles; Child; Child Preschool; Epilepsy; Female; Glutamate Decarboxylase; Humans; Infant; Male; Muscle Hypotonia; Mutation; Neurodevelopmental DisordersMESH: Female[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology030217 neurology & neurosurgeryReports
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