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1.
Ned Tijdschr Geneeskd ; 1662022 05 03.
Artigo em Holandês | MEDLINE | ID: mdl-35899711

RESUMO

A 56-year old female runner is not able to run without tripping over anymore. Only whilst running her right foot repeatedly and involuntary makes an outward twist, which impedes her from continuing. She was diagnosed with Runner's Dystonia based on her presentation and virtually normal physical neurologic examination at rest.


Assuntos
Distúrbios Distônicos , Corrida , Distúrbios Distônicos/diagnóstico , Feminino , , Humanos , Pessoa de Meia-Idade , Exame Físico
2.
J Am Heart Assoc ; 10(17): e021580, 2021 09 07.
Artigo em Inglês | MEDLINE | ID: mdl-34472371

RESUMO

Background Physical exercise is an intervention that might protect against doxorubicin-induced cardiotoxicity. In this meta-analysis and systematic review, we aimed to estimate the effect of exercise on doxorubicin-induced cardiotoxicity and to evaluate mechanisms underlying exercise-mediated cardioprotection using (pre)clinical evidence. Methods and Results We conducted a systematic search in PubMed, Embase, and Cochrane Central Register of Controlled Trials (CENTRAL) databases. Cochrane's and Systematic Review Centre for Laboratory Animal Experimentation (SYRCLE) risk-of-bias tools were used to assess the validity of human and animal studies, respectively. Cardiotoxicity outcomes reported by ≥3 studies were pooled and structured around the type of exercise intervention. Forty articles were included, of which 3 were clinical studies. Overall, in humans (sample sizes ranging from 24 to 61), results were indicative of exercise-mediated cardioprotection, yet they were not sufficient to establish whether physical exercise protects against doxorubicin-induced cardiotoxicity. In animal studies (n=37), a pooled analysis demonstrated that forced exercise interventions significantly mitigated in vivo and ex vivo doxorubicin-induced cardiotoxicity compared with nonexercised controls. Similar yet slightly smaller effects were found for voluntary exercise interventions. We identified oxidative stress and related pathways, and less doxorubicin accumulation as mechanisms underlying exercise-induced cardioprotection, of which the latter could act as an overarching mechanism. Conclusions Animal studies indicate that various exercise interventions can protect against doxorubicin-induced cardiotoxicity in rodents. Less doxorubicin accumulation in cardiac tissue could be a key underlying mechanism. Given the preclinical evidence and limited availability of clinical data, larger and methodologically rigorous clinical studies are needed to clarify the role of physical exercise in preventing cardiotoxicity in patients with cancer. Registration URL: https://www.crd.york.ac.uk/prospero; Unique identifier: CRD42019118218.


Assuntos
Antibióticos Antineoplásicos , Cardiotoxicidade , Doxorrubicina , Exercício Físico , Animais , Antibióticos Antineoplásicos/efeitos adversos , Cardiotoxicidade/prevenção & controle , Doxorrubicina/efeitos adversos , Humanos
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