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Myositis Autoantibodies in Patients with Suspected Post-Treatment Lyme Disease Syndrome

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F23%3A73621444" target="_blank" >RIV/61989592:15110/23:73621444 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00098892:_____/23:10157904

  • Výsledek na webu

    <a href="https://www.mdpi.com/2075-1729/13/2/527" target="_blank" >https://www.mdpi.com/2075-1729/13/2/527</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/life13020527" target="_blank" >10.3390/life13020527</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Myositis Autoantibodies in Patients with Suspected Post-Treatment Lyme Disease Syndrome

  • Popis výsledku v původním jazyce

    Most patients suffering from Lyme disease are effectively treated with antibiotics. Insome patients, however, problems persist for a long time despite appropriate therapy. The termpost-treatment Lyme disease syndrome (PTLDS) is currently used for this condition in scientificliterature. The pathogenesis is still not precisely known, but the involvement of immunopathologicalmechanisms is assumed. In our study, we analyzed the presence of autoantibodies including myositisspecific(MSA) and myositis-associated autoantibodies (MAA) in patients with laboratory provenhistory of Lyme disease and with clinical symptoms of PTLDS. A total of 59 patients meeting thecriteria for PTLDS were enrolled in this study. The control group consisted of 40 patients undergoingdifferential diagnosis of neurological disorders without clinical and/or laboratory-proven history ofLyme disease. The presence of autoantibodies was determined by immunoblot methods and positivesamples were further tested for serum creatine kinase (CK) and myoglobin levels. The presence ofmyositis autoantibodies was detected in 18 subjects with suspected PTLDS (30.5%), but only in 5%of control subjects exhibiting no evidence of Lyme disease history. The difference was statisticallysignificant (p = 0.002). The subsequent biochemical analysis of muscle-damage markers in positivesubjects found a mild elevation in six MSA/MAA-positive PTLDS patients. The study detected raisedMSA/MAA autoantibodies formation in the group of PTLDS patients raising the question abouttheir involvement in the pathogenesis of this syndrome.

  • Název v anglickém jazyce

    Myositis Autoantibodies in Patients with Suspected Post-Treatment Lyme Disease Syndrome

  • Popis výsledku anglicky

    Most patients suffering from Lyme disease are effectively treated with antibiotics. Insome patients, however, problems persist for a long time despite appropriate therapy. The termpost-treatment Lyme disease syndrome (PTLDS) is currently used for this condition in scientificliterature. The pathogenesis is still not precisely known, but the involvement of immunopathologicalmechanisms is assumed. In our study, we analyzed the presence of autoantibodies including myositisspecific(MSA) and myositis-associated autoantibodies (MAA) in patients with laboratory provenhistory of Lyme disease and with clinical symptoms of PTLDS. A total of 59 patients meeting thecriteria for PTLDS were enrolled in this study. The control group consisted of 40 patients undergoingdifferential diagnosis of neurological disorders without clinical and/or laboratory-proven history ofLyme disease. The presence of autoantibodies was determined by immunoblot methods and positivesamples were further tested for serum creatine kinase (CK) and myoglobin levels. The presence ofmyositis autoantibodies was detected in 18 subjects with suspected PTLDS (30.5%), but only in 5%of control subjects exhibiting no evidence of Lyme disease history. The difference was statisticallysignificant (p = 0.002). The subsequent biochemical analysis of muscle-damage markers in positivesubjects found a mild elevation in six MSA/MAA-positive PTLDS patients. The study detected raisedMSA/MAA autoantibodies formation in the group of PTLDS patients raising the question abouttheir involvement in the pathogenesis of this syndrome.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30102 - Immunology

Návaznosti výsledku

  • Projekt

    Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2023

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Life

  • ISSN

    2075-1729

  • e-ISSN

    2075-1729

  • Svazek periodika

    13

  • Číslo periodika v rámci svazku

    2

  • Stát vydavatele periodika

    CH - Švýcarská konfederace

  • Počet stran výsledku

    8

  • Strana od-do

    527

  • Kód UT WoS článku

    000940123400001

  • EID výsledku v databázi Scopus

    2-s2.0-85148956065