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