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The dysregulation of monocyte subpopulations in individuals at risk of developing rheumatoid arthritis

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11510%2F21%3A10428540" target="_blank" >RIV/00216208:11510/21:10428540 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00023728:_____/21:N0000074 RIV/00216208:11110/21:10428540

  • Výsledek na webu

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=GhIwFWUekE" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=GhIwFWUekE</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/rheumatology/keaa518" target="_blank" >10.1093/rheumatology/keaa518</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    The dysregulation of monocyte subpopulations in individuals at risk of developing rheumatoid arthritis

  • Popis výsledku v původním jazyce

    Objectives. Individuals carrying antibodies against citrullinated proteins (ACPA) are at high risk of developing RA. EULAR provided a clinical definition of individuals with arthralgia suspicious for progression to RA (clinically suspect arthralgia, CSA). The alteration of monocyte subpopulations in patients with established RA has been previously described. We analysed peripheral blood monocyte subpopulations in individuals with arthralgia at risk of RA. Methods. We included 70 at-risk individuals, defined as having arthralgia without arthritis and being either ACPA(+) or meeting the clinical CSA definition, 23 patients with early RA (ERA) and 19 healthy controls (HCs). Monocytes classified as classical (CD14(++)CD16(-)), intermediate (CD14(++)CD16(+/++)) and nonclassical (CD14(-/+)CD16(++)) were analysed by flow cytometry. Results. Of the 70 at-risk individuals, 46 were ACPA(+) and 45 met the CSA definition. The at-risk individuals and, especially, ERA patients had a lower percentage of classical monocytes and a higher percentage of nonclassical monocytes than the HCs. ACPA positivity had no effect on the difference in the distribution of the monocyte subsets between at-risk individuals and ERA patients, but a difference was determined in those reaching the ERA phase. However, when compared with HCs, the shift of monocyte subsets was more significant in ACPA(+) than in ACPA(-) individuals with arthralgia. This trend was observed in individuals who did not meet the CSA definition. This finding was, however, determined by a selection bias, as these individuals were solely ACPA(+). Conclusion. The shift from classical to nonclassical monocyte subpopulations was observed already in individuals at risk of developing RA.

  • Název v anglickém jazyce

    The dysregulation of monocyte subpopulations in individuals at risk of developing rheumatoid arthritis

  • Popis výsledku anglicky

    Objectives. Individuals carrying antibodies against citrullinated proteins (ACPA) are at high risk of developing RA. EULAR provided a clinical definition of individuals with arthralgia suspicious for progression to RA (clinically suspect arthralgia, CSA). The alteration of monocyte subpopulations in patients with established RA has been previously described. We analysed peripheral blood monocyte subpopulations in individuals with arthralgia at risk of RA. Methods. We included 70 at-risk individuals, defined as having arthralgia without arthritis and being either ACPA(+) or meeting the clinical CSA definition, 23 patients with early RA (ERA) and 19 healthy controls (HCs). Monocytes classified as classical (CD14(++)CD16(-)), intermediate (CD14(++)CD16(+/++)) and nonclassical (CD14(-/+)CD16(++)) were analysed by flow cytometry. Results. Of the 70 at-risk individuals, 46 were ACPA(+) and 45 met the CSA definition. The at-risk individuals and, especially, ERA patients had a lower percentage of classical monocytes and a higher percentage of nonclassical monocytes than the HCs. ACPA positivity had no effect on the difference in the distribution of the monocyte subsets between at-risk individuals and ERA patients, but a difference was determined in those reaching the ERA phase. However, when compared with HCs, the shift of monocyte subsets was more significant in ACPA(+) than in ACPA(-) individuals with arthralgia. This trend was observed in individuals who did not meet the CSA definition. This finding was, however, determined by a selection bias, as these individuals were solely ACPA(+). Conclusion. The shift from classical to nonclassical monocyte subpopulations was observed already in individuals at risk of developing RA.

Klasifikace

  • Druh

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

  • CEP obor

  • OECD FORD obor

    30226 - Rheumatology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/NV17-32612A" target="_blank" >NV17-32612A: Klinicky suspektní artralgie: charakteristika preklinické fáze revmatoidní artritidy</a><br>

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2021

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    Rheumatology

  • ISSN

    1462-0324

  • e-ISSN

  • Svazek periodika

    60

  • Číslo periodika v rámci svazku

    4

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    9

  • Strana od-do

    1823-1831

  • Kód UT WoS článku

    000644544400044

  • EID výsledku v databázi Scopus

    2-s2.0-85104048166