Long Term Impact of Adalimumab Therapy on Biomarkers of Systemic Inflammation in Psoriasis: Results of a 2 year study
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F20%3A43920316" target="_blank" >RIV/00216208:11120/20:43920316 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00064173:_____/20:N0000028
Výsledek na webu
<a href="https://doi.org/10.1111/dth.14110" target="_blank" >https://doi.org/10.1111/dth.14110</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/dth.14110" target="_blank" >10.1111/dth.14110</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Long Term Impact of Adalimumab Therapy on Biomarkers of Systemic Inflammation in Psoriasis: Results of a 2 year study
Popis výsledku v původním jazyce
Psoriasis patients are at increased risk of atherosclerosis, characterized by endothelial dysfunction, linked through systemic inflammation. Anti-TNF-a therapy seems to decrease this risk. The purpose of this study was to measure the levels of serum markers associated with systemic inflammation in psoriasis patients, compared to healthy individuals and to investigate the change in their levels after 3 months and 2 years of adalimumab therapy. We investigated 4 biomarkers: high-sensitivity C-reactive protein (hsCRP), oxidized low-density lipoproteins (OxLDL), E-selectin and Interleukin 22 (IL-22). These markers were measured in healthy volunteers and in 28 patients with moderate/severe psoriasis before and after 3 and 24 months of treatment with adalimumab. Psoriasis patients had increased levels of markers in comparison to the control group. After 3 months of therapy, E-selectin decreased significantly (P < 0.001), as well as IL-22 (P < 0.001). hsCRP also decreased but did not show a statistical significance, OxLDL were slightly higher than initially. After 24 months, 17 patients were still being treated with adalimumab. In these patients, hsCRP (P < 0.05), E-selectin (P < 0.001) and IL-22 (P < 0.001) were significantly decreased. OxLDL remained at a higher level. The stable decrease of E-selectin, hsCRP and IL-22 after 24 months confirms that adalimumab suppresses systemic inflammation.
Název v anglickém jazyce
Long Term Impact of Adalimumab Therapy on Biomarkers of Systemic Inflammation in Psoriasis: Results of a 2 year study
Popis výsledku anglicky
Psoriasis patients are at increased risk of atherosclerosis, characterized by endothelial dysfunction, linked through systemic inflammation. Anti-TNF-a therapy seems to decrease this risk. The purpose of this study was to measure the levels of serum markers associated with systemic inflammation in psoriasis patients, compared to healthy individuals and to investigate the change in their levels after 3 months and 2 years of adalimumab therapy. We investigated 4 biomarkers: high-sensitivity C-reactive protein (hsCRP), oxidized low-density lipoproteins (OxLDL), E-selectin and Interleukin 22 (IL-22). These markers were measured in healthy volunteers and in 28 patients with moderate/severe psoriasis before and after 3 and 24 months of treatment with adalimumab. Psoriasis patients had increased levels of markers in comparison to the control group. After 3 months of therapy, E-selectin decreased significantly (P < 0.001), as well as IL-22 (P < 0.001). hsCRP also decreased but did not show a statistical significance, OxLDL were slightly higher than initially. After 24 months, 17 patients were still being treated with adalimumab. In these patients, hsCRP (P < 0.05), E-selectin (P < 0.001) and IL-22 (P < 0.001) were significantly decreased. OxLDL remained at a higher level. The stable decrease of E-selectin, hsCRP and IL-22 after 24 months confirms that adalimumab suppresses systemic inflammation.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30216 - Dermatology and venereal diseases
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2020
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Dermatologic Therapy
ISSN
1396-0296
e-ISSN
—
Svazek periodika
33
Číslo periodika v rámci svazku
6
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
6
Strana od-do
"Article e14110"
Kód UT WoS článku
000560662900001
EID výsledku v databázi Scopus
2-s2.0-85089455762