The association between systemic inflammation as measured by calprotectin and autoantibody load in rheumatoid arthritis.
Обработка статьи · этапы, ошибки и управление
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Grönwall Caroline, Alm Linda Mathsson, Westerlind Helga, Gehring Isabel, Ghasemzadeh Nasim, Krogh Niels Steen, Lillegraven Siri, Haavardsholm Espen, Johannesson Martina, Kvien Tore K, Rönnelid Johan, Kragstrup Tue Wenzel, Glintborg Bente, Hetland Merete Lund, Hammer Hilde Berner, Danish Rheumatologic Biobank Study Group, Swedish Rheumatology Quality Register Biobank Study Group(SRQb), Askling Johan, Hendricks Oliver, Høgdall Estrid, Jensen Dorte Vendelbo, Munk Heidi Lausten, Pedersen Jens Kristian, Ellingsen Torkell, Loft Anne Gitte, Hauge Ellen-Margrethe, Kristensen Salome, Dreyer Lene, Linauskas Asta, Jacobsen Søren, Turesson Carl, Dahlqvist Solbritt Rantapää, Björkman Lena, Kastbom Alf, Baecklund Eva
Аннотация
METHODS: Rheumatoid factor (RF), anti-cyclic citrullinated peptide 2 (CCP2) isotypes and plasma calprotectin were centrally measured in a cross-sectional cohort of 4521 Scandinavian RA patients using fluoroenzyme immunoassays. IgG to 15 citrullinated (Cit) and four carbamylated or acetylated (Carb/Acet) peptides were measured by multiplex solid-phase array. CRP and ESR values were obtained from clinical measurements at the time of blood sampling.
RESULTS: Calprotectin levels correlated with ESR (ρ=0.53), CRP (ρ=0.47), VAS pain (ρ=0.24), SJC28 (ρ=0.39), and TJC28 (ρ=0.26; p<0.0001 for all). Patients with both elevated CRP (>10mg/L) and calprotectin (>15 AU/ml) (14%, N=613) had significantly higher VAS pain, SJC28, and TJC28 than patients with only elevated CRP (p<0.0001), in early and established disease. Patients with elevated calprotectin, independent of CRP levels, had significantly higher proportions of AMPA positivity including anti-CCP2. When patients were divided into six groups based on increasing number of Cit/Carb/Acet-reactivities and anti-CCP2 IgG levels, elevated calprotectin was associated with increasing AMPA load, particularly in the presence of RF IgM. The differences between AMPA load groups remained after adjusting for sex, age, RF IgM, and disease duration.
CONCLUSIONS: Plasma calprotectin is positively associated with seropositivity and AMPA load by autoantibody levels and the breadth of the autoantibody response.