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Sökning: WFRF:(Hansson Lotta) > (2020-2022) > Anti-citrullinated ...

Anti-citrullinated protein antibody specificities and pulmonary fibrosis in relation to genetic loci in early rheumatoid arthritis

Brink, Mikael (författare)
Univ Hosp, Rheumatol, Dept Publ Hlth & Clin Med, SE-90185 Umeå, Sweden.
Ljung, Lotta (författare)
Karolinska Institutet
Hansson, Monika (författare)
Karolinska Institutet
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Rönnelid, Johan (författare)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
Holmdahl, Rickard (författare)
Karolinska Institutet
Skriner, Karl (författare)
Charite Univ Med Berlin, Dept Rheumatol & Clin Immunol, Berlin, Germany.
Serre, Guy (författare)
Univ Toulouse, Inst Toulousain Malad Infectieuses & Inflamm, UMR 1291, INSERM,CNRS 5051, Toulouse, France.
Klareskog, Lars (författare)
Karolinska Inst, Karolinska Univ Hosp, Rheumatol Unit, Dept Med, Stockholm, Sweden.
Rantapaa-Dahlqvist, Solbritt (författare)
Univ Hosp, Rheumatol, Dept Publ Hlth & Clin Med, SE-90185 Umeå, Sweden.
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Karolinska Institutet Univ Hosp, Rheumatol, Dept Publ Hlth & Clin Med, SE-90185 Umeå, Sweden (creator_code:org_t)
2022-05-09
2022
Engelska.
Ingår i: Rheumatology. - : Oxford University Press. - 1462-0324 .- 1462-0332. ; 61:12, s. 4985-4990
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Objectives Pulmonary manifestations in RA are common comorbidities, but the underlying mechanisms are largely unknown. The added value of a multiplex of ACPA and genetic risk markers was evaluated for the development of pulmonary fibrosis (PF) in an inception cohort. Methods A total of 1184 patients with early RA were consecutively included and followed prospectively from the index date until death or 31 December 2016. The presence of 21 ACPA fine specificities was analysed using a custom-made microarray chip (Thermo Fisher Scientific, Uppsala, Sweden). Three SNPs, previously found related to PF were evaluated, rs2609255 (FAM13A), rs111521887 (TOLLIP) and rs35705950 (MUC5B). ACPA and genetic data were available for 841 RA patients, of whom 50 developed radiologically defined PF. Results In unadjusted analyses, 11 ACPA specificities were associated with PF development. In multiple variable analyses, six ACPA specificities were associated with increased risk of PF: vimentin (Vim)60-75, fibrinogen (Fib)beta 62-78 (72), Fib alpha 621-635, Bla26, collagen (C)II359-369 and F4-CIT-R (P < 0.01 to P < 0.05). The number of ACPA specificities was also related to PF development (P < 0.05 crude and adjusted models). In multiple variable models respectively adjusted for each of the SNPs, the number of ACPA specificities (P < 0.05 in all models), anti-Vim60-75 (P < 0.05, in all models), anti-Fib beta 62-78 (72) (P < 0.001 to P < 0.05), anti-CII359-369 (P < 0.05 in all models) and anti-F4-CIT-R AQ4 (P < 0.01 to P < 0.05), anti-Fib alpha 621-635 (P < 0.05 in one) and anti-Bla26 (P < 0.05 in two) were significantly associated with PF development. Conclusion The development of PF in an inception cohort of RA patients was associated with both presence of certain ACPA and the number of ACPA specificities and risk genes.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Nyckelord

RA
pulmonary fibrosis
autoantibodies
ACPA specificities
genetic loci

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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