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Pulmonary fibrosis in relation to genetic loci in an inception cohort of patients with early rheumatoid arthritis from northern Sweden

Jönsson, Elias (författare)
Umeå universitet,Reumatologi,Department of Public Health and Medicine/Rheumatology, Umeå University, Umeå
Ljung, Lotta, 1964- (författare)
Umeå universitet,Reumatologi,Department of Public Health and Medicine/Rheumatology, Umeå University, Umeå
Norrman, Eva (författare)
Umeå universitet,Reumatologi,Department of Public Health and Medicine/Rheumatology, Umeå University, Umeå
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Freyhult, Eva, 1979- (författare)
Uppsala universitet,Institutionen för medicinska vetenskaper,Science for Life Laboratory, SciLifeLab
Ärlestig, Lisbeth, 1954- (författare)
Umeå universitet,Reumatologi,Department of Public Health and Medicine/Rheumatology, Umeå University, Umeå
Dahlqvist, Johanna, 1979- (författare)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Rantapää-Dahlqvist, Solbritt (författare)
Umeå universitet,Reumatologi,Department of Public Health and Medicine/Rheumatology, Umeå University, Umeå
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 (creator_code:org_t)
2021-05-16
2022
Engelska.
Ingår i: Rheumatology. - : British Society for Rheumatology. - 1462-0324 .- 1462-0332. ; 61:3, s. 943-952
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • OBJECTIVES: Pulmonary manifestations in RA are common comorbidities. Interstitial lung disease (ILD), both idiopathic and in RA, has been associated with several genetic variants. We assessed pulmonary fibrosis (PF) in an inception cohort of RA patients in relation to genetic variants and disease-related factors.METHODS: A total of 1466 early RA patients were consecutively included and followed prospectively from the index date until death or 31 December 2016. Clinical and laboratory data and treatment were continuously registered according to the Swedish Rheumatology Quality Register. DNA was available from 1184 patients and 571 151 genome-wide single-nucleotide polymorphisms (SNPs) were analysed. Thirteen identified genetic variants were extracted. At follow-up, the patients answered a questionnaire regarding disease progression and lung involvement that was validated by reviewing medical records and analysing radiological examinations.RESULTS: The prevalence of PF was 5.6% and the annualized incidence rate was 5.0/1000 (95% CI 3.80, 6.54). Four SNPs were associated with PF in RA: rs35705950 [MUC5B; OR 2.5 (95% CI 1.5, 4.0), adjusted P-value = 0.00016, q-value = 0.0021]; rs111521887 [TOLLIP; OR 1.9 (95% CI 1.3, 2.8), adjusted P-value = 0.0014, q-value = 0.0092]; rs2609255 [FAM13A; OR 1.7 (95% CI 1.1, 2.5), adjusted P-value = 0.013, q-value = 0.055] and rs2736100 [TERT; OR 1.5 (95% CI 1.0, 2.2), adjusted P-value = 0.046, q-value = 0.15]. Older age and RF positivity were associated with increased risk, while MTX treatment was associated with a lower risk of PF.CONCLUSIONS: Development of PF in an inception cohort of RA patients was associated with 4 of 12 ILD risk genes. RA-related factors except for age at diagnosis and RF positivity were of limited importance in PF development.

Ämnesord

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

Nyckelord

pulmonary fibrosis
rheumatoid arthritis
rs111521887 (TOLLIP)
rs2609255 (FAM13A)
rs2736100 (TERT)
rs35705950 (MUC5B)

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ref (ämneskategori)
art (ämneskategori)

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