Short peripheral blood leukocyte telomere length in rheumatoid arthritis-interstitial lung disease

Tracy J. Doyle*, Pierre Antoine Juge, Anna L. Peljto, Seoyeon Lee, Avram D. Walts, Anthony Joseph Esposito, Sergio Poli, Ritu Gill, Hiroto Hatabu, Mizuki Nishino, Paul F. Dellaripa, Michael E. Weinblatt, Nancy A. Shadick, M. Kristen Demoruelle, Jeffrey A. Sparks, Ivan O. Rosas, Benjamin Granger, Kevin D. Deane, Bruno Crestani, Paul J. WoltersPhilippe Dieudé, Joyce S. Lee

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Shortened telomere lengths (TLs) can be caused by single nucleotide polymorphisms and loss-of-function mutations in telomere-related genes (TRG), as well as ageing and lifestyle factors such as smoking. Our objective was to determine if shortened TL is associated with interstitial lung disease (ILD) in individuals with rheumatoid arthritis (RA). This is the largest study to demonstrate and replicate that shortened peripheral blood leukocytes-TL is associated with ILD in patients with RA compared with RA without ILD in a multinational cohort, and short PBL-TL was associated with baseline disease severity in RA-ILD as measured by forced vital capacity percent predicted.

Original languageEnglish (US)
Pages (from-to)182-185
Number of pages4
JournalThorax
Volume79
Issue number2
DOIs
StatePublished - Dec 7 2023

Funding

This work was supported by the National Institutes of Health [K23 HL119558, R03 HL148484 and R01 HL155522 to T.J.D.; F32 HL151132 to A.J.E.; R01CA203636, 5U01CA209414, 2R01HL111024, R01HL135142, and 1R01HL130974 to HH; P30 AR079369 to KDD and MKD; R01 AR077607, P30 AR070253, and P30 AR072577 to J.A.S; K23 HL138131 to JSL]; Nina Ireland Program for Lung Health to P.J.W. BRASS is funded by grants from Bristol Myers Squibb.

Keywords

  • interstitial fibrosis
  • rheumatoid lung disease

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

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