Faster lung function decline in people living with HIV despite adequate treatment: a longitudinal matched cohort study

Author:

Thudium Rebekka Faber,Ronit Andreas,Afzal ShoaibORCID,Çolak Yunus,Forman Julie Lyng,Mendo Fernando,Chen Fabian,Estrada Vicente,Kumarasamy Nagalingeswaran,Nordestgaard Børge G,Lundgren Jens,Vestbo Jørgen,Kunisaki Ken MORCID,Nielsen Susanne Dam

Abstract

IntroductionChronic lung disease is common among people living with HIV (PLWH). We hypothesised that PLWH receiving antiretroviral therapy (ART) have faster lung function decline than matched controls.MethodsWe performed a prospective matched cohort study by including ART-treated PLWH from the Copenhagen Co-morbidity in HIV Infection Study (n=705) and the INSIGHT Strategic Timing of Antiretroviral Treatment Pulmonary Substudy (n=425) and frequency matched population controls from the Copenhagen General Population Study (n=2895) in a 1:3 ratio. Eligible participants were ≥25 years old and had two spirometry tests separated by at least 2 years of follow-up. Forced expiratory volume in 1 s (FEV1) decline (mL/year) was compared between PLWH and controls using a linear mixed model adjusted for age, sex, ethnicity and smoking status. Effect modification by smoking was investigated in subgroup analyses.ResultsThe majority of PLWH were virally suppressed (96.1%). The adjusted mean annual decline in FEV1was faster in PLWH than in controls with 36.4 (95% CI 33.7 to 39.1) vs 27.9 (95% CI 26.9 to 28.8) mL/year, yielding a difference of 8.5 (95% CI 5.6 to 11.4) mL/year. The association between HIV and FEV1decline was modified by smoking, with the largest difference in current smokers (difference: 16.8 (95% CI 10.5 to 23.0) mL/year) and the smallest difference in never-smokers (difference: 5.0 (95% CI 0.7 to 9.3) mL/year). FEV1decline >40 mL/year was more prevalent in PLWH (adjusted OR: 1.98 (95% CI 1.67 to 2.34)).ConclusionWell-treated PLWH have faster lung function decline than controls and smoking seems to modify this association, suggesting that smoking may lead to more rapid lung function decline in PLWH than in controls.

Funder

Rigshospitalet Research Council

European AIDS Treatment Network

National Institute of Health Reseach Manchester Biomedical research Centre

Gilead Sciences

UK Medical Research Council

Novo Nordisk

Australian National Health and Medical Research Council

National Institute of Allergy and Infectious Diseases

Minneapolis Veterans Affairs Medical Center, Minneapolis, USA

The National Heart Lung and Blood Institute

German Ministry of Education and Research

Publisher

BMJ

Subject

Pulmonary and Respiratory Medicine

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