SUMF1 Common Variant rs793391 Is Associated with Response to Inhaled Corticosteroids in Patients with COPD

This study investigated whether specific <i>sulfatase modifying factor-1</i> (<i>SUMF1</i>) SNPs-previously linked to lung function-are associated with COPD progression and response to inhaled corticosteroid (ICS) treatment, specifically budesonide, given that <i>SUMF1</i> expression is altered in COPD and its variants linked to increased disease risk. A subgroup of 165 COPD patients from the HISTORIC study were genotyped for two common <i>SUMF1</i> SNPs, rs11915920 and rs793391. Patients first underwent a six-week run-in phase with open-label triple inhaled therapy (LAMA/LABA/ICS), then were randomized to receive either LAMA/LABA/placebo or LAMA/LABA/ICS for 12 months. Associations between SNPs, baseline characteristics, and response to ICS-based on FEV<sub>1</sub> change over 12 months-were evaluated. Heterozygotes (TG) for the rs793391 polymorphism treated with LAMA/LABA/ICS showed a significant and clinically meaningful FEV<sub>1</sub> improvement compared to the placebo group. This was supported by improved patient-reported outcomes, with lower SGRQ and CAT scores and a clinically relevant increase in General Health Questionnaire scores. These findings suggest that rs793391 may be linked to both COPD progression and ICS response and could contribute to more personalized treatment strategies in COPD.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-10-21
DOI
https://doi.org/10.3390/ijms262010225
Primary Topic
Chronic Obstructive Pulmonary Disease (COPD) Research
Type
article
Field-Weighted Citation Impact
0.00

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article

SUMF1 Common Variant rs793391 Is Associated with Response to Inhaled Corticosteroids in Patients with COPD

Daiana Stolz, Despoina Ioannidou, Björn C. Frye, Spasenija Savic Prince et al.
International Journal of Molecular Sciences
Chronic Obstructive Pulmonary Disease (COPD) Research
article

SUMF1 Common Variant rs793391 Is Associated with Response to Inhaled Corticosteroids in Patients with COPD

Daiana Stolz, Despoina Ioannidou, Björn C. Frye, Spasenija Savic Prince, Charikleia Ntenti, Maria Grazia Pascarella, Antonis Goulas, Eleni Papakonstantinou, Sebastian Fähndrich, Leticia Grize
article en

Abstract

This study investigated whether specific <i>sulfatase modifying factor-1</i> (<i>SUMF1</i>) SNPs-previously linked to lung function-are associated with COPD progression and response to inhaled corticosteroid (ICS) treatment, specifically budesonide, given that <i>SUMF1</i> expression is altered in COPD and its variants linked to increased disease risk. A subgroup of 165 COPD patients from the HISTORIC study were genotyped for two common <i>SUMF1</i> SNPs, rs11915920 and rs793391. Patients first underwent a six-week run-in phase with open-label triple inhaled therapy (LAMA/LABA/ICS), then were randomized to receive either LAMA/LABA/placebo or LAMA/LABA/ICS for 12 months. Associations between SNPs, baseline characteristics, and response to ICS-based on FEV<sub>1</sub> change over 12 months-were evaluated. Heterozygotes (TG) for the rs793391 polymorphism treated with LAMA/LABA/ICS showed a significant and clinically meaningful FEV<sub>1</sub> improvement compared to the placebo group. This was supported by improved patient-reported outcomes, with lower SGRQ and CAT scores and a clinically relevant increase in General Health Questionnaire scores. These findings suggest that rs793391 may be linked to both COPD progression and ICS response and could contribute to more personalized treatment strategies in COPD.

International Journal of Molecular SciencesVol. 26(20)
University of Freiburg (DE), University of Basel (CH), Aristotle University of Thessaloniki (GR), University Medical Center Freiburg (DE), University Hospital of Basel (CH), Ippokrateio General Hospital of Thessaloniki (GR)
European Commission, Albert-Ludwigs-Universität Freiburg, Medizinische Fakultät der Albert-Ludwigs-Universität Freiburg, European Social Fund
Openalex Percentile: Top 57%
Chronic Obstructive Pulmonary Disease (COPD) Research
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