PMID- 38396308 OWN - NLM STAT- MEDLINE DCOM- 20240516 LR - 20240516 IS - 1432-1041 (Electronic) IS - 0031-6970 (Linking) VI - 80 IP - 6 DP - 2024 Jun TI - Long-acting B-2 agonists (LABA) or long-acting muscarinic antagonists (LAMA): which one may be the first option in group A COPD patients? PG - 847-853 LID - 10.1007/s00228-024-03637-1 [doi] AB - INTRODUCTION: Long-acting muscarinic antagonists (LAMA) or beta-2 agonists (LABA) have been recommended for symptom control in group A COPD patients as a first-line bronchodilator treatment in GOLD guidelines. However, there is no mention of priority/superiority between the two treatment options. We aimed to compare the effectiveness of these treatments in this group. METHODS: The study cohort was formed of all subjects from six pulmonology clinics with an initial diagnosis of COPD who were new users of a LAMA or LABA from January 2020 to December 2021. Seventy-six group A COPD patients, in whom LABA or LAMA therapy had been started in the last 1 month as a first-line treatment, were included in our study. Participants were evaluated with spirometry, COPD Assessment Test (CAT), mMRC scale, and St. George Respiratory Questionnaire (SGRQ) for three times (baseline, 6-12(th) months). RESULTS: There were 76 group A COPD patients with LAMA (67.1%) and LABA (32.9%). The number of patients who improved in CAT score at the end of the first year was significantly higher in patients using LAMA than those using LABA (p = 0.022); the improvement at minimum clinically important difference (MCID) in CAT score of LAMA group at 1(st) year was also significant (p = 0.044). SGRQ total and impact scores were found to be statistically lower at 1(st) year compared to baseline in patients using LAMA (p = 0.010 and 0.006, respectively). Significant improvement was detected in CAT and SGRQ scores at the 6(th) month visit in the LAMA group having emphysema (p = 0.032 and 0.002, respectively). CONCLUSION: According to significant improvements in CAT and SGRQ score, LAMA may be preferred over LABA as a bronchodilator agent in group A COPD patients, especially in emphysema-dominant phenotype. CI - (c) 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. FAU - Turan, Onur AU - Turan O AUID- ORCID: 0000-0001-6320-0470 AD - Chest Diseases Department, Izmir Katip Celebi University, Izmir, Turkey. onurtura@yahoo.com. FAU - Ogan, Nalan AU - Ogan N AUID- ORCID: 0000-0001-5232-3803 AD - Chest Diseases Department, Ufuk University, Ankara, Turkey. FAU - Bozkus, Fulsen AU - Bozkus F AUID- ORCID: 0000-0002-6498-4390 AD - Chest Diseases Department, Kahramanmaras Sutcu Imam University, Kahramanmaras, Turkey. FAU - Sarioglu, Nurhan AU - Sarioglu N AUID- ORCID: 0000-0002-5180-9649 AD - Chest Diseases Department, Balikesir University, Balikesir, Turkey. FAU - Turan, Pakize Ayse AU - Turan PA AUID- ORCID: 0000-0002-9325-4303 AD - Chest Diseases Department, Menemen State Hospital, Izmir, Turkey. FAU - Satici, Celal AU - Satici C AUID- ORCID: 0000-0002-5457-9551 AD - Chest Diseases Department, Istanbul Gaziosmanpasa Research and Training Hospital University, Istanbul, Turkey. LA - eng PT - Comparative Study PT - Journal Article PT - Multicenter Study DEP - 20240223 PL - Germany TA - Eur J Clin Pharmacol JT - European journal of clinical pharmacology JID - 1256165 SB - IM MH - Humans MH - *Pulmonary Disease, Chronic Obstructive/drug therapy MH - Male MH - Female MH - *Adrenergic beta-2 Receptor Agonists/therapeutic use/administration & dosage MH - *Muscarinic Antagonists/administration & dosage/therapeutic use MH - Aged MH - Middle Aged MH - Bronchodilator Agents/therapeutic use/administration & dosage MH - Treatment Outcome MH - Spirometry MH - Muscarinic Agonists/therapeutic use/administration & dosage MH - Delayed-Action Preparations OTO - NOTNLM OT - COPD OT - Group A OT - Long-acting beta-2 agonists (LABA) OT - Long-acting muscarinic antagonists (LAMA) OT - Treatment EDAT- 2024/02/24 11:45 MHDA- 2024/05/16 12:43 CRDT- 2024/02/24 00:07 PHST- 2023/10/09 00:00 [received] PHST- 2024/01/23 00:00 [accepted] PHST- 2024/05/16 12:43 [medline] PHST- 2024/02/24 11:45 [pubmed] PHST- 2024/02/24 00:07 [entrez] AID - 10.1007/s00228-024-03637-1 [pii] AID - 10.1007/s00228-024-03637-1 [doi] PST - ppublish SO - Eur J Clin Pharmacol. 2024 Jun;80(6):847-853. doi: 10.1007/s00228-024-03637-1. Epub 2024 Feb 23.