PMID- 36921671 OWN - NLM STAT- MEDLINE DCOM- 20230515 LR - 20230522 IS - 1538-2990 (Electronic) IS - 0002-9629 (Linking) VI - 365 IP - 6 DP - 2023 Jun TI - Temporal changes in biomarkers in individuals with and without acute mountain sickness following rapid ascent. PG - 510-519 LID - S0002-9629(23)01064-9 [pii] LID - 10.1016/j.amjms.2023.03.004 [doi] AB - BACKGROUND: Field studies have reported conflicting results regarding changes in biomarkers at high altitude. This study measured temporal changes in biomarkers and compared the differences between individuals with and without acute mountain sickness (AMS). MATERIALS AND METHODS: This study included 34 nonacclimatized healthy participants. Ten-milliliters of blood were collected at four time points: 3 days before ascent (T0), on two successive nights at 3150 m (T1 and T2), and 2 days after descent (T3). Participants were transported by bus from 555 m to 3150 m within 3 hours. AMS was diagnosed using the self-reported Lake Louise Scoring (LLS) questionnaire. RESULTS: Compared with T0, significant increases in E-selectin and decreases in vascular endothelial growth factor (VEGF) levels were observed at high altitude. Significantly increased C-reactive protein (CRP), monocyte chemoattractant protein-1 (MCP-1), and S100 calcium-binding protein B (S100B) levels were observed at T2, and significantly decreased vascular cell adhesion molecule-1 (VCAM-1) levels were observed at T3. Eighteen (53%) participants developed AMS. Changes in E-selectin, CRP, MCP-1, and S100B levels were independent of AMS. Relative to individuals without AMS, those with AMS had significantly higher atrial natriuretic peptide (ANP) and VCAM-1 levels and lower plasminogen activator inhibitor-1 (PAI-1) levels at T1 and higher brain natriuretic peptide and lower VEGF and PAI-1 levels at T3. LLSs were positively correlated with ANP and VCAM-1 levels and negatively correlated with PAI-1 levels measured at T1. CONCLUSIONS: After acute ascent, individuals with and without AMS exhibited different trends in biomarkers associated with endothelial cell activation and natriuretic peptides. CI - Copyright (c) 2023 Southern Society for Clinical Investigation. Published by Elsevier Inc. All rights reserved. FAU - Lin, Fang-Chi AU - Lin FC AD - Department of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan. Electronic address: fclin3@vghtpe.gov.tw. FAU - Chao, Heng-Sheng AU - Chao HS AD - Department of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan. FAU - Chou, Chung-Wei AU - Chou CW AD - Department of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan. FAU - Tsai, Han-Chen AU - Tsai HC AD - Department of Nursing, Taipei Veterans General Hospital, Taipei, Taiwan; Institute of Emergency and Critical Care Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan. FAU - Chang, Shi-Chuan AU - Chang SC AD - Pingtung Christian Hospital, Taiwan. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20230313 PL - United States TA - Am J Med Sci JT - The American journal of the medical sciences JID - 0370506 RN - 0 (E-Selectin) RN - 0 (Plasminogen Activator Inhibitor 1) RN - 0 (Vascular Endothelial Growth Factor A) RN - 0 (Vascular Cell Adhesion Molecule-1) RN - 0 (Biomarkers) SB - IM MH - Humans MH - *Altitude Sickness/diagnosis MH - E-Selectin MH - Plasminogen Activator Inhibitor 1 MH - Vascular Endothelial Growth Factor A MH - Vascular Cell Adhesion Molecule-1 MH - Acute Disease MH - Biomarkers OTO - NOTNLM OT - Acute mountain sickness OT - High-altitude illness OT - Lake Louise Score COIS- Declaration of Competing Interest All authors declare that they have no conflicts of interest. EDAT- 2023/03/16 06:00 MHDA- 2023/05/15 06:42 CRDT- 2023/03/15 20:26 PHST- 2022/04/05 00:00 [received] PHST- 2023/02/13 00:00 [revised] PHST- 2023/03/08 00:00 [accepted] PHST- 2023/05/15 06:42 [medline] PHST- 2023/03/16 06:00 [pubmed] PHST- 2023/03/15 20:26 [entrez] AID - S0002-9629(23)01064-9 [pii] AID - 10.1016/j.amjms.2023.03.004 [doi] PST - ppublish SO - Am J Med Sci. 2023 Jun;365(6):510-519. doi: 10.1016/j.amjms.2023.03.004. Epub 2023 Mar 13.