Global REACH 2018: volume regulation in high-altitude Andeans with and without chronic mountain sickness

Author:

Steele Andrew R.1ORCID,Tymko Michael M.1ORCID,Meah Victoria L.123ORCID,Simpson Lydia L.4,Gasho Christopher5,Dawkins Tony G.6ORCID,Williams Alexandra M.78ORCID,Villafuerte Francisco C.9ORCID,Vizcardo-Galindo Gustavo A.10ORCID,Figueroa-Mujíca Rómulo J.9,Ainslie Philip N.10,Stembridge Mike6ORCID,Moore Jonathan P.11ORCID,Steinback Craig D.12312ORCID

Affiliation:

1. Neurovascular Health Lab, Faculty of Kinesiology, Sport, and Recreation, University of Alberta, Edmonton, Alberta, Canada

2. Women and Children’s Health Research Institute, University of Alberta, Edmonton, Alberta, Canada

3. Alberta Diabetes Institute, University of Alberta, Edmonton, Alberta, Canada

4. Division of Physiology, Department of Sport Science, University of Innsbruck, Innsbruck, Austria

5. Division of Pulmonary and Critical Care, School of Medicine, Loma Linda University, Loma Linda, California

6. Cardiff School of Sport and Health Sciences, Cardiff Metropolitan University, Cardiff, United Kingdom

7. Department of Cellular and Physiological Sciences, Faculty of Medicine, University of British Columbia, Kelowna, British Columbia, Canada

8. International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, British Columbia, Canada

9. Department of Biological and Physiological Sciences, Universidad Peruana Cayetano Heredia, Lima, Peru

10. Centre for Heart, Lung, and Vascular Health, University of British Columbia Okanagan, Kelowna, British Columbia, Canada

11. Extremes Research Group, School of Sport, Health and Exercise Sciences, Bangor University, Bangor, United Kingdom

12. Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada

Abstract

The high-altitude maladaptation syndrome known as chronic mountain sickness (CMS) is characterized by polycythemia and is associated with proteinuria despite unaltered glomerular filtration rate. However, it remains unclear if indigenous highlanders with CMS have altered volume regulatory hormones. We assessed NH2-terminal pro-B-type natriuretic peptide (NT pro-BNP), plasma aldosterone concentration, plasma renin activity, kidney function (urinary microalbumin, glomerular filtration rate), blood volume, and estimated pulmonary artery systolic pressure (ePASP) in Andean males without ( n = 14; age = 39 ± 11 yr) and with ( n = 10; age = 40 ± 12 yr) CMS at 4,330 m (Cerro de Pasco, Peru). Plasma renin activity (non-CMS: 15.8 ± 7.9 ng/mL vs. CMS: 8.7 ± 5.4 ng/mL; P = 0.025) and plasma aldosterone concentration (non-CMS: 77.5 ± 35.5 pg/mL vs. CMS: 54.2 ± 28.9 pg/mL; P = 0.018) were lower in highlanders with CMS compared with non-CMS, whereas NT pro-BNP was not different between groups (non-CMS: 1394.9 ± 214.3 pg/mL vs. CMS: 1451.1 ± 327.8 pg/mL; P = 0.15). Highlanders had similar total blood volume (non-CMS: 90 ± 15 mL·kg−1 vs. CMS: 103 ± 18 mL·kg−1; P = 0.071), but Andeans with CMS had greater total red blood cell volume (non-CMS: 46 ± 10 mL·kg−1 vs. CMS: 66 ± 14 mL·kg−1; P < 0.01) and smaller plasma volume (non-CMS: 43 ± 7 mL·kg−1 vs. CMS: 35 ± 5 mL·kg−1; P = 0.03) compared with non-CMS. There were no differences in ePASP between groups (non-CMS: 32 ± 9 mmHg vs. CMS: 31 ± 8 mmHg; P = 0.6). A negative correlation was found between plasma renin activity and glomerular filtration rate in both groups (group: r = −0.66; P < 0.01; non-CMS: r = −0.60; P = 0.022; CMS: r = −0.63; P = 0.049). A smaller plasma volume in Andeans with CMS may indicate an additional CMS maladaptation to high altitude, causing potentially greater polycythemia and clinical symptoms.

Funder

Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada

Gilchrist Educational Trust

Heart and Stroke Foundation of Canada

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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