Higher arterial oxygen saturation during submaximal exercise in Bolivian Aymara compared to European sojourners and Europeans born and raised at high altitude.

Arterial oxygen saturation (SaO(2)) was measured at 3,600-3,850 m by pulse oximetry at rest and during submaximal exercise in three study groups: 1) highland Aymara natives of the Bolivian altiplano (n = 25); 2) lowland European/North American sojourners to the highlands with at least 2 months of acclimatization time to 3,600 m (n = 27); and 3) subjects of European ancestry born and raised at 3,600 m (n = 22). Aymara subjects maintained approximately 1 percentage point higher SaO(2) during submaximal work up to 70% of their maximal work capacity, and showed a smaller rate of decline in SaO(2) with increasing work compared to both European study groups. The higher-exercise SaO(2) of Aymara compared to Europeans born and raised at 3,600 m suggests genetic adaptation. The two European study groups, who differed by exposure to high altitude during their growth and development period, did not show any significant difference in either resting or exercise SaO(2). This suggests that the developmental mode of adaptation is less important than the genetic mode of adaptation in determining exercise SaO(2). A weak correlation was detected (across study groups only) between the residual forced vital capacity (FVC) and the residual SaO(2) measured at the highest level of submaximal work output (P = 0.024, R = 0.26). While firm conclusions based on this correlation are problematic, it is suggested that a part of the higher SaO(2) observed in Aymara natives is due to a larger lung volume and pulmonary diffusion capacity for oxygen. Results from this study are compared to similar studies conducted with Tibetan natives, and are interpreted in light of recent quantitative genetic analyses conducted in both the Andes and Himalayas.

[1]  T. Brutsaert,et al.  Effect of developmental and ancestral high-altitude exposure on VO(2)peak of Andean and European/North American natives. , 1999, American journal of physical anthropology.

[2]  T. Brutsaert,et al.  Effect of developmental and ancestral high altitude exposure on chest morphology and pulmonary function in Andean and European/North American natives , 1999, American journal of human biology : the official journal of the Human Biology Council.

[3]  J Blangero,et al.  Percent of oxygen saturation of arterial hemoglobin among Bolivian Aymara at 3,900-4,000 m. , 1999, American journal of physical anthropology.

[4]  L. Almasy,et al.  Ventilation and hypoxic ventilatory response of Tibetan and Aymara high altitude natives. , 1997, American journal of physical anthropology.

[5]  J. Blangero,et al.  Quantitative genetic analysis of arterial oxygen saturation in Tibetan highlanders. , 1997, Human biology.

[6]  R. Ge,et al.  Exercise performance of Tibetan and Han adolescents at altitudes of 3,417 and 4,300 m. , 1997, Journal of applied physiology.

[7]  B. Groves,et al.  Smaller alveolar-arterial O2 gradients in Tibetan than Han residents of Lhasa (3658 m). , 1996, Respiration physiology.

[8]  L. Moore,et al.  Arterial oxygen saturation in Tibetan and Han infants born in Lhasa, Tibet. , 1995, The New England journal of medicine.

[9]  K. Kubo,et al.  Comparisons of oxygen transport between Tibetan and Han residents at moderate altitude , 1995 .

[10]  W. Coward,et al.  Energy expenditure determined by the doubly labeled water method in Bolivian Aymara living in a high altitude agropastoral community. , 1995, The American journal of clinical nutrition.

[11]  L. Moore,et al.  Hypoxic ventilatory responses in Tibetan residents of 4400 m compared with 3658 m. , 1995, Respiration physiology.

[12]  G. Ferretti,et al.  Maximal exercise performance in chronic hypoxia and acute normoxia in high-altitude natives , 1995 .

[13]  J. Blangero,et al.  Major gene for percent of oxygen saturation of arterial hemoglobin in Tibetan highlanders. , 1994, American journal of physical anthropology.

[14]  K. Kubo,et al.  Higher exercise performance and lower VO2max in Tibetan than Han residents at 4,700 m altitude. , 1994, Journal of applied physiology.

[15]  B. Groves,et al.  Are Tibetans Better Adapted? , 1992, International journal of sports medicine.

[16]  L. Greksa Surnames as indicators of European admixture in Andean Indians , 1992 .

[17]  G. Matheson,et al.  Overall and regional lung function in Andean natives after descent to low altitude. , 1992, Respiration physiology.

[18]  L. Moore,et al.  Greater maximal O2 uptakes and vital capacities in Tibetan than Han residents of Lhasa. , 1990, Respiration physiology.

[19]  R. M. Peters,et al.  Increased diffusion capacity maintains arterial saturation during exercise in the Quechua Indians of Chilean Altiplano , 1990, American journal of human biology : the official journal of the Human Biology Council.

[20]  A. J. Hamilton,et al.  Increased exercise SaO2 independent of ventilatory acclimatization at 4,300 m. , 1989, Journal of applied physiology.

[21]  R. Chakraborty,et al.  Ethnicity determination by names among the Aymara of Chile and Bolivia. , 1989, Human biology.

[22]  S. Powers,et al.  Hemoglobin desaturation in highly trained athletes during heavy exercise. , 1986, Medicine and science in sports and exercise.

[23]  D. Altman,et al.  STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT , 1986, The Lancet.

[24]  R. Johnson,et al.  Functional capacities of lungs and thorax in beagles after prolonged residence at 3,100 m. , 1985, Journal of applied physiology.

[25]  R. Chakraborty,et al.  Immunoglobulin (Gm and Km) allotypes in the Aymara of Chile and Bolivia. , 1985, Annals of human biology.

[26]  L. Moore,et al.  Hypocapnia and sustained hypoxia blunt ventilation on arrival at high altitude. , 1984, Journal of applied physiology: respiratory, environmental and exercise physiology.

[27]  R. Winslow,et al.  Variability of oxygen affinity of blood: human subjects native to high altitude. , 1981, Journal of applied physiology: respiratory, environmental and exercise physiology.

[28]  J. Weiner,et al.  Practical human biology , 1981 .

[29]  F. Rothhammer,et al.  Part IV: Genes and epidemiology in anthropological adaptation studies: Familial correlations in lung function in populations residing at different altitudes in Chile , 1980 .

[30]  P. Pasquis,et al.  Pulmonary gas exchange, diffusing capacity in natives and newcomers at high altitude. , 1978, Respiration physiology.

[31]  J. Weil,et al.  Respiratory failure associated with familial depression of ventilatory response to hypoxia and hypercapnia. , 1976, The New England journal of medicine.

[32]  J. Durnin,et al.  Body fat assessed from total body density and its estimation from skinfold thickness: measurements on 481 men and women aged from 16 to 72 Years , 1974, British Journal of Nutrition.

[33]  J. Dempsey,et al.  Pulmonary gas exchange in nonnative residents of high altitude. , 1973, The Journal of clinical investigation.

[34]  S. Roy,et al.  Pulmonary diffusing capacity at high altitude. , 1971, Journal of applied physiology.

[35]  J. Dempsey,et al.  Effects of acute through life-long hypoxic exposure on exercise pulmonary gas exchange. , 1971, Respiration physiology.

[36]  A. Degraff,et al.  Diffusing capacity of the lung in Caucasians native to 3,100 m. , 1970, Journal of applied physiology.

[37]  G. Lasker Human Biological Adaptability , 1969 .

[38]  J. Remmers,et al.  The carbon monoxide diffusing capacity in permanent residents at high altitudes. , 1969, Respiration physiology.

[39]  A. Beckett,et al.  AKUFO AND IBARAPA. , 1965, Lancet.