4.7 Article

Sex differences in cardiorespiratory fitness are explained by blood volume and oxygen carrying capacity

Journal

CARDIOVASCULAR RESEARCH
Volume 118, Issue 1, Pages 334-343

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/cvr/cvab028

Keywords

Cardiac function; Blood volume; Haemoglobin mass; Aerobic power; Sex

Funding

  1. Swiss National Science Foundation [P2ZHP3-184211]
  2. Natural Sciences and Engineering Research Council of Canada [RGPIN-2019-04833]
  3. Swiss National Science Foundation (SNF) [P2ZHP3_184211] Funding Source: Swiss National Science Foundation (SNF)

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This study confirms that sex differences in cardiorespiratory fitness can be abolished by experimentally matching blood attributes between adult women and men.
Aims Intrinsic sex differences in fundamental blood attributes have long been hypothesized to contribute to the gap in cardiorespiratory fitness between men and women. This study experimentally assessed the role of blood volume and oxygen (O-2) carrying capacity on sex differences in cardiac function and aerobic power. Methods and results Healthy women and men (n = 60) throughout the mature adult lifespan (42-88 yr) were matched by age and physical activity levels. Transthoracic echocardiography, central blood pressure, and O-2 uptake were assessed throughout incremental exercise (cycle ergometry). Main outcomes such as left ventricular end-diastolic volume (LVEDV), stroke volume (SV), cardiac output (Q), and peak O-2 uptake (VO2peak), as well as blood volume (BV) were determined with established methods. Measurements were repeated in men following blood withdrawal and O-2 carrying capacity reduction matching women's levels. Prior to blood normalization, BV and O-2 carrying capacity were markedly reduced in women compared with men (P < 0.001). Blood normalization resulted in a precise match of BV (82.36 +/- 9.83 vs. 82.34 +/- 7.70 ml.kg(-1), P = 0.993) and O-2 carrying capacity (12.0 +/- 0.6 vs. 12.0 +/- 0.7 g.dl(-1), P = 0.562) between women and men. Body size-adjusted cardiac filling and output (LVEDV, SV, Q) during exercise as well as VO2peak (30.8 +/- 7.5 vs. 35.6 +/- 8.7 ml.min(-1).kg(-1), P < 0.001) were lower in women compared with men prior to blood normalization. VO2peak did not differ between women and men after blood normalization (30.8 +/- 7.5 vs. 29.7 +/- 7.4 ml.min(-1).kg(-1), P = 0.551). Conclusions Sex differences in cardiorespiratory fitness are abolished when blood attributes determining O-2 delivery are experimentally matched between adult women and men.

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