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Hemoglobin oxygen affinity in patients suffering from arterial occlusive disease of the legs

K M Braumann1, W Kleemann, U Martens

  • 1Abteilung Sport- und Arbeitsphysiologie, Hochschule Hannover.

Klinische Wochenschrift
|May 2, 1988
PubMed

Insights

Arterial occlusive disease (AOD) patients exhibit altered hemoglobin oxygen affinity due to smoking-induced carboxyhemoglobin (COHb). This impacts oxygen delivery, potentially affecting tissue oxygenation in AOD.

Area of Science:

  • Physiology
  • Cardiovascular Medicine
  • Biochemistry

Background:

  • Arterial occlusive disease (AOD) affects peripheral circulation.
  • Hemoglobin's oxygen affinity is crucial for oxygen transport.
  • Smoking is a common risk factor for AOD and affects blood parameters.

Purpose of the Study:

  • To investigate hemoglobin oxygen affinity in patients with leg arterial occlusive disease (AOD).
  • To compare these parameters with healthy controls.
  • To understand the influence of smoking and potential metabolic factors on oxygen transport in AOD.

Main Methods:

  • Blood samples from 12 male AOD patients and healthy controls were analyzed.
  • Hemoglobin oxygen affinity parameters, including oxygen dissociation curve (ODC), P50, and Bohr coefficients, were measured.
  • Carboxyhemoglobin (COHb) and 2,3-diphosphoglycerate levels were determined.

Main Results:

  • AOD patients, particularly smokers, showed elevated COHb levels, causing a leftward shift in the ODC.
  • The half-saturation pressure (P50) was initially lower in AOD patients but normalized after COHb correction.
  • Corrected ODC steepness (Hill's 'n') and Bohr coefficients (BCLac) were significantly different in AOD patients compared to controls, indicating altered oxygen binding.
  • Elevated 2,3-diphosphoglycerate was observed, but did not fully compensate for COHb effects.

Conclusions:

  • Smoking-induced COHb significantly alters hemoglobin oxygen affinity in AOD patients.
  • AOD is associated with intrinsic changes in hemoglobin oxygen binding characteristics beyond COHb effects.
  • Factors such as reduced erythrocyte age or metabolic byproducts may contribute to these alterations, impacting oxygen delivery in AOD.

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