Mpkj. Engelen et al., Factors contributing to alterations in skeletal muscle and plasma amino acid profiles in patients with chronic obstructive pulmonary disease, AM J CLIN N, 72(6), 2000, pp. 1480-1487
Background: There is increasing evidence of abnormal protein metabolism in
patients with chronic obstructive pulmonary disease (COPD), as reflected by
lower plasma branched-chain amino acid (BCAA) concentrations and different
muscle amino acid (AA) patterns than in age-matched control subjects.
Objective: We examined whether the low plasma BCAA concentrations in COPD r
eflect an imbalance between anabolic and catabolic processes as evidenced b
y a low fat-free mass (FFM) and alterations in the anabolic hormone insulin
and whether discrepancies in muscle AA concentrations between studies are
related to different patient characteristics.
Design: AA profiles in arterial plasma and quadriceps femoris muscle and in
sulin concentrations in venous plasma were analyzed in 28 postabsorptive CO
PD patients (14 with and 14 without macroscopic emphysema) and in 28 contro
l subjects. FFM was measured by dual-energy X-ray absorptiometry.
Results: The lower sum of plasma BCAAs in the COPD group than in the contro
l subjects was the result of a lower leucine concentration (P < 0.001); no
significant difference in valine and isoleucine was found between the group
s. In the COPD group, the lower leucine concentrations were associated with
low FFM (P < 0.01). Compared with the control group, the muscle-to-plasma
leucine gradient was higher in the COPD group (P < 0.001) and was associate
d with a higher insulin concentration (P < 0.01). Several muscle AA concent
rations were higher or tended to be higher in the group without emphysema t
han in the control group, whereas nearly all AA concentrations were lower i
n the group with emphysema.
Conclusions: Leucine metabolism is altered in COPD patients and is associat
ed with low FFM and high insulin concentrations. There were striking differ
ences in the skeletal muscle AA profile between the COPD subtypes.