A. Schmid et al., Lipoproteins and free plasma catecholamines in spinal cord injured men with different injury levels, CLIN PHYSL, 20(4), 2000, pp. 304-310
Persons with spinal cord injury (SCI) are especially prone to atherogenesis
. This is partly explained by an unfavourable lipoprotein profile in these
individuals. The impairment of the sympathetic nervous system, and the fact
that SCI subjects are subject to extreme physical inactivity, may have an
influence on their lipid profile and lipoprotein(a) concentration. We made
a detailed investigation of the lipid profile as well as serum levels of ad
renaline and noradrenaline in 80 men with SCI ranging from tetraplegia to l
ow paraplegia and in 16 control subjects. The lipid profile of tetraplegics
was characterized by elevated very low-density lipoprotein cholesterol and
triglyceride levels and reduced high-density lipoprotein levels. In contra
st, paraplegics had significantly higher low-density lipoprotein and total
cholesterol levels. Tetraplegics had lower and the low-lesion paraplegics h
ad higher adrenaline and noradrenaline levels than the high-lesion parapleg
ics and the control subjects. High-lesion SCI subjects also showed an extre
me reduction in VO2max. The lipoprotein profile was dependent on the injury
level and serum catecholamine concentrations. The lower the noradrenaline
values, the lower the high-density lipoprotein cholesterol. The low-density
lipoprotein also correlated to catecholamines and particularly adrenaline
values. Despite the correlation between lipoprotein(a) and adrenaline, no s
ignificant differences in lipoprotein(a) were found within SCI individuals
as well as between SCI individuals and control subjects, indicating the pre
dominantly genetic determination of lipoprotein(a) and thus the cardiovascu
lar risk. Different serum catecholamine levels due to impairment of sympath
etic nervous system and VO2max levels were observed in SCI subjects. This w
as associated with a higher lipid risk profile for cardiovascular diseases;
however, the risk profile is dependent on the lesion level.