Background Patients treated with lipid apheresis already suffer from famili
al hypercholesterolemia and severe coronary heart disease: any additional r
isk factor is dangerous for these patients. Hyperhomocysteinemia has been r
ecognized as an independent risk factor for atherosclerotic disease. We che
cked the frequency of hyperhomocysteinemia in lipid apheresis patients and
measured the effect of a vitamin therapy.
Materials and Methods Sixteen heterozygous patients (10 males, 6 females) w
ere studied, who were being treated by three different apheresis procedures
. Homocysteine was measured using an enzyme conversion immunoassay. Cystath
ionine and methylmalonic acid were assessed by gas chromatography/mass spec
trometry. Serum levels of folic acid, vitamin B12, and vitamin B6 were also
determined. The patients received a vitamin therapy (3 mg folate, 60 mug c
yanocobalamine, 10 mg pyridoxine hydrochloride daily) for 12 weeks.
Results In 9 out of 16 patients, plasma homocysteine levels were found to b
e elevated (> 12 mu mol L-1). Cystathionine concentrations were also increa
sed, especially in those patients with elevated homocysteine. Methylmalonic
acid levels were not elevated. Serum folic acid, vitamin B6, and vitamin B
12 concentrations were initially in the normal range and not correlated to
plasma homocysteine. The vitamin therapy reduced the plasma homocysteine co
ncentrations in all patients significantly by 33%. Among those patients wit
h elevated homocysteine levels, the optimal range < 12 <mu>mol L-1 for homo
cysteine was rarely reached.
Conclusions In patients treated with lipid apheresis, a hyperhomocysteinemi
a can be frequently seen. The constellation of both elevated homocysteine a
nd cystathionine levels points to the existence of tissue vitamin deficienc
ies, folate and vitamin B-6, which were improved by vitamin supplements. Be
cause methylmalonic acid was mostly normal, a vitamin B-12 deficiency was n
ot proven.