OBJECTIVE - Low birth weight has been associated with hyperlipidemia, hyper
tension, diabetes, and coronary heart disease in adult life, but the precis
e mechanism is debated. The endothelium is thought to play a pivotal role i
n each of the above conditions with abnormalities being detectable before t
he development of overt disease. To investigate the possibility that endoth
elium has a role in mediating the excessive risk of adult vascular disease
associated with low birth weight, endothelial function was assessed in youn
g healthy adults who were either of low or normal birth weight at term.
RESEARCH DESIGN AND METHODS - Twelve low birth weight (2.2 +/- 0.05 kg mean
+/- SEM) subjects (six men/six women; age 28 +/- 0.2 years) and twelve age
- and sex matched normal birth weight (3.3 +/- 0.07 kg) control subjects we
re studied. The L-arginine-nitric oxide pathway was assessed in the forearm
vascular bed by using venous occlusion plethysmography during intra-arteri
al brachial infusion of acetylcholine, sodium nitroprusside, norepinephrine
, and N-G-monomethyl-L-arginine (L-NMMA). Von Willebrand factor, a noninvas
ive marker of endothelial dysfunction, was also measured. Comparisons were
made using Student's t rests.
RESULTS - Von Willebrand factor was significantly elevated in low birth wei
ght compared with normal birth weight subjects (136.9 +/- 12.7 vs. 95.6 +/-
9.5%; P = 0.016). The groups did not differ in the responses to acetylchol
ine (P = 0.76), sodium nitroprusside (P = 0.84), nor epinephrine (P = 0.21)
, or L-NMMA (P = 0.35).
CONCLUSIONS - The finding of elevated von Willebrand factor in low birth Me
ight subjects is suggestive of endothelial cell injury but does not appear
to be associated with dysfunction of the L-arginine-nitric oxide pathway.