beta(2)-Microglobulin (beta(2)-m) is a polypeptide that is freely filt
ered and then mostly reabsorbed and degraded in the proximal renal tub
ule, beta(2)-m is a marker of glomerular filtration (GFR) in renal fai
lure, whereas urinary beta(2)-m is a marker of proximal renal tubular
dysfunction. Preeclampsia (PE) tie, de novo hypertension in pregnancy
with accompanying renal, cerebral, or liver disease or thrombocytopeni
a) often has renal involvement characterized by proteinuria, decreasin
g glomerular filtration, or renal tubular dysfunction. The aim of this
study was to determine whether serum beta(2)-m concentration or urina
ry beta(2)-m excretion were greater in women with PE than in women wit
h gestational hypertension (GH) tie, isolated de novo hypertension in
the second half of pregnancy) and normal pregnant women, Seventy-five
pregnant women (35 with RE, 22 with GH, and 18 normotensives) were stu
died prospectively. Serum creatinine and Pn-m concentrations, 24 hour
proteinuria, and fractional excretion (FE) of beta(2)-m were measured,
Preeclamptics had similar serum creatinine but higher serum beta(2)-m
(3.26 +/- 0.99 mg/L) than gestational hypertensives (2.44 +/- 0.77 mg
/L; P = 0.016), and both groups had higher serum beta(2)-m than contro
ls (1.62 +/- 0.54 mg/L; P = 0.001). FE of beta(2)-m was similar amongs
t groups (PE: 0.27%; interquartile range [IQR]: 0.20-0.86; GH: 0.21%;
IQR: 0.11-0.40; controls: 0.26%, IQR: 0.12-0.69), PE is characterized
by higher serum beta(2)-m but similar serum creatinine to GH. Because
FE beta(2)-m is similar in these groups, this implies reduced filterin
g of Pn-m in PE rather than altered tubular handling of beta(2)-m Furt
her studies are now necessary to assess whether measurement of serum P
n-m is helpful in the clinical management of the hypertensive disorder
s of pregnancy, (C) 1998 by the National Kidney Foundation, Inc.