R. Ramseygoldman et al., PREGNANCY OUTCOME AND ANTICARDIOLIPIN ANTIBODY IN WOMEN WITH SYSTEMICLUPUS-ERYTHEMATOSUS, American journal of epidemiology, 138(12), 1993, pp. 1057-1069
Pregnancies in women with systemic lupus erythematosus are recognized
to result in excessive fetal morbidity and mortality. Maternal autoant
ibody status may explain some of these problems. Anti-cardiolipin anti
body has been associated with recurrent pregnancy losses in some women
with lupus, but the risk of these losses has not been defined. At the
University of Pittsburgh between January 1, 1979, and December 31, 19
89, an unmatched case-control study design was used to determine wheth
er patients with lupus and anti-cardiolipin antibody (81 cases) were a
t increased risk for adverse pregnancy outcomes in comparison with lup
us patients without the antibody (174 controls). Cases had 98 of 192 (
51%) pregnancies with an adverse outcome, while controls had 212 of 49
4 (43%). The odds ratio for having any adverse pregnancy outcome was 1
.40 (95% confidence interval (Cl) 0.98-1.98). When pregnancies were cl
assified according to specific adverse outcome types, the frequency of
late miscarriages (14-20 weeks gestation) in cases and controls was 8
% and 3%, respectively. The odds ratio for late miscarriage was 2.94 (
95% Cl 1.31-6.60). When pregnancies were stratified by birth number an
d by occurrence of pregnancy before or after diagnosis, the increased
frequency of late miscarriages in cases was noted only in the first pr
egnancy when the pregnancy occurred before recognized disease. Preterm
births (before 38 weeks gestation) were increased in cases compared w
ith controls in pregnancies that occurred after diagnosis for second a
nd third pregnancies. If a case had one previous adverse outcome, the
odds ratio for another adverse outcome was 3.00 (95% Cl 1.62-5.57). If
a case had two previous adverse outcomes, the odds ratio for a third
adverse pregnancy outcome was 4.14 (95% Cl 1.62-10.58). Thus, a previo
us adverse pregnancy outcome was the most important risk factor for an
adverse outcome in a subsequent pregnancy.