Why the study?
Are anticardiolipin antibody and anti-cardiolipin beta-2-glycoprotein I-antibody associated with recurrent fetal miscarriage?
Are anticardiolipin antibody and anti-cardiolipin beta-2-glycoprotein I-antibody associated with recurrent fetal miscarriage?
Anticardiolipin antibodies are associated with recurrent fetal miscarriage, while anti-cardiolipin beta-2-glycoprotein I antibodies are specifically linked to second or third-trimester intrauterine fetal death.
Supports aCL-Ab testing in recurrent miscarriage; leaves open causal role and clinical utility of aCL-beta-2-GP I-Ab screening.
To elucidate the association between anticardiolipin antibody (aCL-Ab) or anti-cardiolipin beta-2-glycoprotein I-antibody (aCL-beta-2-GP I-Ab) and recurrent fetal miscarriage, the positive rates of aCL-Ab were assessed in 667 patients with recurrent fetal miscarriages and those of aCL-beta-2-GP I-Ab were assessed in 208 patients. The rates were then compared with the control group. The positive rate of aCL-Ab in the patients group (17.4%) was significantly higher than that in the control group (4.0%). The rate of aCL-Ab was especially high in patients who had experienced two or more fetal miscarriages including at least one or more intrauterine fetal deaths during the second or third trimester (41.3%). The positive rate of aCL-beta-2-GP I-Ab in patients with recurrent fetal miscarriage (3/208 cases, 1.4%) was not significantly different from the control group (0/100 cases, 0%). However, the rate of aCL-beta-2-GP I-Ab was significantly higher in patients who had experienced two or more fetal miscarriages including at least one or more intrauterine fetal deaths during the second or third trimester (8.3%) compared with the control group. In conclusion, the implication of aCL-Ab in the genesis of recurrent fetal miscarriage was confirmed. It was suggested that aCL-beta-2-GP I-Ab was associated with the generation of intrauterine fetal death, although it had little association with the genesis of recurrent fetal miscarriage during the first trimester.
No takes yet. Share an insight, caveat, or question.
Higashino et al. (1998) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: