Key result
Acquired activated protein C resistance was significantly more common in women with recurrent early (8.8%, P=0.02) and late miscarriage (8.7%, P=0.04) compared to controls (3.3%).
Why the study?
Is acquired or congenital activated protein C (APC) resistance associated with recurrent early or late miscarriage in women?
Case-Control (n=1,261)
Is acquired or congenital activated protein C (APC) resistance associated with recurrent early or late miscarriage in women?
Acquired, but not congenital, activated protein C resistance is significantly associated with both early and late recurrent miscarriage.
Answers are grounded in this paper and cite their sources.
Acquired APC resistance was associated with recurrent miscarriage; leaves open whether testing or intervention improves outcomes.
Activated protein C (APC) resistance, both in its congenital form, due to the factor V Leiden mutation, and in its acquired form, are important risk factors for systemic venous thrombosis. In view of the suspected thrombotic aetiology of some cases of recurrent miscarriage, the prevalence of APC resistance was determined among 1111 consecutive Caucasian women with a history of either recurrent early miscarriage (three or more consecutive pregnancy losses at <12 weeks gestation; n = 904) or a history of at least one late miscarriage (>12 weeks gestation; n = 207). A control group of 150 parous Caucasian women with no previous history of adverse pregnancy outcome was also studied. Acquired APC resistance was significantly more common among both women with recurrent early miscarriage (8.8%: 80/904; P = 0.02) and those with late miscarriage (8.7%: 18/207; P = 0.04) compared with controls (3.3%: 5/150). In contrast, the frequency of the factor V Leiden allele was similar among (i) women with recurrent early miscarriage (3.3%:60/1808; 58 heterozygotes and one homozygote), (ii) those with late miscarriage (3.9%:16/414; 14 heterozygotes and one homozygote) and (iii) the control group (4.0%:12/300; 12 heterozygotes). Acquired but not congenital APC resistance (due to the factor V Leiden mutation) is associated with both early and late miscarriage.
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Rai et al. (2001) conducted a case-control in Recurrent miscarriage (n=1,261). Acquired activated protein C (APC) resistance vs. Parous women with no previous history of adverse pregnancy outcome was evaluated on Prevalence of acquired activated protein C (APC) resistance (p=0.02). Acquired activated protein C resistance was significantly more common in women with recurrent early (8.8%, P=0.02) and late miscarriage (8.7%, P=0.04) compared to controls (3.3%).
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