Key result
Protein Z deficiency (< 1 mg/L) was significantly associated with early fetal loss between the 10th and 15th week of gestation (OR 6.7; 95% CI 3.1-14.8; P<10^-3).
Why the study?
Is protein Z deficiency associated with unexplained early fetal loss in nonthrombotic, nonthrombophilic women?
Observational (n=200)
Is protein Z deficiency associated with unexplained early fetal loss in nonthrombotic, nonthrombophilic women?
Odds Ratio: 6.7 (95% CI 3.1–14.8)
p-value: p=< 10(-3)
Protein Z deficiency is significantly associated with unexplained early fetal loss, suggesting it may induce severe placental insufficiency.
The protein Z-protein Z-dependent inhibitor complex is a factor Xa inhibitor. Protein Z deficiencies have recently been described in patients with ischemic stroke. As placenta infarction leads to poor pregnancy outcome, we studied protein Z plasma concentrations in nonthrombotic, nonthrombophilic consecutive patients with unexplained pregnancy wastage. A significant amount of protein Z deficiencies was only found in the early fetal loss group (< 1 mg/L; 44 of 200, P < 10(-4)) and mainly in the case of fetal demise between the beginning of the 10th and the end of the 15th week of gestation (odds ratio, 6.7 [3.1-14.8], P < 10(-3)). These deficiencies were not due to partial vitamin K1 deficiency, and at least some of them were constitutional ones. In women, protein Z deficiency may induce an enhanced risk of severe placental insufficiency soon after the connection of maternal and fetal circulations.
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Gris et al. (2002) conducted an observational in Unexplained pregnancy wastage (n=200). Protein Z deficiency vs. Normal protein Z levels was evaluated on Fetal demise between the 10th and 15th week of gestation (OR 6.7, 95% CI 3.1-14.8, p=< 10(-3)). Protein Z deficiency (< 1 mg/L) was significantly associated with early fetal loss between the 10th and 15th week of gestation (OR 6.7; 95% CI 3.1-14.8; P<10^-3).
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