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Association of AAT/ SERPINA1 PI*Z Variant with Gestational Duration and Prevention of Premature Birth in Knockout Mice by AAT-Supplementation
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Abstract
About 10% of pregnancies end prematurely before 37 weeks, without effective prevention therapies. Previously, we identified rare damaging variants in
SERPINA1
encoding Alpha-1-antitrypsin (AAT) in families with recurrent spontaneous preterm births (SPTB) and detected decreased protein and mRNA levels of AAT/
SERPINA1
from placentas in SPTB. Here, we investigated genetic associations between
SERPINA1
variants and gestational duration and evaluated AAT supplementation as a therapeutic intervention in a mouse model of preterm birth.
SERPINA1
Pi*Z variant (rs28929474-T) was associated with gestational duration (
P
< 5×10
-8
) in European-ancestry mothers with preterm and term deliveries. We detected a nine-day decrease in gestational duration and a fourfold Odds for preterm birth vs. term birth in Pi*Z homozygotes (Pi*ZZ), compared to other genotypes. In transgenic mice without endogenous AAT, exogenous Prolastina
®
treatment inhibited LPS-induced preterm births (
P
< 0.05). Supplemented AAT was preferentially deposited in the placenta. Our findings support AAT’s protective role in SPTB and highlight its therapeutic potential, particularly in
SERPINA1
Pi*ZZ genotype carriers.
Title: Association of AAT/
SERPINA1
PI*Z Variant with Gestational Duration and Prevention of Premature Birth in Knockout Mice by AAT-Supplementation
Description:
Abstract
About 10% of pregnancies end prematurely before 37 weeks, without effective prevention therapies.
Previously, we identified rare damaging variants in
SERPINA1
encoding Alpha-1-antitrypsin (AAT) in families with recurrent spontaneous preterm births (SPTB) and detected decreased protein and mRNA levels of AAT/
SERPINA1
from placentas in SPTB.
Here, we investigated genetic associations between
SERPINA1
variants and gestational duration and evaluated AAT supplementation as a therapeutic intervention in a mouse model of preterm birth.
SERPINA1
Pi*Z variant (rs28929474-T) was associated with gestational duration (
P
< 5×10
-8
) in European-ancestry mothers with preterm and term deliveries.
We detected a nine-day decrease in gestational duration and a fourfold Odds for preterm birth vs.
term birth in Pi*Z homozygotes (Pi*ZZ), compared to other genotypes.
In transgenic mice without endogenous AAT, exogenous Prolastina
®
treatment inhibited LPS-induced preterm births (
P
< 0.
05).
Supplemented AAT was preferentially deposited in the placenta.
Our findings support AAT’s protective role in SPTB and highlight its therapeutic potential, particularly in
SERPINA1
Pi*ZZ genotype carriers.
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