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Published on: January 26, 2024
Serum Fatty Acid Binding Protein 4 (FABP4) Predicts Pre-eclampsia in Women With Type 1 Diabetes
Amy C Wotherspoon1, Ian S Young1, David R McCance2
1Centre for Public Health, Queen's University Belfast, Belfast, U.K.
Insights
Fatty acid binding protein 4 (FABP4) levels were higher in pregnant women with type 1 diabetes who developed pre-eclampsia. Elevated FABP4 in the second trimester independently predicted pre-eclampsia risk.
Area of Science:
- Endocrinology
- Obstetrics
- Metabolic Disorders
Background:
- Pre-eclampsia is a serious pregnancy complication.
- Type 1 diabetes increases pre-eclampsia risk.
- Novel biomarkers are needed for early detection.
Purpose of the Study:
- To investigate the association between fatty acid binding protein 4 (FABP4) and pre-eclampsia risk.
- To evaluate FABP4 as a potential biomarker in women with type 1 diabetes.
Main Methods:
- Serum FABP4 levels measured in 710 women with type 1 diabetes during early and second trimesters.
- Comparison of FABP4 levels between women who developed pre-eclampsia and those who did not.
- Statistical analysis to determine independent prediction of pre-eclampsia.
Main Results:
- FABP4 levels were significantly elevated in early and second trimesters in women who developed pre-eclampsia.
- Elevated second-trimester FABP4 was independently associated with pre-eclampsia (OR 2.87).
- FABP4 improved risk prediction models for pre-eclampsia.
Conclusions:
- Increased second-trimester FABP4 independently predicts pre-eclampsia in women with type 1 diabetes.
- FABP4 demonstrates potential as a novel biomarker for pre-eclampsia prediction.
- Early identification of pre-eclampsia risk can guide management.
Objective:
To examine the association between fatty acid binding protein 4 (FABP4) and pre-eclampsia risk in women with type 1 diabetes.
Research Design And Methods:
Serum FABP4 was measured in 710 women from the Diabetes and Pre-eclampsia Intervention Trial (DAPIT) in early pregnancy and in the second trimester (median 14 and 26 weeks' gestation, respectively).
Results:
FABP4 was significantly elevated in early pregnancy (geometric mean 15.8 ng/mL [interquartile range 11.6-21.4] vs. 12.7 ng/mL [interquartile range 9.6-17]; P < 0.001) and the second trimester (18.8 ng/mL [interquartile range 13.6-25.8] vs. 14.6 ng/mL [interquartile range 10.8-19.7]; P < 0.001) in women in whom pre-eclampsia later developed. Elevated second-trimester FABP4 level was independently associated with pre-eclampsia (odds ratio 2.87 [95% CI 1.24-6.68], P = 0.03). The addition of FABP4 to established risk factors significantly improved net reclassification improvement at both time points and integrated discrimination improvement in the second trimester.
Conclusions:
Increased second-trimester FABP4 independently predicted pre-eclampsia and significantly improved reclassification and discrimination. FABP4 shows potential as a novel biomarker for pre-eclampsia prediction in women with type 1 diabetes.
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