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Lipid Metabolism Affects Fetal Fraction and Screen Failures in Non-invasive Prenatal Testing

Objective: To assess the association between lipid metabolism and fetal fraction, which is a critical factor in ensuring a highly accurate non-invasive prenatal testing (NIPT), and on the rate of screen failures or “no calls” in NIPT. Methods: A total of 4,514 pregnant women at 12–26 weeks of gestat...

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Autores principales: Cao, Jun, Qiao, Longwei, Jin, Jieyu, Zhang, Sheng, Chen, Ping, Tang, Haoyu, Yu, Zheng, Shi, Jingye, Wang, Ting, Liang, Yuting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790535/
https://www.ncbi.nlm.nih.gov/pubmed/35096900
http://dx.doi.org/10.3389/fmed.2021.811385
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author Cao, Jun
Qiao, Longwei
Jin, Jieyu
Zhang, Sheng
Chen, Ping
Tang, Haoyu
Yu, Zheng
Shi, Jingye
Wang, Ting
Liang, Yuting
author_facet Cao, Jun
Qiao, Longwei
Jin, Jieyu
Zhang, Sheng
Chen, Ping
Tang, Haoyu
Yu, Zheng
Shi, Jingye
Wang, Ting
Liang, Yuting
author_sort Cao, Jun
collection PubMed
description Objective: To assess the association between lipid metabolism and fetal fraction, which is a critical factor in ensuring a highly accurate non-invasive prenatal testing (NIPT), and on the rate of screen failures or “no calls” in NIPT. Methods: A total of 4,514 pregnant women at 12–26 weeks of gestation underwent NIPT sequencing and serum lipid measurements. Univariate analysis and multivariate regression models were used to evaluate the associations of serum lipid concentrations with the fetal fraction and the rate of screen failures. Results: The fetal fraction decreased with increased low-density lipoprotein cholesterol and triglyceride (TG) levels, which were significant factors (standardized coefficient: −0.11). Conversely, high-density lipoprotein cholesterol and the interval between the two tests were positively correlated with the fetal fraction. The median fetal fraction was 10.88% (interquartile range, 8.28–13.89%) and this decreased with TG from 11.56% at ≤1.10 mmol/L to 9.51% at >2.30 mmol/L. Meanwhile, multivariate logistic regression analysis revealed that increased TG levels were independently associated with the risk of screen failures. The rate of screen failures showed an increase with TG levels from 1.20% at ≤1.70 mmol/L to 2.41% at >2.30 mmol/L. Conclusions: The fetal fraction and the rate of screen failures in NIPT are affected by TG levels. Meanwhile, in pregnant women with high TG levels, delaying the time between NIPT blood collections can significantly increase the fetal fraction.
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spelling pubmed-87905352022-01-27 Lipid Metabolism Affects Fetal Fraction and Screen Failures in Non-invasive Prenatal Testing Cao, Jun Qiao, Longwei Jin, Jieyu Zhang, Sheng Chen, Ping Tang, Haoyu Yu, Zheng Shi, Jingye Wang, Ting Liang, Yuting Front Med (Lausanne) Medicine Objective: To assess the association between lipid metabolism and fetal fraction, which is a critical factor in ensuring a highly accurate non-invasive prenatal testing (NIPT), and on the rate of screen failures or “no calls” in NIPT. Methods: A total of 4,514 pregnant women at 12–26 weeks of gestation underwent NIPT sequencing and serum lipid measurements. Univariate analysis and multivariate regression models were used to evaluate the associations of serum lipid concentrations with the fetal fraction and the rate of screen failures. Results: The fetal fraction decreased with increased low-density lipoprotein cholesterol and triglyceride (TG) levels, which were significant factors (standardized coefficient: −0.11). Conversely, high-density lipoprotein cholesterol and the interval between the two tests were positively correlated with the fetal fraction. The median fetal fraction was 10.88% (interquartile range, 8.28–13.89%) and this decreased with TG from 11.56% at ≤1.10 mmol/L to 9.51% at >2.30 mmol/L. Meanwhile, multivariate logistic regression analysis revealed that increased TG levels were independently associated with the risk of screen failures. The rate of screen failures showed an increase with TG levels from 1.20% at ≤1.70 mmol/L to 2.41% at >2.30 mmol/L. Conclusions: The fetal fraction and the rate of screen failures in NIPT are affected by TG levels. Meanwhile, in pregnant women with high TG levels, delaying the time between NIPT blood collections can significantly increase the fetal fraction. Frontiers Media S.A. 2022-01-12 /pmc/articles/PMC8790535/ /pubmed/35096900 http://dx.doi.org/10.3389/fmed.2021.811385 Text en Copyright © 2022 Cao, Qiao, Jin, Zhang, Chen, Tang, Yu, Shi, Wang and Liang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Cao, Jun
Qiao, Longwei
Jin, Jieyu
Zhang, Sheng
Chen, Ping
Tang, Haoyu
Yu, Zheng
Shi, Jingye
Wang, Ting
Liang, Yuting
Lipid Metabolism Affects Fetal Fraction and Screen Failures in Non-invasive Prenatal Testing
title Lipid Metabolism Affects Fetal Fraction and Screen Failures in Non-invasive Prenatal Testing
title_full Lipid Metabolism Affects Fetal Fraction and Screen Failures in Non-invasive Prenatal Testing
title_fullStr Lipid Metabolism Affects Fetal Fraction and Screen Failures in Non-invasive Prenatal Testing
title_full_unstemmed Lipid Metabolism Affects Fetal Fraction and Screen Failures in Non-invasive Prenatal Testing
title_short Lipid Metabolism Affects Fetal Fraction and Screen Failures in Non-invasive Prenatal Testing
title_sort lipid metabolism affects fetal fraction and screen failures in non-invasive prenatal testing
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790535/
https://www.ncbi.nlm.nih.gov/pubmed/35096900
http://dx.doi.org/10.3389/fmed.2021.811385
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