Changes in circulating kisspeptin levels during each trimester in women with antenatal complications
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Published version
Author(s)
Type
Journal Article
Abstract
Context
Antenatal complications such as hypertensive disorders of pregnancy (HDP), fetal growth restriction (FGR), gestational diabetes (GDM), and preterm birth (PTB) are associated with placental dysfunction. Kisspeptin has emerged as a putative marker of placental function, but limited data exist describing circulating kisspeptin levels across all three trimesters in women with antenatal complications.
Objective
To assess whether kisspeptin levels are altered in women with antenatal complications.
Design
Women with antenatal complications (n=105) and those with uncomplicated pregnancies (n=265) underwent serial ultrasound scans and blood-sampling at least once during each trimester (March 2014 to March 2017).
Setting
Early Pregnancy Assessment Unit at Hammersmith Hospital, UK.
Participants
Women with antenatal complications: HDP (n=32), FGR (n=17), GDM (n=35) and PTB (n=11), and 10 women with multiple complications, provided 373 blood samples, and a further 265 controls provided 930 samples.
Main outcome
Differences in circulating kisspeptin levels.
Results
Third trimester kisspeptin levels were higher than controls in HDP but lower in FGR. The odds of HDP adjusted for gestational age, maternal age, ethnicity, BMI, smoking and parity were increased by 30% (95%CI 16-47%; p<0.0001), and of FGR were reduced by 28% (95%CI 4-46%; p=0.025), for every 1 nmol/L increase in plasma kisspeptin. Multiple of gestation-specific median values of kisspeptin were higher in pregnancies affected by PTB (p=0.014), and lower in those affected by GDM (p=0.020), but not significantly on multivariable analysis.
Conclusion
We delineate changes in circulating kisspeptin levels at different trimesters and evaluate the potential of kisspeptin as a biomarker for antenatal complications.
Antenatal complications such as hypertensive disorders of pregnancy (HDP), fetal growth restriction (FGR), gestational diabetes (GDM), and preterm birth (PTB) are associated with placental dysfunction. Kisspeptin has emerged as a putative marker of placental function, but limited data exist describing circulating kisspeptin levels across all three trimesters in women with antenatal complications.
Objective
To assess whether kisspeptin levels are altered in women with antenatal complications.
Design
Women with antenatal complications (n=105) and those with uncomplicated pregnancies (n=265) underwent serial ultrasound scans and blood-sampling at least once during each trimester (March 2014 to March 2017).
Setting
Early Pregnancy Assessment Unit at Hammersmith Hospital, UK.
Participants
Women with antenatal complications: HDP (n=32), FGR (n=17), GDM (n=35) and PTB (n=11), and 10 women with multiple complications, provided 373 blood samples, and a further 265 controls provided 930 samples.
Main outcome
Differences in circulating kisspeptin levels.
Results
Third trimester kisspeptin levels were higher than controls in HDP but lower in FGR. The odds of HDP adjusted for gestational age, maternal age, ethnicity, BMI, smoking and parity were increased by 30% (95%CI 16-47%; p<0.0001), and of FGR were reduced by 28% (95%CI 4-46%; p=0.025), for every 1 nmol/L increase in plasma kisspeptin. Multiple of gestation-specific median values of kisspeptin were higher in pregnancies affected by PTB (p=0.014), and lower in those affected by GDM (p=0.020), but not significantly on multivariable analysis.
Conclusion
We delineate changes in circulating kisspeptin levels at different trimesters and evaluate the potential of kisspeptin as a biomarker for antenatal complications.
Date Issued
2022-01
Date Acceptance
2021-08-17
Citation
Journal of Clinical Endocrinology and Metabolism, 2022, 107 (1), pp.e71-e83
ISSN
0021-972X
Publisher
Endocrine Society
Start Page
e71
End Page
e83
Journal / Book Title
Journal of Clinical Endocrinology and Metabolism
Volume
107
Issue
1
Copyright Statement
© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society.
This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
Sponsor
National Institute for Health Research
Medical Research Council
Medical Research Council (MRC)
Identifier
https://academic.oup.com/jcem/advance-article/doi/10.1210/clinem/dgab617/6357057
Grant Number
CS-2018-18-ST2-002
MR/T006242/1
MR/T006242/1
Subjects
Science & Technology
Life Sciences & Biomedicine
Endocrinology & Metabolism
fetal growth restriction (FGR)
intrauterine growth restriction (IUGR)
hypertensive diseases of pregnancy (HDP)
gestational diabetes (GDM)
preterm birth (PTB)
kisspeptin
GESTATIONAL-AGE INFANTS
PLACENTAL EXPRESSION
GROWTH RESTRICTION
PLASMA KISSPEPTIN
FETAL-GROWTH
PREGNANCY
PREECLAMPSIA
METASTIN
WEIGHT
KISS-1
fetal growth restriction (FGR)
gestational diabetes (GDM)
hypertensive diseases of pregnancy (HDP)
intrauterine growth restriction (IUGR)
kisspeptin
preterm birth (PTB)
Endocrinology & Metabolism
1103 Clinical Sciences
1114 Paediatrics and Reproductive Medicine
Publication Status
Published
Date Publish Online
2021-08-24