Changes in Circulating Kisspeptin Levels During Each Trimester in Women With Antenatal Complications

Author:

Abbara Ali1ORCID,Al-Memar Maya2,Phylactou Maria1ORCID,Daniels Elisabeth1,Patel Bijal1,Eng Pei C1,Nadir Rans1,Izzi-Engbeaya Chioma1ORCID,Clarke Sophie A1,Mills Edouard G1,Hunjan Tia1,Pacuszka Ewa1,Yang Lisa1,Bech Paul1,Tan Tricia1,Comninos Alexander N1ORCID,Kelsey Tom W3,Kyriacou Christopher2,Fourie Hanine2,Bourne Tom24ORCID,Dhillo Waljit S1ORCID

Affiliation:

1. Section of Endocrinology and Investigative Medicine, Imperial College London, Hammersmith Hospital, London, W12, UK

2. Tommy’s National Centre for Miscarriage Research, Queen Charlotte’s and Chelsea Hospital, Imperial College London, Du Cane Road, London, UK

3. School of Computer Science, University of St Andrews, St Andrews, UK

4. KU Leuven, Department of Development and Regeneration, Leuven, Belgium

Abstract

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 3 trimesters in women with antenatal complications. Objective We aimed to assess whether kisspeptin levels are altered in women with antenatal complications. Methods Women with antenatal complications (n = 105) and those with uncomplicated pregnancies (n = 265) underwent serial ultrasound scans and blood sampling at the Early Pregnancy Assessment Unit at Hammersmith Hospital, UK, at least once during each trimester (March 2014 to March 2017). The women with antenatal complications (HDP [n = 32], FGR [n = 17], GDM [n = 35], PTB [n = 11], and multiple complications [n=10]) provided 373 blood samples and the controls provided 930 samples. Differences in circulating kisspeptin levels were assessed. 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 with 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.

Funder

NIHR Clinical Scientist Award

Tommy’s National Centre for Miscarriage Research

NIHR Academic Clinical Lectureship

Imperial College-BRC IPPRF Fellowship

MRC clinical training fellowship

NIHR Biomedical Research Centre

NIHR Professorship

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference62 articles.

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