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

被引:15
作者
Abbara, Ali [1 ]
Al-Memar, Maya [2 ]
Phylactou, Maria [1 ]
Daniels, Elisabeth [1 ]
Patel, Bijal [1 ]
Eng, Pei C. [1 ]
Nadir, Rans [1 ]
Izzi-Engbeaya, Chioma [1 ]
Clarke, Sophie A. [1 ]
Mills, Edouard G. [1 ]
Hunjan, Tia [1 ]
Pacuszka, Ewa [1 ]
Yang, Lisa [1 ]
Bech, Paul [1 ]
Tan, Tricia [1 ]
Comninos, Alexander N. [1 ]
Kelsey, Tom W. [3 ]
Kyriacou, Christopher [2 ]
Fourie, Hanine [2 ]
Bourne, Tom [2 ,4 ]
Dhillo, Waljit S. [1 ]
机构
[1] Imperial Coll London, Hammersmith Hosp, Sect Endocrinol & Investigative Med, London W12 0NN, England
[2] Queen Charlottes & Chelsea Hosp, Imperial Coll London, Tommys Natl Ctr Miscarriage Res, Du Cane Rd, London W12 0HS, England
[3] Univ St Andrews, Sch Comp Sci, St Andrews KY16 9SX, Fife, Scotland
[4] Katholieke Univ Leuven, Dept Dev & Regenerat, Leuven, Belgium
基金
英国医学研究理事会;
关键词
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;
D O I
10.1210/clinem/dgab617
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:E71 / E83
页数:13
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