Circulating Growth Differentiation Factor 15 Is Increased Preceding Preeclampsia Diagnosis: Implications as a Disease Biomarker

被引:27
作者
Cruickshank, Tess [1 ,2 ]
MacDonald, Teresa M. [2 ,3 ]
Walker, Susan P. [2 ,3 ]
Keenan, Emerson [2 ]
Dane, Kirsten [3 ]
Middleton, Anna [2 ,3 ]
Kyritsis, Valerie [3 ]
Myers, Jenny [4 ]
Cluver, Catherine [1 ,3 ,5 ]
Hastie, Roxanne [1 ,2 ,3 ]
Bergman, Lina [5 ,6 ,7 ,8 ]
Garcha, Damanpreet [1 ,2 ]
Cannon, Ping [1 ,2 ]
Murray, Elizabeth [1 ,2 ]
Nguyen, Tuong-Vi [1 ,2 ]
Hiscock, Richard [2 ]
Pritchard, Natasha [1 ,2 ,3 ]
Hannan, Natalie J. [1 ,2 ,3 ]
Tong, Stephen [1 ,2 ,3 ]
Kaitu'u-Lino, Tu'uhevaha J. [1 ,2 ,3 ]
机构
[1] Mercy Hosp Women, Translat Obstet Grp, Heidelberg, Vic, Australia
[2] Mercy Hosp Women, Dept Obstet & Gynaecol, Heidelberg, Vic, Australia
[3] Mercy Hosp Women, Mercy Perinatal, Heidelberg, Vic, Australia
[4] Univ Manchester, St Marys Hosp, Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
[5] Univ Stellenbosch, Tygerberg Hosp, Dept Obstet & Gynecol, Cape Town, South Africa
[6] Uppsala Univ, Dept Womens & Childrens Hlth, Uppsala, Sweden
[7] Sahlgrenska Acad Univ Gothenburg, Dept Obstet, Gothenburg, Sweden
[8] Sahlgrenska Acad Univ Gothenburg, Inst Clin Sci, Gothenburg, Sweden
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2021年 / 10卷 / 16期
基金
英国医学研究理事会;
关键词
biomarker; placental growth factor; preeclampsia; pregnancy; MACROPHAGE INHIBITORY CYTOKINE-1; CARDIOVASCULAR EVENTS; RISK; GDF15; WOMEN; SERUM;
D O I
10.1161/JAHA.120.020302
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background We investigated the biomarker potential of growth differentiation factor 15 (GDF-15), a stress response protein highly expressed in placenta, to predict preeclampsia. Methods and Results In 2 prospective cohorts (cohort 1: 960 controls, 39 women who developed preeclampsia; cohort 2: 950 controls, 41 developed preeclampsia), plasma concentrations of GDF-15 at 36 weeks' gestation were significantly increased among those who developed preeclampsia (P<0.001), area under the receiver operating characteristic curves (AUC) of 0.66 and 0.71, respectively. In cohort 2 a ratio of sFlt-1/PlGF (a clinical biomarker for preeclampsia) had a sensitivity of 61.0% at 83.2% specificity to predict those who will develop preeclampsia (AUC of 0.79). A ratio of GDF-15xsFlt-1/PlGF yielded a sensitivity of 68.3% at 83.2% specificity (AUC of 0.82). GDF-15 was consistently elevated across a number of international cohorts: levels were higher in placenta and blood from women delivering <34 weeks' gestation due to preterm preeclampsia in Melbourne, Australia; and in the blood at 26 to 32 weeks' gestation among 57 women attending the Manchester Antenatal Vascular Service (MAViS, UK) who developed preeclampsia (P=0.0002), compared with 176 controls. In the Preeclampsia Obstetric adVerse Events biobank (PROVE, South Africa), plasma GDF-15 was significantly increased in women with preeclampsia with severe features (P=0.02; n=14) compared to controls (n=14). Conclusions We conclude circulating GDF-15 is elevated among women more likely to develop preeclampsia or diagnosed with the condition. It may have value as a clinical biomarker, including the potential to improve the sensitivity of sFlt-1/PlGF ratio.
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