Subtypes of Preeclampsia: Recognition and Determining Clinical Usefulness

被引:186
作者
Roberts, James M. [1 ]
Rich-Edwards, Janet W. [2 ,3 ,4 ]
McElrath, Thomas F. [5 ,6 ]
Garmire, Lana [7 ]
Myatt, Leslie [8 ]
机构
[1] Univ Pittsburgh, Magee Womens Res Inst, Dept Obstet Gynecol & Reprod Sci, Epidemiol & Clin & Translat Res, 10 Georgian Pl, Pittsburgh, PA 15215 USA
[2] Harvard Univ, Dept Epidemiol, Harvard TH Chan Sch Publ Hlth, Boston, MA USA
[3] Brigham & Womens Hosp, Dept Epidemiol, Harvard TH Chan Sch Publ Hlth, Boston, MA USA
[4] Brigham & Womens Hosp, Dept Med, Div Womens Hlth, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Div Maternal Fetal Med, Boston, MA USA
[6] Harvard Med Sch, Boston, MA 02115 USA
[7] Univ Michigan, Med Sch, Dept Computat Med & Bioinformat, Ann Arbor, MI USA
[8] Oregon Hlth & Sci Univ, Dept Obstet & Gynecol, Moore Inst Nutr & Wellness, Portland, OR 97201 USA
关键词
epidemiology; inflammation; prediction; preeclampsia; syndrome; MATERNAL CARDIOVASCULAR-DISEASE; LOW-DOSE ASPIRIN; GENE-EXPRESSION; PREGNANT-WOMEN; CORPUS LUTEAL; RISK; HYPERTENSION; PREDICTION; COMPLICATIONS; OUTCOMES;
D O I
10.1161/HYPERTENSIONAHA.120.14781
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The concept that preeclampsia is a multisystemic syndrome is appreciated in both research and clinical care. Our understanding of pathophysiology recognizes the role of inflammation, oxidative and endoplasm reticulum stress, and angiogenic dysfunction. Yet, we have not progressed greatly toward clinically useful prediction nor had substantial success in prevention or treatment. One possibility is that the maternal syndrome may be reached through different pathophysiological pathways, that is, subtypes of preeclampsia, that in their specificity yield more clinical utility. For example, early and late onset preeclampsia are increasingly acknowledged as different pathophysiological processes leading to a common presentation. Other subtypes of preeclampsia are supported by disparate clinical outcomes, long-range prognosis, organ systems involved, and risk factors. These insights have been supplemented by discovery-driven methods, which cluster preeclampsia cases into groups indicating different pathophysiologies. In this presentation, we review likely subtypes based on current knowledge and suggest others. We present a consideration of the requirements for a clinically meaningful preeclampsia subtype. A useful subtype should (1) identify a specific pathophysiological pathway or (2) specifically indicate maternal or fetal outcome, (3) be recognizable in a clinically useful time frame, and (4) these results should be reproducible and generalizable (but at varying frequency) including in low resource settings. We recommend that the default consideration be that preeclampsia includes several subtypes rather than trying to force all cases into a single pathophysiological pathway. The recognition of subtypes and deciphering their different pathophysiologies will provide specific targets for prevention, prediction, and treatment directing personalized care.
引用
收藏
页码:1430 / 1441
页数:12
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