Literature DB >> 33775113

Subtypes of Preeclampsia: Recognition and Determining Clinical Usefulness.

James M Roberts1, Janet W Rich-Edwards2,3, Thomas F McElrath4, Lana Garmire5, Leslie Myatt6.   

Abstract

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.

Entities:  

Keywords:  epidemiology; inflammation; prediction; preeclampsia; syndrome

Mesh:

Year:  2021        PMID: 33775113      PMCID: PMC8103569          DOI: 10.1161/HYPERTENSIONAHA.120.14781

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  72 in total

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3.  Cardiovascular Disease-Related Morbidity and Mortality in Women With a History of Pregnancy Complications.

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Journal:  Circulation       Date:  2019-02-19       Impact factor: 29.690

4.  A conceptual and methodological framework for investigating etiologic heterogeneity.

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5.  Clinical Course, Associated Factors, and Blood Pressure Profile of Delayed-Onset Postpartum Preeclampsia.

Authors:  Emily K Redman; Alisse Hauspurg; Carl A Hubel; James M Roberts; Arun Jeyabalan
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Review 8.  Pre-eclampsia and risk of cardiovascular disease and cancer in later life: systematic review and meta-analysis.

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  15 in total

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Review 4.  Animal Models of Preeclampsia: Mechanistic Insights and Promising Therapeutics.

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6.  The diagnostic potential of oxidative stress biomarkers for preeclampsia: systematic review and meta-analysis.

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7.  Maternal Levels of Perfluoroalkyl Substances (PFAS) during Early Pregnancy in Relation to Preeclampsia Subtypes and Biomarkers of Preeclampsia Risk.

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10.  A Sharper Focus: Clarifying the PFAS-Preeclampsia Association by Analyzing Disease Subtypes.

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