Key result
Animal models mimic select preeclampsia features, but none fully captures the human disease phenotype.
Why the study?
Preeclampsia is heterogeneous and no single experimental model fully recapitulates the human disease, making mechanistic evaluation essential for developing effective therapies.
Systematic Review (n=609)
Current animal models of preeclampsia reproduce distinct features of the disease but fail to fully recapitulate human heterogeneity, highlighting the need for mechanism-driven model selection and multi-hit approaches.
Requires mechanism-specific interpretation of preeclampsia animal data before clinical translation; extends evidence by advocating multi-hit models incorporating comorbidities.
CLINICAL PROBLEM: Preeclampsia is a heterogeneous hypertensive disorder of pregnancy characterized by new-onset hypertension and end-organ dysfunction, affecting 5% to 10% of pregnancies globally. It is associated with significant maternal and fetal morbidity and mortality, and delivery remains the only definitive treatment. Understanding the underlying mechanisms is essential for the development of effective therapies. RECOMMENDATIONS: Given the heterogeneity of preeclampsia and the absence of a single experimental model that fully recapitulates the human disease, the purpose of this review is to evaluate current animal models of preeclampsia according to the pathophysiological mechanisms they represent. We discuss the strengths, limitations, and translational relevance of these models, identify gaps in the existing experimental framework, and highlight opportunities for future model development and therapeutic discovery. SUMMARY: Current models reproduce distinct features of preeclampsia, including abnormal placentation, placental ischemia, angiogenic imbalance, endothelial dysfunction, immune activation, and metabolic dysregulation. Despite mechanistic insights, translational success has been limited. Future progress will depend on mechanism-driven model selections, development of models that better capture early placentation defects and disease heterogeneity, multi-hit approaches, including the incorporation of maternal comorbidities, and integration of human-relevant experimental systems to improve clinical translation.
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Reckelhoff et al. (2026) conducted a systematic review in Preeclampsia (n=609). Experimental animal models was evaluated. Current experimental animal models reproduce distinct features of preeclampsia, but no single model fully recapitulates the human disease, highlighting the need for mechanism-driven model selection.
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