Related Experiment Video
Updated: Jul 12, 2026

Disruption of the Mouse Blood-Brain Barrier by Small Extracellular Vesicles from Hypoxic Human Placentas
Published on: January 26, 2024
Does Low-dose Aspirin prevent preeclampsia or merely delay it?
Avinash Kavi1, Shivaprasad S Goudar1, Mrityunjay C Metgud1
1Women's and Children's Health Research Unit, Jawaharlal Nehru Medical College, KLE Academy of Higher Education and Research, Belagavi, India.
Low-dose aspirin (LDA) modestly reduces preeclampsia rates. However, LDA may delay early-onset preeclampsia (EOPE) before 34 weeks, a critical outcome for maternal and infant health.
Area of Science:
- Obstetrics and Gynecology
- Perinatal Medicine
- Pharmacology in Pregnancy
Background:
- Low-dose aspirin (LDA) is widely used for preventing preeclampsia.
- Current evidence shows a modest overall reduction in preeclampsia rates with LDA.
Purpose of the Study:
- To investigate the specific impact of LDA on early-onset preeclampsia (EOPE).
- To explore whether different phenotypes of preeclampsia respond differently to aspirin therapy.
Main Methods:
- Analysis of clinical data on preeclampsia incidence and timing.
- Comparative assessment of LDA's effect on early-onset versus late-onset preeclampsia.
Main Results:
- LDA's primary benefit appears to be delaying the onset of preeclampsia before 34 weeks gestation.
- This suggests distinct pathophysiological pathways for early-onset and term preeclampsia, with differential responses to aspirin.
Conclusions:
- LDA may be particularly effective in preventing early-onset preeclampsia (EOPE).
- Preventing EOPE, which causes significant maternal and neonatal morbidity/mortality, offers substantial long-term benefits.
- Targeted use of LDA may be crucial for mitigating the most severe pregnancy complications.
Related Concept Videos
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Adrenergic Antagonists: ɑ and β-Receptor Blockers
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...
Atherosclerosis III: Management
