Seeking the mechanism(s) of action for corticosteroids in HELLP syndrome: SMASH study

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• 作者：Kedra Wallace ; PhD^a ; James N. Martin Jr ; MD^a ; Kiran Tam Tam ; MD^a ; Gerd Wallukat ; PhD^b ; Ralf Dechend ; PhD^b ; Babbette Lamarca ; PhD^a ; Michelle Y. Owens ; MD^a
• 关键词：HELLP (hemolysis ; elevated liver enzymes ; and low platelet count) syndrome ; inflammatory cytokines ; severe preeclampsia ; soluble endoglin ; soluble fms-like tyrosine kinase-1
• 刊名：American Journal of Obstetrics and Gynecology
• 出版年：2013
• 出版时间：May, 2013
• 年：2013
• 卷：208
• 期：5
• 页码：380.e1-380.e8
• 全文大小：1045 K

文摘

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Introduction

Administration of dexamethasone to the hemolysis, elevated liver enzymes, and low platelet count (HELLP) syndrome patients (10 mg intravenously [IV] every 12 hours) shortens the disease course and reduces maternal morbidity in patients treated at the University of Mississippi Medical Center (UMMC), associated with this severe form of preeclampsia. However, the pathophysiological mechanisms involved with this intervention remain unclear.

Objective

We sought to investigate the potential role of IV dexamethasone to restore the imbalance among antiangiogenic and inflammatory factors known to be significantly elevated in women with HELLP syndrome.

Study Design

This was a single-center prospective study of women diagnosed with HELLP syndrome who were treated for IV dexamethasone at UMMC. Blood was drawn prior to dexamethasone administration and again 12 and 24 hours after the initial dexamethasone administration. Enzyme-linked immune assays were used to measure circulating inflammatory cytokines and antiangiogenic factors. A repeated-measures analysis of variance was used to analyze the data collected before, after, and during dexamethasone administration.

Results

Seventeen women with HELLP syndrome were enrolled in this study. Dexamethasone significantly decreased evidence of hemolysis (P = .002) and liver enzymes (P = .003), and significantly increased platelets (P = .0001) within 24 hours of administration. Circulating interleukin-6 levels after 24 hours were decreased (P < .001); soluble fms-like tyrosine kinase-1 and soluble endoglin were also significantly decreased by 24 hours after dexamethasone administration (P < .002 and P < .004, respectively). There were no significant differences in circulating levels of placental growth factor (P = .886) due to dexamethasone administration. Angiotensin II receptor autoantibody levels were unchanged by dexamethasone administration.

Conclusion

We conclude that 1 important mechanism of dexamethasone administration is to blunt the release of both antiangiogenic and inflammatory factors suggested to play role in the pathophysiology of HELLP syndrome.