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Real-time Analyses of Retinol Transport by the Membrane Receptor of Plasma Retinol Binding Protein
Published on: January 28, 2013
Retinol-binding protein 4 and insulin resistance in preeclampsia
Hisashi Masuyama1, Seiji Inoue, Yuji Hiramatsu
1Department of Obstetrics and Gynecology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata, Okayama, Japan. masuyama@cc.okayama-u.ac.jp
Insights
Retinol-binding protein 4 (RBP4) levels and insulin resistance were higher in overweight women with late-onset preeclampsia. This suggests RBP4 may play a role in preeclampsia development in obese pregnant individuals.
Area of Science:
- Obstetrics and Gynecology
- Endocrinology
- Metabolic Disorders
Background:
- Preeclampsia is a pregnancy complication causing high blood pressure and proteinuria, leading to significant maternal and neonatal risks.
- Insulin resistance is increasingly recognized as a factor in preeclampsia development.
- Retinol-binding protein 4 (RBP4), an adipose-derived protein, is implicated in regulating insulin resistance.
Purpose of the Study:
- To investigate the association between RBP4 levels, insulin resistance, and preeclampsia.
- To explore the potential role of RBP4 in the pathophysiology of preeclampsia, particularly in relation to body mass.
Main Methods:
- Retinol-binding protein 4 (RBP4) levels and insulin resistance (Homeostasis Model Assessment - Insulin Resistance [HOMA-IR]) were measured.
- Patients with preeclampsia and healthy pregnant women were compared, stratified by weight status (overweight vs. normal weight) and preeclampsia onset (early-onset vs. late-onset).
- Participants were recruited from Okayama University Hospital.
Main Results:
- No significant differences in RBP4 levels were found between all preeclampsia patients and controls.
- Overweight patients with late-onset preeclampsia exhibited significantly higher RBP4 levels and HOMA-IR compared to overweight controls and normal-weight women with late-onset preeclampsia.
- No significant differences in RBP4 or HOMA-IR were observed between overweight and normal-weight groups in early-onset preeclampsia or in healthy pregnant women.
Conclusions:
- RBP4 may contribute to the pathophysiology of late-onset preeclampsia, particularly in overweight or obese pregnant women.
- Increased insulin resistance associated with RBP4 could be a key mechanism in this subgroup of preeclampsia.
- Further research is warranted to elucidate the precise role of RBP4 in pregnancy complications.
Abstract:
Preeclampsia is characterized by the onset of high blood pressure and proteinuria during pregnancy, which results in substantial maternal and neonatal morbidity and mortality. Insulin resistance has been observed before the onset of preeclampsia, and is implicated in its pathophysiology. Recently, retinol-binding protein 4 (RBP4), which carries retinol in circulation, has been shown to be a potential regulator of insulin resistance originating from adipose tissue. Here we measured insulin resistance and RBP-4 levels in patients with preeclampsia and in women with normal pregnancies matched for gestational age and body mass index at Okayama University Hospital. Our aim was to examine the potential role of RBP4 in the pathophysiology of this disorder. There were no significant differences in RBP4 levels between all patients with preeclampsia and controls. However, the RBP4 level and homeostasis model assessment as an index of insulin resistance (HOMA-IR) in overweight patients with late-onset preeclampsia were significantly higher than in overweight controls carrying normal pregnancies and in normal weight women with late-onset preeclampsia. In contrast, there were no significant differences between the overweight and normal weight groups among patients with early-onset preeclampsia and in healthy pregnant women. These data suggest that RBP4 might act in the pathophysiology of late-onset preeclampsia via increased insulin resistance in obese women.
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