Shawqi S. Saleh’s research while affiliated with University of Jordan and other places

Pre-eclampsia (PE) is a serious pregnancy-related disorder and the leading cause of maternal and fetal mortality and morbidity worldwide. The etiology of PE is poorly understood and a definitive diagnosis is still lacking. Herein, we used synchrotron-FTIR microspectroscopy as a new analytical tool to investigate the molecular changes in the structure and intensity of lipids (spectral range 3050-2800 cm⁻¹) and protein-carbonyl (spectral range 1855–1485 cm⁻¹) components of the plasma and link them to the pathogenesis of the disease. In the lipid region, an increase in the CH2 and CH3 peaks intensity was noticed in PE group compared to normotensive pregnancy reflecting abnormalities in the lipid profile and a high level of LDL. Increased CH2/CH3 ratio and red shifts were observed in the lipid region in PE highlighting structural variations of lipids and transformation of conformation of lipid tails. In the protein-carbonyl region, a decrease in the amide I and II absorption signals in the plasma of PE compared to normotensive controls was evident, and a red shift was noticed in the amide I region reflecting conformational changes and rearrangement in the α-helix secondary structure of the protein. Moreover, malondialdehyde level and lipid carbonyl peak at 1743 cm⁻¹ were higher and more intense in PE due to the oxidative stress condition in PE. Spectral analysis of plasma drop from PE revealed that lipid and protein components tend to concentrate more in the central region of the drop, and that the most intense wavenumber values for the lipid and amide I region in the plasma drop were very comparable to their analogous in plasma film. Taken together, the current work provides evidence of the promising role of synchrotron-FTIR microspectroscopy in providing a better understanding of the pathophysiology of PE.

Pre-eclampsia (PE) is a serious hypertensive disorder with unclear etiology and lack of reliable diagnostic tests. In this study, IR microspectroscopy was applied to identify molecular changes associated with the pathogenesis of PE in placental tissues and plasma samples from pre-eclamptic women and normotensive matched controls. The obtained spectra were analyzed by multivariate analysis in the spectral ranges of 3050–2800 cm⁻¹ and 1855–1485 cm⁻¹ corresponding to lipid and protein-carbonyl components, respectively. In the lipid region, an increase in CH2/CH3 ratio was noticed and higher level of unsaturation index in placenta was evident. New lipid species emerged as a consequence of oxidative stress. The more intense peak at 1740 cm⁻¹ in PE reflected higher level of LDL and VLDL. In the protein region, a decrease in the α-helix structure associated with gain in β-sheet and β-turn structures was detected. Our results revealed significant conformational changes in the protein secondary structure in PE illustrated by peak shifts and intensity alterations, particularly in amide I component. Variations in lipid order, membrane integrity, fatty acid saturation and plasma lipid profile were also detected in PE. The ROC curve generated from plasma samples yielded AUC values of 98.4% and 99.9% for lipid and protein-carbonyl regions, respectively. The current study shed light on the promising role of IR microspectroscopy as a new analytical tool that can aid in providing better diagnosis and understanding of the pathophysiology of PE.