1.Matrix metalloproteinase-9 and tissue inhibitors of metalloproteinases 1 and 2 as potential biomarkers for gestational hypertension.
Jabrullah Ab HAMID ; Norhafizah MOHTARRUDIN ; Malina OSMAN ; Andi Anggeriana Andi ASRI ; Wan Hamilton Wan HASSAN ; Rohani AZIZ
Singapore medical journal 2012;53(10):681-683
INTRODUCTIONGestational hypertension (GH) is a common disorder during pregnancy that can progress to preeclampsia and cause various subsequent fatal complications. A cluster of enzymes, called matrix metalloproteinases (MMPs), and its specific inhibitors, tissue inhibitors of metalloproteinases (TIMPs), have been reported to be involved in the pathophysiology of GH. The purpose of this study was to examine circulating levels of MMP-9, TIMP-1 and TIMP-2 in pregnant women who had GH and those who were normotensive.
METHODSIn a case-control study, the total levels of MMP-9, TIMP-1 and TIMP-2 in the sera of 108 pregnant patients were evaluated using enzyme-linked immunosorbent assays. 54 patients with GH (test group) and 64 normotensive pregnant women (control group) were included in the study.
RESULTSWhile MMP-9 levels showed a high level of expression in the GH group (p = 0.085), TIMP-1 and TIMP-2 levels showed low levels of expression for the same. Weak positive correlations were found on correlation analysis between maternal age and TIMP-1 in the GH group (r = 0.278, p < 0.05), and between gestational age and TIMP-2 in the control group (r = 0.318, p < 0.05).
CONCLUSIONOur findings suggest that MMP-9 may be involved in the pathophysiology of GH. It may be of value to further evaluate MMP-9 as a potential biomarker for predicting preeclampsia in pregnant women.
Adolescent ; Adult ; Biomarkers ; blood ; Case-Control Studies ; Enzyme-Linked Immunosorbent Assay ; Female ; Gestational Age ; Humans ; Hypertension, Pregnancy-Induced ; blood ; diagnosis ; Matrix Metalloproteinase 9 ; blood ; Pregnancy ; Tissue Inhibitor of Metalloproteinase-1 ; blood ; Tissue Inhibitor of Metalloproteinase-2 ; blood ; Young Adult
2.Socioeconomic Status Affecting Inequity of Healthcare Utilisation in Malaysia
Nurul Salwana Abu Bakar ; Adilius Manual ; Jabrullah Ab Hamid
Malaysian Journal of Medical Sciences 2019;26(4):79-85
Background: Equity is one of the important aspects of universal health coverage. Variation
in socioeconomic status (SES) has been proved to contribute discrepancies in the use of healthcare
services. This study aimed to assess equity for inpatient, outpatient and dental care utilisation by
household SES over time.
Methods: This study used five series of National Health and Morbidity Survey data from
1986 to 2015. Healthcare utilisation for inpatient, outpatient and dental care were analysed. SES
was grouped based on household expenditure variables accounting for total number of adults and
children in the household using consumption per adult equivalents approach. The determination
of healthcare utilisation across the SES segments was measured using concentration index.
Results: The overall distribution of inpatient utilisation tended towards the pro-poor,
although only data from 1996 (P-value = 0.017) and 2006 (P-value = 0.021) were statistically
significant (P < 0.05). Out-patient care showed changing trends from initially being pro-rich in
1986 (P < 0.05), then gradually switching to pro-poor in 2015 (P < 0.05). Dental care utilisation
was significantly pro-rich throughout the survey period (P < 0.05). Public providers mostly showed
significantly pro-poor trends for both in- and out-patient care (P < 0.05). Private providers,
meanwhile, constantly showed a significantly pro-rich (P < 0.05) trend of utilisation.
Conclusion: Total health utilisation was close to being equal across SES throughout the
years. However, this overall effect exhibited inequities as the effect of pro-rich utilisation in the
private sector negated the pro-poor utilisation in the public sector. Strategies to improve equity
should be consistent by increasing accessibility to the private sectors, which has been primarily
dominated by the richest population.