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Hubungan Kadar Matrix Metalloproteinase-9 pada Cairan Serebrospinal dan Serum terhadap Derajat Keparahan dan Luaran Pasien Meningitis Tuberkulosis Sonia Hardianti; Yuliarni Syafrita; Fanny Adhy Putri; Syarif Indra; Restu Susanti; Reno Bestari
Journal of Pharmaceutical and Sciences JPS Volume 9 Nomor 2 (2026)
Publisher : Fakultas Farmasi Universitas Tjut Nyak Dhien

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36490/journal-jps.com.v9i2.1632

Abstract

Tuberculous meningitis (TBM) is a severe form of tuberculosis associated with high mortality and neurological morbidity. Disease severity strongly influences outcome; however, reliable biological predictors remain limited. Matrix metalloproteinase-9 (MMP-9) is a proteolytic enzyme involved in neuroinflammation and blood-brain barrier disruption, and it has been reported to be elevated in both the cerebrospinal fluid (CSF) and serum of TBM patients. This study aimed to evaluate the relationship between MMP-9 levels and the severity and outcome of TBM patients. This was an analytical observational study with a cross-sectional design involving TBM patients treated at Dr. M. Djamil General Hospital, Padang, from January to December 2024. CSF and serum MMP-9 levels were measured using the enzyme-linked immunosorbent assay (ELISA) method. Disease severity was assessed using the British Medical Research Council (BMRC) criteria, and outcomes at 14 and 60 days were assessed using the Glasgow Outcome Scale. A total of 41 TBM patients were included in the study. The mean CSF MMP-9 level was 2,034.40 ng/L, while the median serum MMP-9 level was 1,490.14 ng/L. The analysis showed no significant association between CSF MMP-9 levels and disease severity (p = 0.276), 14-day outcome (p = 0.269), or 60-day outcome (p = 0.375). Serum MMP-9 levels were likewise not associated with disease severity (p = 0.248), 14-day outcome (p = 0.224), or 60-day outcome (p = 0.138), but they still showed an increasing pattern in patients with a fatal outcome. CSF and serum MMP-9 levels had no significant association with the severity and outcome of TBM patients. These findings suggest that a single MMP-9 measurement is insufficient as a clinical predictor, so a multibiomarker and longitudinal approach should be considered.
Hubungan Kadar Protein S100B Serum dengan Volume Perdarahan dan Tingkat Keparahan Pasien Perdarahan Intraserebral Spontan Fadrian Herjunio; Syarif Indra; Restu Susanti; Yuliarni Syafrita; Dedi Sutia; Reno Bestari
Journal of Pharmaceutical and Sciences JPS Volume 9 Nomor 2 (2026)
Publisher : Fakultas Farmasi Universitas Tjut Nyak Dhien

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36490/journal-jps.com.v9i2.1662

Abstract

Spontaneous intracerebral hemorrhage is a hemorrhagic stroke with high mortality and morbidity rates. Hemorrhage volume and the degree of neurological severity are important factors influencing prognosis. Brain tissue damage due to hemorrhage triggers the release of biomarkers such as S100B protein, which is secreted by astrocytes. This study aims to determine the relationship between serum S100B protein levels and the volume of bleeding and severity in patients with spontaneous intracerebral hemorrhage. This observational, analytical, cross-sectional study was conducted on 47 patients with primary spontaneous intracerebral hemorrhage aged ≥18 years with onset within 0–24 hours, admitted to Dr. M. Djamil Padang General Hospital between August 2025 and February 2026 and confirmed by head CT scan. Serum S100B protein levels were measured using an enzyme-linked immunosorbent assay (ELISA), hemorrhage volume was assessed using the Broderick method, and severity was assessed using the NIHSS score. Statistical analysis used the Mann-Whitney and Kruskal-Wallis tests. A total of 30 patients (63.8%) had a bleeding volume <30 cc and 27 patients (57.4%) had moderate neurological deficits. The median serum S100B protein level was 0.049 µg/L. There was a significant median difference between serum S100B protein levels and hemorrhage volume (p=0.047), but not with clinical severity based on the NIHSS (p=0.173). Serum S100B protein levels differed significantly between the small and large hemorrhage volume groups, but not across clinical severity groups based on the NIHSS.