Gabriela Valencia Putri Husodho
Faculty of Medicine, Universitas Diponegoro, Jl. Prof. Sudarto, SH, Tembalang, Semarang, Indonesia

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POTENTIAL OF MIRNA-183, MIRNA-29B, AND MIRNA-34A COMBINATION AS A NOVEL ADVANCED SENSORINEURAL HEARING LOSS DIAGNOSTIC AND THERAPEUTIC (THERAGNOSTIC) AGENT Agyta Hanifa Faiza; Gabriela Valencia Putri Husodho; Anatalya Diah Ayu Kumalasari
Jurnal Kedokteran Diponegoro (Diponegoro Medical Journal) Vol 14, No 3 (2025): JURNAL KEDOKTERAN DIPONEGORO (DIPONEGORO MEDICAL JOURNAL)
Publisher : Faculty of Medicine, Universitas Diponegoro, Semarang, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/dmj.v14i3.47640

Abstract

Background: Sensorineural hearing loss (SNHL) is a hearing disability that makes up 90% of all hearing loss in general. This condition reduces quality of life and causes lifelong disability. Current diagnostic and therapeutic agents are considered less than optimal and need to be developed further. MicroRNAs (miRNAs), such as miRNA-34a, miRNA-29b, and miRNA-183, play a role in the pathogenesis of SNHL and thus have potential as specific biomarkers and therapeutic agents. Objective: To open a new perspective regarding the use of diagnostic biomarkers and miRNA therapy as a new step towards the era of personalized medicine in SNHL patients. Methods: This literature review used a non-systematic review method using the search engines PubMed, Science Direct, and ProQuest. Results: Increased expression of miRNA-34a, miRNA-29b, and miRNA-183 causes a decrease in the number of inner hair cells hence causing hearing loss. This means that these miRNAs can be used as biomarkers in the diagnosis of SNHL. Suppression of these miRNAs to certain levels could potentially be a therapy for SNHL, as it showed reduced oxidative stress and apoptosis. Suppression of miRNA-29b expression causes increased proliferation and reduced oxidative stress. However, knock out of miRNA-183 shows disruption in stereociliary bundle development and hair cell maturation hence when using miRNA inhibitors as therapy it is important to take note of dosage. Conclusion: miRNA-34a, miRNA-29b, and miRNA-183 have potential as diagnostic biomarkers and therapeutic agents for SNHL by regulating levels of oxidative stress, apoptosis, and the number of inner hair cells. Utilizing these three miRNAs simultaneously can increase the specificity, sensitivity and effectiveness in the diagnosis and therapy of SNHL.
HOW SUITABLE ARE NDO-LID AND PGL-I IN RAPID DIAGNOSTIC TESTS FOR SCREENING OF LEPROSY? A REVIEW OF DIAGNOSTIC STUDIES Gabriela Valencia Putri Husodho; Anatalya Diah Ayu Kumalasari; Agyta Hanifa Faiza
Jurnal Kedokteran Diponegoro (Diponegoro Medical Journal) Vol 15, No 2 (2026): JURNAL KEDOKTERAN DIPONEGORO (DIPONEGORO MEDICAL JOURNAL)
Publisher : Faculty of Medicine, Universitas Diponegoro, Semarang, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/dmj.v15i2.53438

Abstract

Background: Indonesia has the third highest prevalence of leprosy, a neglected tropical disease caused by the “Mycobacterium leprae complex which causes neuropathy and hypopigmented skin lesions with hypoesthesia. The main problem in eradicating leprosy is due to its negative social stigma and prevalence in lower socioeconomic populations, as the gold standard for leprosy diagnosis is histopathology of skin smears. Hence, cost and time effective screening tools are needed. PGL-I and NDO-LID are antigens that have been developed as biomarkers used in serological assays, one of them being rapid lateral flow tests. Therefore, a rapid test utilizing a combination of PGL-I and NDO-LID as its marker is potentially a suitable tool for leprosy screening in areas with limited access to healthcare. Objective: To evaluate the diagnostic potential of PGL-I and NDO-LID in rapid lateral flow tests for leprosy. Methods: This literature review was done by using the search engines PubMed, Science Direct, and SpringerLink.  Results: Diagnostic potential studies for PGL-I rapid tests using UCP-LFA and Gold-LFA showed high overall sensitivity and specificity for leprosy patients, with more positive results in MB and PB patients. NDO-LID rapid test diagnostic studies which used the also showed similar results. However, these tests are not as accurate as ELISA and histopathology, but modifications such as additional biomarkers can be used to improve its utility. Conclusion: PGL-I and NDO-LID have good sensitivity and specificity from the results of various diagnostic studies, thus are potentially suitable for field screening of leprosy.