Comparison of Mir122 expression in children with biliary atresia and healthy group.

Biliary atresia Liver Micro RNA miR-122

Journal

Molecular biology research communications
ISSN: 2345-2005
Titre abrégé: Mol Biol Res Commun
Pays: Iran
ID NLM: 101613459

Informations de publication

Date de publication:
2024
Historique:
medline: 25 6 2024
pubmed: 25 6 2024
entrez: 25 6 2024
Statut: ppublish

Résumé

Biliary atresia (BA) is the primary cause of neonatal jaundice with various pathological mechanisms. Many BA patients may experience progressive liver dysfunction and eventually need a liver transplant. Therefore, identifying potential non-invasive biomarkers for BA is crucial. miR-122, the most abundant microRNA in the liver, plays significant roles in different liver diseases. This study aimed to assess miR-122 levels in BA patients. Eighteen patients with biliary atresia were selected at random from the Shiraz Pediatric Liver Cirrhosis Cohort Study (SPLCCS), along with 18 healthy controls. Blood samples were collected, and biochemical parameters (such as liver function tests) were measured. Quantitative reverse-transcription PCR (RT-PCR) was conducted on serum samples from both the case and control groups to analyze miR-122 levels. The study results indicated that serum miR-122 expression in BA patients was elevated compared to the control group, although it did not reach statistical significance. Additionally, no correlation was found between miR-122 expression and serum levels of liver enzymes or other laboratory findings in BA cases. miR-122 could be a potential target for diagnosing BA; however, further research with a larger population is necessary to determine if miR-122 could serve as a useful biomarker for diagnosing BA.

Identifiants

pubmed: 38915454
doi: 10.22099/mbrc.2024.49649.1950
pmc: PMC11194029
doi:

Types de publication

Journal Article

Langues

eng

Pagination

147-154

Déclaration de conflit d'intérêts

The authors declare that there is no conflict of interest.

Auteurs

Nasrin Motazedian (N)

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Negar Azarpira (N)

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Kimia Falamarzi (K)

Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.

Seyed Mohsen Dehghani (SM)

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Maryam Ataollahi (M)

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Elaheh Esfandiari (E)

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Mahintaj Dara (M)

Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Razieh Toobafard (R)

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Mehrab Sayadi (M)

Cardiovascular Research Centre, Shiraz University of Medical Sciences, Shiraz, Iran.

Seyed Ali Shekarforoush (SA)

Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Seyed Hossein Owji (SH)

Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Stem Cells Technology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Seyed Ali Malekhosseini (SA)

Abu-Ali Sina Organ Transplant Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Classifications MeSH