Association of genetic and epigenetic changes of insulin like growth factor binding protein-1 in Egyptian patients with type 2 diabetes mellitus.


Journal

Diabetes research and clinical practice
ISSN: 1872-8227
Titre abrégé: Diabetes Res Clin Pract
Pays: Ireland
ID NLM: 8508335

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 26 06 2022
revised: 20 03 2023
accepted: 18 04 2023
medline: 6 6 2023
pubmed: 24 4 2023
entrez: 23 04 2023
Statut: ppublish

Résumé

Diabetes is one of the global health threat. Type 2 Diabetes mellitus (T2DM) is associated with life-threatening complications. This work, aimed to study the association between T2DM and IGFBP-1 gene methylation, gene polymorphism and serum levels of IGFBP-1. We included 100 subjects with T2DM and 100 control. DNA methylation of IGFBP-1 was analyzed using pyrosequencing, IGFBP-1 gene polymorphism was analyzed using real time polymerase chain reaction and serum level of IGFBP-1 was measured by ELISA. There was DNA hyper methylation levels of IGFBP1 gene at each of the six CpG sites in T2DM patients than control (P < 0.001). IGFBP-1 gene polymorphism (rs 2854843) CC pattern was significantly associated with DM, P = 0.002. Also, there was decrease in serum IGFBP-1 in patients with T2DM than control group (P < 0.001). We concluded that DNA hyper methylation of IGFBP-1 gene and CC polymorphism (rs 2854843) of IGFBP-1 gene are associated with T2DM in Egyptian patients, also, decrease serum level of IGFBP-1. Further cohort study is recommended with large sample size to detect which one, epigenetic changes or polymorphism of IGFBP-1 gene, is the cause of T2DM or even both.

Sections du résumé

BACKGROUND BACKGROUND
Diabetes is one of the global health threat. Type 2 Diabetes mellitus (T2DM) is associated with life-threatening complications. This work, aimed to study the association between T2DM and IGFBP-1 gene methylation, gene polymorphism and serum levels of IGFBP-1.
METHOD METHODS
We included 100 subjects with T2DM and 100 control. DNA methylation of IGFBP-1 was analyzed using pyrosequencing, IGFBP-1 gene polymorphism was analyzed using real time polymerase chain reaction and serum level of IGFBP-1 was measured by ELISA.
RESULTS RESULTS
There was DNA hyper methylation levels of IGFBP1 gene at each of the six CpG sites in T2DM patients than control (P < 0.001). IGFBP-1 gene polymorphism (rs 2854843) CC pattern was significantly associated with DM, P = 0.002. Also, there was decrease in serum IGFBP-1 in patients with T2DM than control group (P < 0.001).
CONCLUSION CONCLUSIONS
We concluded that DNA hyper methylation of IGFBP-1 gene and CC polymorphism (rs 2854843) of IGFBP-1 gene are associated with T2DM in Egyptian patients, also, decrease serum level of IGFBP-1. Further cohort study is recommended with large sample size to detect which one, epigenetic changes or polymorphism of IGFBP-1 gene, is the cause of T2DM or even both.

Identifiants

pubmed: 37088243
pii: S0168-8227(23)00438-2
doi: 10.1016/j.diabres.2023.110677
pii:
doi:

Substances chimiques

DNA 9007-49-2
Insulin-Like Growth Factor Binding Protein 1 0
Insulin-Like Growth Factor I 67763-96-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110677

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Nehal Salah Hasan (NS)

Department of Clinical and Chemical Pathology, National Research Centre (NRC), Cairo, Egypt.

Hesham Gamal El Dine (H)

Department of Clinical and Chemical Pathology, National Research Centre (NRC), Cairo, Egypt.

Solaf Ahmed Kamel (SA)

Department of Clinical and Chemical Pathology, National Research Centre (NRC), Cairo, Egypt.

Mona Hamed (M)

Department of Clinical and Chemical Pathology, National Research Centre (NRC), Cairo, Egypt.

Rasha N Youssef (RN)

Department of Clinical and Chemical Pathology, National Research Centre (NRC), Cairo, Egypt.

Eman Mahmoud Hassan (E)

Department of Clinical and Chemical Pathology, National Research Centre (NRC), Cairo, Egypt.

Amany Hosny Abdelrahman (AH)

Department of Clinical and Chemical Pathology, National Research Centre (NRC), Cairo, Egypt.

Nevine Ibrahim Musa (NI)

Department of Internal Medicine, Ain Shams University, Cairo, Egypt.

Asmaa Ali (A)

Department of Pulmonary Medicine, Abbassia Chest Hospital, Ministry of Health, Cairo, Egypt; Department of Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, PR China.

Eman Awadallah (E)

Department of Clinical and Chemical Pathology, National Research Centre (NRC), Cairo, Egypt. Electronic address: emanawad_28@yahoo.com.

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Classifications MeSH