Synergistic interactions of Angiotensin Converting Enzyme (ACE) gene and Apolipoprotein E (APOE) gene polymorphisms with T1DM susceptibility in south India
| Autor: | Dharmarajan Pannerselvam, Padma-Malini Ravi, Murali Vijayan, Ramgopal Sivanadham, S. Pushkala, Balakrishnan Karuppiah, Rathika Chinniah |
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| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Apolipoprotein E medicine.medical_specialty Autoantibody Angiotensin-converting enzyme 030204 cardiovascular system & hematology Biology medicine.disease 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Endocrinology Internal medicine Diabetes mellitus Genotype Genetic model Genetics medicine biology.protein Allele Allele frequency Genetics (clinical) |
| Zdroj: | Meta Gene. 18:39-45 |
| ISSN: | 2214-5400 |
| Popis: | Type 1 diabetes mellitus (T1DM) is an autoimmune endocrine disease, in which both gene-gene and gene-environmental factors play a key role in the development and progression of the disease. The main aim of the present study was to determine the association of Angiotensin Converting Enzyme (ACE) and Apolipoprotein E (APOE) gene polymorphisms in T1DM patients. A cohort of 196 T1DM patients (n = 196) and age/sex matched controls (n = 196) were enrolled for typing of ACE and APOE by PCR-SSP and PCR-RFLP methods. We observed an increased frequencies of ‘DD’ (P: OR = 2.40; M: OR = 2.08 and F: OR = 2.90), ‘ID’ (P: OR = 1.94; M: OR = 2.01; F: OR = 1.84) genotypes and ‘D’ allele (P: OR = 2.43; M: OR = 2.21; F: OR = 2.74) in patients confirmed their susceptible association. Whereas, the ‘II’ genotype (P: OR = 0.25; M: OR = 0.28; F: OR = 0.21) and ‘I’ allele frequencies (P: OR = 0.41; M: OR = 0.45; F: OR = 0.36) were decreased in patients suggested their protective association. Multivariate analysis revealed that the ‘GAD65+’, ‘IA2+’ and ‘GAD65+ + IA2+’ autoantibodies were significantly associated with patients. Genetic model of inheritance analysis showed that, the additive (P: OR = 5.15; M: OR = 5.52; F: OR = 4.66), recessive (P: OR = 2.40; M: OR = 2.41; F: OR = 2.41), dominant (P: OR = 3.99; M: OR = 4.79; F: OR = 3.21) and co-dominant (P: OR = 1.94; M: OR = 2.60) models were significantly associated in patients. No significant association was observed for the APOE genotypes with T1DM. However, ‘e3’ allele (M: OR = 0.191; F: OR = 0.128) was decreased in patients confirming its moderate protection. Analysis on synergistic association have revealed that: ‘DD + e3/e4’ (P: OR = 11.59) and ‘ID + e3/e3’ (P: OR = 1.66) were susceptible; and ‘II + e3/e3’ (P: OR = 0.25) as the protective combinations. Thus, the present study conclude the stronger susceptible risks for the combinations ‘DD’ + ‘e3/e4’ and ‘ID’ + ‘e3/e3’ towards the development of T1D in south India. |
| Databáze: | OpenAIRE |
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