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Study of the LMNA 1908 C/T gene polymorphism in type 2 diabetic Egyptians with vascular complications

Abstract

Aims/introduction

Vascular complications are the main cause of morbidity and mortality in type 2 diabetic patients. Genetic susceptibility is associated with the evolution of diabetic complications. One such gene is the lamin A and C gene located on chromosome 1q21, a susceptibility locus for type 2 diabetes mellitus, and encodes nuclear lamins A and C. The LMNA 1908 C/T polymorphism has been reported to be associated with dyslipidemia, metabolic syndrome, and obesity, suggesting that this polymorphism increases the risk of atherosclerosis and vascular disease. The present study aims to elucidate the association between the LMNA 1908 C/T single nucleotide polymorphism and the prevalence of vascular complications in a sample of type 2 diabetic Egyptian patients.

Materials and methods

Genomic DNA from 47 type 2 diabetic patients with vascular complications and 20 control participants was analyzed for the LMNA 1908 C/T polymorphism using PCR- RFLP.

Results

Carriers of the LMNA 1908 T-allele showed a significantly higher prevalence in patients with diabetic nephropathy than carriers of the C-allele (P < 0.05). Multiple regression analysis showed that the LMNA 1908 T-allele tended to be independent risk factor for diabetic nephropathy (P = 0.012, odds ratio = 5.460).

Conclusion

The findings of this study suggest that the LMNA 1908 C/T single nucleotide polymorphism is associated with the development of diabetic nephropathy in Egyptian type 2 diabetic patients.

References

  1. International Diabetes Federation. IDF diabetes atlas. 5th ed. Brussels, Belgium: International Diabetes Federation 2011.

  2. Bos M, Agyemang C. Prevalence and complications of diabetes mellitus in Northern Africa: a systematic review. BMC Public Health 2013; 13: 387.

    Article  Google Scholar 

  3. Badran M, Laher I. Type II diabetes mellitus in Arabic-speaking countries. Int J Endocrinol 2012; 2012: 902873.

    Article  Google Scholar 

  4. Doria A, Patti ME, Kahn CR. The emerging genetic architecture of type 2 diabetes. Cell Metab 2008; 8: 186–200.

    Article  CAS  Google Scholar 

  5. Liang H, Murase Y, Katuta Y, Asano A, Kobayashi J, Mabuchi H. Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes. Clin Endocrinol (Oxf) 2005; 63: 317–322.

    Article  CAS  Google Scholar 

  6. Bansal S, Chawla D, Banerjee BD, Madhu SV, Tripathi AK. Association of RAGE gene polymorphism with circulating AGEs level and paraoxonase activity in relation to macro-vascular complications in Indian type 2 diabetes mellitus patients. Gene 2013; 526: 325–330.

    Article  CAS  Google Scholar 

  7. Owen KR, Groves CJ, Hanson RL, Knowler WC, Shuldiner AR, Elbein SC, et al. Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9518 subjects. Diabetes 2007; 56: 879–883.

    Article  CAS  Google Scholar 

  8. Mory PB, Crispim F, Kasamatsu T, Gabbay MA, Dib SA, Moisés RS. Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation. Arq Bras Endocrinol Metabol 2008; 52: 1252–1256.

    Article  Google Scholar 

  9. Yokoyama H, Emoto M, Fujiwara S, Motoyama K, Morioka TK, omatsu M, et al. Quantitative insulin sensitive check index and the reciporcal index of homeostasis model assessment in normal range weight and moderately obese type 2 diabetic patients. Diabetic Care 2003; 26: 2426–2432.

    Article  CAS  Google Scholar 

  10. Fontaine-Bisson B, Alessi MC, Saut N, Fumeron F, Marre M, Dutour A, et al. Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study. J Mol Med (Berl) 2010; 88: 193–201.

    Article  CAS  Google Scholar 

  11. Wegner L, Andersen G, Sparso T, Grarup N, Glümer C, Borch-Johnsen K, et al. Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: studies of 7495 Danish whites. Diabetes 2007; 56: 694–698.

    Article  CAS  Google Scholar 

  12. Murase Y, Yagi K, Katsuda Y, Asano A, Koizumi J, Mabuchi H. An LMNA variant is associated with dyslipidemia and insulin resistance in the Japanese. Metabolism 2002; 51: 1017–1021.

    Article  CAS  Google Scholar 

  13. Mukti S, Annop M, Naval V, Bhatt S, Shivani C, Neha G, et al. Genotype of the LMNA 1908 C/T variant is assaociated with generalized obesity in Asian Indians in north India. Clin Endocrinol (Oxf) 2011; 75: 642–645.

    Article  Google Scholar 

  14. Wolford JK, Hanson RL, Bogardus C, Prochazka M. Analysis of the lamin A/C gene as a candidate for type II diabetes susceptibility in Pima Indians. Diabetologia 2001; 44: 779–782.

    Article  CAS  Google Scholar 

  15. Hegele RA, Cao H, Harris SB, Zinman B, Hanley AJ, Anderson CM. Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians. Physiol Genomics 2000; 3: 39–44.

    Article  CAS  Google Scholar 

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Correspondence to Ahmed Hamdy MD.

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Mostafa, H., Eldeeb, M., Hamdy, A. et al. Study of the LMNA 1908 C/T gene polymorphism in type 2 diabetic Egyptians with vascular complications. Egypt J Intern Med 27, 103–107 (2015). https://doi.org/10.4103/1110-7782.165440

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