Association of Soluble ? - Klotho and Klotho Polymorphisms (KL-VS and G-395A) with Essential Hypertension in Indian Population

Authors

  • Gauri Pathare Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Center
  • Sunila Raju Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Center
  • Vinod Shah Sir H.N. Reliance Foundation Hospital and Research Center
  • Manoj Mashru Sir H.N. Reliance Foundation Hospital and Research Center
  • Kavita Shalia Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Center

DOI:

https://doi.org/10.7439/ijbar.v9i12.4969

Keywords:

Gene polymorphism, ? - Klotho, anti - aging protein, Cardiovascular disease

Abstract

Klotho, a novel anti-aging gene, is known to ameliorate aging phenotypes and extend lifespan. Recent studies have highlighted arterial aging as a risk factor for hypertension. Thus, Klotho appears to be a link between aging and cardiovascular diseases (CVD) including hypertension. KL-VS and G-395A polymorphisms of Klotho and its soluble levels have been associated with CVD incidence. We analyzed the prevalence of alfa-Klotho polymorphisms KL-VS and G-395A and their influence on soluble alfa-Klotho levels in essential hypertension (EH) patients in Indian population. One-hundred-twelve EH patients and age, BMI-matched 103 normotensive controls were recruited. Soluble alfa-Klotho levels were measured by Enzyme-Linked-Immunosorbent-Assay. Genotyping of single nucleotide polymorphisms (SNP) was performed using TaqMan assays. Soluble alfa-Klotho levels in patients were significantly lower (26.9%,p=0.001) than controls. ROC curve analysis for soluble α-Klotho showed a cut-off of 580pg/ml with AUC 0.798(SE=0.031, 95%CI=0.737-0.859). Genotype distributions for both polymorphisms did not differ between the groups. Distribution of soluble alfa-Klotho levels in both groups did not vary across KL-VS genotypes. In patient group, GA and AA genotypes of G-395A polymorphism were associated with significantly lower (15.4%,p=0.014) soluble alfa-Klotho levels compared to GG genotype. Soluble alfa-Klotho levels were significantly lower in EH patients as compared to healthy normotensive individuals.

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Author Biographies

  • Gauri Pathare, Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Center

    Ms. Gauri Pathare, M.Sc.

    Designation: Ph.D. Fellow, Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Centre, Court House, L. T. Road, Mumbai 400002, India.

  • Sunila Raju, Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Center

    Ms. Sunila Raju, M.Sc.

    Designation: Research Assistant, Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Centre, Court House, L. T. Road, Mumbai 400002, India.

  • Vinod Shah, Sir H.N. Reliance Foundation Hospital and Research Center

    Dr. Vinod Shah, DM (Card.), MD (Med.), FISE

    Designation: Interventional Cardiologist; Consultant, Department of Cardiology, Sir H.N. Reliance Foundation Hospital and Research Center, Raja Ram Mohan Roy Road, Mumbai 400004, India

  • Manoj Mashru, Sir H.N. Reliance Foundation Hospital and Research Center

    Dr. Manoj Mashru, MD (Med), DM (Card)

    Designation: Interventional Cardiologist; Mentor, Department of Cardiology,

    Sir H.N. Reliance Foundation Hospital and Research Center, Raja Ram Mohan Roy Road, Mumbai 400004, India

  • Kavita Shalia, Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Center

    Dr. Kavita Shalia, Ph.D.

    Designation: Senior Scientist, Sir H.N. Medical Research Society, Sir H.N. Reliance Foundation Hospital and Research Centre, Court House, L. T. Road, Mumbai 400002, India.

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Published

2018-12-08

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Original Research Articles

How to Cite

Association of Soluble ? - Klotho and Klotho Polymorphisms (KL-VS and G-395A) with Essential Hypertension in Indian Population. (2018). International Journal of Biomedical and Advance Research, 9(12), 392-399. https://doi.org/10.7439/ijbar.v9i12.4969