Klotho locus, metabolic traits, and serum hemoglobin in hospitalized older patients: A genetic association analysis

Giulia Paroni, Davide Seripa, Francesco Panza, Filomena Addante, Massimiliano Copetti, Grazia D'Onofrio, Fabio Pellegrini, Luigi Fontana, Alberto Pilotto

Research output: Contribution to journalArticle

Abstract

Klotho (KL) gene has been involved in severe alterations of physiological biochemical parameters leading to premature aging-like phenotypes and strikingly shortening lifespan. KL participates to the regulation of a number of intracellular biochemical pathways, including lipid profile and glucose metabolism. Aim of this study was to investigate the possible association between KL locus and biological parameters commonly accepted as indicators of the clinical status in hospitalized older patients. We genotyped the single-nucleotide polymorphisms (SNPs) rs9536314, rs1207568, and rs564481 at the KL locus in 594 hospitalized older patients (65-99 years), consecutively attending a geriatric ward, and tested the association of these KL variants with biological quantitative traits using analyses of covariance and genetic risk score models. Significant associations of rs9536314 with serum levels of hemoglobin, albumin, and high-density lipoprotein cholesterol (HDL-C) as well as significant associations of rs564481 with serum levels of hemoglobin, fasting insulin, and fasting glucose were observed. Gender-segregated analyses confirmed these associations, and suggested that the associations of KL genotypes with HDL-C, fasting glucose and fasting insulin levels may be driven by the female gender, while the association with serum levels of hemoglobin may be driven by the male gender. The association of KL genotypes with creatinine levels was found only in females, while the association with insulin-like growth factor-1 (IGF-1) and lymphocytes count (LC) was found only in males. The genetic risk score (GRS) models further confirmed significant associations among KL SNPs and hemoglobin, total cholesterol, and HDL-C. Gender-segregated analyses with the GRS-tagged approach confirmed the associations with HDL-C, fasting glucose, and fasting insulin levels in females, and with hemoglobin and LC in males. Our findings suggested that KL locus may influence quantitative traits such as serum levels of lipid, fasting glucose, albumin and hemoglobin in hospitalized older patients, with some gender differences suggested for creatinine, IGF-1 levels, and LC, thus being one of the genetic factors possibly contributing to age-related diseases and longevity.

Original languageEnglish
Pages (from-to)949-968
Number of pages20
JournalAge
Volume34
Issue number4
DOIs
Publication statusPublished - Aug 2012

Fingerprint

Fasting
Hemoglobins
HDL Cholesterol
Serum
Lymphocyte Count
Glucose
Somatomedins
Insulin
Single Nucleotide Polymorphism
Albumins
Creatinine
Genotype
Premature Aging
Lipids
Geriatrics
Phenotype
Genes

Keywords

  • Albumin
  • Chromosome 13
  • Creatinine
  • Fasting glucose
  • Fasting insulin
  • Hemoglobin
  • High-density lipoprotein cholesterol
  • Insulin-like growth factor-1
  • Klotho
  • Lymphocytes
  • Total cholesterol

ASJC Scopus subject areas

  • Ageing
  • Geriatrics and Gerontology

Cite this

Klotho locus, metabolic traits, and serum hemoglobin in hospitalized older patients : A genetic association analysis. / Paroni, Giulia; Seripa, Davide; Panza, Francesco; Addante, Filomena; Copetti, Massimiliano; D'Onofrio, Grazia; Pellegrini, Fabio; Fontana, Luigi; Pilotto, Alberto.

In: Age, Vol. 34, No. 4, 08.2012, p. 949-968.

Research output: Contribution to journalArticle

Paroni, Giulia ; Seripa, Davide ; Panza, Francesco ; Addante, Filomena ; Copetti, Massimiliano ; D'Onofrio, Grazia ; Pellegrini, Fabio ; Fontana, Luigi ; Pilotto, Alberto. / Klotho locus, metabolic traits, and serum hemoglobin in hospitalized older patients : A genetic association analysis. In: Age. 2012 ; Vol. 34, No. 4. pp. 949-968.
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AU - Copetti, Massimiliano

AU - D'Onofrio, Grazia

AU - Pellegrini, Fabio

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N2 - Klotho (KL) gene has been involved in severe alterations of physiological biochemical parameters leading to premature aging-like phenotypes and strikingly shortening lifespan. KL participates to the regulation of a number of intracellular biochemical pathways, including lipid profile and glucose metabolism. Aim of this study was to investigate the possible association between KL locus and biological parameters commonly accepted as indicators of the clinical status in hospitalized older patients. We genotyped the single-nucleotide polymorphisms (SNPs) rs9536314, rs1207568, and rs564481 at the KL locus in 594 hospitalized older patients (65-99 years), consecutively attending a geriatric ward, and tested the association of these KL variants with biological quantitative traits using analyses of covariance and genetic risk score models. Significant associations of rs9536314 with serum levels of hemoglobin, albumin, and high-density lipoprotein cholesterol (HDL-C) as well as significant associations of rs564481 with serum levels of hemoglobin, fasting insulin, and fasting glucose were observed. Gender-segregated analyses confirmed these associations, and suggested that the associations of KL genotypes with HDL-C, fasting glucose and fasting insulin levels may be driven by the female gender, while the association with serum levels of hemoglobin may be driven by the male gender. The association of KL genotypes with creatinine levels was found only in females, while the association with insulin-like growth factor-1 (IGF-1) and lymphocytes count (LC) was found only in males. The genetic risk score (GRS) models further confirmed significant associations among KL SNPs and hemoglobin, total cholesterol, and HDL-C. Gender-segregated analyses with the GRS-tagged approach confirmed the associations with HDL-C, fasting glucose, and fasting insulin levels in females, and with hemoglobin and LC in males. Our findings suggested that KL locus may influence quantitative traits such as serum levels of lipid, fasting glucose, albumin and hemoglobin in hospitalized older patients, with some gender differences suggested for creatinine, IGF-1 levels, and LC, thus being one of the genetic factors possibly contributing to age-related diseases and longevity.

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