The association between Single Nucleotide Polymorphisms of Klotho Gene and Mortality in Elderly Men: The MrOS Sweden Study

• Published in: Scientific reports Vol. 10; no. 1; p. 10243
• Main Authors: Wu, Ping-Hsun, Westerberg, Per-Anton, Kindmark, Andreas, Tivesten, Åsa, Karlsson, Magnus K., Mellström, Dan, Ohlsson, Claes, Fellström, Bengt, Linde, Torbjörn, Ljunggren, Östen
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 24.06.2020; Nature Publishing Group
• Subjects: 38/39; 692/308/2056; 692/53/2422; Aged; Aged, 80 and over; annotation; Basic Medicine; blood-pressure; Cardiac and Cardiovascular Systems; Cardiovascular diseases; Cause of Death; Clinical Medicine; Computer applications; Computer Simulation; density; disease; functional variant; genome-wide association; Genomes; glucose-metabolism; Glucuronidase - genetics; Health risk assessment; Homeostasis; Humanities and Social Sciences; Humans; Kardiologi; Klinisk medicin; Klotho protein; Male; Medical and Health Sciences; Medical Genetics; Medicin och hälsovetenskap; Medicinsk genetik; Medicinska och farmaceutiska grundvetenskaper; Mortality; multidisciplinary; Osteoporosis; Osteoporotic Fractures - genetics; Osteoporotic Fractures - mortality; pathogenicity; Polymorphism, Single Nucleotide; Prospective Studies; risk; Science; Science & Technology - Other Topics; Science (multidisciplinary); sequence; Single-nucleotide polymorphism; Sweden - epidemiology; Sweden
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-66517-5

The Klotho ( KL ) gene is involved in phosphate homeostasis. Polymorphisms in this gene have been reported to be associated with the risk of cardiovascular disease. Here we used computational tools to predict the damage-associated single nucleotide polymorphisms (SNPs) in the human KL gene. We further investigated the association of SNPs in the KL gene and mortality in the Swedish multicenter prospective Osteoporotic Fractures in Men (MrOS) cohort. This study included 2921 men (aged 69–81 years) with mean 4.49 ± 1.03 years follow-up. 18 SNPs in the KL gene were genotyped using Sequenom. These SNPs were identified by in silico tools for the coding and noncoding genome to predict the damaging SNPs. After quality analyses, SNPs were analyzed for mortality risk using two steps approach on logistic regression model screening and then Cox regression model confirmation. Two non-synonymous SNPs rs9536314 and rs9527025 were found to be potentially damaging SNPs that affect KL protein stability and expression. However, these two SNPs were not statistically significantly associated with all-cause mortality (crude Hazard ratio [HR] 1.72, 95% confidence interval [CI] 0.96–3.07 in rs9536314; crude HR 1.82, 95% CI 0.998–3.33 in rs9527025) or cardiovascular mortality (crude HR 1.52, 95% CI 0.56–4.14 in rs9536314; crude HR 1.54, 95% CI 0.55–4.33 in rs9527025) in additive model using Cox regression analysis. In conclusion, these two potentially damaging SNPs (rs9536314 and rs9527025) in the KL gene were not associated with all-cause mortality or cardiovascular mortality in MrOs cohort. Larger scales studies and meta-analysis are needed to confirm the correlation between polymorphisms of the KL gene and mortality.