Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

The Klotho gene G-395A polymorphism and metabolic syndrome in very elderly people

BMC Geriatrics volume 16, Article number: 46 (2016) Cite this article

Abstract

Background

To investigate the possible association of the Klotho G-395A polymorphism and metabolic syndrome (MetS) among a population of Chinese nonagenarians and centenarians.

Methods

Subjects were from the Project of Longevity and Aging in Dujiangyan (PLAD). The genotyping of G-395A (rs1207568) in the promoter region of the Klotho gene was performed using the TaqMan allelic discrimination assay. MetS was diagnosed according to the International Diabetes Federation criteria.

Results

We included 695 subjects aged 93.5 ± 3.2 years. G and A allele frequencies were 0.852 and 0.148, respectively. In the whole population, the frequency of MetS was 10.8 % and 5.9 % in the GG and GA + AA genotype group, respectively (p = 0.004). The -395A allele carriers had significantly lower risk of MetS in the whole population (odd ratio [OR] 0.50, 95 % confidential interval [CI] 0.25 to 0.98) and in women (OR 0.51, 95 % CI 0.24 to 0.97), but not in men (OR 0.42, 95 % CI 0.05 to 3.85). In the whole population and women, the relationship between the Klotho G-395A SNP and MetS might due to its influence on high blood pressure (OR 0.48, 95 % CI 0.34 to 0.67; OR 0.47, 95 % CI 0.31 to 0.71, respectively) and hypertriglyceridemia (OR 0.66, 95 % CI 0.39 to 0.95; OR 0.54, 95 % CI 0.31 to 0.98, respectively). In men, this relationship might due to its influence on high blood pressure (OR 0.47, 95 % CI 0.25 to 0.90) and low HDL-C (OR 0.69, 95 % CI 0.27 to 0.93).

Conclusions

The -395A allele carriers of the Klotho gene were correlated with lower risk of MetS among Chinese nonagenarians and centenarians, especially in women.

Peer Review reports

Background

Metabolic syndrome (MetS), a cluster of cardiometabolic risk factors including abdominal obesity, hyperglycemia, dyslipidemia and hypertension, increases with aging [1]. In elderly adults, MetS not only increases the risk of cardiovascular diseases and type 2 diabetes [2], but also is associated with cognitive decline [3] and disability [1]. Current evidence suggests that MetS is partly heritable, and genetic factors plays a greater role than environment factors on the incidence of MetS [4, 5]. Single nucleotide polymorphism (SNP) is one of the most active research fields of genetic researches. A recent systematic review found that eight SNPs in six genes (GNB3, TCF7L2, APOA5, APOC3, APOE, and CETP) were associated with MetS [6].

Klotho gene is an aging associated gene discovered by Kuro-o et al. during the development of hypertensive transgenic mice models [7]. Since then, more than 10 SNPs in the human Klotho gene have been identified [8], among which, the G-395A (rs1207568) SNP in the promoter region of Klotho gene was related to hypertension [9] or high systolic blood pressure 10 in previous studies [10] in previous studies. In addition, Shimoyama and colleagues found that the Klotho G-395A SNP was related to lipid metabolism in men and glucose metabolism in women among Japanese health subjects [11]. The same research team also found that the Klotho G-395A SNP was associated with low levels of low-density lipoprotein cholesterol (LDL-C) in Japanese hemodialysis patients [12].

Based on these findings, we speculated that the Klotho G-395A SNP may be a candidate SNP related to MetS. In 2005, we performed a cross-sectional study [13, 14] including 870 Chinese adults aged 90 years and older, and built a relevant DNA specimen database. Most of these participants lived in their homeland during their entire lifetime and were never exposed to immigrants, which can represent Chinese well. It offered us an opportunity to investigate the genetic factors of MetS in this special population. In this study, we aimed to examine the possible association between the Klotho G-395A SNP and MetS among this long-lived population.

Methods

Study subjects

Subjects were from the Project of Longevity and Aging in Dujiangyan (PLAD) [13, 14], a cross-sectional study conducted in the rural area of Dujiangyan, a small town in southwest China, in April 2005. This study was conducted in order to investigate the relationship between environment, lifestyle and age-related diseases, and longevity. A total of 1115 adults aged 90 years and older dwelling in this area were screened, among which, 870 subjects (men: 280 cases; women: 590 cases) agreed to participant. Trained staff visited all study participants at their homes or at community centers. Face-to-face interviews were performed for data collection. Anthropometric measurements were performed and biological specimens were collected by trained staff. Subjects without DNA samples (160 cases) or the results of waist circumference (4 cases) and high density lipoprotein cholesterol (HDL-C, 11 cases) were excluded from the current analyses. As a result, the study population ultimately consisted of 695 subjects (men: 220 cases; women: 475 cases). The Research Ethics Committee of Sichuan University approved the study protocol. Written informed consent was obtained from all of the participants or their legal proxies.

Genotyping of the Klotho gene G-395A polymorphism

Genomic DNA was isolated from the whole blood samples, drawn from antecubital vein, using commercial DNA isolation kits from QIAGEN (Chatsworth, CA, USA), according to standard procedures. The genotyping of G-395A (rs1207568) in the promoter region of the Klotho gene was performed using the TaqMan allelic discrimination assay as previously reported by Wang et al. [9].

The following primers and probes (Takara, Dalian, China) were used:

  • Forward primer 5′-TAGGGCCCGGCAGGAT-3′;

  • Reverse primer 5’-CCTGGAGCGGCTTCGTC-3’;

  • Probe A 5’-(FAM) CCCCAAGTCGGGAAAAGTTGGTC (TAMRA)-3’;

  • Probe G 5’-(HEX) CCCCCAAGTCGGGGAAAGTTGGTC (TAMRA)-3’.

The PCR reaction was performed in 20 μl reaction volumes containing 10 μl of Premix Ex Taq, 1.5 μl of each primer, 0.5 μl of probe A, 1 μl of probe G, 1 μl of genomic DNA, and 4.25 μl of sterile double distilled water. The reaction conditions were as follows: an initial denaturation step at 95 °C for 30 s, followed by 40 cycles of denaturation at 95 °C for 5 s, and annealing for 30 s at 60 °C. The PCR reaction was performed and analyzed on a Thermal Cycler Dice Real Time System (Takara, Dalian, China).

In addition, we randomly selected 10 % of the samples for sequencing in both the forward and reverse directions to confirm the genotypes of G-395A in the promoter of Klotho gene. The results of the sequencing were identical to the results of the TaqMan allelic discrimination assay.

Diagnosis of MetS

MetS was diagnosed according to the International Diabetes Federation (IDF) criteria [15]: abdominal obesity (for Chinese people, waist circumference [WC] ≥ 90 cm in men and ≥ 80 cm in women), combined with any two or more of the following four factors: 1) fasting plasma glucose (FPG) ≥ 5.6 mmol/L or previously diagnosed type 2 diabetes; 2) systolic blood pressure (SBP) ≥ 130 mm Hg and/or diastolic blood pressure (DBP) ≥ 85 mm Hg or currently use of anti-hypertensive agents; 3) HDL-C < 1.29 mmol/L in women and <1.03 mmol/L in men or specific treatment for this lipid abnormality; 4) triglyceride (TG) ≥ 1.7 mmol/L or specific treatment for this lipid abnormality.

Measurement of covariates

Body height and weight were measured using a wall-mounted stadiometer and a digital floor scale to the nearest 0.1 cm and 0.1 kg, respectively. Body mass index (BMI) was calculated by dividing body weight in kilograms by height in squared meters (kg/m2). In addition, the following information were included in the analyses: age, gender, and cigarette smoking habits, alcoholic habits, and exercise habits. Venous blood samples were collected after an overnight fast to measure the following biochemistry indicators: FPG, total cholesterol (TC), TG, HDL-C, LDL-C, and serum uric acid (SUA).

Statistical analysis

All of the statistical analyses for this study were performed with SPSS for Windows software package, version 11.5 (SPSS Inc., Chicago, Illinois, USA). A two-tailed P <0.05 was considered statistically significant. The categorical variables are presented as percentage, whereas the continuous data are presented as the mean ± SD. A Chi-square test was performed to evaluate the allelic and genotypic frequencies that were calculated from the observed genotypic counts. Using Chi-square tests for categorical variables and one-way ANOVA for continuous variables, characteristics of subjects were compared between those with or without MetS and between those with or without the -395A allele, respectively. Because the prevalence of MetS was generally higher in women than in men [16], we reported the results in men and women, respectively, as well as in the whole population. In addition, odds ratios (OR) and 95 % confidential intervals (CI) for MetS were determined using binary logistic regression models.

Results

Clinical characteristics of study subjects

Among the 695 subjects for the current analyses, the mean age was 93.5 ± 3.2 years (range 90–108 years), 475 (68.3 %) were women. MetS was presented in 9.4 % of the whole population and it was more prevalent in women (12.2 %) than men (3.2 %) (p < 0.001). There was a significant difference in the distribution of many clinical parameters between subjects with or without MetS (Table 1). There were more women in the MetS group than in the non-MetS group (89.2 % vs. 66.2 %, p < 0.001). The mean values of WC, SBP, DBP, FPG, TG, LDL-C, SUA, and BMI were significantly higher in subjects with MetS compared to those without MetS, whereas the mean value of HDL-C was significantly lower in the MetS group. However, no significant difference was found between the two groups with respect to the mean value of TC.

Table 1 Characteristics of subjects according to MetS (N = 695)
Full size table

Subgroup analysis showed similar results in women, except that the mean value of TG were significantly higher in women with MetS compared with those without MetS. In men, subjects with MetS had significantly higher mean values of BMI, WC, SBP, FPG, and TG compared with those without MetS, but no significant difference was observed between the MetS and non-MetS groups in terms of the mean values of DBP, TC, H DL-C, LDL-C, and SUA (Table 1).

Incidence of the Klotho G-395A SNP

In the whole population, the genotype frequencies of the Klotho G-395A SNP were 70.4 % for GG genotype (n = 489), 29.5 % for GA genotype (n = 194), and 1.7 % for AA genotype (n = 12). These frequencies were in compliance with the Hardy-Weinberg equilibrium (X 2 = 2.14; p = 0.14). G and A allele frequencies were 0.852 and 0.148, respectively. Incidence of each genotype of the Klotho G-395A SNP according to MetS and gender is shown in Table 1. The distribution of the Klotho G-395A genotypes was significantly different between the MetS and non-MetS groups in the whole population and in women, but not in men.

The Klotho G-395A SNP and MetS

The characteristics of subjects according to the Klotho G-395A SNP was shown in Table 2. In the whole population, the frequency of MetS was 10.8 % in the GG genotype group and 5.9 % in the GA + AA genotype group (p = 0.004), and the result of logistic regression indicated that the -395A allele carriers had significantly lower risk of MetS after adjusting for age, gender, smoking habits, alcohol habits, exercise habits, BMI, and SUA (OR 0.50, 95 % CI 0.25 to 0.98) (Table 3).

Table 2 Characteristics of subjects according to the klotho G-395A polymorphism (N = 695)
Full size table
Table 3 Estimate of the effect of klotho G-392A polymorphism on MetS and its components with logistic regression
Full size table

In women, the frequencies of MetS were 14.3 % and 7.5 % in the GG and GA + AA groups, respectively (p = 0.038). The result of logistic regression showed that the -395A allele carriers had significantly lower risk of MetS after adjusting for relevant confounders (OR 0.51, 95 % CI 0.24 to 0.97) (Table 3).

In men, the frequencies of MetS were 3.7 % and 1.7 % in the GG and GA + AA groups, but the difference was not statistically significant (p = 0.447). Logistic regression analysis failed to find a significantly association between the Klotho G-395A SNP and MetS adjusting for relevant confounders (OR 0.42, 95 % CI 0.05 to 3.85) (Table 3).

The Klotho G-395A SNP and components of MetS

In the whole population, the -395A allele carriers, compared with the control subjects, had significantly lower frequencies of high blood pressure (49.8 % vs. 66.3 %, p < 0.001) and hypertriglyceridemia (11.7 % vs. 19.2 %, p = 0.017). There was no significant association of the Klotho G-395A SNP with abdominal obesity, Low HDL-C, and high FPG (Table 2). After adjusting for relevant confounders, logistic regression analysis revealed that the Klotho G-395A SNP was significantly associated with high blood pressure (OR 0.48, 95 % CI 0.34 to 0.67) and hypertriglyceridemia (OR 0.66, 95 % CI 0.39 to 0.95) (Table 3).

In women, the −395 allele carriers also had significantly lower frequencies of high blood pressure (51.4 % vs 68.4 %, p < 0.001) and hypertriglyceridemia (12.3 % vs. 20.7, p = 0.029). In addition, the -395A allele carriers had a trend of higher frequency of high FPG, but it was not statistically significant (15.8 % vs. 10.3 %, p = 0.094). After adjusting for relevant confounders, logistic regression analysis showed that the Klotho G-395A SNP was significantly associated with high blood pressure (OR 0.47, 95 % CI 0.31 to 0.71) and hypertriglyceridemia (OR 0.54, 95 % CI 0.31 to 0.98) (Table 3).

In men, the −395 allele carriers had significantly lower frequencies of high blood pressure (45.8 % vs 62.1 %, p = 0.030) and low HDL-C (1.7 % vs. 9.9 %). After adjusting for relevant confounders, logistic regression analysis showed that the Klotho G-395A SNP was significantly associated with high blood pressure (OR 0.47, 95 % CI 0.25 to 0.90) and low HDL-C (OR 0.69, 95 % CI 0.27 to 0.93) (Table 3).

Discussion

To the best of our knowledge, this is the first study to investigate the relationship between the Klotho G-395A SNP and MetS. The results of this study indicated that the -395A allele carriers of the Klotho gene were related to lower risk of MetS among Chinese nonagenarians and centenarians, especially in women. The association of the Klotho G-395A SNP with MetS could be linked to its observed influence on high blood pressure in both men and women, and hypertriglyceridemia in women. These findings were supported by previous studies which demonstrated that Klotho gene had an impact on multiple aspects of MetS including blood pressure, lipid metabolism and insulin resistance in different populations [11, 12, 17].

The association of the Klotho variant with the metabolic syndrome could be linked to its observed influence on high blood glucose, high blood pressure, insulin resistance, hypertriglyceridemia and endothelial function [17, 18]. The potential involvement of SNP G-395A in KLOTHO gene function and pathogenesis of the metabolic syndrome and these components remains speculative. Previous studies reported G-395A can influence the affinity of binding transcription factors, G-395A has strong Linkage Disequilibrium with other SNP and other gene (PPAR-γ), which could also act as a surrogate for other functional variant(s) nearby (such as G110C, C1818T and C2298T) [9, 17, 19, 20]. Furthermore, a previous study indicated that the G-395A SNP in the promoter region of Klotho gene might influence the function of Klotho gene by upregulating its expression and the Klotho protein may function as a humoral factor [9]. Thus, we speculated that the up-regulation of Klotho expression and functional link with other gene could also explain the observed association between the G-395A and the metabolic syndrome.

The minor allele frequency (MAF), the frequency of the -395A allele in this study, was 0.148. In previous studies, the MAF of the Klotho G-395A SNP were 0.191 in a Chinese Han population [9], from 0.155 to 0.171 in Korean populations [10] [21], from 0.128 to 0.168 in Japanese populations [11, 19], and 0.277 in a Turkish population [22]. Our finding was similar with the results of those studies conducted in East Asian populations, but inconsistent with the Turkish study [22]. One possible reason was the MAF of the Klotho G-395A SNP varied across ethnic populations. In addition, we did not identify the AA genotype in our population, whereas it varied from 1.7 % to 5.9 % in previous studies [10, 11, 21, 22]. The survival effect might account for this result as only nonagenarians and centenarians were included in this study.

In our study, the frequency of high blood pressure (defined as SBP ≥ 130 mm Hg and/or DBP ≥ 85 mm Hg) was significantly lower in the -395A allele carriers than the non-carriers among both men and women. Another Chinese study found similar results in women but not in men [9]. On the contrary, Rhee and colleague found that the mean SBP was significantly higher in the -395A allele carriers in health Korean women [10]. In addition, Shimoyama and colleagues reported no significant difference in the mean SBP between the -395A carriers and the non-carriers in healthy Japanese subjects [11]. Putting all these findings together, we may speculate that the association between blood pressure and the Klotho G-395A SNP varies in different ethnic populations.

The reason of the gender difference in the association of the Klotho G-395A SNP with lipid metabolism in this study remains unclear. Shimoyama et al. also found gender difference in the association between the Klotho G-395A SNP and lipid metabolism in Japanese people. The possible reason may be the gender-based difference in free radical homeostasis maintenance [23]. The Klotho gene has been reported to reduce oxidative stress by inhibiting the insulin/IGF-1 signaling pathway [8], whereas oxidative stress appears to be related to lipid metabolism [24].

It is notable that the prevalence of MetS in our study (9.4 %) was lower than that reported in other studies [1, 2]. In most developed countries the prevalence of MetS is approximately 20 % in the overall population, and increases with advancing age [1]. In China, a recent study reported that the prevalence of MetS was 18.4 % in adults according to the IDF criteria [25]. One possible reason for the low prevalence of MetS in our population was that people with MetS were prone to multiple morbidities and therefore might have low probability to live to more than ninety. However, to our knowledge, there was no other study regarding the prevalence of MetS in long-lived populations. Therefore, we could not found more evidence to support this inference.

There is robust evidence that hyperuricemia is associated with MetS, and some researchers argue that hyperuricemia should be considered as a new marker for MetS [26]. In this study, we found that the mean value of uric acid was significantly higher in subjects with MetS compared with those without MetS in all and female subjects, but the difference was not significant in men. In addition, we did not find the association between uric acid and the Klotho G-395A SNP. However, Shimoyama et al. reported that uric acid was significantly high in the -395A allele carriers of the Klotho gene compared with non-carriers in Japanese hemodialysis patients [12].

This study has some limitations. First, there were 870 subjects in the PLAD study, however, 175 subjects were excluded in the current analyses because of missing essential data. The exclusion of participants might induce selection bias. Second, because women generally have a longer life expectancy than men, a significant gender imbalance existed in our study population. The relatively small sample size of men (220 cases) reduced the possibility for detecting the possible association of Klotho G-395A SNP with MetS and its components and some conclusion may biased by the small sample size. Third, we only included the very old people in this study (90 or older), there might be survival bias. However, this is inherent to a study of individuals of this age-group. In conclusion, the Klotho G-395A SNP is associated with MetS in very elderly people, especially in women. This association could be linked to its influence on blood pressure and lipid metabolism. Further cross-sectional and longitudinal studies with larger sample size are warranted to investigate this association in different ethnic populations.

Conclusion

The results of this study indicates that the -395A allele carriers of the Klotho gene are correlated with lower risk of MetS in a sample of Chinese nonagenarians and centenarians, especially in women. This relationship needs to be further investigated in the future.

Ethics approval and consent to participate

The study protocol was approved by the Research Ethics Committee of Sichuan University. Written informed consent was obtained from all of the participants (or their legal proxies).

Consent for publication

Not applicable.

Availability of data and materials

The anonymized genetic dataset supporting the conclusions of this article is included within the article and its Additional file 1. The other data in this study will not be shared because many information are from local government and medical records, we are not allowed to share these data due to the privacy policy.

Abbreviations

MetS:

Metabolic syndrome

PLAD:

the Project of Longevity and Aging in Dujiangyan

OR:

Odd ratio

CI:

Confidential interval

SNP:

Single nucleotide polymorphism

LDL-C:

Low density lipoprotein cholesterol

HDL-C:

High density lipoprotein cholesterol

IDF:

the International diabetes federation

WC:

Waist circumference

FPG:

Asting plasma glucose

SBP:

Systolic blood pressure

DBP:

Diastolic blood pressure

TG:

Triglyceride

BMI:

Body mass index

TC:

Total cholesterol

SUA:

Serum uric acid

MAF:

The minor allele frequency

References

  1. Lechleitner M. Obesity and the metabolic syndrome in the elderly--a mini-review. Gerontology. 2008;54(5):253–9.

    Article  CAS  PubMed  Google Scholar 

  2. Balkau B, Valensi P, Eschwege E, Slama G. A review of the metabolic syndrome. Diabetes Metab. 2007;33(6):405–13.

    Article  CAS  PubMed  Google Scholar 

  3. Yaffe K. Metabolic syndrome and cognitive disorders: is the sum greater than its parts? Alzheimer Dis Assoc Disord. 2007;21(2):167–71.

    Article  PubMed  Google Scholar 

  4. Vattikuti S, Guo J, Chow CC. Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits. PLoS Genet. 2012;8(3):e1002637.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Gharipour M, Sadeghi M. Pivotal role of microRNA-33 in metabolic syndrome: A systematic review. ARYA Atheroscler. 2013;9(6):372–6.

    PubMed Central  PubMed  Google Scholar 

  6. Povel CM, Boer JM, Reiling E, Feskens EJ. Genetic variants and the metabolic syndrome: a systematic review. Obes Rev. 2011;12(11):952–67.

    Article  CAS  PubMed  Google Scholar 

  7. Kuro-o M, Hanaoka K, Hiroi Y, Noguchi T, Fujimori Y, Takewaki S, Hayasaka M, Katoh H, Miyagishi A, Nagai R et al. Salt-sensitive hypertension in transgenic mice overexpressing Na(+)-proton exchanger. Circ Res. 1995;76(1):148–53.

  8. Wang Y, Sun Z. Current understanding of klotho. Ageing Res Rev. 2009;8(1):43–51.

    Article  PubMed Central  PubMed  Google Scholar 

  9. Wang HL, Xu Q, Wang Z, Zhang YH, Si LY, Li XJ, Yang QH, Xiao H. A potential regulatory single nucleotide polymorphism in the promoter of the Klotho gene may be associated with essential hypertension in the Chinese Han population. Clin Chim Acta. 2010;411(5–6):386–90.

  10. Rhee EJ, Oh KW, Yun EJ, Jung CH, Lee WY, Kim SW, Baek KH, Kang MI, Park SW. Relationship between polymorphisms G395A in promoter and C1818T in exon 4 of the KLOTHO gene with glucose metabolism and cardiovascular risk factors in Korean women. J Endocrinol Investig. 2006;29(7):613–8.

  11. Shimoyama Y, Nishio K, Hamajima N, Niwa T. KLOTHO gene polymorphisms G-395A and C1818T are associated with lipid and glucose metabolism, bone mineral density and systolic blood pressure in Japanese healthy subjects. Clin Chim Acta. 2009;406(1–2):134–8.

    Article  CAS  PubMed  Google Scholar 

  12. Shimoyama Y, Taki K, Mitsuda Y, Tsuruta Y, Hamajima N, Niwa T. KLOTHO gene polymorphisms G-395A and C1818T are associated with low-density lipoprotein cholesterol and uric acid in Japanese hemodialysis patients. Am J Nephrol. 2009;30(4):383–8.

    Article  CAS  PubMed  Google Scholar 

  13. Yue JR, Dong BR, Huang CQ, Lu ZC, Wu HM, Zhang YL. Pro12Ala polymorphism in PPAR-gamma2 and dementia in Chinese nonagenarians/centenarians. Age (Dordr). 2010;32(3):397–404.

    Article  CAS  Google Scholar 

  14. Yue JR, Huang CQ, Dong BR. Association of serum uric acid with body mass index among long-lived Chinese. Exp Gerontol. 2012;47(8):595–600.

    Article  CAS  PubMed  Google Scholar 

  15. Lu YH, Lu JM, Wang SY, Li CL, Liu LS, Zheng RP, Tian H, Wang XL, Yang LJ, Zhang YQ et al. Comparison of the diagnostic criteria of metabolic syndrome by International Diabetes Federation and that by Chinese Medical Association Diabetes Branch. Zhonghua Yi Xue Za Zhi. 2006;86(6):386–9.

  16. Beigh SH, Jain S. Prevalence of metabolic syndrome and gender differences. Bioinformation. 2012;8(13):613–6.

    Article  PubMed Central  PubMed  Google Scholar 

  17. Majumdar V, Christopher R. Association of exonic variants of Klotho with metabolic syndrome in Asian Indians. Clin Chim Acta. 2011;412(11–12):1116–21.

    Article  CAS  PubMed  Google Scholar 

  18. Saito Y, Nakamura T, Ohyama Y, Suzuki T, Iida A, Shiraki-Iida T, Kuro-o M, Nabeshima Y, Kurabayashi M, Nagai R. In vivo klotho gene delivery protects against endothelial dysfunction in multiple risk factor syndrome. Biochem Biophys Res Commun. 2000;276(2):767–72.

  19. Kawano K, Ogata N, Chiano M, Molloy H, Kleyn P, Spector TD, Uchida M, Hosoi T, Suzuki T, Orimo H et al. Klotho gene polymorphisms associated with bone density of aged postmenopausal women. J Bone Miner Res. 2002;17(10):1744–51.

  20. Zhang F, Zhai G, Kato BS, Hart DJ, Hunter D, Spector TD, Ahmadi KR. Association between KLOTHO gene and hand osteoarthritis in a female Caucasian population. Osteoarthritis Cartilage. 2007;15(6):624–9.

  21. Kim Y, Jeong SJ, Lee HS, Kim EJ, Song YR, Kim SG, Oh JE, Lee YK, Seo JW, Yoon JW et al. Polymorphism in the promoter region of the klotho gene (G-395A) is associated with early dysfunction in vascular access in hemodialysis patients. Korean J Intern Med. 2008;23(4):201–7.

  22. Telci D, Dogan AU, Ozbek E, Polat EC, Simsek A, Cakir SS, Yeloglu HO, Sahin F. KLOTHO gene polymorphism of G395A is associated with kidney stones. Am J Nephrol. 2011;33(4):337–43.

    Article  CAS  PubMed  Google Scholar 

  23. Ali SS, Xiong C, Lucero J, Behrens MM, Dugan LL, Quick KL. Gender differences in free radical homeostasis during aging: shorter-lived female C57BL6 mice have increased oxidative stress. Aging Cell. 2006;5(6):565–74.

    Article  CAS  PubMed  Google Scholar 

  24. Sekiya M, Hiraishi A, Touyama M, Sakamoto K. Oxidative stress induced lipid accumulation via SREBP1c activation in HepG2 cells. Biochem Biophys Res Commun. 2008;375(4):602–7.

    Article  CAS  PubMed  Google Scholar 

  25. Xi B, He D, Hu Y, Zhou D. Prevalence of metabolic syndrome and its influencing factors among the Chinese adults: the China Health and Nutrition Survey in 2009. Prev Med. 2013;57(6):867–71.

    Article  PubMed Central  PubMed  Google Scholar 

  26. Billiet L, Doaty S, Katz JD, Velasquez MT. Review of Hyperuricemia as New Marker for Metabolic Syndrome. ISRN rheumatology. 2014;2014:852954.

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Acknowledgments

The authors appreciate the staff of the department of Geriatrics, Dujiangyan Hospital; and all participants, as well as their legal proxies, for their great contributions.

Funding

This work was supported by the project of Science and technology Bureau of Sichuan Province (2006Z09-006-4) and the Cadres health care committee of Sichuan Province Health Department (2012-GANJIANBAN-7). The sponsor has no role in the design, methods, data collection, analysis and preparation of this paper.

Author information

Author notes

    Authors and Affiliations

    1. The Center of Gerontology and Geriatrics, West China Hospital, Sichuan University, No.37 Guoxue Lane, Chengdu, Sichuan, China

      Li Luo, Qiukui Hao, Birong Dong & Ming Yang

    Authors
    1. Li Luo
      View author publications

      You can also search for this author in PubMed Google Scholar

    2. Qiukui Hao
      View author publications

      You can also search for this author in PubMed Google Scholar

    3. Birong Dong
      View author publications

      You can also search for this author in PubMed Google Scholar

    4. Ming Yang
      View author publications

      You can also search for this author in PubMed Google Scholar

    Corresponding author

    Correspondence to Ming Yang.

    Additional information

    Competing interests

    No author of this paper has any competing interests with this study.

    Authors’ contributions

    LL carried out the molecular genetic studies, performed some of the statistical analysis and drafted the manuscript. QH participated in some part of the study and drafted the manuscript and revised it (contributed equally with LL to this work). BD participated in the design of the study. MY conceived of the study, participated in its design and coordination, performed the statistical analysis and revised the manuscript. All authors read and approved the final manuscript.

    Authors’ information

    All The authors are staff in The Center of Gerontology and Geriatrics, West China Hospital, Sichuan University, China.

    Additional file

    Additional file 1:

    the SNP data of the study population. (XLS 36 kb)

    Rights and permissions

    Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

    Reprints and permissions

    About this article

    Check for updates. Verify currency and authenticity via CrossMark

    Cite this article

    Luo, L., Hao, Q., Dong, B. et al. The Klotho gene G-395A polymorphism and metabolic syndrome in very elderly people. BMC Geriatr 16, 46 (2016). https://doi.org/10.1186/s12877-016-0221-6

    Download citation

    • Received:

    • Accepted:

    • Published:

    • DOI: https://doi.org/10.1186/s12877-016-0221-6

    Keywords

    BMC Geriatrics

    ISSN: 1471-2318

    Contact us