Non-alcoholic Fatty Liver Disease
|
0.320 |
GeneticVariation
|
disease |
BEFREE |
<i>KLB</i> rs7674434 and rs12152703 had associations with alanine aminotransferase (ALT) (<i>P</i> = 0.03 and <i>P</i> = 0.04, respectively) and gamma-glutamyltransferase (<i>P</i> = 0.03 and <i>P</i> = 0.02, respectively) levels in all subjects, but the associations were especially strong with ALT in the NAFLD group (<i>P</i> = 0.005 and <i>P</i> = 0.008, respectively).
|
31548436 |
2019 |
Non-alcoholic Fatty Liver Disease
|
0.320 |
Biomarker
|
disease |
CTD_human |
Hepatic regulation of VLDL receptor by PPARβ/δ and FGF21 modulates non-alcoholic fatty liver disease.
|
29289645 |
2018 |
Non-alcoholic Fatty Liver Disease
|
0.320 |
GeneticVariation
|
disease |
BEFREE |
We evaluated the impact of the rs17618244 G>A β-Klotho (KLB) variant on liver damage in 249 pediatric patients with biopsy-proven NAFLD and the association of this variant with the expression of hepatic and soluble KLB.
|
31655133 |
2020 |
Congenital hypogonadotropic hypogonadism
|
0.310 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.
|
28754744 |
2017 |
Congenital hypogonadotropic hypogonadism
|
0.310 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Congenital hypogonadotropic hypogonadism
|
0.310 |
GeneticVariation
|
disease |
BEFREE |
<i>KLB</i>, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.
|
28754744 |
2017 |
Nonalcoholic Steatohepatitis
|
0.300 |
Biomarker
|
disease |
CTD_human |
Hepatic regulation of VLDL receptor by PPARβ/δ and FGF21 modulates non-alcoholic fatty liver disease.
|
29289645 |
2018 |
Obesity
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
KLB and FGFR1 were upregulated in AT in relation to obesity, and both were further increased 12 months after RYGB.
|
28552744 |
2017 |
Obesity
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
In addition to higher FGF21 levels, reduced KLB expression in liver and adipose tissue has been noted in these same individuals, suggesting that obesity may represent an FGF21 resistant state.
|
26901091 |
2016 |
Obesity
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Since obesity has been reported to be associated with reduced expression of FGFR1 and βKlotho receptor in white adipose tissues in mice, our results suggest that the distribution in adipose tissues was influenced by target expression levels.
|
28895785 |
2018 |
Obesity
|
0.100 |
Biomarker
|
disease |
BEFREE |
However, further studies are needed to explore the possibility that Klotho could be a novel therapeutic target to reduce obesity and related complications, and to determine whether and how Klotho might influence the regulation and function of a related protein, β-Klotho, which is also involved in energy metabolism.
|
22641000 |
2012 |
Obesity
|
0.100 |
Biomarker
|
disease |
BEFREE |
Recent microRNA (miR) studies have revealed that aberrantly elevated miR-34a in obesity directly targets β-Klotho, the obligate coreceptor for both FGF19 and FGF21, and attenuates metabolic signaling of these hormones.
|
27125742 |
2016 |
Obesity
|
0.100 |
Biomarker
|
disease |
BEFREE |
These results indicate that aberrantly elevated miR-34a in obesity attenuates hepatic FGF19 signaling by directly targeting βKL.
|
22988100 |
2012 |
Obesity
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The G-allele frequency of <i>KLB</i> rs7674434 and T-allele frequency of rs12152703 were higher in the obese with NAFLD than obese without NAFLD group (<i>P</i> = 0.004 and <i>P</i> = 0.006), but the genotype distribution between two non-obese groups did not differ.
|
31548436 |
2019 |
Obesity
|
0.100 |
Biomarker
|
disease |
BEFREE |
Replenishment of recombinant FGF21 to a level equivalent to that in obesity restores SAT mass and reverses insulin resistance in FGF21KO, but not in adipose-specific βklotho knockout mice.
|
29348470 |
2018 |
Obesity
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
In WAT, overweight/obesity with and without type 2 diabetes led to reduced expression of KLB, but increased FGFR1c expression.
|
28721439 |
2017 |
Obesity
|
0.100 |
Biomarker
|
disease |
BEFREE |
β-Klotho deficiency protects against obesity through a crosstalk between liver, microbiota, and brown adipose tissue.
|
28422755 |
2017 |
Liver carcinoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
These data suggest βKlotho suppresses tumor growth in hepatocellular carcinoma.
|
23383245 |
2013 |
Liver carcinoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
Although it is well established that FGF19 acts through the receptor complex FGFR4-β-Klotho (KLB) to regulate bile acid metabolism, FGF19 is also implicated in the development of HCC.
|
24728076 |
2014 |
Liver carcinoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
The restricted tissue expression profile of KLB, together with the anti-proliferative effect observed with KLB-silencing, also qualifies it as a specific and potent therapeutic target for HCC patients.
|
22439738 |
2012 |
Liver carcinoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Here we show that βklotho expression is more consistently down-regulated in human and mouse hepatomas than FGFR4.
|
20657013 |
2010 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
In WAT, overweight/obesity with and without type 2 diabetes led to reduced expression of KLB, but increased FGFR1c expression.
|
28721439 |
2017 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Our findings indicate that serum Klotho levels were associated with the development of T2DM, and long-term control of blood glucose will be beneficial in ameliorating changes to α-Klotho and β-Klotho levels in patients with T2DM and complications.
|
30042059 |
2018 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Serum levels of α-Klotho and β-Klotho are down-regulated in patients with T2DM.
|
27916483 |
2017 |
Malignant neoplasm of breast
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Quantitative real-time RT-PCR of ITGA7, SVEP1, TNS1, LPHN3, SEMA3G, KLB and MMP13 mRNA expression in breast cancer.
|
23317273 |
2012 |