Soluble serum Klotho levels in healthy subjects. Comparison of two different immunoassays
Soluble serum Klotho is a new biomarker linked to chronic kidney disease, cardiovascular disease and diabetes. This study describes the evaluation and comparison of two different immunoassays and establishment of assay specific reference intervals in adults. Serum Klotho concentrations were determin...
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Published in | Clinical biochemistry Vol. 46; no. 12; pp. 1079 - 1083 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.08.2013
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Online Access | Get full text |
ISSN | 0009-9120 1873-2933 1873-2933 |
DOI | 10.1016/j.clinbiochem.2013.05.046 |
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Abstract | Soluble serum Klotho is a new biomarker linked to chronic kidney disease, cardiovascular disease and diabetes. This study describes the evaluation and comparison of two different immunoassays and establishment of assay specific reference intervals in adults.
Serum Klotho concentrations were determined in 120 healthy adults aged 19–66years. Blood samples were collected, and stored sera were assayed for Klotho according to age and gender. In addition several other clinical and laboratory characteristics were determined in the cohort and compared to the levels of serum Klotho.
Serum Klotho levels were significantly higher in time-resolved fluorescence immunoassay (TRF) compared to an ELISA (IBL) and no correlation was found between the assays. No signal was obtained in either assay when the standard curve was switched between the two different immunoassays. The median serum Klotho concentration using TRF was 61ng/mL (2.5–97.5% reference limits; 11–181ng/mL) for males and 99ng/mL (2.5–97.5% reference limits; 19–316ng/mL) for females while the ELISA gave a mean value of 472pg/mL (2.5–97.5% reference limits; 204–741pg/mL) with no difference between genders. Concentrations of serum Klotho were independently associated with estimated glomerular filtration rate (eGFR) and body weight using TRF whereas serum Klotho concentrations were associated with age using the ELISA.
Comparison of two different immunoassays for serum Klotho indicate, that the protein exists in human beings in different forms which may function as independent factors and whose role and potential value as biomarkers needs to be evaluated separately. Reference intervals specific for the different forms recognized by the different assays were calculated in this study.
•Assay specific reference values for soluble serum Klotho in adults are established.•Two Klotho immunoassays showed a significant difference in serum Klotho levels.•Serum Klotho was negatively correlated with eGFR and body weight using TRF immunoassay.•Serum Klotho was negatively correlated with age using ELISA.•Both assays showed acceptable performance for quantification of serum Klotho. |
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AbstractList | Soluble serum Klotho is a new biomarker linked to chronic kidney disease, cardiovascular disease and diabetes. This study describes the evaluation and comparison of two different immunoassays and establishment of assay specific reference intervals in adults.
Serum Klotho concentrations were determined in 120 healthy adults aged 19–66years. Blood samples were collected, and stored sera were assayed for Klotho according to age and gender. In addition several other clinical and laboratory characteristics were determined in the cohort and compared to the levels of serum Klotho.
Serum Klotho levels were significantly higher in time-resolved fluorescence immunoassay (TRF) compared to an ELISA (IBL) and no correlation was found between the assays. No signal was obtained in either assay when the standard curve was switched between the two different immunoassays. The median serum Klotho concentration using TRF was 61ng/mL (2.5–97.5% reference limits; 11–181ng/mL) for males and 99ng/mL (2.5–97.5% reference limits; 19–316ng/mL) for females while the ELISA gave a mean value of 472pg/mL (2.5–97.5% reference limits; 204–741pg/mL) with no difference between genders. Concentrations of serum Klotho were independently associated with estimated glomerular filtration rate (eGFR) and body weight using TRF whereas serum Klotho concentrations were associated with age using the ELISA.
Comparison of two different immunoassays for serum Klotho indicate, that the protein exists in human beings in different forms which may function as independent factors and whose role and potential value as biomarkers needs to be evaluated separately. Reference intervals specific for the different forms recognized by the different assays were calculated in this study.
•Assay specific reference values for soluble serum Klotho in adults are established.•Two Klotho immunoassays showed a significant difference in serum Klotho levels.•Serum Klotho was negatively correlated with eGFR and body weight using TRF immunoassay.•Serum Klotho was negatively correlated with age using ELISA.•Both assays showed acceptable performance for quantification of serum Klotho. Soluble serum Klotho is a new biomarker linked to chronic kidney disease, cardiovascular disease and diabetes. This study describes the evaluation and comparison of two different immunoassays and establishment of assay specific reference intervals in adults.OBJECTIVESoluble serum Klotho is a new biomarker linked to chronic kidney disease, cardiovascular disease and diabetes. This study describes the evaluation and comparison of two different immunoassays and establishment of assay specific reference intervals in adults.Serum Klotho concentrations were determined in 120 healthy adults aged 19-66 years. Blood samples were collected, and stored sera were assayed for Klotho according to age and gender. In addition several other clinical and laboratory characteristics were determined in the cohort and compared to the levels of serum Klotho.DESIGN AND METHODSSerum Klotho concentrations were determined in 120 healthy adults aged 19-66 years. Blood samples were collected, and stored sera were assayed for Klotho according to age and gender. In addition several other clinical and laboratory characteristics were determined in the cohort and compared to the levels of serum Klotho.Serum Klotho levels were significantly higher in time-resolved fluorescence immunoassay (TRF) compared to an ELISA (IBL) and no correlation was found between the assays. No signal was obtained in either assay when the standard curve was switched between the two different immunoassays. The median serum Klotho concentration using TRF was 61 ng/mL (2.5-97.5% reference limits; 11-181 ng/mL) for males and 99 ng/mL (2.5-97.5% reference limits; 19-316 ng/mL) for females while the ELISA gave a mean value of 472 pg/mL (2.5-97.5% reference limits; 204-741 pg/mL) with no difference between genders. Concentrations of serum Klotho were independently associated with estimated glomerular filtration rate (eGFR) and body weight using TRF whereas serum Klotho concentrations were associated with age using the ELISA.RESULTSSerum Klotho levels were significantly higher in time-resolved fluorescence immunoassay (TRF) compared to an ELISA (IBL) and no correlation was found between the assays. No signal was obtained in either assay when the standard curve was switched between the two different immunoassays. The median serum Klotho concentration using TRF was 61 ng/mL (2.5-97.5% reference limits; 11-181 ng/mL) for males and 99 ng/mL (2.5-97.5% reference limits; 19-316 ng/mL) for females while the ELISA gave a mean value of 472 pg/mL (2.5-97.5% reference limits; 204-741 pg/mL) with no difference between genders. Concentrations of serum Klotho were independently associated with estimated glomerular filtration rate (eGFR) and body weight using TRF whereas serum Klotho concentrations were associated with age using the ELISA.Comparison of two different immunoassays for serum Klotho indicate, that the protein exists in human beings in different forms which may function as independent factors and whose role and potential value as biomarkers needs to be evaluated separately. Reference intervals specific for the different forms recognized by the different assays were calculated in this study.CONCLUSIONComparison of two different immunoassays for serum Klotho indicate, that the protein exists in human beings in different forms which may function as independent factors and whose role and potential value as biomarkers needs to be evaluated separately. Reference intervals specific for the different forms recognized by the different assays were calculated in this study. Soluble serum Klotho is a new biomarker linked to chronic kidney disease, cardiovascular disease and diabetes. This study describes the evaluation and comparison of two different immunoassays and establishment of assay specific reference intervals in adults. Serum Klotho concentrations were determined in 120 healthy adults aged 19-66 years. Blood samples were collected, and stored sera were assayed for Klotho according to age and gender. In addition several other clinical and laboratory characteristics were determined in the cohort and compared to the levels of serum Klotho. Serum Klotho levels were significantly higher in time-resolved fluorescence immunoassay (TRF) compared to an ELISA (IBL) and no correlation was found between the assays. No signal was obtained in either assay when the standard curve was switched between the two different immunoassays. The median serum Klotho concentration using TRF was 61 ng/mL (2.5-97.5% reference limits; 11-181 ng/mL) for males and 99 ng/mL (2.5-97.5% reference limits; 19-316 ng/mL) for females while the ELISA gave a mean value of 472 pg/mL (2.5-97.5% reference limits; 204-741 pg/mL) with no difference between genders. Concentrations of serum Klotho were independently associated with estimated glomerular filtration rate (eGFR) and body weight using TRF whereas serum Klotho concentrations were associated with age using the ELISA. Comparison of two different immunoassays for serum Klotho indicate, that the protein exists in human beings in different forms which may function as independent factors and whose role and potential value as biomarkers needs to be evaluated separately. Reference intervals specific for the different forms recognized by the different assays were calculated in this study. |
Author | Pedersen, Lise Pedersen, Susanne Møller Brasen, Claus Lohman Rasmussen, Lars Melholt |
Author_xml | – sequence: 1 givenname: Lise surname: Pedersen fullname: Pedersen, Lise email: Lise-Pedersen@ouh.regionsyddanmark.dk organization: Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark – sequence: 2 givenname: Susanne Møller surname: Pedersen fullname: Pedersen, Susanne Møller organization: Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark – sequence: 3 givenname: Claus Lohman surname: Brasen fullname: Brasen, Claus Lohman organization: Department of Clinical Biochemistry, Vejle Hospital, Denmark – sequence: 4 givenname: Lars Melholt surname: Rasmussen fullname: Rasmussen, Lars Melholt organization: Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23707222$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/S0014-5793(98)00127-6 10.1007/s10157-011-0511-4 10.1073/pnas.0803223105 10.1093/ndt/gfr645 10.1006/bbrc.1998.9576 10.4061/2011/102686 10.1210/jc.2002-021105 10.1007/978-1-4614-0887-1_2 10.5414/CN107204 10.1073/pnas.0709805104 10.1016/j.febslet.2004.03.090 10.1016/j.bbrc.2010.06.110 10.1126/science.1114245 10.1006/bbrc.1997.8019 10.1126/science.1143578 10.1016/S0006-291X(02)03056-5 10.1385/ENDO:25:3:229 10.1309/AJCPGPMAF7SFRBO4 10.1681/ASN.2009121311 10.1053/meta.2000.8606 |
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Keywords | eGFR PTH Phosphate Ionized calcium Klotho Reference ranges FGF23 Immunoassays Age BMI |
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References | Chen, Podvin, Gillespie, Leeman, Abraham (bb0015) 2007; 104 Hostmark, Sogaard, Alvaer, Meyer (bb0025) 2011; 2011 Sugiura, Tsuchiya, Nitta (bb0080) 2011; 15 Imai, Ishikawa, Matsukawa, Kida, Ohta, Ikushima (bb0040) 2004; 25 Yang, Matsukawa, Rakugi, Imai, Kida, Nagai (bb0100) 2003; 301 Shiraki-Iida, Aizawa, Matsumura, Sekine, Iida, Anazawa (bb0075) 1998; 424 Liu, Fergusson, Castilho, Liu, Cao, Chen (bb0060) 2007; 317 Yamazaki, Okazaki, Shibata, Hasegawa, Satoh, Tajima (bb0095) 2002; 87 Kuro (bb0055) 2012; 728 Matsumura, Aizawa, Shiraki-Iida, Nagai, Kuro-O, Nabeshima (bb0065) 1998; 242 Utsugi, Ohno, Ohyama, Uchiyama, Saito, Matsumara (bb0085) 2000; 49 Chang, Hoefs, van der Kemp, Topala, Bindels, Hoenderop (bb0010) 2005; 310 Komaba, Koizumi, Tanaka, Takahashi, Sawada, Kakuta (bb0050) 2012; 27 Yokoyama, Imura, Ohkido, Maruyama, Yamazaki, Hasegawa (bb0105) 2012; 77 Ohyama, Kurabayashi, Masuda, Nakamura, Aihara, Kaname (bb0070) 1998; 251 Yamazaki, Imura, Urakawa, Shimada, Murakami, Aano (bb0090) 2010; 398 Devaraj, Syed, Chien, Jialal (bb0020) 2012; 137 Hu, Shi, Zhang, Quiñones, Griffith, Kuro-O (bb0035) 2011; 22 Imura, Iwano, Tohyama, Tsuji, Nozaki, Hashimoto (bb0045) 2004; 565 Hu, Kuro-o, Moe (bb0030) 2012 Cha, Ortega, Kurosu, Rosenblatt, Kuro-O, Huang (bb0005) 2008; 105 Devaraj (10.1016/j.clinbiochem.2013.05.046_bb0020) 2012; 137 Hostmark (10.1016/j.clinbiochem.2013.05.046_bb0025) 2011; 2011 Chen (10.1016/j.clinbiochem.2013.05.046_bb0015) 2007; 104 Kuro (10.1016/j.clinbiochem.2013.05.046_bb0055) 2012; 728 Ohyama (10.1016/j.clinbiochem.2013.05.046_bb0070) 1998; 251 Liu (10.1016/j.clinbiochem.2013.05.046_bb0060) 2007; 317 Matsumura (10.1016/j.clinbiochem.2013.05.046_bb0065) 1998; 242 Utsugi (10.1016/j.clinbiochem.2013.05.046_bb0085) 2000; 49 Hu (10.1016/j.clinbiochem.2013.05.046_bb0035) 2011; 22 Sugiura (10.1016/j.clinbiochem.2013.05.046_bb0080) 2011; 15 Imai (10.1016/j.clinbiochem.2013.05.046_bb0040) 2004; 25 Yamazaki (10.1016/j.clinbiochem.2013.05.046_bb0095) 2002; 87 Hu (10.1016/j.clinbiochem.2013.05.046_bb0030) 2012 Shiraki-Iida (10.1016/j.clinbiochem.2013.05.046_bb0075) 1998; 424 Yang (10.1016/j.clinbiochem.2013.05.046_bb0100) 2003; 301 Chang (10.1016/j.clinbiochem.2013.05.046_bb0010) 2005; 310 Yamazaki (10.1016/j.clinbiochem.2013.05.046_bb0090) 2010; 398 Yokoyama (10.1016/j.clinbiochem.2013.05.046_bb0105) 2012; 77 Imura (10.1016/j.clinbiochem.2013.05.046_bb0045) 2004; 565 Komaba (10.1016/j.clinbiochem.2013.05.046_bb0050) 2012; 27 Cha (10.1016/j.clinbiochem.2013.05.046_bb0005) 2008; 105 |
References_xml | – volume: 104 start-page: 19796 year: 2007 end-page: 19801 ident: bb0015 article-title: Insulin stimulates the cleavage and release of the extracellular domain of Klotho by ADAM10 and ADAM17 publication-title: Proc Natl Acad Sci U S A – volume: 137 start-page: 479 year: 2012 end-page: 485 ident: bb0020 article-title: Validation of an immunoassay for soluble klotho protein: decreased levels in diabetes and increased levels in chronic kidney disease publication-title: Am J Clin Pathol – volume: 424 start-page: 6 year: 1998 end-page: 10 ident: bb0075 article-title: Structure of the mouse klotho gene and its two transcripts encoding membrane and secreted protein publication-title: FEBS Lett – volume: 49 start-page: 1118 year: 2000 end-page: 1123 ident: bb0085 article-title: Decreased insulin production and increased insulin sensitivity in the klotho mutant mouse, a novel animal model for human aging publication-title: Metabolism – volume: 27 start-page: 1967 year: 2012 end-page: 1969 ident: bb0050 article-title: Effects of cinacalcet treatment on serum soluble Klotho levels in haemodialysis patients with secondary hyperparathyroidism publication-title: Nephrol Dial Transplant – volume: 242 start-page: 626 year: 1998 end-page: 630 ident: bb0065 article-title: Identification of the human klotho gene and its two transcripts encoding membrane and secreted klotho protein publication-title: Biochem Biophys Res Commun – volume: 77 start-page: 347 year: 2012 end-page: 351 ident: bb0105 article-title: Serum soluble alpha-klotho in hemodialysis patients publication-title: Clin Nephrol – volume: 251 start-page: 920 year: 1998 end-page: 925 ident: bb0070 article-title: Molecular cloning of rat klotho cDNA: markedly decreased expression of klotho by acute inflammatory stress publication-title: Biochem Biophys Res Commun – volume: 15 start-page: 795 year: 2011 end-page: 796 ident: bb0080 article-title: Circulating levels of soluble alpha-Klotho in patients with chronic kidney disease publication-title: Clin Exp Nephrol – volume: 398 start-page: 513 year: 2010 end-page: 518 ident: bb0090 article-title: Establishment of sandwich ELISA for soluble alpha-Klotho measurement: age-dependent change of soluble alpha-Klotho levels in healthy subjects publication-title: Biochem Biophys Res Commun – volume: 22 start-page: 124 year: 2011 end-page: 136 ident: bb0035 article-title: Klotho deficiency causes vascular calcification in chronic kidney disease publication-title: J Am Soc Nephrol – volume: 2011 start-page: 102686 year: 2011 ident: bb0025 article-title: The oslo health study: a dietary index estimating frequent intake of soft drinks and rare intake of fruit and vegetables is negatively associated with bone mineral density publication-title: J Osteoporos – volume: 728 start-page: 25 year: 2012 end-page: 40 ident: bb0055 article-title: Klotho and betaKlotho publication-title: Adv Exp Med Biol – volume: 310 start-page: 490 year: 2005 end-page: 493 ident: bb0010 article-title: The beta-glucuronidase klotho hydrolyzes and activates the TRPV5 channel publication-title: Science – volume: 301 start-page: 424 year: 2003 end-page: 429 ident: bb0100 article-title: Upregulation of cAMP is a new functional signal pathway of Klotho in endothelial cells publication-title: Biochem Biophys Res Commun – volume: 105 start-page: 9805 year: 2008 end-page: 9810 ident: bb0005 article-title: Removal of sialic acid involving Klotho causes cell-surface retention of TRPV5 channel via binding to galectin-1 publication-title: Proc Natl Acad Sci U S A – volume: 25 start-page: 229 year: 2004 end-page: 234 ident: bb0040 article-title: Klotho protein activates the PKC pathway in the kidney and testis and suppresses 25-hydroxyvitamin D3 1alpha-hydroxylase gene expression publication-title: Endocrine – volume: 87 start-page: 4957 year: 2002 end-page: 4960 ident: bb0095 article-title: Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia publication-title: J Clin Endocrinol Metab – start-page: 126 year: 2012 end-page: 157 ident: bb0030 publication-title: Endocrine FGFs and Klothos – volume: 565 start-page: 143 year: 2004 end-page: 147 ident: bb0045 article-title: Secreted Klotho protein in sera and CSF: implication for post-translational cleavage in release of Klotho protein from cell membrane publication-title: FEBS Lett – volume: 317 start-page: 803 year: 2007 end-page: 806 ident: bb0060 article-title: Augmented Wnt signaling in a mammalian model of accelerated aging publication-title: Science – volume: 424 start-page: 6 year: 1998 ident: 10.1016/j.clinbiochem.2013.05.046_bb0075 article-title: Structure of the mouse klotho gene and its two transcripts encoding membrane and secreted protein publication-title: FEBS Lett doi: 10.1016/S0014-5793(98)00127-6 – volume: 15 start-page: 795 year: 2011 ident: 10.1016/j.clinbiochem.2013.05.046_bb0080 article-title: Circulating levels of soluble alpha-Klotho in patients with chronic kidney disease publication-title: Clin Exp Nephrol doi: 10.1007/s10157-011-0511-4 – volume: 105 start-page: 9805 year: 2008 ident: 10.1016/j.clinbiochem.2013.05.046_bb0005 article-title: Removal of sialic acid involving Klotho causes cell-surface retention of TRPV5 channel via binding to galectin-1 publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0803223105 – volume: 27 start-page: 1967 year: 2012 ident: 10.1016/j.clinbiochem.2013.05.046_bb0050 article-title: Effects of cinacalcet treatment on serum soluble Klotho levels in haemodialysis patients with secondary hyperparathyroidism publication-title: Nephrol Dial Transplant doi: 10.1093/ndt/gfr645 – volume: 251 start-page: 920 year: 1998 ident: 10.1016/j.clinbiochem.2013.05.046_bb0070 article-title: Molecular cloning of rat klotho cDNA: markedly decreased expression of klotho by acute inflammatory stress publication-title: Biochem Biophys Res Commun doi: 10.1006/bbrc.1998.9576 – volume: 2011 start-page: 102686 year: 2011 ident: 10.1016/j.clinbiochem.2013.05.046_bb0025 article-title: The oslo health study: a dietary index estimating frequent intake of soft drinks and rare intake of fruit and vegetables is negatively associated with bone mineral density publication-title: J Osteoporos doi: 10.4061/2011/102686 – volume: 87 start-page: 4957 year: 2002 ident: 10.1016/j.clinbiochem.2013.05.046_bb0095 article-title: Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2002-021105 – volume: 728 start-page: 25 year: 2012 ident: 10.1016/j.clinbiochem.2013.05.046_bb0055 article-title: Klotho and betaKlotho publication-title: Adv Exp Med Biol doi: 10.1007/978-1-4614-0887-1_2 – start-page: 126 year: 2012 ident: 10.1016/j.clinbiochem.2013.05.046_bb0030 – volume: 77 start-page: 347 year: 2012 ident: 10.1016/j.clinbiochem.2013.05.046_bb0105 article-title: Serum soluble alpha-klotho in hemodialysis patients publication-title: Clin Nephrol doi: 10.5414/CN107204 – volume: 104 start-page: 19796 year: 2007 ident: 10.1016/j.clinbiochem.2013.05.046_bb0015 article-title: Insulin stimulates the cleavage and release of the extracellular domain of Klotho by ADAM10 and ADAM17 publication-title: Proc Natl Acad Sci U S A doi: 10.1073/pnas.0709805104 – volume: 565 start-page: 143 year: 2004 ident: 10.1016/j.clinbiochem.2013.05.046_bb0045 article-title: Secreted Klotho protein in sera and CSF: implication for post-translational cleavage in release of Klotho protein from cell membrane publication-title: FEBS Lett doi: 10.1016/j.febslet.2004.03.090 – volume: 398 start-page: 513 year: 2010 ident: 10.1016/j.clinbiochem.2013.05.046_bb0090 article-title: Establishment of sandwich ELISA for soluble alpha-Klotho measurement: age-dependent change of soluble alpha-Klotho levels in healthy subjects publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2010.06.110 – volume: 310 start-page: 490 year: 2005 ident: 10.1016/j.clinbiochem.2013.05.046_bb0010 article-title: The beta-glucuronidase klotho hydrolyzes and activates the TRPV5 channel publication-title: Science doi: 10.1126/science.1114245 – volume: 242 start-page: 626 year: 1998 ident: 10.1016/j.clinbiochem.2013.05.046_bb0065 article-title: Identification of the human klotho gene and its two transcripts encoding membrane and secreted klotho protein publication-title: Biochem Biophys Res Commun doi: 10.1006/bbrc.1997.8019 – volume: 317 start-page: 803 year: 2007 ident: 10.1016/j.clinbiochem.2013.05.046_bb0060 article-title: Augmented Wnt signaling in a mammalian model of accelerated aging publication-title: Science doi: 10.1126/science.1143578 – volume: 301 start-page: 424 year: 2003 ident: 10.1016/j.clinbiochem.2013.05.046_bb0100 article-title: Upregulation of cAMP is a new functional signal pathway of Klotho in endothelial cells publication-title: Biochem Biophys Res Commun doi: 10.1016/S0006-291X(02)03056-5 – volume: 25 start-page: 229 year: 2004 ident: 10.1016/j.clinbiochem.2013.05.046_bb0040 article-title: Klotho protein activates the PKC pathway in the kidney and testis and suppresses 25-hydroxyvitamin D3 1alpha-hydroxylase gene expression publication-title: Endocrine doi: 10.1385/ENDO:25:3:229 – volume: 137 start-page: 479 year: 2012 ident: 10.1016/j.clinbiochem.2013.05.046_bb0020 article-title: Validation of an immunoassay for soluble klotho protein: decreased levels in diabetes and increased levels in chronic kidney disease publication-title: Am J Clin Pathol doi: 10.1309/AJCPGPMAF7SFRBO4 – volume: 22 start-page: 124 year: 2011 ident: 10.1016/j.clinbiochem.2013.05.046_bb0035 article-title: Klotho deficiency causes vascular calcification in chronic kidney disease publication-title: J Am Soc Nephrol doi: 10.1681/ASN.2009121311 – volume: 49 start-page: 1118 year: 2000 ident: 10.1016/j.clinbiochem.2013.05.046_bb0085 article-title: Decreased insulin production and increased insulin sensitivity in the klotho mutant mouse, a novel animal model for human aging publication-title: Metabolism doi: 10.1053/meta.2000.8606 |
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Snippet | Soluble serum Klotho is a new biomarker linked to chronic kidney disease, cardiovascular disease and diabetes. This study describes the evaluation and... |
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SubjectTerms | Adult Age Aged BMI eGFR Enzyme-Linked Immunosorbent Assay Female FGF23 Fibroblast Growth Factors - blood Glucuronidase - blood Health Humans Immunoassay - methods Immunoassays Ionized calcium Klotho Male Middle Aged Phosphate PTH Reference ranges Reference Values Regression Analysis Solubility Statistics, Nonparametric Young Adult |
Title | Soluble serum Klotho levels in healthy subjects. Comparison of two different immunoassays |
URI | https://dx.doi.org/10.1016/j.clinbiochem.2013.05.046 https://www.ncbi.nlm.nih.gov/pubmed/23707222 https://www.proquest.com/docview/1411626736 |
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