Increased circulating sclerostin levels in end-stage renal disease predict biopsy-verified vascular medial calcification and coronary artery calcification
Sclerostin, an osteocyte-derived inhibitor of bone formation, is linked to mineral bone disorder. In order to validate its potential as a predictor of vascular calcification, we explored associations of circulating sclerostin with measures of calcification in 89 epigastric artery biopsies from patie...
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Published in | Kidney international Vol. 88; no. 6; pp. 1356 - 1364 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.12.2015
Elsevier Limited |
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Abstract | Sclerostin, an osteocyte-derived inhibitor of bone formation, is linked to mineral bone disorder. In order to validate its potential as a predictor of vascular calcification, we explored associations of circulating sclerostin with measures of calcification in 89 epigastric artery biopsies from patients with end-stage renal disease. Significantly higher sclerostin levels were found in the serum of patients with epigastric and coronary artery calcification (calcification score 100 or more). In Spearman’s rank correlations, sclerostin levels significantly associated with age, intact parathyroid hormone, bone-specific alkaline phosphatase, and percent calcification. Multivariable regression showed that age, male gender, and sclerostin each significantly associated with the presence of medial vascular calcification. Receiver operating characteristic curve analysis showed that sclerostin (AUC 0.68) predicted vascular calcification. Vascular sclerostin mRNA and protein expressions were low or absent, and did not differ between calcified and non-calcified vessels, suggesting that the vasculature is not a major contributor to circulating levels. Thus, high serum sclerostin levels associate with the extent of vascular calcification as evaluated both by coronary artery CT and scoring of epigastric artery calcification. Among circulating biomarkers of mineral bone disorder, only sclerostin predicted vascular calcification. |
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AbstractList | Sclerostin, an osteocyte-derived inhibitor of bone formation, is linked to mineral bone disorder. In order to validate its potential as a predictor of vascular calcification, we explored associations of circulating sclerostin with measures of calcification in 89 epigastric artery biopsies from patients with end-stage renal disease. Significantly higher sclerostin levels were found in the serum of patients with epigastric and coronary artery calcification (calcification score 100 or more). In Spearman's rank correlations, sclerostin levels significantly associated with age, intact parathyroid hormone, bone-specific alkaline phosphatase, and percent calcification. Multivariable regression showed that age, male gender, and sclerostin each significantly associated with the presence of medial vascular calcification. Receiver operating characteristic curve analysis showed that sclerostin (AUC 0.68) predicted vascular calcification. Vascular sclerostin mRNA and protein expressions were low or absent, and did not differ between calcified and non-calcified vessels, suggesting that the vasculature is not a major contributor to circulating levels. Thus, high serum sclerostin levels associate with the extent of vascular calcification as evaluated both by coronary artery CT and scoring of epigastric artery calcification. Among circulating biomarkers of mineral bone disorder, only sclerostin predicted vascular calcification. |
Author | Lindholm, Bengt Barany, Peter Ripsweden, Jonaz Olauson, Hannes Witasp, Anna Brandenburg, Vincent Qureshi, Abdul Rashid Nordfors, Louise Stenvinkel, Peter Wernerson, Annika Haarhaus, Mathias Wennberg, Lars Söderberg, Magnus |
Author_xml | – sequence: 1 givenname: Abdul Rashid surname: Qureshi fullname: Qureshi, Abdul Rashid organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 2 givenname: Hannes surname: Olauson fullname: Olauson, Hannes organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 3 givenname: Anna surname: Witasp fullname: Witasp, Anna organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 4 givenname: Mathias surname: Haarhaus fullname: Haarhaus, Mathias organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 5 givenname: Vincent surname: Brandenburg fullname: Brandenburg, Vincent organization: Department of Cardiology, University Hospital RWTH Aachen, Aachen, Germany – sequence: 6 givenname: Annika surname: Wernerson fullname: Wernerson, Annika organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 7 givenname: Bengt surname: Lindholm fullname: Lindholm, Bengt organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 8 givenname: Magnus surname: Söderberg fullname: Söderberg, Magnus organization: Pathology, Drug Safety and Metabolism, AstraZeneca, Mölndal, Sweden – sequence: 9 givenname: Lars surname: Wennberg fullname: Wennberg, Lars organization: Division of Transplantation Surgery, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 10 givenname: Louise surname: Nordfors fullname: Nordfors, Louise organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 11 givenname: Jonaz surname: Ripsweden fullname: Ripsweden, Jonaz organization: Division of Radiology, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 12 givenname: Peter surname: Barany fullname: Barany, Peter organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden – sequence: 13 givenname: Peter surname: Stenvinkel fullname: Stenvinkel, Peter email: peter.stenvinkel@ki.se organization: Division of Renal Medicine and Baxter Novum, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden |
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Keywords | end-stage renal disease inflammation mineral-bone disease vascular calcification sclerostin |
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SubjectTerms | end-stage renal disease inflammation Medicin och hälsovetenskap mineral-bone disease sclerostin vascular calcification |
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Title | Increased circulating sclerostin levels in end-stage renal disease predict biopsy-verified vascular medial calcification and coronary artery calcification |
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