Risk Factors for Fracture in Patients with Coexisting Chronic Kidney Disease and Type 2 Diabetes: An Observational Analysis from the CREDENCE Trial

Background. The fracture pathophysiology associated with type 2 diabetes and chronic kidney disease (CKD) is incompletely understood. We examined individual fracture predictors and prediction sets based on different pathophysiological hypotheses, testing whether any of the sets improved prediction b...

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Main Authors: Tamara K. Young, Nigel D. Toussaint, Gian Luca Di Tanna, Clare Arnott, Carinna Hockham, Amy Kang, Aletta E. Schutte, Vlado Perkovic, Kenneth W. Mahaffey, Rajiv Agarwal, George L. Bakris, David M. Charytan, Hiddo J. L. Heerspink, Adeera Levin, Carol Pollock, David C. Wheeler, Hong Zhang, Meg J. Jardine
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Journal of Diabetes Research
Online Access:http://dx.doi.org/10.1155/2022/9998891
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author Tamara K. Young
Nigel D. Toussaint
Gian Luca Di Tanna
Clare Arnott
Carinna Hockham
Amy Kang
Aletta E. Schutte
Vlado Perkovic
Kenneth W. Mahaffey
Rajiv Agarwal
George L. Bakris
David M. Charytan
Hiddo J. L. Heerspink
Adeera Levin
Carol Pollock
David C. Wheeler
Hong Zhang
Meg J. Jardine
author_facet Tamara K. Young
Nigel D. Toussaint
Gian Luca Di Tanna
Clare Arnott
Carinna Hockham
Amy Kang
Aletta E. Schutte
Vlado Perkovic
Kenneth W. Mahaffey
Rajiv Agarwal
George L. Bakris
David M. Charytan
Hiddo J. L. Heerspink
Adeera Levin
Carol Pollock
David C. Wheeler
Hong Zhang
Meg J. Jardine
author_sort Tamara K. Young
collection DOAJ
description Background. The fracture pathophysiology associated with type 2 diabetes and chronic kidney disease (CKD) is incompletely understood. We examined individual fracture predictors and prediction sets based on different pathophysiological hypotheses, testing whether any of the sets improved prediction beyond that based on traditional osteoporotic risk factors. Methods. Within the CREDENCE cohort with adjudicated fracture outcomes, we assessed the association of individual factors with fracture using Cox regression models. We used the Akaike information criteria (AIC) and Schwartz Bayes Criterion (SBC) to assess six separate variable sets based on hypothesized associations with fracture, namely, traditional osteoporosis, exploratory general population findings, cardiovascular risk, CKD-mineral and bone disorder, diabetic osteodystrophy, and an all-inclusive set containing all variables. Results. Fracture occurred in 135 (3.1%) participants over a median 2.35 [1.88–2.93] years. Independent fracture predictors were older age (hazard ratio [HR] 1.04, confidence interval [CI] 1.01–1.06), female sex (HR 2.49, CI 1.70–3.65), previous fracture (HR 2.30, CI 1.58–3.34), Asian race (HR 1.74, CI 1.09–2.78), vitamin D therapy requirement (HR 2.05, CI 1.31–3.21), HbA1c (HR 1.14, CI 1.00–1.32), prior cardiovascular event (HR 1.60, CI 1.10–2.33), and serum albumin (HR 0.41, CI 0.23–0.74) (lower albumin associated with greater risk). The goodness of fit of the various hypothesis sets was similar (AIC range 1870.92–1849.51, SBC range 1875.60–1948.04). Conclusion. Independent predictors of fracture were identified in the CREDENCE participants with type 2 diabetes and CKD. Fracture prediction was not improved by models built on alternative pathophysiology hypotheses compared with traditional osteoporosis predictors.
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spelling doaj-art-e95efd5aefe248e7bd867a88ada5f5aa2025-02-03T01:07:36ZengWileyJournal of Diabetes Research2314-67532022-01-01202210.1155/2022/9998891Risk Factors for Fracture in Patients with Coexisting Chronic Kidney Disease and Type 2 Diabetes: An Observational Analysis from the CREDENCE TrialTamara K. Young0Nigel D. Toussaint1Gian Luca Di Tanna2Clare Arnott3Carinna Hockham4Amy Kang5Aletta E. Schutte6Vlado Perkovic7Kenneth W. Mahaffey8Rajiv Agarwal9George L. Bakris10David M. Charytan11Hiddo J. L. Heerspink12Adeera Levin13Carol Pollock14David C. Wheeler15Hong Zhang16Meg J. Jardine17The George Institute for Global HealthDepartment of NephrologyThe George Institute for Global HealthThe George Institute for Global HealthThe George Institute for Global HealthThe George Institute for Global HealthThe George Institute for Global HealthThe George Institute for Global HealthStanford Center for Clinical ResearchIndiana University School of Medicine and Veterans Affairs Medical CenterDepartment of MedicineNephrology DivisionThe George Institute for Global HealthDivision of NephrologyKolling Institute of Medical ResearchDepartment of Renal MedicineRenal Division of Peking University First HospitalThe George Institute for Global HealthBackground. The fracture pathophysiology associated with type 2 diabetes and chronic kidney disease (CKD) is incompletely understood. We examined individual fracture predictors and prediction sets based on different pathophysiological hypotheses, testing whether any of the sets improved prediction beyond that based on traditional osteoporotic risk factors. Methods. Within the CREDENCE cohort with adjudicated fracture outcomes, we assessed the association of individual factors with fracture using Cox regression models. We used the Akaike information criteria (AIC) and Schwartz Bayes Criterion (SBC) to assess six separate variable sets based on hypothesized associations with fracture, namely, traditional osteoporosis, exploratory general population findings, cardiovascular risk, CKD-mineral and bone disorder, diabetic osteodystrophy, and an all-inclusive set containing all variables. Results. Fracture occurred in 135 (3.1%) participants over a median 2.35 [1.88–2.93] years. Independent fracture predictors were older age (hazard ratio [HR] 1.04, confidence interval [CI] 1.01–1.06), female sex (HR 2.49, CI 1.70–3.65), previous fracture (HR 2.30, CI 1.58–3.34), Asian race (HR 1.74, CI 1.09–2.78), vitamin D therapy requirement (HR 2.05, CI 1.31–3.21), HbA1c (HR 1.14, CI 1.00–1.32), prior cardiovascular event (HR 1.60, CI 1.10–2.33), and serum albumin (HR 0.41, CI 0.23–0.74) (lower albumin associated with greater risk). The goodness of fit of the various hypothesis sets was similar (AIC range 1870.92–1849.51, SBC range 1875.60–1948.04). Conclusion. Independent predictors of fracture were identified in the CREDENCE participants with type 2 diabetes and CKD. Fracture prediction was not improved by models built on alternative pathophysiology hypotheses compared with traditional osteoporosis predictors.http://dx.doi.org/10.1155/2022/9998891
spellingShingle Tamara K. Young
Nigel D. Toussaint
Gian Luca Di Tanna
Clare Arnott
Carinna Hockham
Amy Kang
Aletta E. Schutte
Vlado Perkovic
Kenneth W. Mahaffey
Rajiv Agarwal
George L. Bakris
David M. Charytan
Hiddo J. L. Heerspink
Adeera Levin
Carol Pollock
David C. Wheeler
Hong Zhang
Meg J. Jardine
Risk Factors for Fracture in Patients with Coexisting Chronic Kidney Disease and Type 2 Diabetes: An Observational Analysis from the CREDENCE Trial
Journal of Diabetes Research
title Risk Factors for Fracture in Patients with Coexisting Chronic Kidney Disease and Type 2 Diabetes: An Observational Analysis from the CREDENCE Trial
title_full Risk Factors for Fracture in Patients with Coexisting Chronic Kidney Disease and Type 2 Diabetes: An Observational Analysis from the CREDENCE Trial
title_fullStr Risk Factors for Fracture in Patients with Coexisting Chronic Kidney Disease and Type 2 Diabetes: An Observational Analysis from the CREDENCE Trial
title_full_unstemmed Risk Factors for Fracture in Patients with Coexisting Chronic Kidney Disease and Type 2 Diabetes: An Observational Analysis from the CREDENCE Trial
title_short Risk Factors for Fracture in Patients with Coexisting Chronic Kidney Disease and Type 2 Diabetes: An Observational Analysis from the CREDENCE Trial
title_sort risk factors for fracture in patients with coexisting chronic kidney disease and type 2 diabetes an observational analysis from the credence trial
url http://dx.doi.org/10.1155/2022/9998891
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