Longer Duration of Diabetes Strongly Impacts Fracture Risk Assessment: The Manitoba BMD Cohort

Context: Type 2 diabetes is associated with a higher risk for major osteoporotic fracture (MOF) and hip fracture than predicted by the World Health Organization fracture risk assessment (FRAX) tool. Objective: The objective of the study was to examine the impact of diabetes duration on fracture risk...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2016-11, Vol.101 (11), p.4489-4496
Hauptverfasser: Majumdar, Sumit R, Leslie, William D, Lix, Lisa M, Morin, Suzanne N, Johansson, Helena, Oden, Anders, McCloskey, Eugene V, Kanis, John A
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container_end_page 4496
container_issue 11
container_start_page 4489
container_title The journal of clinical endocrinology and metabolism
container_volume 101
creator Majumdar, Sumit R
Leslie, William D
Lix, Lisa M
Morin, Suzanne N
Johansson, Helena
Oden, Anders
McCloskey, Eugene V
Kanis, John A
description Context: Type 2 diabetes is associated with a higher risk for major osteoporotic fracture (MOF) and hip fracture than predicted by the World Health Organization fracture risk assessment (FRAX) tool. Objective: The objective of the study was to examine the impact of diabetes duration on fracture risk. Methods: Using a clinical dual-energy x-ray absorptiometry registry linked with the Manitoba administrative databases, we identified all women age 40 years or older with 10 or more years of prior health care coverage undergoing hip dual-energy x-ray absorptiometry measurements (1996–2013). Incident MOF and incident hip fractures were each studied over 7 years. Cox proportional hazards models were adjusted for FRAX (FRAX adjusted) and then FRAX plus comorbidity, falls, osteoporosis therapy, or insulin (fully adjusted). FRAX calibration was assessed comparing observed vs predicted probabilities. Results: There were 49 098 women without and 8840 women with diabetes (31.4% >10 y duration; 20.1% 5–10 y; 23.7% 10 y vs HR 1.32, 95% CI 1.03–1.69 for new onset). FRAX significantly underestimated the MOF risk (calibration ratio 1.24, 95% CI 1.08–1.39) and hip fracture risk (1.93, 95% CI 1.50–2.35) in those with a diabetes duration longer than 10 years. Conclusion: Diabetes is a FRAX-independent risk factor for MOF only in women with a long duration of diabetes, but diabetes increases hip fracture risk, regardless of duration. Those with diabetes longer than 10 years are at particularly high risk of fracture, and this elevated risk is currently underestimated by FRAX. In a large study we found it was long duration of diabetes that was more important than the diagnosis itself in predicting fracture risk, and that FRAX under-estimates risk in women with diabetes.
doi_str_mv 10.1210/jc.2016-2569
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Objective: The objective of the study was to examine the impact of diabetes duration on fracture risk. Methods: Using a clinical dual-energy x-ray absorptiometry registry linked with the Manitoba administrative databases, we identified all women age 40 years or older with 10 or more years of prior health care coverage undergoing hip dual-energy x-ray absorptiometry measurements (1996–2013). Incident MOF and incident hip fractures were each studied over 7 years. Cox proportional hazards models were adjusted for FRAX (FRAX adjusted) and then FRAX plus comorbidity, falls, osteoporosis therapy, or insulin (fully adjusted). FRAX calibration was assessed comparing observed vs predicted probabilities. Results: There were 49 098 women without and 8840 women with diabetes (31.4% &gt;10 y duration; 20.1% 5–10 y; 23.7% &lt;5 y; 24.8% new onset). In FRAX-adjusted analyses, only duration longer than 10 years was associated with a higher risk for MOF (hazard ratio [HR] 1.47, 95% confidence interval [CI] 1.30–1.66), and this was similar in the fully adjusted models (HR 1.34, 95% CI 1.17–1.54). In contrast, a higher risk for hip fracture was seen for all durations in a dose-dependent fashion (eg, FRAX adjusted HR 2.10, 95% CI 1.71–2.59 for duration &gt;10 y vs HR 1.32, 95% CI 1.03–1.69 for new onset). FRAX significantly underestimated the MOF risk (calibration ratio 1.24, 95% CI 1.08–1.39) and hip fracture risk (1.93, 95% CI 1.50–2.35) in those with a diabetes duration longer than 10 years. Conclusion: Diabetes is a FRAX-independent risk factor for MOF only in women with a long duration of diabetes, but diabetes increases hip fracture risk, regardless of duration. Those with diabetes longer than 10 years are at particularly high risk of fracture, and this elevated risk is currently underestimated by FRAX. In a large study we found it was long duration of diabetes that was more important than the diagnosis itself in predicting fracture risk, and that FRAX under-estimates risk in women with diabetes.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/jc.2016-2569</identifier><identifier>PMID: 27603908</identifier><language>eng</language><publisher>United States: Endocrine Society</publisher><subject>Absorptiometry, Photon ; Adult ; Aged ; Bone Density ; Diabetes Mellitus, Type 2 - complications ; Female ; Follow-Up Studies ; Hip Fractures - epidemiology ; Hip Fractures - etiology ; Humans ; Manitoba - epidemiology ; Middle Aged ; Original ; Osteoporotic Fractures - epidemiology ; Osteoporotic Fractures - etiology ; Registries ; Risk Assessment ; Time Factors</subject><ispartof>The journal of clinical endocrinology and metabolism, 2016-11, Vol.101 (11), p.4489-4496</ispartof><rights>Copyright © 2016 by The Endocrine Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5391-aa3ffb1f4f92d4bfee355ad887bc19826037b046c4cfbd6fbbecf3bfcb86d1883</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27603908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Majumdar, Sumit R</creatorcontrib><creatorcontrib>Leslie, William D</creatorcontrib><creatorcontrib>Lix, Lisa M</creatorcontrib><creatorcontrib>Morin, Suzanne N</creatorcontrib><creatorcontrib>Johansson, Helena</creatorcontrib><creatorcontrib>Oden, Anders</creatorcontrib><creatorcontrib>McCloskey, Eugene V</creatorcontrib><creatorcontrib>Kanis, John A</creatorcontrib><title>Longer Duration of Diabetes Strongly Impacts Fracture Risk Assessment: The Manitoba BMD Cohort</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>Context: Type 2 diabetes is associated with a higher risk for major osteoporotic fracture (MOF) and hip fracture than predicted by the World Health Organization fracture risk assessment (FRAX) tool. Objective: The objective of the study was to examine the impact of diabetes duration on fracture risk. Methods: Using a clinical dual-energy x-ray absorptiometry registry linked with the Manitoba administrative databases, we identified all women age 40 years or older with 10 or more years of prior health care coverage undergoing hip dual-energy x-ray absorptiometry measurements (1996–2013). Incident MOF and incident hip fractures were each studied over 7 years. Cox proportional hazards models were adjusted for FRAX (FRAX adjusted) and then FRAX plus comorbidity, falls, osteoporosis therapy, or insulin (fully adjusted). FRAX calibration was assessed comparing observed vs predicted probabilities. Results: There were 49 098 women without and 8840 women with diabetes (31.4% &gt;10 y duration; 20.1% 5–10 y; 23.7% &lt;5 y; 24.8% new onset). In FRAX-adjusted analyses, only duration longer than 10 years was associated with a higher risk for MOF (hazard ratio [HR] 1.47, 95% confidence interval [CI] 1.30–1.66), and this was similar in the fully adjusted models (HR 1.34, 95% CI 1.17–1.54). In contrast, a higher risk for hip fracture was seen for all durations in a dose-dependent fashion (eg, FRAX adjusted HR 2.10, 95% CI 1.71–2.59 for duration &gt;10 y vs HR 1.32, 95% CI 1.03–1.69 for new onset). FRAX significantly underestimated the MOF risk (calibration ratio 1.24, 95% CI 1.08–1.39) and hip fracture risk (1.93, 95% CI 1.50–2.35) in those with a diabetes duration longer than 10 years. Conclusion: Diabetes is a FRAX-independent risk factor for MOF only in women with a long duration of diabetes, but diabetes increases hip fracture risk, regardless of duration. Those with diabetes longer than 10 years are at particularly high risk of fracture, and this elevated risk is currently underestimated by FRAX. In a large study we found it was long duration of diabetes that was more important than the diagnosis itself in predicting fracture risk, and that FRAX under-estimates risk in women with diabetes.</description><subject>Absorptiometry, Photon</subject><subject>Adult</subject><subject>Aged</subject><subject>Bone Density</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hip Fractures - epidemiology</subject><subject>Hip Fractures - etiology</subject><subject>Humans</subject><subject>Manitoba - epidemiology</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Osteoporotic Fractures - epidemiology</subject><subject>Osteoporotic Fractures - etiology</subject><subject>Registries</subject><subject>Risk Assessment</subject><subject>Time Factors</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkcFrFDEUxoModq3ePEuOHpyaTCYzGQ9C3bVa2CK0FTwZksxLZ7YzyTbJWPrfm2XbUsFAeIT3e18-3ofQW0qOaEnJx405Kgmti5LX7TO0oG3Fi4a2zXO0IKSkRduUvw7Qqxg3hNCq4uwlOiibmrCWiAX6vfbuCgJezUGlwTvsLV4NSkOCiC9SyN3xDp9OW2VSxCchlzkAPh_iNT6OEWKcwKVP-LIHfKbckLxW-MvZCi9970N6jV5YNUZ4c18P0c-Tr5fL78X6x7fT5fG6MJy1tFCKWauprWxbdpW2AIxz1QnRaENbUWa3jSZVbSpjdVdbrcFYpq3Rou6oEOwQfd7rbmc9QWeyp6BGuQ3DpMKd9GqQ_3bc0Msr_0dy0vK8uSzw_l4g-JsZYpLTEA2Mo3Lg5yipYDwvjxOe0Q971AQfYwD7-A0lcheJ3Bi5i0TuIsn4u6fWHuGHDDJQ7YFbPyYI8XqcbyHIHtSYeknyqepGFDtFSvOryLeheYztx8B13oTBwTbkOOTGz8HlXf_fzV8xbaoh</recordid><startdate>201611</startdate><enddate>201611</enddate><creator>Majumdar, Sumit R</creator><creator>Leslie, William D</creator><creator>Lix, Lisa M</creator><creator>Morin, Suzanne N</creator><creator>Johansson, Helena</creator><creator>Oden, Anders</creator><creator>McCloskey, Eugene V</creator><creator>Kanis, John A</creator><general>Endocrine Society</general><general>Copyright by The Endocrine Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201611</creationdate><title>Longer Duration of Diabetes Strongly Impacts Fracture Risk Assessment: The Manitoba BMD Cohort</title><author>Majumdar, Sumit R ; Leslie, William D ; Lix, Lisa M ; Morin, Suzanne N ; Johansson, Helena ; Oden, Anders ; McCloskey, Eugene V ; Kanis, John A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5391-aa3ffb1f4f92d4bfee355ad887bc19826037b046c4cfbd6fbbecf3bfcb86d1883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Absorptiometry, Photon</topic><topic>Adult</topic><topic>Aged</topic><topic>Bone Density</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hip Fractures - epidemiology</topic><topic>Hip Fractures - etiology</topic><topic>Humans</topic><topic>Manitoba - epidemiology</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Osteoporotic Fractures - epidemiology</topic><topic>Osteoporotic Fractures - etiology</topic><topic>Registries</topic><topic>Risk Assessment</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Majumdar, Sumit R</creatorcontrib><creatorcontrib>Leslie, William D</creatorcontrib><creatorcontrib>Lix, Lisa M</creatorcontrib><creatorcontrib>Morin, Suzanne N</creatorcontrib><creatorcontrib>Johansson, Helena</creatorcontrib><creatorcontrib>Oden, Anders</creatorcontrib><creatorcontrib>McCloskey, Eugene V</creatorcontrib><creatorcontrib>Kanis, John A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The journal of clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Majumdar, Sumit R</au><au>Leslie, William D</au><au>Lix, Lisa M</au><au>Morin, Suzanne N</au><au>Johansson, Helena</au><au>Oden, Anders</au><au>McCloskey, Eugene V</au><au>Kanis, John A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longer Duration of Diabetes Strongly Impacts Fracture Risk Assessment: The Manitoba BMD Cohort</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>2016-11</date><risdate>2016</risdate><volume>101</volume><issue>11</issue><spage>4489</spage><epage>4496</epage><pages>4489-4496</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><abstract>Context: Type 2 diabetes is associated with a higher risk for major osteoporotic fracture (MOF) and hip fracture than predicted by the World Health Organization fracture risk assessment (FRAX) tool. Objective: The objective of the study was to examine the impact of diabetes duration on fracture risk. Methods: Using a clinical dual-energy x-ray absorptiometry registry linked with the Manitoba administrative databases, we identified all women age 40 years or older with 10 or more years of prior health care coverage undergoing hip dual-energy x-ray absorptiometry measurements (1996–2013). Incident MOF and incident hip fractures were each studied over 7 years. Cox proportional hazards models were adjusted for FRAX (FRAX adjusted) and then FRAX plus comorbidity, falls, osteoporosis therapy, or insulin (fully adjusted). FRAX calibration was assessed comparing observed vs predicted probabilities. Results: There were 49 098 women without and 8840 women with diabetes (31.4% &gt;10 y duration; 20.1% 5–10 y; 23.7% &lt;5 y; 24.8% new onset). In FRAX-adjusted analyses, only duration longer than 10 years was associated with a higher risk for MOF (hazard ratio [HR] 1.47, 95% confidence interval [CI] 1.30–1.66), and this was similar in the fully adjusted models (HR 1.34, 95% CI 1.17–1.54). In contrast, a higher risk for hip fracture was seen for all durations in a dose-dependent fashion (eg, FRAX adjusted HR 2.10, 95% CI 1.71–2.59 for duration &gt;10 y vs HR 1.32, 95% CI 1.03–1.69 for new onset). FRAX significantly underestimated the MOF risk (calibration ratio 1.24, 95% CI 1.08–1.39) and hip fracture risk (1.93, 95% CI 1.50–2.35) in those with a diabetes duration longer than 10 years. Conclusion: Diabetes is a FRAX-independent risk factor for MOF only in women with a long duration of diabetes, but diabetes increases hip fracture risk, regardless of duration. Those with diabetes longer than 10 years are at particularly high risk of fracture, and this elevated risk is currently underestimated by FRAX. In a large study we found it was long duration of diabetes that was more important than the diagnosis itself in predicting fracture risk, and that FRAX under-estimates risk in women with diabetes.</abstract><cop>United States</cop><pub>Endocrine Society</pub><pmid>27603908</pmid><doi>10.1210/jc.2016-2569</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Absorptiometry, Photon
Adult
Aged
Bone Density
Diabetes Mellitus, Type 2 - complications
Female
Follow-Up Studies
Hip Fractures - epidemiology
Hip Fractures - etiology
Humans
Manitoba - epidemiology
Middle Aged
Original
Osteoporotic Fractures - epidemiology
Osteoporotic Fractures - etiology
Registries
Risk Assessment
Time Factors
title Longer Duration of Diabetes Strongly Impacts Fracture Risk Assessment: The Manitoba BMD Cohort
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