Bone Mineral Density is Negatively Associated with Risk of All-Cause and Cardiovascular Mortality among Adults with Type 2 Diabetes Mellitus: A Cross-sectional Study of the NHANES 2005–2010, 2013–2014

Background: With ageing and lifestyle changes, the coexistence of osteoporosis and type 2 diabetes (T2DM) is becoming more common, which greatly increases patient disability and mortality. However, the association of low bone mineral density (BMD) with cardiovascular disease (CVD) and all-cause mort...

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Published inReviews in cardiovascular medicine Vol. 25; no. 12; p. 434
Main Authors Li, Haipeng, Wang, Baolong, Xu, Dongshuo, Zhang, Jialu, Wang, Changhui
Format Journal Article
LanguageEnglish
Published Singapore IMR Press 01.12.2024
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Abstract Background: With ageing and lifestyle changes, the coexistence of osteoporosis and type 2 diabetes (T2DM) is becoming more common, which greatly increases patient disability and mortality. However, the association of low bone mineral density (BMD) with cardiovascular disease (CVD) and all-cause mortality in T2DM patients have not been conclusively established. Methods: Using the National Health and Nutrition Examination Survey (NHANES) to obtain a nationally representative sample of the US population, we sought to determine the independent and incremental value of low BMD, particularly in patients with osteoporosis in assessing all-cause and CVD mortality in adults with T2DM. Results: We demonstrated that increased BMD was significantly related to decreased mortality from all-causes and CVDs among US adults with T2DM. In addition, we found that, after multivariate adjustment, osteoporosis and osteopenia were independently associated with an increased risk of all-cause and CVD mortality in T2DM patients at long-term follow-up. Conclusions: The clinical diagnosis of osteopenia or osteoporosis in adults with T2DM provides independent prognostic value for CVD and all-cause mortality.
AbstractList With ageing and lifestyle changes, the coexistence of osteoporosis and type 2 diabetes (T2DM) is becoming more common, which greatly increases patient disability and mortality. However, the association of low bone mineral density (BMD) with cardiovascular disease (CVD) and all-cause mortality in T2DM patients have not been conclusively established. Using the National Health and Nutrition Examination Survey (NHANES) to obtain a nationally representative sample of the US population, we sought to determine the independent and incremental value of low BMD, particularly in patients with osteoporosis in assessing all-cause and CVD mortality in adults with T2DM. We demonstrated that increased BMD was significantly related to decreased mortality from all-causes and CVDs among US adults with T2DM. In addition, we found that, after multivariate adjustment, osteoporosis and osteopenia were independently associated with an increased risk of all-cause and CVD mortality in T2DM patients at long-term follow-up. The clinical diagnosis of osteopenia or osteoporosis in adults with T2DM provides independent prognostic value for CVD and all-cause mortality.
Background: With ageing and lifestyle changes, the coexistence of osteoporosis and type 2 diabetes (T2DM) is becoming more common, which greatly increases patient disability and mortality. However, the association of low bone mineral density (BMD) with cardiovascular disease (CVD) and all-cause mortality in T2DM patients have not been conclusively established. Methods: Using the National Health and Nutrition Examination Survey (NHANES) to obtain a nationally representative sample of the US population, we sought to determine the independent and incremental value of low BMD, particularly in patients with osteoporosis in assessing all-cause and CVD mortality in adults with T2DM. Results: We demonstrated that increased BMD was significantly related to decreased mortality from all-causes and CVDs among US adults with T2DM. In addition, we found that, after multivariate adjustment, osteoporosis and osteopenia were independently associated with an increased risk of all-cause and CVD mortality in T2DM patients at long-term follow-up. Conclusions: The clinical diagnosis of osteopenia or osteoporosis in adults with T2DM provides independent prognostic value for CVD and all-cause mortality.
With ageing and lifestyle changes, the coexistence of osteoporosis and type 2 diabetes (T2DM) is becoming more common, which greatly increases patient disability and mortality. However, the association of low bone mineral density (BMD) with cardiovascular disease (CVD) and all-cause mortality in T2DM patients have not been conclusively established.BackgroundWith ageing and lifestyle changes, the coexistence of osteoporosis and type 2 diabetes (T2DM) is becoming more common, which greatly increases patient disability and mortality. However, the association of low bone mineral density (BMD) with cardiovascular disease (CVD) and all-cause mortality in T2DM patients have not been conclusively established.Using the National Health and Nutrition Examination Survey (NHANES) to obtain a nationally representative sample of the US population, we sought to determine the independent and incremental value of low BMD, particularly in patients with osteoporosis in assessing all-cause and CVD mortality in adults with T2DM.MethodsUsing the National Health and Nutrition Examination Survey (NHANES) to obtain a nationally representative sample of the US population, we sought to determine the independent and incremental value of low BMD, particularly in patients with osteoporosis in assessing all-cause and CVD mortality in adults with T2DM.We demonstrated that increased BMD was significantly related to decreased mortality from all-causes and CVDs among US adults with T2DM. In addition, we found that, after multivariate adjustment, osteoporosis and osteopenia were independently associated with an increased risk of all-cause and CVD mortality in T2DM patients at long-term follow-up.ResultsWe demonstrated that increased BMD was significantly related to decreased mortality from all-causes and CVDs among US adults with T2DM. In addition, we found that, after multivariate adjustment, osteoporosis and osteopenia were independently associated with an increased risk of all-cause and CVD mortality in T2DM patients at long-term follow-up.The clinical diagnosis of osteopenia or osteoporosis in adults with T2DM provides independent prognostic value for CVD and all-cause mortality.ConclusionsThe clinical diagnosis of osteopenia or osteoporosis in adults with T2DM provides independent prognostic value for CVD and all-cause mortality.
Author Wang, Changhui
Xu, Dongshuo
Zhang, Jialu
Li, Haipeng
Wang, Baolong
AuthorAffiliation 1 Department of Cardiology, The First Affiliated Hospital of Anhui Medical University, 230022 Hefei, Anhui, China
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Cites_doi 10.1359/JBMR.050711
10.1016/j.neubiorev.2024.105641
10.1016/j.injury.2011.03.021
10.3389/fendo.2022.938399
10.1016/j.bone.2011.09.055
10.1016/j.ajog.2020.05.051
10.1007/s00198-018-4578-6
10.1210/jc.2005-2672
10.1210/jc.2017-00042
10.1002/jcb.26174
10.1111/1753-0407.13530
10.1016/j.bone.2009.10.005
10.1210/er.2003-0015
10.1016/j.ecl.2021.03.005
10.2174/138945011798829456
10.2337/dc06-0062
10.1056/NEJMcp2307353
10.2337/dc07-2426
10.1007/s10654-004-1706-8
10.1016/j.vph.2012.06.004
10.1007/s00198-022-06317-x
10.1016/S0140-6736(22)01655-5
10.3390/ijms20194873
10.1016/S2213-8587(18)30110-4
10.7326/AITC202401160
10.1016/j.regg.2019.08.009
10.1016/j.exger.2010.09.014
10.1016/j.jbiomech.2010.10.016
10.1136/heartjnl-2020-318764
10.1038/s41574-023-00866-9
10.1016/j.jocd.2009.02.001
10.1016/S0140-6736(96)90075-6
10.3390/biom13040616
10.1016/j.bone.2005.11.024
10.1016/j.mayocp.2021.07.019
10.1002/jbmr.5650100517
10.1016/j.jocd.2023.101442
10.1016/j.bone.2020.115597
10.1007/s11657-015-0219-2
10.1007/s11914-007-0004-2
10.1615/CritRevEukarGeneExpr.v21.i2.70
10.1007/s00774-020-01189-9
10.2337/dc06-0440
10.1002/jbmr.2269
10.1038/nrendo.2017.151
10.1111/j.1600-0501.2010.01923.x
10.1007/s00198-014-2676-7
10.1093/ajcn/83.1.146
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Keywords cardiovascular mortality
bone mineral density
type 2 diabetes
NHANES database
osteoporosis
all-cause mortality
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References ref13
ref12
ref15
ref14
ref11
ref10
ref17
ref16
ref19
ref18
ref50
ref46
ref45
ref48
ref47
ref42
ref41
ref44
ref43
ref49
ref8
ref7
ref9
ref4
ref3
ref6
ref5
ref40
ref35
ref34
ref37
ref36
ref31
ref30
ref33
ref32
ref2
ref1
ref39
ref38
ref24
ref23
ref26
ref25
ref20
ref22
ref21
ref28
ref27
ref29
References_xml – ident: ref14
  doi: 10.1359/JBMR.050711
– ident: ref19
  doi: 10.1016/j.neubiorev.2024.105641
– ident: ref50
  doi: 10.1016/j.injury.2011.03.021
– ident: ref20
– ident: ref22
  doi: 10.3389/fendo.2022.938399
– ident: ref36
  doi: 10.1016/j.bone.2011.09.055
– ident: ref15
  doi: 10.1016/j.ajog.2020.05.051
– ident: ref25
  doi: 10.1007/s00198-018-4578-6
– ident: ref38
  doi: 10.1210/jc.2005-2672
– ident: ref10
  doi: 10.1210/jc.2017-00042
– ident: ref31
  doi: 10.1002/jcb.26174
– ident: ref43
  doi: 10.1111/1753-0407.13530
– ident: ref4
  doi: 10.1016/j.bone.2009.10.005
– ident: ref2
– ident: ref39
  doi: 10.1210/er.2003-0015
– ident: ref11
  doi: 10.1016/j.ecl.2021.03.005
– ident: ref35
  doi: 10.2174/138945011798829456
– ident: ref3
  doi: 10.2337/dc06-0062
– ident: ref13
  doi: 10.1056/NEJMcp2307353
– ident: ref37
  doi: 10.2337/dc07-2426
– ident: ref40
  doi: 10.1007/s10654-004-1706-8
– ident: ref32
  doi: 10.1016/j.vph.2012.06.004
– ident: ref24
  doi: 10.1007/s00198-022-06317-x
– ident: ref1
  doi: 10.1016/S0140-6736(22)01655-5
– ident: ref8
  doi: 10.3390/ijms20194873
– ident: ref29
  doi: 10.1016/S2213-8587(18)30110-4
– ident: ref5
  doi: 10.7326/AITC202401160
– ident: ref12
  doi: 10.1016/j.regg.2019.08.009
– ident: ref30
  doi: 10.1016/j.exger.2010.09.014
– ident: ref33
  doi: 10.1016/j.jbiomech.2010.10.016
– ident: ref16
  doi: 10.1136/heartjnl-2020-318764
– ident: ref18
  doi: 10.1038/s41574-023-00866-9
– ident: ref41
  doi: 10.1016/j.jocd.2009.02.001
– ident: ref42
  doi: 10.1016/S0140-6736(96)90075-6
– ident: ref46
  doi: 10.3390/biom13040616
– ident: ref6
  doi: 10.1016/j.bone.2005.11.024
– ident: ref23
  doi: 10.1016/j.mayocp.2021.07.019
– ident: ref17
  doi: 10.1002/jbmr.5650100517
– ident: ref44
  doi: 10.1016/j.jocd.2023.101442
– ident: ref21
  doi: 10.1016/j.bone.2020.115597
– ident: ref45
  doi: 10.1007/s11657-015-0219-2
– ident: ref34
  doi: 10.1007/s11914-007-0004-2
– ident: ref28
  doi: 10.1615/CritRevEukarGeneExpr.v21.i2.70
– ident: ref48
  doi: 10.1007/s00774-020-01189-9
– ident: ref26
  doi: 10.2337/dc06-0440
– ident: ref7
  doi: 10.1002/jbmr.2269
– ident: ref9
  doi: 10.1038/nrendo.2017.151
– ident: ref49
  doi: 10.1111/j.1600-0501.2010.01923.x
– ident: ref27
  doi: 10.1007/s00198-014-2676-7
– ident: ref47
  doi: 10.1093/ajcn/83.1.146
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Snippet Background: With ageing and lifestyle changes, the coexistence of osteoporosis and type 2 diabetes (T2DM) is becoming more common, which greatly increases...
With ageing and lifestyle changes, the coexistence of osteoporosis and type 2 diabetes (T2DM) is becoming more common, which greatly increases patient...
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SubjectTerms all-cause mortality
bone mineral density
cardiovascular mortality
nhanes database
Original Research
osteoporosis
type 2 diabetes
Title Bone Mineral Density is Negatively Associated with Risk of All-Cause and Cardiovascular Mortality among Adults with Type 2 Diabetes Mellitus: A Cross-sectional Study of the NHANES 2005–2010, 2013–2014
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