Intensive Glycemic Control Is Not Associated With Fractures or Falls in the ACCORD Randomized Trial
Older adults with type 2 diabetes are at high risk of fractures and falls, but the effect of glycemic control on these outcomes is unknown. To determine the effect of intensive versus standard glycemic control, we assessed fractures and falls as outcomes in the Action to Control Cardiovascular Risk...
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Published in | Diabetes care Vol. 35; no. 7; pp. 1525 - 1531 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Alexandria, VA
American Diabetes Association
01.07.2012
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Subjects | |
Online Access | Get full text |
ISSN | 0149-5992 1935-5548 1935-5548 |
DOI | 10.2337/dc11-2184 |
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Abstract | Older adults with type 2 diabetes are at high risk of fractures and falls, but the effect of glycemic control on these outcomes is unknown. To determine the effect of intensive versus standard glycemic control, we assessed fractures and falls as outcomes in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) randomized trial.
ACCORD participants were randomized to intensive or standard glycemia strategies, with an achieved median A1C of 6.4 and 7.5%, respectively. In the ACCORD BONE ancillary study, fractures were assessed at 54 of the 77 ACCORD clinical sites that included 7,287 of the 10,251 ACCORD participants. At annual visits, 6,782 participants were asked about falls in the previous year.
During an average follow-up of 3.8 (SD 1.3) years, 198 of 3,655 participants in the intensive glycemia and 189 of 3,632 participants in the standard glycemia group experienced at least one nonspine fracture. The average rate of first nonspine fracture was 13.9 and 13.3 per 1,000 person-years in the intensive and standard groups, respectively (hazard ratio 1.04 [95% CI 0.86-1.27]). During an average follow-up of 2.0 years, 1,122 of 3,364 intensive- and 1,133 of 3,418 standard-therapy participants reported at least one fall. The average rate of falls was 60.8 and 55.3 per 100 person-years in the intensive and standard glycemia groups, respectively (1.10 [0.84-1.43]).
Compared with standard glycemia, intensive glycemia did not increase or decrease fracture or fall risk in ACCORD. |
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AbstractList | Older adults with type 2 diabetes are at high risk of fractures and falls, but the effect of glycemic control on these outcomes is unknown. To determine the effect of intensive versus standard glycemic control, we assessed fractures and falls as outcomes in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) randomized trial. ACCORD participants were randomized to intensive or standard glycemia strategies, with an achieved median A1C of 6.4 and 7.5%, respectively. In the ACCORD BONE ancillary study, fractures were assessed at 54 of the 77 ACCORD clinical sites that included 7,287 of the 10,251 ACCORD participants. At annual visits, 6,782 participants were asked about falls in the previous year. During an average follow-up of 3.8 (SD 1.3) years, 198 of 3,655 participants in the intensive glycemia and 189 of 3,632 participants in the standard glycemia group experienced at least one nonspine fracture. The average rate of first nonspine fracture was 13.9 and 13.3 per 1,000 person-years in the intensive and standard groups, respectively (hazard ratio 1.04 [95% CI 0.86-1.271). During an average follow-up of 2.0 years, 1,122 of 3,364 intensive- and 1,133 of 3,418 standard-therapy participants reported at least one fall. The average rate of falls was 60.8 and 55.3 per 100 person-years in the intensive and standard glycemia groups, respectively (1.10 [0.84-1.43]). Compared with standard glycemia, intensive glycemia did not increase or decrease fracture or fall risk in ACCORD. Older adults with type 2 diabetes are at high risk of fractures and falls, but the effect of glycemic control on these outcomes is unknown. To determine the effect of intensive versus standard glycemic control, we assessed fractures and falls as outcomes in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) randomized trial.OBJECTIVEOlder adults with type 2 diabetes are at high risk of fractures and falls, but the effect of glycemic control on these outcomes is unknown. To determine the effect of intensive versus standard glycemic control, we assessed fractures and falls as outcomes in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) randomized trial.ACCORD participants were randomized to intensive or standard glycemia strategies, with an achieved median A1C of 6.4 and 7.5%, respectively. In the ACCORD BONE ancillary study, fractures were assessed at 54 of the 77 ACCORD clinical sites that included 7,287 of the 10,251 ACCORD participants. At annual visits, 6,782 participants were asked about falls in the previous year.RESEARCH DESIGN AND METHODSACCORD participants were randomized to intensive or standard glycemia strategies, with an achieved median A1C of 6.4 and 7.5%, respectively. In the ACCORD BONE ancillary study, fractures were assessed at 54 of the 77 ACCORD clinical sites that included 7,287 of the 10,251 ACCORD participants. At annual visits, 6,782 participants were asked about falls in the previous year.During an average follow-up of 3.8 (SD 1.3) years, 198 of 3,655 participants in the intensive glycemia and 189 of 3,632 participants in the standard glycemia group experienced at least one nonspine fracture. The average rate of first nonspine fracture was 13.9 and 13.3 per 1,000 person-years in the intensive and standard groups, respectively (hazard ratio 1.04 [95% CI 0.86-1.27]). During an average follow-up of 2.0 years, 1,122 of 3,364 intensive- and 1,133 of 3,418 standard-therapy participants reported at least one fall. The average rate of falls was 60.8 and 55.3 per 100 person-years in the intensive and standard glycemia groups, respectively (1.10 [0.84-1.43]).RESULTSDuring an average follow-up of 3.8 (SD 1.3) years, 198 of 3,655 participants in the intensive glycemia and 189 of 3,632 participants in the standard glycemia group experienced at least one nonspine fracture. The average rate of first nonspine fracture was 13.9 and 13.3 per 1,000 person-years in the intensive and standard groups, respectively (hazard ratio 1.04 [95% CI 0.86-1.27]). During an average follow-up of 2.0 years, 1,122 of 3,364 intensive- and 1,133 of 3,418 standard-therapy participants reported at least one fall. The average rate of falls was 60.8 and 55.3 per 100 person-years in the intensive and standard glycemia groups, respectively (1.10 [0.84-1.43]).Compared with standard glycemia, intensive glycemia did not increase or decrease fracture or fall risk in ACCORD.CONCLUSIONSCompared with standard glycemia, intensive glycemia did not increase or decrease fracture or fall risk in ACCORD. Older adults with type 2 diabetes are at high risk of fractures and falls, but the effect of glycemic control on these outcomes is unknown. To determine the effect of intensive versus standard glycemic control, we assessed fractures and falls as outcomes in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) randomized trial. ACCORD participants were randomized to intensive or standard glycemia strategies, with an achieved median A1C of 6.4 and 7.5%, respectively. In the ACCORD BONE ancillary study, fractures were assessed at 54 of the 77 ACCORD clinical sites that included 7,287 of the 10,251 ACCORD participants. At annual visits, 6,782 participants were asked about falls in the previous year. During an average follow-up of 3.8 (SD 1.3) years, 198 of 3,655 participants in the intensive glycemia and 189 of 3,632 participants in the standard glycemia group experienced at least one nonspine fracture. The average rate of first nonspine fracture was 13.9 and 13.3 per 1,000 person-years in the intensive and standard groups, respectively (hazard ratio 1.04 [95% CI 0.86-1.27]). During an average follow-up of 2.0 years, 1,122 of 3,364 intensive- and 1,133 of 3,418 standard-therapy participants reported at least one fall. The average rate of falls was 60.8 and 55.3 per 100 person-years in the intensive and standard glycemia groups, respectively (1.10 [0.84-1.43]). Compared with standard glycemia, intensive glycemia did not increase or decrease fracture or fall risk in ACCORD. |
Audience | Professional |
Author | Bauer, Douglas C. Schnall, Adrian M. Hamilton, Bruce P. Vittinghoff, Eric Atkinson, Hal H. Simmons, Debra L. Palermo, Lisa Green, Jennifer B. Sellmeyer, Deborah E. Margolis, Karen L. Bonds, Denise E. Josse, Robert G. O’Connor, Patrick J. Force, Rex W. Schwartz, Ann V. Hue, Trisha F. Ambrosius, Walter T. |
Author_xml | – sequence: 1 givenname: Ann V. surname: Schwartz fullname: Schwartz, Ann V. organization: Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California – sequence: 2 givenname: Karen L. surname: Margolis fullname: Margolis, Karen L. organization: HealthPartners Research Foundation, Minneapolis, Minnesota – sequence: 3 givenname: Deborah E. surname: Sellmeyer fullname: Sellmeyer, Deborah E. organization: Division of Endocrinology, Johns Hopkins School of Medicine, Baltimore, Maryland – sequence: 4 givenname: Eric surname: Vittinghoff fullname: Vittinghoff, Eric organization: Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California – sequence: 5 givenname: Walter T. surname: Ambrosius fullname: Ambrosius, Walter T. organization: Department of Biostatistics, Wake Forest School of Medicine, Winston-Salem, North Carolina – sequence: 6 givenname: Denise E. surname: Bonds fullname: Bonds, Denise E. organization: Division of Prevention and Population Sciences, National Heart, Lung, and Blood Institute, Bethesda, Maryland – sequence: 7 givenname: Robert G. surname: Josse fullname: Josse, Robert G. organization: Department of Medicine, University of Toronto, Toronto, Ontario, Canada – sequence: 8 givenname: Adrian M. surname: Schnall fullname: Schnall, Adrian M. organization: Department of Medicine, Case Western Reserve School of Medicine, Cleveland, Ohio – sequence: 9 givenname: Debra L. surname: Simmons fullname: Simmons, Debra L. organization: Department of Endocrinology and Metabolism, Central Arkansas Veterans Healthcare System and University of Arkansas for Medical Sciences, Little Rock, Arkansas – sequence: 10 givenname: Trisha F. surname: Hue fullname: Hue, Trisha F. organization: Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California – sequence: 11 givenname: Lisa surname: Palermo fullname: Palermo, Lisa organization: Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California – sequence: 12 givenname: Bruce P. surname: Hamilton fullname: Hamilton, Bruce P. organization: Department of Medicine, University of Maryland School of Medicine, Baltimore VA Medical Center, Baltimore, Maryland – sequence: 13 givenname: Jennifer B. surname: Green fullname: Green, Jennifer B. organization: Department of Medicine, Endocrinology and Metabolism, Duke University Medical Center, Durham, North Carolina – sequence: 14 givenname: Hal H. surname: Atkinson fullname: Atkinson, Hal H. organization: Department of Biostatistics, Wake Forest School of Medicine, Winston-Salem, North Carolina – sequence: 15 givenname: Patrick J. surname: O’Connor fullname: O’Connor, Patrick J. organization: HealthPartners Research Foundation, Minneapolis, Minnesota – sequence: 16 givenname: Rex W. surname: Force fullname: Force, Rex W. organization: College of Pharmacy, Idaho State University, Pocatello, Idaho – sequence: 17 givenname: Douglas C. surname: Bauer fullname: Bauer, Douglas C. organization: Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California |
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Keywords | Endocrinopathy Human Glycemic control Nutrition Diseases of the osteoarticular system Metabolic diseases Fracture Trauma Target tissue resistance Association Clinical trial Insulin resistance Fall Endocrinology Glycemia |
Language | English |
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PublicationDate | 2012-07-01 |
PublicationDateYYYYMMDD | 2012-07-01 |
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PublicationDecade | 2010 |
PublicationPlace | Alexandria, VA |
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PublicationTitle | Diabetes care |
PublicationTitleAlternate | Diabetes Care |
PublicationYear | 2012 |
Publisher | American Diabetes Association |
Publisher_xml | – name: American Diabetes Association |
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between the number of prescription medications and incident falls in a multi-ethnic population of adult type-2 diabetes patients: the diabetes and aging study publication-title: J Gen Intern Med doi: 10.1007/s11606-009-1179-2 |
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Snippet | Older adults with type 2 diabetes are at high risk of fractures and falls, but the effect of glycemic control on these outcomes is unknown. To determine the... |
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SubjectTerms | Accidental Falls - statistics & numerical data Adult Aged Biological and medical sciences Blood Glucose - drug effects Blood pressure Bone Density Cardiovascular diseases Cardiovascular Diseases - prevention & control Care and treatment Complications and side effects Diabetes Mellitus, Type 2 - complications Diabetes therapy Diabetes. Impaired glucose tolerance Endocrine pancreas. Apud cells (diseases) Endocrinopathies Female Fractures Fractures, Bone - prevention & control Glycated Hemoglobin Health aspects Humans Hypoglycemic Agents - administration & dosage Male Medical sciences Metabolic diseases Middle Aged Miscellaneous Mortality Older people Original Research Patient outcomes Prevention Public health. Hygiene Public health. Hygiene-occupational medicine Risk assessment Risk Factors Type 2 diabetes |
Title | Intensive Glycemic Control Is Not Associated With Fractures or Falls in the ACCORD Randomized Trial |
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