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Article: HbA1c variability, in addition to mean HbA1c, predicts incident hip fractures in Chinese people with type 2 diabetes

TitleHbA1c variability, in addition to mean HbA1c, predicts incident hip fractures in Chinese people with type 2 diabetes
Authors
KeywordsChinese
Diabetes mellitus
Glycated hemoglobin A
Hip fractures
Hypoglycemia
Osteoporosis
Postmenopause
Type 2
Issue Date2020
PublisherSpringer UK. The Journal's web site is located at http://www.springer.com/medicine/orthopedics/journal/198
Citation
Osteoporosis International: with other metabolic bone diseases, 2020, v. 31 n. 10, p. 1955-1964 How to Cite?
Abstractype 2 diabetes is associated with an increased risk of hip fractures. We hypothesize that long-term glycemic variability predicts incident hip fractures. We demonstrated that HbA1c variability predicted incident hip fractures independent of mean HbA1c, suggesting the potential benefits of minimizing glycemic variability in addition to optimizing mean glycemia for bone health. Introduction: Type 2 diabetes is associated with an increased risk of hip fractures, and a linear relationship between HbA1c levels and hip fracture incidence has been observed. We hypothesize that HbA1c variability also predicts incident hip fractures in type 2 diabetes. Methods: Chinese individuals with type 2 diabetes aged ≥ 60 years were identified from electronic health records in Hong Kong between 2008 and 2012 and observed for incident hip fractures. Hip fracture was defined by the International Classification of Diseases (Ninth Revision) code 820. HbA1c variability was determined using standard deviation, adjusted standard deviation, and coefficient of variation of HbA1c measurements in the 5 years preceding the entry date. Multivariable Cox regression analysis was used to evaluate associations between HbA1c variability and incident hip fractures. Results: A total of 83,282 participants were included. Their mean age was 71.3 ± 7.5 years, duration of diabetes 11.7 ± 7.7 years, baseline HbA1c 56.6 ± 13.5 mmol/mol (7.33 ± 1.23%), and median follow-up 6.8 years. All indices of HbA1c variability were significant independent predictors of incident hip fractures, with an adjusted hazard ratio of up to 1.29 (all p < 0.001), and remained to be independent predictors across groups of different intensity of glycemic control. Mean HbA1c ≥ 64 mmol/mol (8.0%) was associated with a 25% increase in incident hip fractures compared with mean HbA1c < 53 mmol/mol (7.0%). Conclusion: HbA1c variability is an independent positive predictor of hip fracture in type 2 diabetes, across the spectrum of varying degree of glycemic control, while a high HbA1c is also not advisable from the perspective of bone health.
Persistent Identifierhttp://hdl.handle.net/10722/293757
ISSN
2021 Impact Factor: 5.071
2020 SCImago Journal Rankings: 1.280
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLui, DTW-
dc.contributor.authorLee, CH-
dc.contributor.authorChan, YH-
dc.contributor.authorChow, WS-
dc.contributor.authorFong, CHY-
dc.contributor.authorSiu, DCW-
dc.contributor.authorTse, HF-
dc.contributor.authorWoo, YC-
dc.contributor.authorLam, KSL-
dc.date.accessioned2020-11-23T08:21:22Z-
dc.date.available2020-11-23T08:21:22Z-
dc.date.issued2020-
dc.identifier.citationOsteoporosis International: with other metabolic bone diseases, 2020, v. 31 n. 10, p. 1955-1964-
dc.identifier.issn0937-941X-
dc.identifier.urihttp://hdl.handle.net/10722/293757-
dc.description.abstractype 2 diabetes is associated with an increased risk of hip fractures. We hypothesize that long-term glycemic variability predicts incident hip fractures. We demonstrated that HbA1c variability predicted incident hip fractures independent of mean HbA1c, suggesting the potential benefits of minimizing glycemic variability in addition to optimizing mean glycemia for bone health. Introduction: Type 2 diabetes is associated with an increased risk of hip fractures, and a linear relationship between HbA1c levels and hip fracture incidence has been observed. We hypothesize that HbA1c variability also predicts incident hip fractures in type 2 diabetes. Methods: Chinese individuals with type 2 diabetes aged ≥ 60 years were identified from electronic health records in Hong Kong between 2008 and 2012 and observed for incident hip fractures. Hip fracture was defined by the International Classification of Diseases (Ninth Revision) code 820. HbA1c variability was determined using standard deviation, adjusted standard deviation, and coefficient of variation of HbA1c measurements in the 5 years preceding the entry date. Multivariable Cox regression analysis was used to evaluate associations between HbA1c variability and incident hip fractures. Results: A total of 83,282 participants were included. Their mean age was 71.3 ± 7.5 years, duration of diabetes 11.7 ± 7.7 years, baseline HbA1c 56.6 ± 13.5 mmol/mol (7.33 ± 1.23%), and median follow-up 6.8 years. All indices of HbA1c variability were significant independent predictors of incident hip fractures, with an adjusted hazard ratio of up to 1.29 (all p < 0.001), and remained to be independent predictors across groups of different intensity of glycemic control. Mean HbA1c ≥ 64 mmol/mol (8.0%) was associated with a 25% increase in incident hip fractures compared with mean HbA1c < 53 mmol/mol (7.0%). Conclusion: HbA1c variability is an independent positive predictor of hip fracture in type 2 diabetes, across the spectrum of varying degree of glycemic control, while a high HbA1c is also not advisable from the perspective of bone health.-
dc.languageeng-
dc.publisherSpringer UK. The Journal's web site is located at http://www.springer.com/medicine/orthopedics/journal/198-
dc.relation.ispartofOsteoporosis International: with other metabolic bone diseases-
dc.subjectChinese-
dc.subjectDiabetes mellitus-
dc.subjectGlycated hemoglobin A-
dc.subjectHip fractures-
dc.subjectHypoglycemia-
dc.subjectOsteoporosis-
dc.subjectPostmenopause-
dc.subjectType 2-
dc.titleHbA1c variability, in addition to mean HbA1c, predicts incident hip fractures in Chinese people with type 2 diabetes-
dc.typeArticle-
dc.identifier.emailLui, DTW: dtwlui@hku.hk-
dc.identifier.emailLee, CH: pchlee@hku.hk-
dc.identifier.emailChow, WS: chowws01@hkucc.hku.hk-
dc.identifier.emailFong, CHY: kalofong@hku.hk-
dc.identifier.emailSiu, DCW: cwdsiu@hkucc.hku.hk-
dc.identifier.emailTse, HF: hftse@hkucc.hku.hk-
dc.identifier.emailWoo, YC: wooyucho@hku.hk-
dc.identifier.emailLam, KSL: ksllam@hku.hk-
dc.identifier.authorityLui, DTW=rp02803-
dc.identifier.authorityLee, CH=rp02043-
dc.identifier.authoritySiu, DCW=rp00534-
dc.identifier.authorityTse, HF=rp00428-
dc.identifier.authorityLam, KSL=rp00343-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s00198-020-05395-z-
dc.identifier.pmid32385660-
dc.identifier.scopuseid_2-s2.0-85084458599-
dc.identifier.hkuros319893-
dc.identifier.hkuros323137-
dc.identifier.volume31-
dc.identifier.issue10-
dc.identifier.spage1955-
dc.identifier.epage1964-
dc.identifier.isiWOS:000531122400001-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0937-941X-

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