Glycated Hemoglobin Variability Is Associated With Adverse Outcomes in Patients With Heart Failure Irrespective of Diabetic Status
The effect of glycated hemoglobin (HbA ) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the predictive value of HbA variability on the risks of all-cause death and HF rehospitalization in patients with HF irrespective of their diabetic status. U...
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Published in | Journal of the American Heart Association Vol. 13; no. 9; p. e034109 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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England
John Wiley and Sons Inc
07.05.2024
Wiley |
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Abstract | The effect of glycated hemoglobin (HbA
) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the predictive value of HbA
variability on the risks of all-cause death and HF rehospitalization in patients with HF irrespective of their diabetic status.
Using a previously validated territory-wide clinical data registry, HbA
variability was assessed by average successive variability (ASV) or SD of all HbA
measurements after HF diagnosis. Multivariable Cox proportional hazards models were used to estimate the adjusted hazard ratio (HR) and its corresponding 95% CI. A total of 65 950 patients with HF were included in the study. Over a median follow-up of 6.7 (interquartile range, 4.0-10.6) years, 34 508 patients died and 52 446 required HF rehospitalization. Every unit increment of variability in HbA
was significantly associated with higher HF rehospitalization (HR ASV, 1.20 [95% CI, 1.18-1.23]) and all-cause death (HR ASV, 1.50 [95% CI, 1.47-1.53]). Diabetes significantly modified the association between HbA
variability and outcomes (
<0.001). HbA
variability in patients with HF without diabetes conferred a higher risk of rehospitalization (HR ASV, 1.92 [95% CI, 1.70-2.17] versus HR ASV, 1.19 [95% CI, 1.17-1.21]), and all-cause death (HR ASV, 3.90 [95% CI, 3.31-4.61] versus HR ASV, 1.47 [95% CI, 1.43-1.50] compared with patients with diabetes).
HbA
variability is significantly associated with greater risk of rehospitalization and all-cause death in patients with HF, irrespective of their diabetic status. These observations were more pronounced in patients with HF without diabetes. |
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AbstractList | Background The effect of glycated hemoglobin (HbA1c) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the predictive value of HbA1c variability on the risks of all‐cause death and HF rehospitalization in patients with HF irrespective of their diabetic status. Methods and Results Using a previously validated territory‐wide clinical data registry, HbA1c variability was assessed by average successive variability (ASV) or SD of all HbA1c measurements after HF diagnosis. Multivariable Cox proportional hazards models were used to estimate the adjusted hazard ratio (HR) and its corresponding 95% CI. A total of 65 950 patients with HF were included in the study. Over a median follow‐up of 6.7 (interquartile range, 4.0–10.6) years, 34 508 patients died and 52 446 required HF rehospitalization. Every unit increment of variability in HbA1c was significantly associated with higher HF rehospitalization (HR ASV, 1.20 [95% CI, 1.18–1.23]) and all‐cause death (HR ASV, 1.50 [95% CI, 1.47–1.53]). Diabetes significantly modified the association between HbA1c variability and outcomes (Pinteraction<0.001). HbA1c variability in patients with HF without diabetes conferred a higher risk of rehospitalization (HR ASV, 1.92 [95% CI, 1.70–2.17] versus HR ASV, 1.19 [95% CI, 1.17–1.21]), and all‐cause death (HR ASV, 3.90 [95% CI, 3.31–4.61] versus HR ASV, 1.47 [95% CI, 1.43–1.50] compared with patients with diabetes). Conclusions HbA1c variability is significantly associated with greater risk of rehospitalization and all‐cause death in patients with HF, irrespective of their diabetic status. These observations were more pronounced in patients with HF without diabetes. The effect of glycated hemoglobin (HbA ) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the predictive value of HbA variability on the risks of all-cause death and HF rehospitalization in patients with HF irrespective of their diabetic status. Using a previously validated territory-wide clinical data registry, HbA variability was assessed by average successive variability (ASV) or SD of all HbA measurements after HF diagnosis. Multivariable Cox proportional hazards models were used to estimate the adjusted hazard ratio (HR) and its corresponding 95% CI. A total of 65 950 patients with HF were included in the study. Over a median follow-up of 6.7 (interquartile range, 4.0-10.6) years, 34 508 patients died and 52 446 required HF rehospitalization. Every unit increment of variability in HbA was significantly associated with higher HF rehospitalization (HR ASV, 1.20 [95% CI, 1.18-1.23]) and all-cause death (HR ASV, 1.50 [95% CI, 1.47-1.53]). Diabetes significantly modified the association between HbA variability and outcomes ( <0.001). HbA variability in patients with HF without diabetes conferred a higher risk of rehospitalization (HR ASV, 1.92 [95% CI, 1.70-2.17] versus HR ASV, 1.19 [95% CI, 1.17-1.21]), and all-cause death (HR ASV, 3.90 [95% CI, 3.31-4.61] versus HR ASV, 1.47 [95% CI, 1.43-1.50] compared with patients with diabetes). HbA variability is significantly associated with greater risk of rehospitalization and all-cause death in patients with HF, irrespective of their diabetic status. These observations were more pronounced in patients with HF without diabetes. The effect of glycated hemoglobin (HbA1c) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the predictive value of HbA1c variability on the risks of all-cause death and HF rehospitalization in patients with HF irrespective of their diabetic status.BACKGROUNDThe effect of glycated hemoglobin (HbA1c) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the predictive value of HbA1c variability on the risks of all-cause death and HF rehospitalization in patients with HF irrespective of their diabetic status.Using a previously validated territory-wide clinical data registry, HbA1c variability was assessed by average successive variability (ASV) or SD of all HbA1c measurements after HF diagnosis. Multivariable Cox proportional hazards models were used to estimate the adjusted hazard ratio (HR) and its corresponding 95% CI. A total of 65 950 patients with HF were included in the study. Over a median follow-up of 6.7 (interquartile range, 4.0-10.6) years, 34 508 patients died and 52 446 required HF rehospitalization. Every unit increment of variability in HbA1c was significantly associated with higher HF rehospitalization (HR ASV, 1.20 [95% CI, 1.18-1.23]) and all-cause death (HR ASV, 1.50 [95% CI, 1.47-1.53]). Diabetes significantly modified the association between HbA1c variability and outcomes (Pinteraction<0.001). HbA1c variability in patients with HF without diabetes conferred a higher risk of rehospitalization (HR ASV, 1.92 [95% CI, 1.70-2.17] versus HR ASV, 1.19 [95% CI, 1.17-1.21]), and all-cause death (HR ASV, 3.90 [95% CI, 3.31-4.61] versus HR ASV, 1.47 [95% CI, 1.43-1.50] compared with patients with diabetes).METHODS AND RESULTSUsing a previously validated territory-wide clinical data registry, HbA1c variability was assessed by average successive variability (ASV) or SD of all HbA1c measurements after HF diagnosis. Multivariable Cox proportional hazards models were used to estimate the adjusted hazard ratio (HR) and its corresponding 95% CI. A total of 65 950 patients with HF were included in the study. Over a median follow-up of 6.7 (interquartile range, 4.0-10.6) years, 34 508 patients died and 52 446 required HF rehospitalization. Every unit increment of variability in HbA1c was significantly associated with higher HF rehospitalization (HR ASV, 1.20 [95% CI, 1.18-1.23]) and all-cause death (HR ASV, 1.50 [95% CI, 1.47-1.53]). Diabetes significantly modified the association between HbA1c variability and outcomes (Pinteraction<0.001). HbA1c variability in patients with HF without diabetes conferred a higher risk of rehospitalization (HR ASV, 1.92 [95% CI, 1.70-2.17] versus HR ASV, 1.19 [95% CI, 1.17-1.21]), and all-cause death (HR ASV, 3.90 [95% CI, 3.31-4.61] versus HR ASV, 1.47 [95% CI, 1.43-1.50] compared with patients with diabetes).HbA1c variability is significantly associated with greater risk of rehospitalization and all-cause death in patients with HF, irrespective of their diabetic status. These observations were more pronounced in patients with HF without diabetes.CONCLUSIONSHbA1c variability is significantly associated with greater risk of rehospitalization and all-cause death in patients with HF, irrespective of their diabetic status. These observations were more pronounced in patients with HF without diabetes. |
Author | Wu, Mei‐Zhen Huang, Jia‐Yi Xu, Xin Wang, Fang Lam, Carolyn S.P. Ren, Qing‐Wen Liu, Ming‐Ya Chandramouli, Chanchal Tse, Yi‐Kei Li, Xin‐Li Tsang, Christopher Tze‐Wei Yiu, Kai‐Hang Ng, Ming‐Yen Cheang, Iok‐Fai Yang, Jie‐Fu |
AuthorAffiliation | 4 Duke‐NUS Medical School Singapore 5 Department of Diagnostic Radiology, School of Clinical Medicine The University of Hong Kong, Li Ka Shing Faculty of Medicine Hong Kong China 1 Cardiology Division, Department of Medicine The University of Hong Kong–Shen Zhen Hospital Shenzhen China 2 Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China 7 Department of Cardiology The First Affiliated Hospital of Nanjing Medical University Nanjing China 3 Department of Cardiology National Heart Center Singapore Singapore 6 Department of Medical Imaging The University of Hong Kong‐Shen Zhen Hospital Shenzhen China 8 Department of Cardiology, Beijing Hospital, National Center of Gerontology Institute of Geriatric Medicine, Chinese Academy of Medical Sciences Beijing China 9 Baim Institute for Clinical Research Boston MA USA |
AuthorAffiliation_xml | – name: 2 Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China – name: 4 Duke‐NUS Medical School Singapore – name: 1 Cardiology Division, Department of Medicine The University of Hong Kong–Shen Zhen Hospital Shenzhen China – name: 9 Baim Institute for Clinical Research Boston MA USA – name: 3 Department of Cardiology National Heart Center Singapore Singapore – name: 6 Department of Medical Imaging The University of Hong Kong‐Shen Zhen Hospital Shenzhen China – name: 7 Department of Cardiology The First Affiliated Hospital of Nanjing Medical University Nanjing China – name: 5 Department of Diagnostic Radiology, School of Clinical Medicine The University of Hong Kong, Li Ka Shing Faculty of Medicine Hong Kong China – name: 8 Department of Cardiology, Beijing Hospital, National Center of Gerontology Institute of Geriatric Medicine, Chinese Academy of Medical Sciences Beijing China |
Author_xml | – sequence: 1 givenname: Xin orcidid: 0000-0001-6795-4296 surname: Xu fullname: Xu, Xin organization: Cardiology Division, Department of Medicine The University of Hong Kong–Shen Zhen Hospital Shenzhen China, Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China – sequence: 2 givenname: Qing‐Wen orcidid: 0000-0003-0712-9299 surname: Ren fullname: Ren, Qing‐Wen organization: Cardiology Division, Department of Medicine The University of Hong Kong–Shen Zhen Hospital Shenzhen China, Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China – sequence: 3 givenname: Chanchal orcidid: 0000-0001-8256-902X surname: Chandramouli fullname: Chandramouli, Chanchal organization: Department of Cardiology National Heart Center Singapore Singapore, Duke‐NUS Medical School Singapore – sequence: 4 givenname: Ming‐Yen orcidid: 0000-0001-9533-3892 surname: Ng fullname: Ng, Ming‐Yen organization: Department of Diagnostic Radiology, School of Clinical Medicine The University of Hong Kong, Li Ka Shing Faculty of Medicine Hong Kong China, Department of Medical Imaging The University of Hong Kong‐Shen Zhen Hospital Shenzhen China – sequence: 5 givenname: Christopher Tze‐Wei orcidid: 0000-0003-3394-6604 surname: Tsang fullname: Tsang, Christopher Tze‐Wei organization: Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China – sequence: 6 givenname: Yi‐Kei surname: Tse fullname: Tse, Yi‐Kei organization: Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China – sequence: 7 givenname: Xin‐Li orcidid: 0000-0002-7889-6359 surname: Li fullname: Li, Xin‐Li organization: Department of Cardiology The First Affiliated Hospital of Nanjing Medical University Nanjing China – sequence: 8 givenname: Ming‐Ya surname: Liu fullname: Liu, Ming‐Ya organization: Cardiology Division, Department of Medicine The University of Hong Kong–Shen Zhen Hospital Shenzhen China – sequence: 9 givenname: Mei‐Zhen orcidid: 0000-0003-2674-5097 surname: Wu fullname: Wu, Mei‐Zhen organization: Cardiology Division, Department of Medicine The University of Hong Kong–Shen Zhen Hospital Shenzhen China, Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China – sequence: 10 givenname: Jia‐Yi surname: Huang fullname: Huang, Jia‐Yi organization: Cardiology Division, Department of Medicine The University of Hong Kong–Shen Zhen Hospital Shenzhen China, Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China – sequence: 11 givenname: Iok‐Fai orcidid: 0000-0002-9950-9696 surname: Cheang fullname: Cheang, Iok‐Fai organization: Department of Cardiology The First Affiliated Hospital of Nanjing Medical University Nanjing China – sequence: 12 givenname: Jie‐Fu orcidid: 0000-0002-2273-4860 surname: Yang fullname: Yang, Jie‐Fu organization: Department of Cardiology, Beijing Hospital, National Center of Gerontology Institute of Geriatric Medicine, Chinese Academy of Medical Sciences Beijing China – sequence: 13 givenname: Fang orcidid: 0000-0002-6674-5537 surname: Wang fullname: Wang, Fang organization: Department of Cardiology, Beijing Hospital, National Center of Gerontology Institute of Geriatric Medicine, Chinese Academy of Medical Sciences Beijing China – sequence: 14 givenname: Carolyn S.P. orcidid: 0000-0003-1903-0018 surname: Lam fullname: Lam, Carolyn S.P. organization: Department of Cardiology National Heart Center Singapore Singapore, Duke‐NUS Medical School Singapore, Baim Institute for Clinical Research Boston MA USA – sequence: 15 givenname: Kai‐Hang orcidid: 0000-0003-2145-3108 surname: Yiu fullname: Yiu, Kai‐Hang organization: Cardiology Division, Department of Medicine The University of Hong Kong–Shen Zhen Hospital Shenzhen China, Cardiology Division, Department of Medicine The University of Hong Kong, Queen Mary Hospital Hong Kong China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38686852$$D View this record in MEDLINE/PubMed |
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Keywords | heart failure diabetes HbA1c variability |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This work was presented in part at the European Society of Cardiology Heart Failure Congress, May 20–23, 2023, in Prague, Czech Republic. This manuscript was sent to Tazeen H. Jafar, MD MPH, Associate Editor, for review by expert referees, editorial decision, and final disposition. Supplemental Material is available at https://www.ahajournals.org/doi/suppl/10.1161/JAHA.123.034109 For Sources of Funding and Disclosures, see page 10. X. Xu and Q. W. Ren are co‐first authors. |
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Snippet | The effect of glycated hemoglobin (HbA
) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the predictive... The effect of glycated hemoglobin (HbA1c) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the predictive... Background The effect of glycated hemoglobin (HbA1c) variability on adverse outcomes in patients with heart failure (HF) is unclear. We aim to investigate the... |
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StartPage | e034109 |
SubjectTerms | diabetes HbA1c variability heart failure Original Research |
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Title | Glycated Hemoglobin Variability Is Associated With Adverse Outcomes in Patients With Heart Failure Irrespective of Diabetic Status |
URI | https://www.ncbi.nlm.nih.gov/pubmed/38686852 https://www.proquest.com/docview/3049721042 https://pubmed.ncbi.nlm.nih.gov/PMC11179906 https://doaj.org/article/cd2c370063cd48acb293a8cbe72e1bac |
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