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- Publisher Website: 10.1016/j.diabres.2021.109071
- Scopus: eid_2-s2.0-85116692126
- PMID: 34592391
- WOS: WOS:000708521100008
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Article: Cardio-renal outcomes and the direct medical cost of type 2 diabetes patients treated with sodium glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists: A population-based cohort study
Title | Cardio-renal outcomes and the direct medical cost of type 2 diabetes patients treated with sodium glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists: A population-based cohort study |
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Authors | |
Keywords | Cardiovascular disease Glucagon-like peptide-1 receptor agonists Sodium glucose cotransporter-2 inhibitors Costs Type 2 diabetes |
Issue Date | 2021 |
Publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/diabres |
Citation | Diabetes Research and Clinical Practice, 2021, v. 180, article no. 109071 How to Cite? |
Abstract | Aims:
To compare cardio-renal outcomes and incurred direct medical costs of patients initiating sodium glucose cotransporter-2 inhibitors (SGLT2i) versus glucagon-like peptide-1 receptor agonists (GLP-1RA).
Methods:
A population-based cohort of patients with type 2 diabetes was identified from Hong Kong Hospital Authority. Patients who were free from cardiovascular and end-stage renal diseases at baseline, and newly treated with SGLT2i (n = 2,541) or GLP-1RA (n = 303), were included. Risks of developing cardio-renal complications, incurred direct medical costs, and changes in clinical parameters were assessed between groups.
Results:
Over a median follow-up of 12.5 months in SGLT2i group and 25.5 months in GLP-1RA group, SGLT2i users were associated with significantly lower risk of heart failure compared with those on GLP-1RA [hazard ratio = 0.183, 95 %CI = (0.045, 0.745)]. 1-year change in clinical parameters also favored use of SGLT2i over GLP-1RA, where the former was associated with a larger reduction in fasting glucose level [difference-in-difference = −0.87 mmol/L, 95 %CI = (−1.42, −0.33), p = 0.002]. The two groups had comparable direct medical costs after 1-year of follow-up.
Conclusion:
Patients initiating SGLT2i experienced a significantly lower risk of heart failure than those on GLP-1RA, alongside better glycemic control through a larger reduction in fasting glucose level over one-year follow-up, while direct medical cost incurred was comparable to that of GLP-1RA. |
Persistent Identifier | http://hdl.handle.net/10722/304680 |
ISSN | 2023 Impact Factor: 6.1 2023 SCImago Journal Rankings: 1.340 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Tang, EHM | - |
dc.contributor.author | Wong, CKH | - |
dc.contributor.author | Lau, KTK | - |
dc.contributor.author | Fei, Y | - |
dc.contributor.author | Cheung, BMY | - |
dc.date.accessioned | 2021-10-05T02:33:36Z | - |
dc.date.available | 2021-10-05T02:33:36Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Diabetes Research and Clinical Practice, 2021, v. 180, article no. 109071 | - |
dc.identifier.issn | 0168-8227 | - |
dc.identifier.uri | http://hdl.handle.net/10722/304680 | - |
dc.description.abstract | Aims: To compare cardio-renal outcomes and incurred direct medical costs of patients initiating sodium glucose cotransporter-2 inhibitors (SGLT2i) versus glucagon-like peptide-1 receptor agonists (GLP-1RA). Methods: A population-based cohort of patients with type 2 diabetes was identified from Hong Kong Hospital Authority. Patients who were free from cardiovascular and end-stage renal diseases at baseline, and newly treated with SGLT2i (n = 2,541) or GLP-1RA (n = 303), were included. Risks of developing cardio-renal complications, incurred direct medical costs, and changes in clinical parameters were assessed between groups. Results: Over a median follow-up of 12.5 months in SGLT2i group and 25.5 months in GLP-1RA group, SGLT2i users were associated with significantly lower risk of heart failure compared with those on GLP-1RA [hazard ratio = 0.183, 95 %CI = (0.045, 0.745)]. 1-year change in clinical parameters also favored use of SGLT2i over GLP-1RA, where the former was associated with a larger reduction in fasting glucose level [difference-in-difference = −0.87 mmol/L, 95 %CI = (−1.42, −0.33), p = 0.002]. The two groups had comparable direct medical costs after 1-year of follow-up. Conclusion: Patients initiating SGLT2i experienced a significantly lower risk of heart failure than those on GLP-1RA, alongside better glycemic control through a larger reduction in fasting glucose level over one-year follow-up, while direct medical cost incurred was comparable to that of GLP-1RA. | - |
dc.language | eng | - |
dc.publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/diabres | - |
dc.relation.ispartof | Diabetes Research and Clinical Practice | - |
dc.subject | Cardiovascular disease | - |
dc.subject | Glucagon-like peptide-1 receptor agonists | - |
dc.subject | Sodium glucose cotransporter-2 inhibitors | - |
dc.subject | Costs | - |
dc.subject | Type 2 diabetes | - |
dc.title | Cardio-renal outcomes and the direct medical cost of type 2 diabetes patients treated with sodium glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists: A population-based cohort study | - |
dc.type | Article | - |
dc.identifier.email | Tang, EHM: erichm@hku.hk | - |
dc.identifier.email | Wong, CKH: carlosho@hku.hk | - |
dc.identifier.email | Lau, KTK: kristytk@hku.hk | - |
dc.identifier.email | Cheung, BMY: mycheung@hkucc.hku.hk | - |
dc.identifier.authority | Wong, CKH=rp01931 | - |
dc.identifier.authority | Cheung, BMY=rp01321 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.diabres.2021.109071 | - |
dc.identifier.pmid | 34592391 | - |
dc.identifier.scopus | eid_2-s2.0-85116692126 | - |
dc.identifier.hkuros | 326377 | - |
dc.identifier.volume | 180 | - |
dc.identifier.spage | article no. 109071 | - |
dc.identifier.epage | article no. 109071 | - |
dc.identifier.isi | WOS:000708521100008 | - |
dc.publisher.place | Ireland | - |