The association of the treatment with glucagon-like peptide-1 receptor agonist exenatide or insulin with cardiovascular outcomes in patients with type 2 diabetes : a retrospective observational study
BACKGROUND: To evaluate the association of treatment with glucagon-like peptide-1 (GLP-1) receptor agonist exenatide and/or insulin on macrovascular outcomes in patients with type 2 diabetes (T2DM).
METHODS: We conducted a retrospective longitudinal pharmaco-epidemiological study using large ambulatory care data to evaluate the risks of heart failure (HF), myocardial infarction (MI) and stroke in established T2DM patients who received a first prescription of exenatide twice daily (EBID) or insulin between June 2005 and May 2009, with follow-up data available until December 2012. Three treatment groups were: EBID with oral antidiabetes drugs (OADs) (EBID, n = 2804), insulin with OADs (Insulin, n = 28551), and those who changed medications between EBID and insulin or had combination of EBID and insulin during follow-up, along with OADs (EBID + insulin, n = 7870). Multivariate Cox-regression models were used to evaluate the association of treatment groups with the risks of macrovascular events.
RESULTS: During a median 3.5 years of follow-up, cardiovascular event rates per 1000 person-years were significantly lower for the EBID and EBID + insulin groups compared to the insulin group (HF: 4.4 and 6.1 vs. 17.9; MI: 1.1 and 1.2 vs. 2.5; stroke: 2.4 and 1.8 vs. 6.1). Patients in the EBID/EBID + insulin group had significantly reduced risk of HF, MI and stroke by 61/56%, 50/38% and 52/63% respectively, compared to patients in the insulin group (p < 0.01).
CONCLUSIONS: Treatment with exenatide, with or without concomitant insulin was associated with reduced macrovascular risks compared to insulin; although inherent potential bias in epidemiological studies should be considered.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2015 |
---|---|
Erschienen: |
2015 |
Enthalten in: |
Zur Gesamtaufnahme - volume:14 |
---|---|
Enthalten in: |
Cardiovascular diabetology - 14(2015) vom: 24. Jan., Seite 10 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Paul, Sanjoy K [VerfasserIn] |
---|
Links: |
---|
Themen: |
9P1872D4OL |
---|
Anmerkungen: |
Date Completed 15.01.2016 Date Revised 22.03.2024 published: Electronic Citation Status MEDLINE |
---|
doi: |
10.1186/s12933-015-0178-3 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM245614079 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM245614079 | ||
003 | DE-627 | ||
005 | 20240322234945.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231224s2015 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1186/s12933-015-0178-3 |2 doi | |
028 | 5 | 2 | |a pubmed24n1340.xml |
035 | |a (DE-627)NLM245614079 | ||
035 | |a (NLM)25616979 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Paul, Sanjoy K |e verfasserin |4 aut | |
245 | 1 | 4 | |a The association of the treatment with glucagon-like peptide-1 receptor agonist exenatide or insulin with cardiovascular outcomes in patients with type 2 diabetes |b a retrospective observational study |
264 | 1 | |c 2015 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 15.01.2016 | ||
500 | |a Date Revised 22.03.2024 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a BACKGROUND: To evaluate the association of treatment with glucagon-like peptide-1 (GLP-1) receptor agonist exenatide and/or insulin on macrovascular outcomes in patients with type 2 diabetes (T2DM) | ||
520 | |a METHODS: We conducted a retrospective longitudinal pharmaco-epidemiological study using large ambulatory care data to evaluate the risks of heart failure (HF), myocardial infarction (MI) and stroke in established T2DM patients who received a first prescription of exenatide twice daily (EBID) or insulin between June 2005 and May 2009, with follow-up data available until December 2012. Three treatment groups were: EBID with oral antidiabetes drugs (OADs) (EBID, n = 2804), insulin with OADs (Insulin, n = 28551), and those who changed medications between EBID and insulin or had combination of EBID and insulin during follow-up, along with OADs (EBID + insulin, n = 7870). Multivariate Cox-regression models were used to evaluate the association of treatment groups with the risks of macrovascular events | ||
520 | |a RESULTS: During a median 3.5 years of follow-up, cardiovascular event rates per 1000 person-years were significantly lower for the EBID and EBID + insulin groups compared to the insulin group (HF: 4.4 and 6.1 vs. 17.9; MI: 1.1 and 1.2 vs. 2.5; stroke: 2.4 and 1.8 vs. 6.1). Patients in the EBID/EBID + insulin group had significantly reduced risk of HF, MI and stroke by 61/56%, 50/38% and 52/63% respectively, compared to patients in the insulin group (p < 0.01) | ||
520 | |a CONCLUSIONS: Treatment with exenatide, with or without concomitant insulin was associated with reduced macrovascular risks compared to insulin; although inherent potential bias in epidemiological studies should be considered | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Observational Study | |
650 | 7 | |a Glucagon-Like Peptide-1 Receptor |2 NLM | |
650 | 7 | |a Hypoglycemic Agents |2 NLM | |
650 | 7 | |a Insulin |2 NLM | |
650 | 7 | |a Peptides |2 NLM | |
650 | 7 | |a Venoms |2 NLM | |
650 | 7 | |a Exenatide |2 NLM | |
650 | 7 | |a 9P1872D4OL |2 NLM | |
700 | 1 | |a Klein, Kerenaftali |e verfasserin |4 aut | |
700 | 1 | |a Maggs, David |e verfasserin |4 aut | |
700 | 1 | |a Best, Jennie H |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Cardiovascular diabetology |d 2002 |g 14(2015) vom: 24. Jan., Seite 10 |w (DE-627)NLM119878380 |x 1475-2840 |7 nnns |
773 | 1 | 8 | |g volume:14 |g year:2015 |g day:24 |g month:01 |g pages:10 |
856 | 4 | 0 | |u http://dx.doi.org/10.1186/s12933-015-0178-3 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 14 |j 2015 |b 24 |c 01 |h 10 |