See the published version of this preprint at Cardiovascular Diabetology.
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Original investigation
Hiromichi Wakui
Yokohama City University Graduate School of Medicine
Corresponding Author
License:
This work is licensed under a CC BY 4.0 License. Read Full License
Background
Both sodium-glucose cotransporter-2 (SGLT-2) inhibitors and glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are known to reduce cardiovascular and renal events in type 2 diabetes mellitus (DM) patients. However, no study to date has compared the effect of SGLT-2 inhibitors with that of GLP-1 RAs in type 2 DM patients with chronic kidney disease (CKD). We herein investigated the benefits of SGLT-2 inhibitors and GLP-1 RAs in CKD patients.
Methods
We performed a systematic literature search through July 2020. We selected randomized control trials that compared the risk of major adverse cardiovascular events (MACE) and a composite of renal outcomes. We performed a network meta-analysis to compare SGLT-2 inhibitors with GLP-1 RA indirectly. Risk ratios (RRs) with corresponding 95 % confidence interval (CI) were synthesized.
Results
Fifteen studies were selected with a total of 20,947 patients. SGLT-2 inhibitors led to a risk reduction in MACE (RR [95 % CI]; 0.80 [0.70-0.91]) , but GLP-1 RAs did not (RR 0.89 [0.78-1.00]). Compared to GLP-1 RAs, SGLT-2 inhibitors did not demonstrate a significant difference (RR 0.90 [0.75-1.08]). Similarly, SGLT-2 inhibitors significantly decreased renal events (RR 0.66 [0.58-0.75]), but GLP-1 RAs did not (RR 0.80 [0.90-1.00]). SGLT-2 inhibitors were also associated with a lower risk of renal events compared to GLP-1 RAs (RR 0.73 [0.62-0.87]).
Conclusions
In patients with type 2 DM and CKD, SGLT-2 inhibitors were associated with a decreased risk of cardiovascular and renal events, but GLP-1 RA were not. SGLT-2 inhibitors significantly decreased the risk of renal events compared to GLP-1 RAs.
Keywords
SGLT2 inhibitors, GLP-1 receptor agonist, meta-analysis, Cardiovascular disease, renal outcomes, diabetes mellitus, chronic kidney disease
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Peer Review Timeline
CURRENT STATUS: Published
View the published article at Cardiovascular Diabetology.
No community comments so far
Editorial decision: Accept
On 13 Dec, 2020
Editor assigned
On 08 Dec, 2020
Submission checks complete
On 08 Dec, 2020
Editor invited
On 08 Dec, 2020
No comments provided
Editorial decision: Major Revision
On 15 Nov, 2020
Review #3 received
Received 13 Nov, 2020
Review #1 received
Received 09 Nov, 2020
Reviewer #3 agreed
On 08 Nov, 2020
Reviewer #2 agreed
On 08 Nov, 2020
Review #2 received
Received 08 Nov, 2020
Editor assigned
On 05 Nov, 2020
Reviewers invited
Invitations sent on 05 Nov, 2020
Reviewer #1 agreed
On 05 Nov, 2020
Submission checks complete
On 05 Nov, 2020
Editor invited
On 05 Nov, 2020
Version 1
Posted 09 Sep, 2020
No comments provided
Review #1 received
Received 30 Sep, 2020
Review #3 received
Received 30 Sep, 2020
Editorial decision: Major Revision
On 30 Sep, 2020
Review #2 received
Received 29 Sep, 2020
Reviewer #3 agreed
On 11 Sep, 2020
Reviewers invited
Invitations sent on 10 Sep, 2020
Reviewer #1 agreed
On 10 Sep, 2020
Reviewer #2 agreed
On 10 Sep, 2020
Editor assigned
On 08 Sep, 2020
Editor invited
On 07 Sep, 2020
Submission checks complete
On 06 Sep, 2020
First submitted
On 24 Aug, 2020
Metrics
Comments: 0
PDF Downloads: ...
HTML Views: ...
Subject Areas
Cardiac & Cardiovascular Systems
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A new preprint design is coming!
We have improved readability, clarity, accessibility, and opportunities for engagement.
See the published version of this preprint at Cardiovascular Diabetology.
This is a preprint, a preliminary version of a manuscript that has not completed peer review at a journal. Research Square does not conduct peer review prior to posting preprints. The posting of a preprint on this server should not be interpreted as an endorsement of its validity or suitability for dissemination as established information or for guiding clinical practice.
Learn more about In Review
Original investigation
Hiromichi Wakui
Yokohama City University Graduate School of Medicine
Corresponding Author
Badges
Prescreen
This manuscript passed our Prescreen assessment
Complete author information
Appropriate declaration statements
Potential risks to human health
Prescreen
Peer Review Timeline
CURRENT STATUS: Published
View the published article at Cardiovascular Diabetology.
No community comments so far
Editorial decision: Accept
On 13 Dec, 2020
Editor assigned
On 08 Dec, 2020
Submission checks complete
On 08 Dec, 2020
Editor invited
On 08 Dec, 2020
No comments provided
Editorial decision: Major Revision
On 15 Nov, 2020
Review #3 received
Received 13 Nov, 2020
Review #1 received
Received 09 Nov, 2020
Reviewer #3 agreed
On 08 Nov, 2020
Reviewer #2 agreed
On 08 Nov, 2020
Review #2 received
Received 08 Nov, 2020
Editor assigned
On 05 Nov, 2020
Reviewers invited
Invitations sent on 05 Nov, 2020
Reviewer #1 agreed
On 05 Nov, 2020
Submission checks complete
On 05 Nov, 2020
Editor invited
On 05 Nov, 2020
Version 1
Posted 09 Sep, 2020
No comments provided
Review #1 received
Received 30 Sep, 2020
Review #3 received
Received 30 Sep, 2020
Editorial decision: Major Revision
On 30 Sep, 2020
Review #2 received
Received 29 Sep, 2020
Reviewer #3 agreed
On 11 Sep, 2020
Reviewers invited
Invitations sent on 10 Sep, 2020
Reviewer #1 agreed
On 10 Sep, 2020
Reviewer #2 agreed
On 10 Sep, 2020
Editor assigned
On 08 Sep, 2020
Editor invited
On 07 Sep, 2020
Submission checks complete
On 06 Sep, 2020
First submitted
On 24 Aug, 2020
Metrics
Comments: 0
PDF Downloads: ...
HTML Views: ...
Subject Areas
Cardiac & Cardiovascular Systems
License:
This work is licensed under a CC BY 4.0 License. Read Full License
View the published article at Cardiovascular Diabetology.
Background
Both sodium-glucose cotransporter-2 (SGLT-2) inhibitors and glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are known to reduce cardiovascular and renal events in type 2 diabetes mellitus (DM) patients. However, no study to date has compared the effect of SGLT-2 inhibitors with that of GLP-1 RAs in type 2 DM patients with chronic kidney disease (CKD). We herein investigated the benefits of SGLT-2 inhibitors and GLP-1 RAs in CKD patients.
Methods
We performed a systematic literature search through July 2020. We selected randomized control trials that compared the risk of major adverse cardiovascular events (MACE) and a composite of renal outcomes. We performed a network meta-analysis to compare SGLT-2 inhibitors with GLP-1 RA indirectly. Risk ratios (RRs) with corresponding 95 % confidence interval (CI) were synthesized.
Results
Fifteen studies were selected with a total of 20,947 patients. SGLT-2 inhibitors led to a risk reduction in MACE (RR [95 % CI]; 0.80 [0.70-0.91]) , but GLP-1 RAs did not (RR 0.89 [0.78-1.00]). Compared to GLP-1 RAs, SGLT-2 inhibitors did not demonstrate a significant difference (RR 0.90 [0.75-1.08]). Similarly, SGLT-2 inhibitors significantly decreased renal events (RR 0.66 [0.58-0.75]), but GLP-1 RAs did not (RR 0.80 [0.90-1.00]). SGLT-2 inhibitors were also associated with a lower risk of renal events compared to GLP-1 RAs (RR 0.73 [0.62-0.87]).
Conclusions
In patients with type 2 DM and CKD, SGLT-2 inhibitors were associated with a decreased risk of cardiovascular and renal events, but GLP-1 RA were not. SGLT-2 inhibitors significantly decreased the risk of renal events compared to GLP-1 RAs.
Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
This is a list of supplementary files associated with this preprint. Click to download.
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