Loading…
Dipeptidyl peptidase‐4 inhibitor and insulin combination treatment in type 2 diabetes and chronic kidney disease: A meta‐analysis
ABSTRACT Aims/Introduction The union of dipeptidyl peptidase‐4 inhibitors and insulin in patients with type 2 diabetes and chronic kidney disease provides satisfactory glucose management without increasing adverse events (AEs). This research appraised the therapeutic effect and safety of combination...
Saved in:
Published in: | Journal of diabetes investigation 2022-03, Vol.13 (3), p.468-477 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c4935-16a2b9aa6315f870fe40597331a075e9fed7e4b0aef133499a30f3e27d928f803 |
container_end_page | 477 |
container_issue | 3 |
container_start_page | 468 |
container_title | Journal of diabetes investigation |
container_volume | 13 |
creator | Zhou, Xianling Shi, Heng Zhu, Shiping Wang, Haixia Sun, Shengyun |
description | ABSTRACT
Aims/Introduction
The union of dipeptidyl peptidase‐4 inhibitors and insulin in patients with type 2 diabetes and chronic kidney disease provides satisfactory glucose management without increasing adverse events (AEs). This research appraised the therapeutic effect and safety of combination therapy in patients with type 2 diabetes and chronic kidney disease.
Materials and Methods
We carried out a meta‐analysis of randomized controlled trials to analyze AEs, hypoglycemia, serious AEs, severe hypoglycemia, estimated glomerular filtration rate, fasting plasma glucose, glycated hemoglobin, insulin dose, low‐density lipoprotein cholesterol, uric acid and weight between combination treatment groups and control groups by searching the Cochrane Library, Excerpta Medica Database (Embase), PubMed and Web of Science databanks until October 2020.
Results
Five studies (6 trials, 1,278 participants) met the inclusion criteria. The evidence quality ranged from moderate to high. Glycated hemoglobin (standardized mean difference −0.29, 95% confidence interval −0.44 to −0.14) and insulin dose (standardized mean difference −0.16, 95% confidence interval −0.29 to −0.02) were obviously smaller in the combination cure patients than in the control patients. Compared with the control groups, combination treatment did not increase AEs, hypoglycemia, serious AEs or severe hypoglycemia.
Conclusions
This study showed the effectiveness and safety of dipeptidyl peptidase‐4 inhibitors bonded with insulin in patients with type 2 diabetes and chronic kidney disease, but the protective actions of this cure on kidney and cardiovascular outcomes, as well as the functions of other dipeptidyl peptidase‐4 inhibitors, need to be affirmed by more good‐quality randomized controlled trials.
It is difficult to control blood glucose in patients with type 2 diabetes complicated with chronic kidney disease, and they are more likely to have adverse events, such as hypoglycemia. Dipeptidyl peptidase‐4 inhibitors combined with insulin can reduce glycated hemoglobin and insulin dose in patients with type 2 diabetes complicated with chronic kidney disease, and there is no significant increase in the incidence of adverse events, such as hypoglycemia. This study provides strong evidence for the application of dipeptidyl peptidase‐4 inhibitors combined with insulin in patients with type 2 diabetes complicated with chronic kidney disease. |
doi_str_mv | 10.1111/jdi.13675 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_b7ec4aef009245e3b50d9942cc7323a1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_b7ec4aef009245e3b50d9942cc7323a1</doaj_id><sourcerecordid>2637062289</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4935-16a2b9aa6315f870fe40597331a075e9fed7e4b0aef133499a30f3e27d928f803</originalsourceid><addsrcrecordid>eNp1ks9u1DAQxiMEolXpgRdAkbjAYVv_SxxzQKraAosqcYGzNXEmXS-JvdheUG7cKm48I0-CuykrioQvHnu--Xk8-oriKSUnNK_TdWdPKK9l9aA4ZESQBaVMPNzHtD4ojmNck7x409S1fFwccFFVlJH6sLi5sBvcJNtNQzkHEPHX95-itG5lW5t8KMF1-RS3g3Wl8WNrHSTrXZkCQhrRpZwt07TJdT9Y2VloMWHclZlV8M6a8rPtHE45FzHzX5Vn5YgJ8jvgYJiijU-KRz0MEY_v9qPi05vLj-fvFlcf3i7Pz64WRiheLWgNrFUANadV30jSoyCVkpxTILJC1WMnUbQEsKecC6WAk54jk51iTd8QflQsZ27nYa03wY4QJu3B6t2FD9caQrJmQN1KNCKDCFFMVMjbinRKCWaM5IwDzazXM2uzbUfsTJ5EgOEe9H7G2ZW-9l91owgThGXAiztA8F-2GJMebTQ4DODQb6Nmlaya_FN52_fzf6Rrvw15eFlVc0lqxhqVVS9nlQk-xoD9vhlK9K1bdHaL3rkla5_93f1e-ccbWXA6C77ZAaf_k_T7i-WM_A2Hbs0E</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2637062289</pqid></control><display><type>article</type><title>Dipeptidyl peptidase‐4 inhibitor and insulin combination treatment in type 2 diabetes and chronic kidney disease: A meta‐analysis</title><source>Wiley Online Library Open Access</source><source>Publicly Available Content (ProQuest)</source><source>PubMed Central</source><creator>Zhou, Xianling ; Shi, Heng ; Zhu, Shiping ; Wang, Haixia ; Sun, Shengyun</creator><creatorcontrib>Zhou, Xianling ; Shi, Heng ; Zhu, Shiping ; Wang, Haixia ; Sun, Shengyun</creatorcontrib><description>ABSTRACT
Aims/Introduction
The union of dipeptidyl peptidase‐4 inhibitors and insulin in patients with type 2 diabetes and chronic kidney disease provides satisfactory glucose management without increasing adverse events (AEs). This research appraised the therapeutic effect and safety of combination therapy in patients with type 2 diabetes and chronic kidney disease.
Materials and Methods
We carried out a meta‐analysis of randomized controlled trials to analyze AEs, hypoglycemia, serious AEs, severe hypoglycemia, estimated glomerular filtration rate, fasting plasma glucose, glycated hemoglobin, insulin dose, low‐density lipoprotein cholesterol, uric acid and weight between combination treatment groups and control groups by searching the Cochrane Library, Excerpta Medica Database (Embase), PubMed and Web of Science databanks until October 2020.
Results
Five studies (6 trials, 1,278 participants) met the inclusion criteria. The evidence quality ranged from moderate to high. Glycated hemoglobin (standardized mean difference −0.29, 95% confidence interval −0.44 to −0.14) and insulin dose (standardized mean difference −0.16, 95% confidence interval −0.29 to −0.02) were obviously smaller in the combination cure patients than in the control patients. Compared with the control groups, combination treatment did not increase AEs, hypoglycemia, serious AEs or severe hypoglycemia.
Conclusions
This study showed the effectiveness and safety of dipeptidyl peptidase‐4 inhibitors bonded with insulin in patients with type 2 diabetes and chronic kidney disease, but the protective actions of this cure on kidney and cardiovascular outcomes, as well as the functions of other dipeptidyl peptidase‐4 inhibitors, need to be affirmed by more good‐quality randomized controlled trials.
It is difficult to control blood glucose in patients with type 2 diabetes complicated with chronic kidney disease, and they are more likely to have adverse events, such as hypoglycemia. Dipeptidyl peptidase‐4 inhibitors combined with insulin can reduce glycated hemoglobin and insulin dose in patients with type 2 diabetes complicated with chronic kidney disease, and there is no significant increase in the incidence of adverse events, such as hypoglycemia. This study provides strong evidence for the application of dipeptidyl peptidase‐4 inhibitors combined with insulin in patients with type 2 diabetes complicated with chronic kidney disease.</description><identifier>ISSN: 2040-1116</identifier><identifier>ISSN: 2040-1124</identifier><identifier>EISSN: 2040-1124</identifier><identifier>DOI: 10.1111/jdi.13675</identifier><identifier>PMID: 34551206</identifier><language>eng</language><publisher>Japan: John Wiley & Sons, Inc</publisher><subject>Bias ; Cholesterol ; Chronic kidney disease ; Clinical trials ; Collaboration ; Diabetes ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - drug therapy ; Dipeptidyl peptidase‐4 inhibitor ; Dipeptidyl-peptidase IV ; Dipeptidyl-Peptidase IV Inhibitors - therapeutic use ; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - therapeutic use ; Drug dosages ; Glomerular filtration rate ; Glucose ; Glycated Hemoglobin - therapeutic use ; Hemodialysis ; Hemoglobin ; Humans ; Hypoglycemia ; Hypoglycemic Agents - therapeutic use ; Insulin ; Insulin - therapeutic use ; Kidney diseases ; Meta-analysis ; Original ; Patients ; Peptidase ; Renal Insufficiency, Chronic - complications ; Renal Insufficiency, Chronic - drug therapy ; Treatment Outcome ; Type 2 diabetes ; Uric acid ; Working groups</subject><ispartof>Journal of diabetes investigation, 2022-03, Vol.13 (3), p.468-477</ispartof><rights>2021 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd.</rights><rights>2022. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4935-16a2b9aa6315f870fe40597331a075e9fed7e4b0aef133499a30f3e27d928f803</cites><orcidid>0000-0002-2087-3322</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2637062289/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2637062289?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,11538,25728,27898,27899,36986,36987,44563,46024,46448,53763,53765,75093</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34551206$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Xianling</creatorcontrib><creatorcontrib>Shi, Heng</creatorcontrib><creatorcontrib>Zhu, Shiping</creatorcontrib><creatorcontrib>Wang, Haixia</creatorcontrib><creatorcontrib>Sun, Shengyun</creatorcontrib><title>Dipeptidyl peptidase‐4 inhibitor and insulin combination treatment in type 2 diabetes and chronic kidney disease: A meta‐analysis</title><title>Journal of diabetes investigation</title><addtitle>J Diabetes Investig</addtitle><description>ABSTRACT
Aims/Introduction
The union of dipeptidyl peptidase‐4 inhibitors and insulin in patients with type 2 diabetes and chronic kidney disease provides satisfactory glucose management without increasing adverse events (AEs). This research appraised the therapeutic effect and safety of combination therapy in patients with type 2 diabetes and chronic kidney disease.
Materials and Methods
We carried out a meta‐analysis of randomized controlled trials to analyze AEs, hypoglycemia, serious AEs, severe hypoglycemia, estimated glomerular filtration rate, fasting plasma glucose, glycated hemoglobin, insulin dose, low‐density lipoprotein cholesterol, uric acid and weight between combination treatment groups and control groups by searching the Cochrane Library, Excerpta Medica Database (Embase), PubMed and Web of Science databanks until October 2020.
Results
Five studies (6 trials, 1,278 participants) met the inclusion criteria. The evidence quality ranged from moderate to high. Glycated hemoglobin (standardized mean difference −0.29, 95% confidence interval −0.44 to −0.14) and insulin dose (standardized mean difference −0.16, 95% confidence interval −0.29 to −0.02) were obviously smaller in the combination cure patients than in the control patients. Compared with the control groups, combination treatment did not increase AEs, hypoglycemia, serious AEs or severe hypoglycemia.
Conclusions
This study showed the effectiveness and safety of dipeptidyl peptidase‐4 inhibitors bonded with insulin in patients with type 2 diabetes and chronic kidney disease, but the protective actions of this cure on kidney and cardiovascular outcomes, as well as the functions of other dipeptidyl peptidase‐4 inhibitors, need to be affirmed by more good‐quality randomized controlled trials.
It is difficult to control blood glucose in patients with type 2 diabetes complicated with chronic kidney disease, and they are more likely to have adverse events, such as hypoglycemia. Dipeptidyl peptidase‐4 inhibitors combined with insulin can reduce glycated hemoglobin and insulin dose in patients with type 2 diabetes complicated with chronic kidney disease, and there is no significant increase in the incidence of adverse events, such as hypoglycemia. This study provides strong evidence for the application of dipeptidyl peptidase‐4 inhibitors combined with insulin in patients with type 2 diabetes complicated with chronic kidney disease.</description><subject>Bias</subject><subject>Cholesterol</subject><subject>Chronic kidney disease</subject><subject>Clinical trials</subject><subject>Collaboration</subject><subject>Diabetes</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Dipeptidyl peptidase‐4 inhibitor</subject><subject>Dipeptidyl-peptidase IV</subject><subject>Dipeptidyl-Peptidase IV Inhibitors - therapeutic use</subject><subject>Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - therapeutic use</subject><subject>Drug dosages</subject><subject>Glomerular filtration rate</subject><subject>Glucose</subject><subject>Glycated Hemoglobin - therapeutic use</subject><subject>Hemodialysis</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Hypoglycemia</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Insulin</subject><subject>Insulin - therapeutic use</subject><subject>Kidney diseases</subject><subject>Meta-analysis</subject><subject>Original</subject><subject>Patients</subject><subject>Peptidase</subject><subject>Renal Insufficiency, Chronic - complications</subject><subject>Renal Insufficiency, Chronic - drug therapy</subject><subject>Treatment Outcome</subject><subject>Type 2 diabetes</subject><subject>Uric acid</subject><subject>Working groups</subject><issn>2040-1116</issn><issn>2040-1124</issn><issn>2040-1124</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1ks9u1DAQxiMEolXpgRdAkbjAYVv_SxxzQKraAosqcYGzNXEmXS-JvdheUG7cKm48I0-CuykrioQvHnu--Xk8-oriKSUnNK_TdWdPKK9l9aA4ZESQBaVMPNzHtD4ojmNck7x409S1fFwccFFVlJH6sLi5sBvcJNtNQzkHEPHX95-itG5lW5t8KMF1-RS3g3Wl8WNrHSTrXZkCQhrRpZwt07TJdT9Y2VloMWHclZlV8M6a8rPtHE45FzHzX5Vn5YgJ8jvgYJiijU-KRz0MEY_v9qPi05vLj-fvFlcf3i7Pz64WRiheLWgNrFUANadV30jSoyCVkpxTILJC1WMnUbQEsKecC6WAk54jk51iTd8QflQsZ27nYa03wY4QJu3B6t2FD9caQrJmQN1KNCKDCFFMVMjbinRKCWaM5IwDzazXM2uzbUfsTJ5EgOEe9H7G2ZW-9l91owgThGXAiztA8F-2GJMebTQ4DODQb6Nmlaya_FN52_fzf6Rrvw15eFlVc0lqxhqVVS9nlQk-xoD9vhlK9K1bdHaL3rkla5_93f1e-ccbWXA6C77ZAaf_k_T7i-WM_A2Hbs0E</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Zhou, Xianling</creator><creator>Shi, Heng</creator><creator>Zhu, Shiping</creator><creator>Wang, Haixia</creator><creator>Sun, Shengyun</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PKEHL</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2087-3322</orcidid></search><sort><creationdate>202203</creationdate><title>Dipeptidyl peptidase‐4 inhibitor and insulin combination treatment in type 2 diabetes and chronic kidney disease: A meta‐analysis</title><author>Zhou, Xianling ; Shi, Heng ; Zhu, Shiping ; Wang, Haixia ; Sun, Shengyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4935-16a2b9aa6315f870fe40597331a075e9fed7e4b0aef133499a30f3e27d928f803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Bias</topic><topic>Cholesterol</topic><topic>Chronic kidney disease</topic><topic>Clinical trials</topic><topic>Collaboration</topic><topic>Diabetes</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Dipeptidyl peptidase‐4 inhibitor</topic><topic>Dipeptidyl-peptidase IV</topic><topic>Dipeptidyl-Peptidase IV Inhibitors - therapeutic use</topic><topic>Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - therapeutic use</topic><topic>Drug dosages</topic><topic>Glomerular filtration rate</topic><topic>Glucose</topic><topic>Glycated Hemoglobin - therapeutic use</topic><topic>Hemodialysis</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Hypoglycemia</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Insulin</topic><topic>Insulin - therapeutic use</topic><topic>Kidney diseases</topic><topic>Meta-analysis</topic><topic>Original</topic><topic>Patients</topic><topic>Peptidase</topic><topic>Renal Insufficiency, Chronic - complications</topic><topic>Renal Insufficiency, Chronic - drug therapy</topic><topic>Treatment Outcome</topic><topic>Type 2 diabetes</topic><topic>Uric acid</topic><topic>Working groups</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Xianling</creatorcontrib><creatorcontrib>Shi, Heng</creatorcontrib><creatorcontrib>Zhu, Shiping</creatorcontrib><creatorcontrib>Wang, Haixia</creatorcontrib><creatorcontrib>Sun, Shengyun</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of diabetes investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Xianling</au><au>Shi, Heng</au><au>Zhu, Shiping</au><au>Wang, Haixia</au><au>Sun, Shengyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dipeptidyl peptidase‐4 inhibitor and insulin combination treatment in type 2 diabetes and chronic kidney disease: A meta‐analysis</atitle><jtitle>Journal of diabetes investigation</jtitle><addtitle>J Diabetes Investig</addtitle><date>2022-03</date><risdate>2022</risdate><volume>13</volume><issue>3</issue><spage>468</spage><epage>477</epage><pages>468-477</pages><issn>2040-1116</issn><issn>2040-1124</issn><eissn>2040-1124</eissn><abstract>ABSTRACT
Aims/Introduction
The union of dipeptidyl peptidase‐4 inhibitors and insulin in patients with type 2 diabetes and chronic kidney disease provides satisfactory glucose management without increasing adverse events (AEs). This research appraised the therapeutic effect and safety of combination therapy in patients with type 2 diabetes and chronic kidney disease.
Materials and Methods
We carried out a meta‐analysis of randomized controlled trials to analyze AEs, hypoglycemia, serious AEs, severe hypoglycemia, estimated glomerular filtration rate, fasting plasma glucose, glycated hemoglobin, insulin dose, low‐density lipoprotein cholesterol, uric acid and weight between combination treatment groups and control groups by searching the Cochrane Library, Excerpta Medica Database (Embase), PubMed and Web of Science databanks until October 2020.
Results
Five studies (6 trials, 1,278 participants) met the inclusion criteria. The evidence quality ranged from moderate to high. Glycated hemoglobin (standardized mean difference −0.29, 95% confidence interval −0.44 to −0.14) and insulin dose (standardized mean difference −0.16, 95% confidence interval −0.29 to −0.02) were obviously smaller in the combination cure patients than in the control patients. Compared with the control groups, combination treatment did not increase AEs, hypoglycemia, serious AEs or severe hypoglycemia.
Conclusions
This study showed the effectiveness and safety of dipeptidyl peptidase‐4 inhibitors bonded with insulin in patients with type 2 diabetes and chronic kidney disease, but the protective actions of this cure on kidney and cardiovascular outcomes, as well as the functions of other dipeptidyl peptidase‐4 inhibitors, need to be affirmed by more good‐quality randomized controlled trials.
It is difficult to control blood glucose in patients with type 2 diabetes complicated with chronic kidney disease, and they are more likely to have adverse events, such as hypoglycemia. Dipeptidyl peptidase‐4 inhibitors combined with insulin can reduce glycated hemoglobin and insulin dose in patients with type 2 diabetes complicated with chronic kidney disease, and there is no significant increase in the incidence of adverse events, such as hypoglycemia. This study provides strong evidence for the application of dipeptidyl peptidase‐4 inhibitors combined with insulin in patients with type 2 diabetes complicated with chronic kidney disease.</abstract><cop>Japan</cop><pub>John Wiley & Sons, Inc</pub><pmid>34551206</pmid><doi>10.1111/jdi.13675</doi><tpages>477</tpages><orcidid>https://orcid.org/0000-0002-2087-3322</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2040-1116 |
ispartof | Journal of diabetes investigation, 2022-03, Vol.13 (3), p.468-477 |
issn | 2040-1116 2040-1124 2040-1124 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_b7ec4aef009245e3b50d9942cc7323a1 |
source | Wiley Online Library Open Access; Publicly Available Content (ProQuest); PubMed Central |
subjects | Bias Cholesterol Chronic kidney disease Clinical trials Collaboration Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - drug therapy Dipeptidyl peptidase‐4 inhibitor Dipeptidyl-peptidase IV Dipeptidyl-Peptidase IV Inhibitors - therapeutic use Dipeptidyl-Peptidases and Tripeptidyl-Peptidases - therapeutic use Drug dosages Glomerular filtration rate Glucose Glycated Hemoglobin - therapeutic use Hemodialysis Hemoglobin Humans Hypoglycemia Hypoglycemic Agents - therapeutic use Insulin Insulin - therapeutic use Kidney diseases Meta-analysis Original Patients Peptidase Renal Insufficiency, Chronic - complications Renal Insufficiency, Chronic - drug therapy Treatment Outcome Type 2 diabetes Uric acid Working groups |
title | Dipeptidyl peptidase‐4 inhibitor and insulin combination treatment in type 2 diabetes and chronic kidney disease: A meta‐analysis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-25T16%3A01%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dipeptidyl%20peptidase%E2%80%904%20inhibitor%20and%20insulin%20combination%20treatment%20in%20type%E2%80%892%20diabetes%20and%20chronic%20kidney%20disease:%20A%20meta%E2%80%90analysis&rft.jtitle=Journal%20of%20diabetes%20investigation&rft.au=Zhou,%20Xianling&rft.date=2022-03&rft.volume=13&rft.issue=3&rft.spage=468&rft.epage=477&rft.pages=468-477&rft.issn=2040-1116&rft.eissn=2040-1124&rft_id=info:doi/10.1111/jdi.13675&rft_dat=%3Cproquest_doaj_%3E2637062289%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4935-16a2b9aa6315f870fe40597331a075e9fed7e4b0aef133499a30f3e27d928f803%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2637062289&rft_id=info:pmid/34551206&rfr_iscdi=true |