Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study
AbstractObjectiveTo assess the association between use of sodium-glucose co-transporter 2 (SGLT2) inhibitors and risk of serious renal events in data from routine clinical practice.DesignCohort study using an active comparator, new user design and nationwide register data.SettingSweden, Denmark, and...
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creator | Pasternak, Björn Wintzell, Viktor Melbye, Mads Eliasson, Björn Svensson, Ann-Marie Franzén, Stefan Gudbjörnsdottir, Soffia Hveem, Kristian Jonasson, Christian Svanström, Henrik Ueda, Peter |
description | AbstractObjectiveTo assess the association between use of sodium-glucose co-transporter 2 (SGLT2) inhibitors and risk of serious renal events in data from routine clinical practice.DesignCohort study using an active comparator, new user design and nationwide register data.SettingSweden, Denmark, and Norway, 2013-18.ParticipantsCohort of 29 887 new users of SGLT2 inhibitors (follow-up time: dapagliflozin 66.1%; empagliflozin 32.6%; canagliflozin 1.3%) and 29 887 new users of an active comparator, dipeptidyl peptidase-4 inhibitors, matched 1:1 on the basis of a propensity score with 57 variables. Mean follow-up time was 1.7 (SD 1.0) years.ExposuresSGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors, defined by filled prescriptions and analysed according to intention to treat.Main outcome measuresThe main outcome was serious renal events, a composite including renal replacement therapy, death from renal causes, and hospital admission for renal events. Secondary outcomes were the individual components of the main outcome.ResultsThe mean age of the study population was 61.3 (SD 10.5) years; 11 108 (19%) had cardiovascular disease, and 1974 (3%) had chronic kidney disease. Use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a reduced risk of serious renal events (2.6 events per 1000 person years versus 6.2 events per 1000 person years; hazard ratio 0.42 (95% confidence interval 0.34 to 0.53); absolute difference −3.6 (–4.4 to −2.8) events per 1000 person years). In secondary outcome analyses, the hazard ratio for use of SGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors was 0.32 (0.22 to 0.47) for renal replacement therapy, 0.41 (0.32 to 0.52) for hospital admission for renal events, and 0.77 (0.26 to 2.23) for death from renal causes. In sensitivity analyses in each of the Swedish and Danish parts of the cohort, the model was further adjusted for glycated haemoglobin and estimated glomerular filtration rate (Sweden and Denmark) and for blood pressure, body mass index, and smoking (Sweden only); in these analyses, the hazard ratio moved from 0.41 (0.26 to 0.66) to 0.50 (0.31 to 0.81) in Sweden and from 0.42 (0.32 to 0.56) to 0.55 (0.41 to 0.74) in Denmark.ConclusionsIn this analysis using nationwide data from three countries, use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a significantly reduced risk of serious renal events. |
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Mean follow-up time was 1.7 (SD 1.0) years.ExposuresSGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors, defined by filled prescriptions and analysed according to intention to treat.Main outcome measuresThe main outcome was serious renal events, a composite including renal replacement therapy, death from renal causes, and hospital admission for renal events. Secondary outcomes were the individual components of the main outcome.ResultsThe mean age of the study population was 61.3 (SD 10.5) years; 11 108 (19%) had cardiovascular disease, and 1974 (3%) had chronic kidney disease. Use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a reduced risk of serious renal events (2.6 events per 1000 person years versus 6.2 events per 1000 person years; hazard ratio 0.42 (95% confidence interval 0.34 to 0.53); absolute difference −3.6 (–4.4 to −2.8) events per 1000 person years). In secondary outcome analyses, the hazard ratio for use of SGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors was 0.32 (0.22 to 0.47) for renal replacement therapy, 0.41 (0.32 to 0.52) for hospital admission for renal events, and 0.77 (0.26 to 2.23) for death from renal causes. In sensitivity analyses in each of the Swedish and Danish parts of the cohort, the model was further adjusted for glycated haemoglobin and estimated glomerular filtration rate (Sweden and Denmark) and for blood pressure, body mass index, and smoking (Sweden only); in these analyses, the hazard ratio moved from 0.41 (0.26 to 0.66) to 0.50 (0.31 to 0.81) in Sweden and from 0.42 (0.32 to 0.56) to 0.55 (0.41 to 0.74) in Denmark.ConclusionsIn this analysis using nationwide data from three countries, use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a significantly reduced risk of serious renal events.</description><identifier>ISSN: 1756-1833</identifier><identifier>ISSN: 0959-8138</identifier><identifier>ISSN: 0959-535X</identifier><identifier>EISSN: 1756-1833</identifier><identifier>DOI: 10.1136/bmj.m1186</identifier><identifier>PMID: 32349963</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Acute Kidney Injury - epidemiology ; Adult ; Aged ; Aged, 80 and over ; Benzhydryl Compounds - therapeutic use ; Blood pressure ; Body mass index ; Canagliflozin - therapeutic use ; Cardiovascular diseases ; Cardiovascular Diseases - epidemiology ; cardiovascular outcomes ; Case-Control Studies ; Clinical Medicine ; Clinical trials ; Cohort analysis ; Cohort Studies ; Comorbidity ; Denmark - epidemiology ; Diabetes ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes Mellitus, Type 2 - epidemiology ; diabetes-mellitus ; Dipeptidyl-peptidase IV ; Dipeptidyl-Peptidase IV Inhibitors - therapeutic use ; Female ; General & Internal Medicine ; Glomerular filtration rate ; Glucose transporter ; Glucosides - therapeutic use ; Hemoglobin ; Hospitalization - statistics & numerical data ; Hospitals ; Humans ; Kidney diseases ; Kidney Diseases - epidemiology ; Kidney Diseases - mortality ; Kidney Diseases - therapy ; Klinisk medicin ; Male ; Middle Aged ; Norway - epidemiology ; Patients ; Peptidase ; Population studies ; Prescription drugs ; Proportional Hazards Models ; Renal Insufficiency, Chronic - epidemiology ; Renal Replacement Therapy - statistics & numerical data ; Sensitivity analysis ; Sodium-Glucose Transporter 2 Inhibitors - therapeutic use ; Sweden - epidemiology ; type-2</subject><ispartof>BMJ (Online), 2020-04, Vol.369, p.m1186</ispartof><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2020 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. BMJ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2020 BMJ</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b574t-65219967cf9640d76bb30ca4e8b60ca3da35b6c59b83c3b6888ee7b2bd4923ad3</citedby><cites>FETCH-LOGICAL-b574t-65219967cf9640d76bb30ca4e8b60ca3da35b6c59b83c3b6888ee7b2bd4923ad3</cites><orcidid>0000-0002-3275-8743</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,550,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32349963$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://gup.ub.gu.se/publication/293615$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:143624602$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Pasternak, Björn</creatorcontrib><creatorcontrib>Wintzell, Viktor</creatorcontrib><creatorcontrib>Melbye, Mads</creatorcontrib><creatorcontrib>Eliasson, Björn</creatorcontrib><creatorcontrib>Svensson, Ann-Marie</creatorcontrib><creatorcontrib>Franzén, Stefan</creatorcontrib><creatorcontrib>Gudbjörnsdottir, Soffia</creatorcontrib><creatorcontrib>Hveem, Kristian</creatorcontrib><creatorcontrib>Jonasson, Christian</creatorcontrib><creatorcontrib>Svanström, Henrik</creatorcontrib><creatorcontrib>Ueda, Peter</creatorcontrib><title>Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study</title><title>BMJ (Online)</title><addtitle>BMJ</addtitle><description>AbstractObjectiveTo assess the association between use of sodium-glucose co-transporter 2 (SGLT2) inhibitors and risk of serious renal events in data from routine clinical practice.DesignCohort study using an active comparator, new user design and nationwide register data.SettingSweden, Denmark, and Norway, 2013-18.ParticipantsCohort of 29 887 new users of SGLT2 inhibitors (follow-up time: dapagliflozin 66.1%; empagliflozin 32.6%; canagliflozin 1.3%) and 29 887 new users of an active comparator, dipeptidyl peptidase-4 inhibitors, matched 1:1 on the basis of a propensity score with 57 variables. Mean follow-up time was 1.7 (SD 1.0) years.ExposuresSGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors, defined by filled prescriptions and analysed according to intention to treat.Main outcome measuresThe main outcome was serious renal events, a composite including renal replacement therapy, death from renal causes, and hospital admission for renal events. Secondary outcomes were the individual components of the main outcome.ResultsThe mean age of the study population was 61.3 (SD 10.5) years; 11 108 (19%) had cardiovascular disease, and 1974 (3%) had chronic kidney disease. Use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a reduced risk of serious renal events (2.6 events per 1000 person years versus 6.2 events per 1000 person years; hazard ratio 0.42 (95% confidence interval 0.34 to 0.53); absolute difference −3.6 (–4.4 to −2.8) events per 1000 person years). In secondary outcome analyses, the hazard ratio for use of SGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors was 0.32 (0.22 to 0.47) for renal replacement therapy, 0.41 (0.32 to 0.52) for hospital admission for renal events, and 0.77 (0.26 to 2.23) for death from renal causes. In sensitivity analyses in each of the Swedish and Danish parts of the cohort, the model was further adjusted for glycated haemoglobin and estimated glomerular filtration rate (Sweden and Denmark) and for blood pressure, body mass index, and smoking (Sweden only); in these analyses, the hazard ratio moved from 0.41 (0.26 to 0.66) to 0.50 (0.31 to 0.81) in Sweden and from 0.42 (0.32 to 0.56) to 0.55 (0.41 to 0.74) in Denmark.ConclusionsIn this analysis using nationwide data from three countries, use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a significantly reduced risk of serious renal events.</description><subject>Acute Kidney Injury - epidemiology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Benzhydryl Compounds - therapeutic use</subject><subject>Blood pressure</subject><subject>Body mass index</subject><subject>Canagliflozin - therapeutic use</subject><subject>Cardiovascular diseases</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>cardiovascular outcomes</subject><subject>Case-Control Studies</subject><subject>Clinical Medicine</subject><subject>Clinical trials</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Comorbidity</subject><subject>Denmark - epidemiology</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Diabetes Mellitus, Type 2 - epidemiology</subject><subject>diabetes-mellitus</subject><subject>Dipeptidyl-peptidase IV</subject><subject>Dipeptidyl-Peptidase IV Inhibitors - therapeutic use</subject><subject>Female</subject><subject>General & Internal Medicine</subject><subject>Glomerular filtration rate</subject><subject>Glucose transporter</subject><subject>Glucosides - therapeutic use</subject><subject>Hemoglobin</subject><subject>Hospitalization - statistics & numerical data</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Kidney diseases</subject><subject>Kidney Diseases - epidemiology</subject><subject>Kidney Diseases - mortality</subject><subject>Kidney Diseases - therapy</subject><subject>Klinisk medicin</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Norway - epidemiology</subject><subject>Patients</subject><subject>Peptidase</subject><subject>Population studies</subject><subject>Prescription drugs</subject><subject>Proportional Hazards Models</subject><subject>Renal Insufficiency, Chronic - epidemiology</subject><subject>Renal Replacement Therapy - statistics & numerical data</subject><subject>Sensitivity analysis</subject><subject>Sodium-Glucose Transporter 2 Inhibitors - therapeutic use</subject><subject>Sweden - 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of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study</title><author>Pasternak, Björn ; Wintzell, Viktor ; Melbye, Mads ; Eliasson, Björn ; Svensson, Ann-Marie ; Franzén, Stefan ; Gudbjörnsdottir, Soffia ; Hveem, Kristian ; Jonasson, Christian ; Svanström, Henrik ; Ueda, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b574t-65219967cf9640d76bb30ca4e8b60ca3da35b6c59b83c3b6888ee7b2bd4923ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acute Kidney Injury - epidemiology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Benzhydryl Compounds - therapeutic use</topic><topic>Blood pressure</topic><topic>Body mass index</topic><topic>Canagliflozin - therapeutic use</topic><topic>Cardiovascular diseases</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>cardiovascular outcomes</topic><topic>Case-Control Studies</topic><topic>Clinical Medicine</topic><topic>Clinical trials</topic><topic>Cohort analysis</topic><topic>Cohort Studies</topic><topic>Comorbidity</topic><topic>Denmark - epidemiology</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Diabetes Mellitus, Type 2 - epidemiology</topic><topic>diabetes-mellitus</topic><topic>Dipeptidyl-peptidase IV</topic><topic>Dipeptidyl-Peptidase IV Inhibitors - therapeutic use</topic><topic>Female</topic><topic>General & Internal Medicine</topic><topic>Glomerular filtration rate</topic><topic>Glucose transporter</topic><topic>Glucosides - therapeutic use</topic><topic>Hemoglobin</topic><topic>Hospitalization - statistics & numerical data</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Kidney diseases</topic><topic>Kidney Diseases - epidemiology</topic><topic>Kidney Diseases - mortality</topic><topic>Kidney Diseases - therapy</topic><topic>Klinisk medicin</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Norway - epidemiology</topic><topic>Patients</topic><topic>Peptidase</topic><topic>Population studies</topic><topic>Prescription drugs</topic><topic>Proportional Hazards Models</topic><topic>Renal Insufficiency, Chronic - epidemiology</topic><topic>Renal Replacement Therapy - statistics & numerical data</topic><topic>Sensitivity analysis</topic><topic>Sodium-Glucose Transporter 2 Inhibitors - therapeutic use</topic><topic>Sweden - epidemiology</topic><topic>type-2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pasternak, Björn</creatorcontrib><creatorcontrib>Wintzell, Viktor</creatorcontrib><creatorcontrib>Melbye, Mads</creatorcontrib><creatorcontrib>Eliasson, Björn</creatorcontrib><creatorcontrib>Svensson, Ann-Marie</creatorcontrib><creatorcontrib>Franzén, Stefan</creatorcontrib><creatorcontrib>Gudbjörnsdottir, Soffia</creatorcontrib><creatorcontrib>Hveem, 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Prep</collection><collection>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</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>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Göteborgs universitet</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>BMJ (Online)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pasternak, Björn</au><au>Wintzell, Viktor</au><au>Melbye, Mads</au><au>Eliasson, Björn</au><au>Svensson, Ann-Marie</au><au>Franzén, Stefan</au><au>Gudbjörnsdottir, Soffia</au><au>Hveem, Kristian</au><au>Jonasson, Christian</au><au>Svanström, Henrik</au><au>Ueda, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study</atitle><jtitle>BMJ (Online)</jtitle><addtitle>BMJ</addtitle><date>2020-04-29</date><risdate>2020</risdate><volume>369</volume><spage>m1186</spage><pages>m1186-</pages><issn>1756-1833</issn><issn>0959-8138</issn><issn>0959-535X</issn><eissn>1756-1833</eissn><abstract>AbstractObjectiveTo assess the association between use of sodium-glucose co-transporter 2 (SGLT2) inhibitors and risk of serious renal events in data from routine clinical practice.DesignCohort study using an active comparator, new user design and nationwide register data.SettingSweden, Denmark, and Norway, 2013-18.ParticipantsCohort of 29 887 new users of SGLT2 inhibitors (follow-up time: dapagliflozin 66.1%; empagliflozin 32.6%; canagliflozin 1.3%) and 29 887 new users of an active comparator, dipeptidyl peptidase-4 inhibitors, matched 1:1 on the basis of a propensity score with 57 variables. Mean follow-up time was 1.7 (SD 1.0) years.ExposuresSGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors, defined by filled prescriptions and analysed according to intention to treat.Main outcome measuresThe main outcome was serious renal events, a composite including renal replacement therapy, death from renal causes, and hospital admission for renal events. Secondary outcomes were the individual components of the main outcome.ResultsThe mean age of the study population was 61.3 (SD 10.5) years; 11 108 (19%) had cardiovascular disease, and 1974 (3%) had chronic kidney disease. Use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a reduced risk of serious renal events (2.6 events per 1000 person years versus 6.2 events per 1000 person years; hazard ratio 0.42 (95% confidence interval 0.34 to 0.53); absolute difference −3.6 (–4.4 to −2.8) events per 1000 person years). In secondary outcome analyses, the hazard ratio for use of SGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors was 0.32 (0.22 to 0.47) for renal replacement therapy, 0.41 (0.32 to 0.52) for hospital admission for renal events, and 0.77 (0.26 to 2.23) for death from renal causes. In sensitivity analyses in each of the Swedish and Danish parts of the cohort, the model was further adjusted for glycated haemoglobin and estimated glomerular filtration rate (Sweden and Denmark) and for blood pressure, body mass index, and smoking (Sweden only); in these analyses, the hazard ratio moved from 0.41 (0.26 to 0.66) to 0.50 (0.31 to 0.81) in Sweden and from 0.42 (0.32 to 0.56) to 0.55 (0.41 to 0.74) in Denmark.ConclusionsIn this analysis using nationwide data from three countries, use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a significantly reduced risk of serious renal events.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>32349963</pmid><doi>10.1136/bmj.m1186</doi><orcidid>https://orcid.org/0000-0002-3275-8743</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1756-1833 |
ispartof | BMJ (Online), 2020-04, Vol.369, p.m1186 |
issn | 1756-1833 0959-8138 0959-535X 1756-1833 |
language | eng |
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source | Jstor Complete Legacy; MEDLINE; SWEPUB Freely available online |
subjects | Acute Kidney Injury - epidemiology Adult Aged Aged, 80 and over Benzhydryl Compounds - therapeutic use Blood pressure Body mass index Canagliflozin - therapeutic use Cardiovascular diseases Cardiovascular Diseases - epidemiology cardiovascular outcomes Case-Control Studies Clinical Medicine Clinical trials Cohort analysis Cohort Studies Comorbidity Denmark - epidemiology Diabetes Diabetes Mellitus, Type 2 - drug therapy Diabetes Mellitus, Type 2 - epidemiology diabetes-mellitus Dipeptidyl-peptidase IV Dipeptidyl-Peptidase IV Inhibitors - therapeutic use Female General & Internal Medicine Glomerular filtration rate Glucose transporter Glucosides - therapeutic use Hemoglobin Hospitalization - statistics & numerical data Hospitals Humans Kidney diseases Kidney Diseases - epidemiology Kidney Diseases - mortality Kidney Diseases - therapy Klinisk medicin Male Middle Aged Norway - epidemiology Patients Peptidase Population studies Prescription drugs Proportional Hazards Models Renal Insufficiency, Chronic - epidemiology Renal Replacement Therapy - statistics & numerical data Sensitivity analysis Sodium-Glucose Transporter 2 Inhibitors - therapeutic use Sweden - epidemiology type-2 |
title | Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study |
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