Metformin and Sulfonylurea Use and Risk of Incident Dementia
To compare incident dementia risk among patients who initiated treatment with metformin or sulfonylurea in Veterans Health Affairs (VHA) patients with replication in Kaiser Permanente Washington (KPW) patients to determine whether first-choice antidiabetic medications are associated with reduced ris...
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Veröffentlicht in: | Mayo Clinic proceedings 2019-08, Vol.94 (8), p.1444-1456 |
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description | To compare incident dementia risk among patients who initiated treatment with metformin or sulfonylurea in Veterans Health Affairs (VHA) patients with replication in Kaiser Permanente Washington (KPW) patients to determine whether first-choice antidiabetic medications are associated with reduced risk of dementia.
Cohorts contained 75,187 VHA patients and 10,866 KPW patients, 50 years and older, who initiated monotherapy with metformin or sulfonylurea. Patients were free of dementia diagnoses and any diabetes treatment for 2 years before cohort entry. Variables were extracted from electronic health data from VHA (1999-2015) and KPW (1996-2015), which included diagnosis codes, pharmacy data, laboratory values, and demographic characteristics. Propensity scores and inverse probability of treatment weighting controlled for confounding.
Veterans Health Affairs patients were 60.8±6.8 years of age on average, and KPW patients were 63.1±9.5 years of age. In the VHA sample, 72,769 (96.8%) were male; and in the KPW sample, 5480 (50.4%). After adjusting for confounding, metformin initiation was associated with a significantly (P=.02) lower risk of dementia in VHA (hazard ratio, 0.9; 95% CI, 0.9-1.0), with a similar point estimate in KPW (hazard ratio, 0.9; 95% CI, 0.7-1.1). Metformin was not associated with dementia risk in patients 75 years and older.
Existing epidemiological studies of metformin and incident dementia have been inconsistent. Using a similar study design in 2 patient populations that differed in clinical and demographic characteristics, our results provide robust evidence that metformin use is associated with a modestly lower risk of incident dementia. |
doi_str_mv | 10.1016/j.mayocp.2019.01.004 |
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Cohorts contained 75,187 VHA patients and 10,866 KPW patients, 50 years and older, who initiated monotherapy with metformin or sulfonylurea. Patients were free of dementia diagnoses and any diabetes treatment for 2 years before cohort entry. Variables were extracted from electronic health data from VHA (1999-2015) and KPW (1996-2015), which included diagnosis codes, pharmacy data, laboratory values, and demographic characteristics. Propensity scores and inverse probability of treatment weighting controlled for confounding.
Veterans Health Affairs patients were 60.8±6.8 years of age on average, and KPW patients were 63.1±9.5 years of age. In the VHA sample, 72,769 (96.8%) were male; and in the KPW sample, 5480 (50.4%). After adjusting for confounding, metformin initiation was associated with a significantly (P=.02) lower risk of dementia in VHA (hazard ratio, 0.9; 95% CI, 0.9-1.0), with a similar point estimate in KPW (hazard ratio, 0.9; 95% CI, 0.7-1.1). Metformin was not associated with dementia risk in patients 75 years and older.
Existing epidemiological studies of metformin and incident dementia have been inconsistent. Using a similar study design in 2 patient populations that differed in clinical and demographic characteristics, our results provide robust evidence that metformin use is associated with a modestly lower risk of incident dementia.</description><identifier>ISSN: 0025-6196</identifier><identifier>ISSN: 1942-5546</identifier><identifier>EISSN: 1942-5546</identifier><identifier>DOI: 10.1016/j.mayocp.2019.01.004</identifier><identifier>PMID: 31378227</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Age Factors ; Aged ; Alzheimer's disease ; Animal models ; Antidiabetics ; c-Jun protein ; Care and treatment ; Cognitive ability ; Databases, Factual ; Dementia ; Dementia - chemically induced ; Dementia - epidemiology ; Dementia - physiopathology ; Dementia disorders ; Diabetes ; Diabetes Mellitus, Type 2 - diagnosis ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes therapy ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Drugstores ; Epidemiology ; Female ; Health care delivery ; Health maintenance organizations ; Hospitals, Veterans ; Humans ; Hypoglycemia ; Hypoglycemic agents ; Incidence ; JNK protein ; Laboratories ; Male ; Medicare ; Memantine ; Metformin ; Metformin - adverse effects ; Metformin - therapeutic use ; Middle Aged ; Older people ; Oxidative stress ; Patients ; Pharmacy ; Phosphorylation ; Prognosis ; Proportional Hazards Models ; Retrospective Studies ; Risk Assessment ; Risk factors ; Sex Factors ; Studies ; Sulfonylurea ; Sulfonylurea Compounds - adverse effects ; Sulfonylurea Compounds - therapeutic use ; Synaptophysin ; Systematic review ; Transcription factors ; Type 2 diabetes ; United States ; β-Amyloid</subject><ispartof>Mayo Clinic proceedings, 2019-08, Vol.94 (8), p.1444-1456</ispartof><rights>2019 Mayo Foundation for Medical Education and Research</rights><rights>Copyright © 2019 Mayo Foundation for Medical Education and Research. All rights reserved.</rights><rights>COPYRIGHT 2019 Frontline Medical Communications Inc.</rights><rights>Copyright Mayo Foundation for Medical Education and Research Aug 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c561t-667248ba5791953c982eb46fc90990dd745a7cd1785cfd5374dc950d5df8ce843</citedby><cites>FETCH-LOGICAL-c561t-667248ba5791953c982eb46fc90990dd745a7cd1785cfd5374dc950d5df8ce843</cites><orcidid>0000-0002-9148-2863 ; 0000-0002-5604-7954</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31378227$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Scherrer, Jeffrey F.</creatorcontrib><creatorcontrib>Salas, Joanne</creatorcontrib><creatorcontrib>Floyd, James S.</creatorcontrib><creatorcontrib>Farr, Susan A.</creatorcontrib><creatorcontrib>Morley, John E.</creatorcontrib><creatorcontrib>Dublin, Sascha</creatorcontrib><title>Metformin and Sulfonylurea Use and Risk of Incident Dementia</title><title>Mayo Clinic proceedings</title><addtitle>Mayo Clin Proc</addtitle><description>To compare incident dementia risk among patients who initiated treatment with metformin or sulfonylurea in Veterans Health Affairs (VHA) patients with replication in Kaiser Permanente Washington (KPW) patients to determine whether first-choice antidiabetic medications are associated with reduced risk of dementia.
Cohorts contained 75,187 VHA patients and 10,866 KPW patients, 50 years and older, who initiated monotherapy with metformin or sulfonylurea. Patients were free of dementia diagnoses and any diabetes treatment for 2 years before cohort entry. Variables were extracted from electronic health data from VHA (1999-2015) and KPW (1996-2015), which included diagnosis codes, pharmacy data, laboratory values, and demographic characteristics. Propensity scores and inverse probability of treatment weighting controlled for confounding.
Veterans Health Affairs patients were 60.8±6.8 years of age on average, and KPW patients were 63.1±9.5 years of age. In the VHA sample, 72,769 (96.8%) were male; and in the KPW sample, 5480 (50.4%). After adjusting for confounding, metformin initiation was associated with a significantly (P=.02) lower risk of dementia in VHA (hazard ratio, 0.9; 95% CI, 0.9-1.0), with a similar point estimate in KPW (hazard ratio, 0.9; 95% CI, 0.7-1.1). Metformin was not associated with dementia risk in patients 75 years and older.
Existing epidemiological studies of metformin and incident dementia have been inconsistent. Using a similar study design in 2 patient populations that differed in clinical and demographic characteristics, our results provide robust evidence that metformin use is associated with a modestly lower risk of incident dementia.</description><subject>Age Factors</subject><subject>Aged</subject><subject>Alzheimer's disease</subject><subject>Animal models</subject><subject>Antidiabetics</subject><subject>c-Jun protein</subject><subject>Care and treatment</subject><subject>Cognitive ability</subject><subject>Databases, Factual</subject><subject>Dementia</subject><subject>Dementia - chemically induced</subject><subject>Dementia - epidemiology</subject><subject>Dementia - physiopathology</subject><subject>Dementia disorders</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - diagnosis</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Diabetes therapy</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Drugstores</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Health care delivery</subject><subject>Health maintenance organizations</subject><subject>Hospitals, Veterans</subject><subject>Humans</subject><subject>Hypoglycemia</subject><subject>Hypoglycemic agents</subject><subject>Incidence</subject><subject>JNK protein</subject><subject>Laboratories</subject><subject>Male</subject><subject>Medicare</subject><subject>Memantine</subject><subject>Metformin</subject><subject>Metformin - adverse effects</subject><subject>Metformin - therapeutic use</subject><subject>Middle Aged</subject><subject>Older people</subject><subject>Oxidative stress</subject><subject>Patients</subject><subject>Pharmacy</subject><subject>Phosphorylation</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk factors</subject><subject>Sex Factors</subject><subject>Studies</subject><subject>Sulfonylurea</subject><subject>Sulfonylurea Compounds - adverse effects</subject><subject>Sulfonylurea Compounds - therapeutic use</subject><subject>Synaptophysin</subject><subject>Systematic review</subject><subject>Transcription factors</subject><subject>Type 2 diabetes</subject><subject>United States</subject><subject>β-Amyloid</subject><issn>0025-6196</issn><issn>1942-5546</issn><issn>1942-5546</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kV1rFDEUhoModq3-A5EBQbzZMcnkYwIilPpVqAhqr0M2OelmnUnWZKaw_95st9bWC8nFgZPnvC_nvAg9J7glmIg3m3Y0u2S3LcVEtZi0GLMHaEEUo0vOmXiIFhhTvhREiSP0pJQNxlgqxR6jo450sqdULtDbLzD5lMcQGxNd830efIq7Yc5gmosC181vofxskm_Oog0O4tS8h7GWYJ6iR94MBZ7d1GN08fHDj9PPy_Ovn85OT86XlgsyLYWQlPUrw6UiindW9RRWTHirsFLYOcm4kdYR2XPrHe8kc1Zx7LjzvYWedcfo3UF3O69GcLaaZzPobQ6jyTudTND3f2JY68t0pSWmSvZdFXh9I5DTrxnKpMdQLAyDiZDmoikVPZdMcFLRl_-gmzTnWNfbU6qXVHWqUu2BujQD6BB9qr62PgdjsCmCD7V_IurJO0GuZV_dGViDGaZ1ScM8hRTLfZAdQJtTKRn87ZoE633weqMPwet98BoTXYOvYy_unuh26E_Sf28INairAFkXGyBacCGDnbRL4f8OvwEjQb6-</recordid><startdate>201908</startdate><enddate>201908</enddate><creator>Scherrer, Jeffrey F.</creator><creator>Salas, Joanne</creator><creator>Floyd, James S.</creator><creator>Farr, Susan A.</creator><creator>Morley, John E.</creator><creator>Dublin, Sascha</creator><general>Elsevier Inc</general><general>Frontline Medical Communications Inc</general><general>Elsevier Limited</general><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>4U-</scope><scope>7RV</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9148-2863</orcidid><orcidid>https://orcid.org/0000-0002-5604-7954</orcidid></search><sort><creationdate>201908</creationdate><title>Metformin and Sulfonylurea Use and Risk of Incident Dementia</title><author>Scherrer, Jeffrey F. ; Salas, Joanne ; Floyd, James S. ; Farr, Susan A. ; Morley, John E. ; Dublin, Sascha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c561t-667248ba5791953c982eb46fc90990dd745a7cd1785cfd5374dc950d5df8ce843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Age Factors</topic><topic>Aged</topic><topic>Alzheimer's disease</topic><topic>Animal models</topic><topic>Antidiabetics</topic><topic>c-Jun protein</topic><topic>Care and treatment</topic><topic>Cognitive ability</topic><topic>Databases, Factual</topic><topic>Dementia</topic><topic>Dementia - chemically induced</topic><topic>Dementia - epidemiology</topic><topic>Dementia - physiopathology</topic><topic>Dementia disorders</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - diagnosis</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Diabetes therapy</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Administration Schedule</topic><topic>Drugstores</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Health care delivery</topic><topic>Health maintenance organizations</topic><topic>Hospitals, Veterans</topic><topic>Humans</topic><topic>Hypoglycemia</topic><topic>Hypoglycemic agents</topic><topic>Incidence</topic><topic>JNK protein</topic><topic>Laboratories</topic><topic>Male</topic><topic>Medicare</topic><topic>Memantine</topic><topic>Metformin</topic><topic>Metformin - adverse effects</topic><topic>Metformin - therapeutic use</topic><topic>Middle Aged</topic><topic>Older people</topic><topic>Oxidative stress</topic><topic>Patients</topic><topic>Pharmacy</topic><topic>Phosphorylation</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Risk factors</topic><topic>Sex Factors</topic><topic>Studies</topic><topic>Sulfonylurea</topic><topic>Sulfonylurea Compounds - adverse effects</topic><topic>Sulfonylurea Compounds - therapeutic use</topic><topic>Synaptophysin</topic><topic>Systematic review</topic><topic>Transcription factors</topic><topic>Type 2 diabetes</topic><topic>United States</topic><topic>β-Amyloid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scherrer, Jeffrey F.</creatorcontrib><creatorcontrib>Salas, Joanne</creatorcontrib><creatorcontrib>Floyd, James S.</creatorcontrib><creatorcontrib>Farr, Susan A.</creatorcontrib><creatorcontrib>Morley, John E.</creatorcontrib><creatorcontrib>Dublin, Sascha</creatorcontrib><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>University Readers</collection><collection>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Public Health Database</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</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>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Mayo Clinic proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scherrer, Jeffrey F.</au><au>Salas, Joanne</au><au>Floyd, James S.</au><au>Farr, Susan A.</au><au>Morley, John E.</au><au>Dublin, Sascha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metformin and Sulfonylurea Use and Risk of Incident Dementia</atitle><jtitle>Mayo Clinic proceedings</jtitle><addtitle>Mayo Clin Proc</addtitle><date>2019-08</date><risdate>2019</risdate><volume>94</volume><issue>8</issue><spage>1444</spage><epage>1456</epage><pages>1444-1456</pages><issn>0025-6196</issn><issn>1942-5546</issn><eissn>1942-5546</eissn><abstract>To compare incident dementia risk among patients who initiated treatment with metformin or sulfonylurea in Veterans Health Affairs (VHA) patients with replication in Kaiser Permanente Washington (KPW) patients to determine whether first-choice antidiabetic medications are associated with reduced risk of dementia.
Cohorts contained 75,187 VHA patients and 10,866 KPW patients, 50 years and older, who initiated monotherapy with metformin or sulfonylurea. Patients were free of dementia diagnoses and any diabetes treatment for 2 years before cohort entry. Variables were extracted from electronic health data from VHA (1999-2015) and KPW (1996-2015), which included diagnosis codes, pharmacy data, laboratory values, and demographic characteristics. Propensity scores and inverse probability of treatment weighting controlled for confounding.
Veterans Health Affairs patients were 60.8±6.8 years of age on average, and KPW patients were 63.1±9.5 years of age. In the VHA sample, 72,769 (96.8%) were male; and in the KPW sample, 5480 (50.4%). After adjusting for confounding, metformin initiation was associated with a significantly (P=.02) lower risk of dementia in VHA (hazard ratio, 0.9; 95% CI, 0.9-1.0), with a similar point estimate in KPW (hazard ratio, 0.9; 95% CI, 0.7-1.1). Metformin was not associated with dementia risk in patients 75 years and older.
Existing epidemiological studies of metformin and incident dementia have been inconsistent. Using a similar study design in 2 patient populations that differed in clinical and demographic characteristics, our results provide robust evidence that metformin use is associated with a modestly lower risk of incident dementia.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>31378227</pmid><doi>10.1016/j.mayocp.2019.01.004</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-9148-2863</orcidid><orcidid>https://orcid.org/0000-0002-5604-7954</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age Factors Aged Alzheimer's disease Animal models Antidiabetics c-Jun protein Care and treatment Cognitive ability Databases, Factual Dementia Dementia - chemically induced Dementia - epidemiology Dementia - physiopathology Dementia disorders Diabetes Diabetes Mellitus, Type 2 - diagnosis Diabetes Mellitus, Type 2 - drug therapy Diabetes therapy Dose-Response Relationship, Drug Drug Administration Schedule Drugstores Epidemiology Female Health care delivery Health maintenance organizations Hospitals, Veterans Humans Hypoglycemia Hypoglycemic agents Incidence JNK protein Laboratories Male Medicare Memantine Metformin Metformin - adverse effects Metformin - therapeutic use Middle Aged Older people Oxidative stress Patients Pharmacy Phosphorylation Prognosis Proportional Hazards Models Retrospective Studies Risk Assessment Risk factors Sex Factors Studies Sulfonylurea Sulfonylurea Compounds - adverse effects Sulfonylurea Compounds - therapeutic use Synaptophysin Systematic review Transcription factors Type 2 diabetes United States β-Amyloid |
title | Metformin and Sulfonylurea Use and Risk of Incident Dementia |
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