Incidence of diabetes mellitus in a population-based cohort of HIV-infected and non-HIV-infected persons: the impact of clinical and therapeutic factors over time

Aims To examine incidence density rate and correlates of incident diabetes mellitus in a cohort of HIV‐infected individuals compared with matched non‐HIV‐infected persons. Methods Data were obtained from the South Carolina Medicaid system and the enhanced HIV/AIDS Reporting System surveillance datab...

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Veröffentlicht in:Diabetic medicine 2014-10, Vol.31 (10), p.1185-1193
Hauptverfasser: Tripathi, A., Liese, A. D., Jerrell, J. M., Zhang, J., Rizvi, A. A., Albrecht, H., Duffus, W. A.
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container_end_page 1193
container_issue 10
container_start_page 1185
container_title Diabetic medicine
container_volume 31
creator Tripathi, A.
Liese, A. D.
Jerrell, J. M.
Zhang, J.
Rizvi, A. A.
Albrecht, H.
Duffus, W. A.
description Aims To examine incidence density rate and correlates of incident diabetes mellitus in a cohort of HIV‐infected individuals compared with matched non‐HIV‐infected persons. Methods Data were obtained from the South Carolina Medicaid system and the enhanced HIV/AIDS Reporting System surveillance database for persons ≥ 18 years of age who had been attended to during the period 1994 to 2011. Time‐dependent proportional hazards analysis and marginal structural models were used to analyse the data. Results A total of 13 632 individuals (6816, 1:1 matched HIV‐infected and non‐HIV‐infected persons; median age 39 years; 57% male) contributed 88 359 person‐years of follow‐up. Incidence rate of diabetes was higher in the non‐HIV‐infected group compared with the HIV‐infected group (13.60 vs. 11.35 per 1000 person‐years). Multivariable hazards analysis suggested a significantly lower risk of incident diabetes among HIV‐infected persons treated with combination antiretroviral therapy compared with the matched non‐HIV‐infected persons (adjusted hazards ratio 0.55; 95% CI 0.46–0.65). Among HIV‐infected persons, marginal structural modelling suggested a significantly higher risk of diabetes with cumulative exposure to protease inhibitors over the observation period (adjusted relative risk 1.35; 95% CI 1.03–1.78), but this association was not significant for exposure to non‐nucleoside reverse transcriptase inhibitors. Overall, female gender, older age, non‐white race/ethnicity, and pre‐existing hypertension, dyslipidaemia, obesity and hepatitis C infection were associated with higher risk of diabetes incidence. Conclusions HIV infection may not be independently associated with increased risk of diabetes. Among HIV‐infected persons, exposure to protease inhibitor‐based regimens may increase the risk of diabetes. Healthcare providers should make every effort to use combination antiretroviral therapy regimens with a better cardiometabolic profile. What's new? This is the first study to examine the incidence density rate of diabetes among HIV‐infected persons compared with a non‐HIV‐infected control group in the Southern USA, which has disproportionally both HIV and cardiometabolic disorders, especially obesity. Time‐dependent statistical methodology was used to examine the retrospective observation data over an 18‐year study period for the pertinent risk factors associated with new‐onset diabetes. Results empirically reiterate the importance of monitoring and managing risk fac
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D. ; Jerrell, J. M. ; Zhang, J. ; Rizvi, A. A. ; Albrecht, H. ; Duffus, W. A.</creator><creatorcontrib>Tripathi, A. ; Liese, A. D. ; Jerrell, J. M. ; Zhang, J. ; Rizvi, A. A. ; Albrecht, H. ; Duffus, W. A.</creatorcontrib><description>Aims To examine incidence density rate and correlates of incident diabetes mellitus in a cohort of HIV‐infected individuals compared with matched non‐HIV‐infected persons. Methods Data were obtained from the South Carolina Medicaid system and the enhanced HIV/AIDS Reporting System surveillance database for persons ≥ 18 years of age who had been attended to during the period 1994 to 2011. Time‐dependent proportional hazards analysis and marginal structural models were used to analyse the data. Results A total of 13 632 individuals (6816, 1:1 matched HIV‐infected and non‐HIV‐infected persons; median age 39 years; 57% male) contributed 88 359 person‐years of follow‐up. Incidence rate of diabetes was higher in the non‐HIV‐infected group compared with the HIV‐infected group (13.60 vs. 11.35 per 1000 person‐years). Multivariable hazards analysis suggested a significantly lower risk of incident diabetes among HIV‐infected persons treated with combination antiretroviral therapy compared with the matched non‐HIV‐infected persons (adjusted hazards ratio 0.55; 95% CI 0.46–0.65). Among HIV‐infected persons, marginal structural modelling suggested a significantly higher risk of diabetes with cumulative exposure to protease inhibitors over the observation period (adjusted relative risk 1.35; 95% CI 1.03–1.78), but this association was not significant for exposure to non‐nucleoside reverse transcriptase inhibitors. Overall, female gender, older age, non‐white race/ethnicity, and pre‐existing hypertension, dyslipidaemia, obesity and hepatitis C infection were associated with higher risk of diabetes incidence. Conclusions HIV infection may not be independently associated with increased risk of diabetes. Among HIV‐infected persons, exposure to protease inhibitor‐based regimens may increase the risk of diabetes. Healthcare providers should make every effort to use combination antiretroviral therapy regimens with a better cardiometabolic profile. What's new? This is the first study to examine the incidence density rate of diabetes among HIV‐infected persons compared with a non‐HIV‐infected control group in the Southern USA, which has disproportionally both HIV and cardiometabolic disorders, especially obesity. Time‐dependent statistical methodology was used to examine the retrospective observation data over an 18‐year study period for the pertinent risk factors associated with new‐onset diabetes. Results empirically reiterate the importance of monitoring and managing risk factors among HIV‐infected persons, especially among those exposed to combination antiretroviral therapy.</description><identifier>ISSN: 0742-3071</identifier><identifier>EISSN: 1464-5491</identifier><identifier>DOI: 10.1111/dme.12455</identifier><identifier>PMID: 24673640</identifier><identifier>CODEN: DIMEEV</identifier><language>eng</language><publisher>Oxford: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Anti-HIV Agents - adverse effects ; Anti-HIV Agents - therapeutic use ; Antiretroviral drugs ; Biological and medical sciences ; Cohort Studies ; Diabetes ; Diabetes Mellitus, Type 1 - chemically induced ; Diabetes Mellitus, Type 1 - complications ; Diabetes Mellitus, Type 1 - epidemiology ; Diabetes Mellitus, Type 1 - microbiology ; Diabetes Mellitus, Type 2 - chemically induced ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - epidemiology ; Diabetes Mellitus, Type 2 - microbiology ; Diabetes. Impaired glucose tolerance ; Drug therapy ; Drug Therapy, Combination - adverse effects ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Epidemiological Monitoring ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Feeding. Feeding behavior ; Female ; Follow-Up Studies ; Fundamental and applied biological sciences. Psychology ; HIV ; HIV Infections - complications ; HIV Infections - drug therapy ; HIV Infections - microbiology ; HIV Protease Inhibitors - adverse effects ; HIV Protease Inhibitors - therapeutic use ; Human immunodeficiency virus ; Humans ; Incidence ; Longitudinal Studies ; Male ; Medicaid ; Medical sciences ; Middle Aged ; Proportional Hazards Models ; Retrospective Studies ; Risk Factors ; South Carolina - epidemiology ; United States - epidemiology ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vertebrates: endocrinology ; Young Adult</subject><ispartof>Diabetic medicine, 2014-10, Vol.31 (10), p.1185-1193</ispartof><rights>2014 The Authors. Diabetic Medicine © 2014 Diabetes UK</rights><rights>2015 INIST-CNRS</rights><rights>2014 The Authors. 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D.</creatorcontrib><creatorcontrib>Jerrell, J. M.</creatorcontrib><creatorcontrib>Zhang, J.</creatorcontrib><creatorcontrib>Rizvi, A. A.</creatorcontrib><creatorcontrib>Albrecht, H.</creatorcontrib><creatorcontrib>Duffus, W. A.</creatorcontrib><title>Incidence of diabetes mellitus in a population-based cohort of HIV-infected and non-HIV-infected persons: the impact of clinical and therapeutic factors over time</title><title>Diabetic medicine</title><addtitle>Diabet. Med</addtitle><description>Aims To examine incidence density rate and correlates of incident diabetes mellitus in a cohort of HIV‐infected individuals compared with matched non‐HIV‐infected persons. Methods Data were obtained from the South Carolina Medicaid system and the enhanced HIV/AIDS Reporting System surveillance database for persons ≥ 18 years of age who had been attended to during the period 1994 to 2011. Time‐dependent proportional hazards analysis and marginal structural models were used to analyse the data. Results A total of 13 632 individuals (6816, 1:1 matched HIV‐infected and non‐HIV‐infected persons; median age 39 years; 57% male) contributed 88 359 person‐years of follow‐up. Incidence rate of diabetes was higher in the non‐HIV‐infected group compared with the HIV‐infected group (13.60 vs. 11.35 per 1000 person‐years). Multivariable hazards analysis suggested a significantly lower risk of incident diabetes among HIV‐infected persons treated with combination antiretroviral therapy compared with the matched non‐HIV‐infected persons (adjusted hazards ratio 0.55; 95% CI 0.46–0.65). Among HIV‐infected persons, marginal structural modelling suggested a significantly higher risk of diabetes with cumulative exposure to protease inhibitors over the observation period (adjusted relative risk 1.35; 95% CI 1.03–1.78), but this association was not significant for exposure to non‐nucleoside reverse transcriptase inhibitors. Overall, female gender, older age, non‐white race/ethnicity, and pre‐existing hypertension, dyslipidaemia, obesity and hepatitis C infection were associated with higher risk of diabetes incidence. Conclusions HIV infection may not be independently associated with increased risk of diabetes. Among HIV‐infected persons, exposure to protease inhibitor‐based regimens may increase the risk of diabetes. Healthcare providers should make every effort to use combination antiretroviral therapy regimens with a better cardiometabolic profile. What's new? This is the first study to examine the incidence density rate of diabetes among HIV‐infected persons compared with a non‐HIV‐infected control group in the Southern USA, which has disproportionally both HIV and cardiometabolic disorders, especially obesity. Time‐dependent statistical methodology was used to examine the retrospective observation data over an 18‐year study period for the pertinent risk factors associated with new‐onset diabetes. Results empirically reiterate the importance of monitoring and managing risk factors among HIV‐infected persons, especially among those exposed to combination antiretroviral therapy.</description><subject>Adult</subject><subject>Aged</subject><subject>Anti-HIV Agents - adverse effects</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>Antiretroviral drugs</subject><subject>Biological and medical sciences</subject><subject>Cohort Studies</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 1 - chemically induced</subject><subject>Diabetes Mellitus, Type 1 - complications</subject><subject>Diabetes Mellitus, Type 1 - epidemiology</subject><subject>Diabetes Mellitus, Type 1 - microbiology</subject><subject>Diabetes Mellitus, Type 2 - chemically induced</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - epidemiology</subject><subject>Diabetes Mellitus, Type 2 - microbiology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Drug therapy</subject><subject>Drug Therapy, Combination - adverse effects</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Epidemiological Monitoring</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>HIV</subject><subject>HIV Infections - complications</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - microbiology</subject><subject>HIV Protease Inhibitors - adverse effects</subject><subject>HIV Protease Inhibitors - therapeutic use</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Incidence</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medicaid</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Proportional Hazards Models</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>South Carolina - epidemiology</subject><subject>United States - epidemiology</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vertebrates: endocrinology</subject><subject>Young Adult</subject><issn>0742-3071</issn><issn>1464-5491</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1TAQhSMEopfCghdAllAlWKS1E9u5YVdKf65UQCpQKjbWxBmrLokd7ATa1-mT4vvTIpDwxtL4O3PGc7LsOaO7LJ29tsddVnAhHmQzxiXPBa_Zw2xGK17kJa3YVvYkxitKWVGX9eNsq-CyKiWns-x24bRt0Wkk3pDWQoMjRtJj19lxisQ6AmTww9TBaL3LG4jYEu0vfRiXipPFeW6dQT2mMriWuAT9VRwwRO_iGzJeIrH9AHol1J11VkO3EqWnAANOo9XEJMCHSPxPDGS0PT7NHhnoIj7b3NvZl6PDzwcn-enH48XB_mmu029FDnNWQCUpp7JppWFgKpxLKlrkFDmvQdeMN1ALbKExKOrCaDGvpQRdUYqi3M5erfsOwf-YMI6qt1GnRYBDP0XFhCxpkkmW0Jf_oFd-Ci5Nt6SKQtaUy0S9XlM6-BgDGjUE20O4UYyqZXAqBadWwSX2xabj1PTY3pN3SSVgZwNATGszAVJw8Q83r6qaSZ64vTX3y3Z4839H9e794Z11vlbYOOL1vQLCd5W8K6G-fjhWn47O3p59O79QF-VvbTG_tA</recordid><startdate>201410</startdate><enddate>201410</enddate><creator>Tripathi, A.</creator><creator>Liese, A. D.</creator><creator>Jerrell, J. M.</creator><creator>Zhang, J.</creator><creator>Rizvi, A. A.</creator><creator>Albrecht, H.</creator><creator>Duffus, W. A.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</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>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201410</creationdate><title>Incidence of diabetes mellitus in a population-based cohort of HIV-infected and non-HIV-infected persons: the impact of clinical and therapeutic factors over time</title><author>Tripathi, A. ; Liese, A. D. ; Jerrell, J. M. ; Zhang, J. ; Rizvi, A. A. ; Albrecht, H. ; Duffus, W. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4915-a812a760406bd6f1af7e8605de40e449ac914ba95edabfe592fc58966ac700e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Anti-HIV Agents - adverse effects</topic><topic>Anti-HIV Agents - therapeutic use</topic><topic>Antiretroviral drugs</topic><topic>Biological and medical sciences</topic><topic>Cohort Studies</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 1 - chemically induced</topic><topic>Diabetes Mellitus, Type 1 - complications</topic><topic>Diabetes Mellitus, Type 1 - epidemiology</topic><topic>Diabetes Mellitus, Type 1 - microbiology</topic><topic>Diabetes Mellitus, Type 2 - chemically induced</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - epidemiology</topic><topic>Diabetes Mellitus, Type 2 - microbiology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Drug therapy</topic><topic>Drug Therapy, Combination - adverse effects</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Epidemiological Monitoring</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HIV</topic><topic>HIV Infections - complications</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - microbiology</topic><topic>HIV Protease Inhibitors - adverse effects</topic><topic>HIV Protease Inhibitors - therapeutic use</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Incidence</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medicaid</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Proportional Hazards Models</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>South Carolina - epidemiology</topic><topic>United States - epidemiology</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Vertebrates: endocrinology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tripathi, A.</creatorcontrib><creatorcontrib>Liese, A. D.</creatorcontrib><creatorcontrib>Jerrell, J. M.</creatorcontrib><creatorcontrib>Zhang, J.</creatorcontrib><creatorcontrib>Rizvi, A. A.</creatorcontrib><creatorcontrib>Albrecht, H.</creatorcontrib><creatorcontrib>Duffus, W. A.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetic medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tripathi, A.</au><au>Liese, A. D.</au><au>Jerrell, J. M.</au><au>Zhang, J.</au><au>Rizvi, A. A.</au><au>Albrecht, H.</au><au>Duffus, W. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incidence of diabetes mellitus in a population-based cohort of HIV-infected and non-HIV-infected persons: the impact of clinical and therapeutic factors over time</atitle><jtitle>Diabetic medicine</jtitle><addtitle>Diabet. Med</addtitle><date>2014-10</date><risdate>2014</risdate><volume>31</volume><issue>10</issue><spage>1185</spage><epage>1193</epage><pages>1185-1193</pages><issn>0742-3071</issn><eissn>1464-5491</eissn><coden>DIMEEV</coden><abstract>Aims To examine incidence density rate and correlates of incident diabetes mellitus in a cohort of HIV‐infected individuals compared with matched non‐HIV‐infected persons. Methods Data were obtained from the South Carolina Medicaid system and the enhanced HIV/AIDS Reporting System surveillance database for persons ≥ 18 years of age who had been attended to during the period 1994 to 2011. Time‐dependent proportional hazards analysis and marginal structural models were used to analyse the data. Results A total of 13 632 individuals (6816, 1:1 matched HIV‐infected and non‐HIV‐infected persons; median age 39 years; 57% male) contributed 88 359 person‐years of follow‐up. Incidence rate of diabetes was higher in the non‐HIV‐infected group compared with the HIV‐infected group (13.60 vs. 11.35 per 1000 person‐years). Multivariable hazards analysis suggested a significantly lower risk of incident diabetes among HIV‐infected persons treated with combination antiretroviral therapy compared with the matched non‐HIV‐infected persons (adjusted hazards ratio 0.55; 95% CI 0.46–0.65). Among HIV‐infected persons, marginal structural modelling suggested a significantly higher risk of diabetes with cumulative exposure to protease inhibitors over the observation period (adjusted relative risk 1.35; 95% CI 1.03–1.78), but this association was not significant for exposure to non‐nucleoside reverse transcriptase inhibitors. Overall, female gender, older age, non‐white race/ethnicity, and pre‐existing hypertension, dyslipidaemia, obesity and hepatitis C infection were associated with higher risk of diabetes incidence. Conclusions HIV infection may not be independently associated with increased risk of diabetes. Among HIV‐infected persons, exposure to protease inhibitor‐based regimens may increase the risk of diabetes. Healthcare providers should make every effort to use combination antiretroviral therapy regimens with a better cardiometabolic profile. What's new? This is the first study to examine the incidence density rate of diabetes among HIV‐infected persons compared with a non‐HIV‐infected control group in the Southern USA, which has disproportionally both HIV and cardiometabolic disorders, especially obesity. Time‐dependent statistical methodology was used to examine the retrospective observation data over an 18‐year study period for the pertinent risk factors associated with new‐onset diabetes. Results empirically reiterate the importance of monitoring and managing risk factors among HIV‐infected persons, especially among those exposed to combination antiretroviral therapy.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>24673640</pmid><doi>10.1111/dme.12455</doi><tpages>9</tpages></addata></record>
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subjects Adult
Aged
Anti-HIV Agents - adverse effects
Anti-HIV Agents - therapeutic use
Antiretroviral drugs
Biological and medical sciences
Cohort Studies
Diabetes
Diabetes Mellitus, Type 1 - chemically induced
Diabetes Mellitus, Type 1 - complications
Diabetes Mellitus, Type 1 - epidemiology
Diabetes Mellitus, Type 1 - microbiology
Diabetes Mellitus, Type 2 - chemically induced
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - epidemiology
Diabetes Mellitus, Type 2 - microbiology
Diabetes. Impaired glucose tolerance
Drug therapy
Drug Therapy, Combination - adverse effects
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Epidemiological Monitoring
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Feeding. Feeding behavior
Female
Follow-Up Studies
Fundamental and applied biological sciences. Psychology
HIV
HIV Infections - complications
HIV Infections - drug therapy
HIV Infections - microbiology
HIV Protease Inhibitors - adverse effects
HIV Protease Inhibitors - therapeutic use
Human immunodeficiency virus
Humans
Incidence
Longitudinal Studies
Male
Medicaid
Medical sciences
Middle Aged
Proportional Hazards Models
Retrospective Studies
Risk Factors
South Carolina - epidemiology
United States - epidemiology
Vertebrates: anatomy and physiology, studies on body, several organs or systems
Vertebrates: endocrinology
Young Adult
title Incidence of diabetes mellitus in a population-based cohort of HIV-infected and non-HIV-infected persons: the impact of clinical and therapeutic factors over time
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