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Effect of Lower Targets for Blood Pressure and LDL Cholesterol on Atherosclerosis in Diabetes: The SANDS Randomized Trial

CONTEXT Individuals with diabetes are at increased risk for cardiovascular disease (CVD), but more aggressive targets for risk factor control have not been tested. OBJECTIVE To compare progression of subclinical atherosclerosis in adults with type 2 diabetes treated to reach aggressive targets of lo...

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Published in:JAMA : the journal of the American Medical Association 2008-04, Vol.299 (14), p.1678-1689
Main Authors: Howard, Barbara V, Roman, Mary J, Devereux, Richard B, Fleg, Jerome L, Galloway, James M, Henderson, Jeffrey A, Howard, Wm. James, Lee, Elisa T, Mete, Mihriye, Poolaw, Bryce, Ratner, Robert E, Russell, Marie, Silverman, Angela, Stylianou, Mario, Umans, Jason G, Wang, Wenyu, Weir, Matthew R, Weissman, Neil J, Wilson, Charlton, Yeh, Fawn, Zhu, Jianhui
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container_issue 14
container_start_page 1678
container_title JAMA : the journal of the American Medical Association
container_volume 299
creator Howard, Barbara V
Roman, Mary J
Devereux, Richard B
Fleg, Jerome L
Galloway, James M
Henderson, Jeffrey A
Howard, Wm. James
Lee, Elisa T
Mete, Mihriye
Poolaw, Bryce
Ratner, Robert E
Russell, Marie
Silverman, Angela
Stylianou, Mario
Umans, Jason G
Wang, Wenyu
Weir, Matthew R
Weissman, Neil J
Wilson, Charlton
Yeh, Fawn
Zhu, Jianhui
description CONTEXT Individuals with diabetes are at increased risk for cardiovascular disease (CVD), but more aggressive targets for risk factor control have not been tested. OBJECTIVE To compare progression of subclinical atherosclerosis in adults with type 2 diabetes treated to reach aggressive targets of low-density lipoprotein cholesterol (LDL-C) of 70 mg/dL or lower and systolic blood pressure (SBP) of 115 mm Hg or lower vs standard targets of LDL-C of 100 mg/dL or lower and SBP of 130 mm Hg or lower. DESIGN, SETTING, AND PARTICIPANTS A randomized, open-label, blinded-to-end point, 3-year trial from April 2003-July 2007 at 4 clinical centers in Oklahoma, Arizona, and South Dakota. Participants were 499 American Indian men and women aged 40 years or older with type 2 diabetes and no prior CVD events. INTERVENTIONS Participants were randomized to aggressive (n=252) vs standard (n=247) treatment groups with stepped treatment algorithms defined for both. MAIN OUTCOME MEASURES Primary end point was progression of atherosclerosis measured by common carotid artery intimal medial thickness (IMT). Secondary end points were other carotid and cardiac ultrasonographic measures and clinical events. RESULTS Mean target LDL-C and SBP levels for both groups were reached and maintained. Mean (95% confidence interval) levels for LDL-C in the last 12 months were 72 (69-75) and 104 (101-106) mg/dL and SBP levels were 117 (115-118) and 129 (128-130) mm Hg in the aggressive vs standard groups, respectively. Compared with baseline, IMT regressed in the aggressive group and progressed in the standard group (−0.012 mm vs 0.038 mm; P 
doi_str_mv 10.1001/jama.299.14.1678
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James ; Lee, Elisa T ; Mete, Mihriye ; Poolaw, Bryce ; Ratner, Robert E ; Russell, Marie ; Silverman, Angela ; Stylianou, Mario ; Umans, Jason G ; Wang, Wenyu ; Weir, Matthew R ; Weissman, Neil J ; Wilson, Charlton ; Yeh, Fawn ; Zhu, Jianhui</creator><creatorcontrib>Howard, Barbara V ; Roman, Mary J ; Devereux, Richard B ; Fleg, Jerome L ; Galloway, James M ; Henderson, Jeffrey A ; Howard, Wm. James ; Lee, Elisa T ; Mete, Mihriye ; Poolaw, Bryce ; Ratner, Robert E ; Russell, Marie ; Silverman, Angela ; Stylianou, Mario ; Umans, Jason G ; Wang, Wenyu ; Weir, Matthew R ; Weissman, Neil J ; Wilson, Charlton ; Yeh, Fawn ; Zhu, Jianhui</creatorcontrib><description>CONTEXT Individuals with diabetes are at increased risk for cardiovascular disease (CVD), but more aggressive targets for risk factor control have not been tested. OBJECTIVE To compare progression of subclinical atherosclerosis in adults with type 2 diabetes treated to reach aggressive targets of low-density lipoprotein cholesterol (LDL-C) of 70 mg/dL or lower and systolic blood pressure (SBP) of 115 mm Hg or lower vs standard targets of LDL-C of 100 mg/dL or lower and SBP of 130 mm Hg or lower. DESIGN, SETTING, AND PARTICIPANTS A randomized, open-label, blinded-to-end point, 3-year trial from April 2003-July 2007 at 4 clinical centers in Oklahoma, Arizona, and South Dakota. Participants were 499 American Indian men and women aged 40 years or older with type 2 diabetes and no prior CVD events. INTERVENTIONS Participants were randomized to aggressive (n=252) vs standard (n=247) treatment groups with stepped treatment algorithms defined for both. MAIN OUTCOME MEASURES Primary end point was progression of atherosclerosis measured by common carotid artery intimal medial thickness (IMT). Secondary end points were other carotid and cardiac ultrasonographic measures and clinical events. RESULTS Mean target LDL-C and SBP levels for both groups were reached and maintained. Mean (95% confidence interval) levels for LDL-C in the last 12 months were 72 (69-75) and 104 (101-106) mg/dL and SBP levels were 117 (115-118) and 129 (128-130) mm Hg in the aggressive vs standard groups, respectively. Compared with baseline, IMT regressed in the aggressive group and progressed in the standard group (−0.012 mm vs 0.038 mm; P &lt; .001); carotid arterial cross-sectional area also regressed (−0.02 mm2 vs 1.05 mm2; P &lt; .001); and there was greater decrease in left ventricular mass index (−2.4 g/m2.7 vs −1.2 g/m2.7; P = .03) in the aggressive group. Rates of adverse events (38.5% and 26.7%; P = .005) and serious adverse events (n = 4 vs 1; P = .18) related to blood pressure medications were higher in the aggressive group. Clinical CVD events (1.6/100 and 1.5/100 person-years; P = .87) did not differ significantly between groups. CONCLUSIONS Reducing LDL-C and SBP to lower targets resulted in regression of carotid IMT and greater decrease in left ventricular mass in individuals with type 2 diabetes. Clinical events were lower than expected and did not differ significantly between groups. Further follow-up is needed to determine whether these improvements will result in lower long-term CVD event rates and costs and favorable risk-benefit outcomes. 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James</creatorcontrib><creatorcontrib>Lee, Elisa T</creatorcontrib><creatorcontrib>Mete, Mihriye</creatorcontrib><creatorcontrib>Poolaw, Bryce</creatorcontrib><creatorcontrib>Ratner, Robert E</creatorcontrib><creatorcontrib>Russell, Marie</creatorcontrib><creatorcontrib>Silverman, Angela</creatorcontrib><creatorcontrib>Stylianou, Mario</creatorcontrib><creatorcontrib>Umans, Jason G</creatorcontrib><creatorcontrib>Wang, Wenyu</creatorcontrib><creatorcontrib>Weir, Matthew R</creatorcontrib><creatorcontrib>Weissman, Neil J</creatorcontrib><creatorcontrib>Wilson, Charlton</creatorcontrib><creatorcontrib>Yeh, Fawn</creatorcontrib><creatorcontrib>Zhu, Jianhui</creatorcontrib><title>Effect of Lower Targets for Blood Pressure and LDL Cholesterol on Atherosclerosis in Diabetes: The SANDS Randomized Trial</title><title>JAMA : the journal of the American Medical Association</title><addtitle>JAMA</addtitle><description>CONTEXT Individuals with diabetes are at increased risk for cardiovascular disease (CVD), but more aggressive targets for risk factor control have not been tested. OBJECTIVE To compare progression of subclinical atherosclerosis in adults with type 2 diabetes treated to reach aggressive targets of low-density lipoprotein cholesterol (LDL-C) of 70 mg/dL or lower and systolic blood pressure (SBP) of 115 mm Hg or lower vs standard targets of LDL-C of 100 mg/dL or lower and SBP of 130 mm Hg or lower. DESIGN, SETTING, AND PARTICIPANTS A randomized, open-label, blinded-to-end point, 3-year trial from April 2003-July 2007 at 4 clinical centers in Oklahoma, Arizona, and South Dakota. Participants were 499 American Indian men and women aged 40 years or older with type 2 diabetes and no prior CVD events. INTERVENTIONS Participants were randomized to aggressive (n=252) vs standard (n=247) treatment groups with stepped treatment algorithms defined for both. MAIN OUTCOME MEASURES Primary end point was progression of atherosclerosis measured by common carotid artery intimal medial thickness (IMT). Secondary end points were other carotid and cardiac ultrasonographic measures and clinical events. RESULTS Mean target LDL-C and SBP levels for both groups were reached and maintained. Mean (95% confidence interval) levels for LDL-C in the last 12 months were 72 (69-75) and 104 (101-106) mg/dL and SBP levels were 117 (115-118) and 129 (128-130) mm Hg in the aggressive vs standard groups, respectively. Compared with baseline, IMT regressed in the aggressive group and progressed in the standard group (−0.012 mm vs 0.038 mm; P &lt; .001); carotid arterial cross-sectional area also regressed (−0.02 mm2 vs 1.05 mm2; P &lt; .001); and there was greater decrease in left ventricular mass index (−2.4 g/m2.7 vs −1.2 g/m2.7; P = .03) in the aggressive group. Rates of adverse events (38.5% and 26.7%; P = .005) and serious adverse events (n = 4 vs 1; P = .18) related to blood pressure medications were higher in the aggressive group. Clinical CVD events (1.6/100 and 1.5/100 person-years; P = .87) did not differ significantly between groups. CONCLUSIONS Reducing LDL-C and SBP to lower targets resulted in regression of carotid IMT and greater decrease in left ventricular mass in individuals with type 2 diabetes. Clinical events were lower than expected and did not differ significantly between groups. Further follow-up is needed to determine whether these improvements will result in lower long-term CVD event rates and costs and favorable risk-benefit outcomes. 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James ; Lee, Elisa T ; Mete, Mihriye ; Poolaw, Bryce ; Ratner, Robert E ; Russell, Marie ; Silverman, Angela ; Stylianou, Mario ; Umans, Jason G ; Wang, Wenyu ; Weir, Matthew R ; Weissman, Neil J ; Wilson, Charlton ; Yeh, Fawn ; Zhu, Jianhui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a286t-aa11eb135c30d9037195e3e6684de8b7856eb6f6de1881f7d0bb2c508b0cf6f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Adults</topic><topic>Antihypertensive Agents - therapeutic use</topic><topic>Atherosclerosis - ethnology</topic><topic>Atherosclerosis - etiology</topic><topic>Atherosclerosis - prevention &amp; control</topic><topic>Blood Pressure</topic><topic>Cardiovascular disease</topic><topic>Carotid Artery, Common - diagnostic imaging</topic><topic>Cholesterol</topic><topic>Cholesterol, LDL - blood</topic><topic>Clinical trials</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - ethnology</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Female</topic><topic>Humans</topic><topic>Hyperlipidemias - complications</topic><topic>Hyperlipidemias - drug therapy</topic><topic>Hypertension - complications</topic><topic>Hypertension - drug therapy</topic><topic>Hypertrophy, Left Ventricular - complications</topic><topic>Hypertrophy, Left Ventricular - diagnostic imaging</topic><topic>Hypolipidemic Agents - therapeutic use</topic><topic>Indians, North American</topic><topic>Low density lipoprotein</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Risk factors</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Howard, Barbara V</creatorcontrib><creatorcontrib>Roman, Mary J</creatorcontrib><creatorcontrib>Devereux, Richard B</creatorcontrib><creatorcontrib>Fleg, Jerome L</creatorcontrib><creatorcontrib>Galloway, James M</creatorcontrib><creatorcontrib>Henderson, Jeffrey A</creatorcontrib><creatorcontrib>Howard, Wm. 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James</au><au>Lee, Elisa T</au><au>Mete, Mihriye</au><au>Poolaw, Bryce</au><au>Ratner, Robert E</au><au>Russell, Marie</au><au>Silverman, Angela</au><au>Stylianou, Mario</au><au>Umans, Jason G</au><au>Wang, Wenyu</au><au>Weir, Matthew R</au><au>Weissman, Neil J</au><au>Wilson, Charlton</au><au>Yeh, Fawn</au><au>Zhu, Jianhui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Lower Targets for Blood Pressure and LDL Cholesterol on Atherosclerosis in Diabetes: The SANDS Randomized Trial</atitle><jtitle>JAMA : the journal of the American Medical Association</jtitle><addtitle>JAMA</addtitle><date>2008-04-09</date><risdate>2008</risdate><volume>299</volume><issue>14</issue><spage>1678</spage><epage>1689</epage><pages>1678-1689</pages><issn>0098-7484</issn><eissn>1538-3598</eissn><coden>JAMAAP</coden><abstract>CONTEXT Individuals with diabetes are at increased risk for cardiovascular disease (CVD), but more aggressive targets for risk factor control have not been tested. OBJECTIVE To compare progression of subclinical atherosclerosis in adults with type 2 diabetes treated to reach aggressive targets of low-density lipoprotein cholesterol (LDL-C) of 70 mg/dL or lower and systolic blood pressure (SBP) of 115 mm Hg or lower vs standard targets of LDL-C of 100 mg/dL or lower and SBP of 130 mm Hg or lower. DESIGN, SETTING, AND PARTICIPANTS A randomized, open-label, blinded-to-end point, 3-year trial from April 2003-July 2007 at 4 clinical centers in Oklahoma, Arizona, and South Dakota. Participants were 499 American Indian men and women aged 40 years or older with type 2 diabetes and no prior CVD events. INTERVENTIONS Participants were randomized to aggressive (n=252) vs standard (n=247) treatment groups with stepped treatment algorithms defined for both. MAIN OUTCOME MEASURES Primary end point was progression of atherosclerosis measured by common carotid artery intimal medial thickness (IMT). Secondary end points were other carotid and cardiac ultrasonographic measures and clinical events. RESULTS Mean target LDL-C and SBP levels for both groups were reached and maintained. Mean (95% confidence interval) levels for LDL-C in the last 12 months were 72 (69-75) and 104 (101-106) mg/dL and SBP levels were 117 (115-118) and 129 (128-130) mm Hg in the aggressive vs standard groups, respectively. Compared with baseline, IMT regressed in the aggressive group and progressed in the standard group (−0.012 mm vs 0.038 mm; P &lt; .001); carotid arterial cross-sectional area also regressed (−0.02 mm2 vs 1.05 mm2; P &lt; .001); and there was greater decrease in left ventricular mass index (−2.4 g/m2.7 vs −1.2 g/m2.7; P = .03) in the aggressive group. Rates of adverse events (38.5% and 26.7%; P = .005) and serious adverse events (n = 4 vs 1; P = .18) related to blood pressure medications were higher in the aggressive group. Clinical CVD events (1.6/100 and 1.5/100 person-years; P = .87) did not differ significantly between groups. CONCLUSIONS Reducing LDL-C and SBP to lower targets resulted in regression of carotid IMT and greater decrease in left ventricular mass in individuals with type 2 diabetes. Clinical events were lower than expected and did not differ significantly between groups. Further follow-up is needed to determine whether these improvements will result in lower long-term CVD event rates and costs and favorable risk-benefit outcomes. TRIAL REGISTRATION clinicaltrials.gov Identifier: NCT00047424</abstract><cop>United States</cop><pub>American Medical Association</pub><pmid>18398080</pmid><doi>10.1001/jama.299.14.1678</doi><tpages>12</tpages></addata></record>
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identifier ISSN: 0098-7484
ispartof JAMA : the journal of the American Medical Association, 2008-04, Vol.299 (14), p.1678-1689
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1538-3598
language eng
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source AMA Current Titles
subjects Adult
Adults
Antihypertensive Agents - therapeutic use
Atherosclerosis - ethnology
Atherosclerosis - etiology
Atherosclerosis - prevention & control
Blood Pressure
Cardiovascular disease
Carotid Artery, Common - diagnostic imaging
Cholesterol
Cholesterol, LDL - blood
Clinical trials
Diabetes
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - ethnology
Diabetes Mellitus, Type 2 - physiopathology
Female
Humans
Hyperlipidemias - complications
Hyperlipidemias - drug therapy
Hypertension - complications
Hypertension - drug therapy
Hypertrophy, Left Ventricular - complications
Hypertrophy, Left Ventricular - diagnostic imaging
Hypolipidemic Agents - therapeutic use
Indians, North American
Low density lipoprotein
Male
Middle Aged
Risk factors
Ultrasonography
title Effect of Lower Targets for Blood Pressure and LDL Cholesterol on Atherosclerosis in Diabetes: The SANDS Randomized Trial
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