The Cross-sectional and Longitudinal Associations of Diabetic Retinopathy With Cognitive Function and Brain MRI Findings: The Action to Control Cardiovascular Risk in Diabetes (ACCORD) Trial

被引:55
|
作者
Hugenschmidt, Christina E. [1 ]
Lovato, James F. [2 ]
Ambrosius, Walter T. [2 ]
Bryan, R. Nick [3 ]
Gerstein, Hertzel C. [4 ,5 ,6 ]
Horowitz, Karen R. [7 ]
Launer, Lenore J. [8 ]
Lazar, Ronald M. [9 ,10 ]
Murray, Anne M. [11 ,12 ]
Chew, Emily Y. [13 ]
Danis, Ronald P. [14 ]
Williamson, Jeff D. [1 ]
Miller, Michael E. [2 ]
Ding, Jingzhong [1 ]
机构
[1] Wake Forest Sch Med, Sect Gerontol & Geriatr Med, Dept Internal Med, Winston Salem, NC 27157 USA
[2] Wake Forest Sch Med, Dept Biostat Sci, Div Publ Hlth Sci, Winston Salem, NC USA
[3] Univ Penn, Sch Med, Dept Radiol, Philadelphia, PA 19104 USA
[4] McMaster Univ, Dept Med, Hamilton, ON, Canada
[5] McMaster Univ, Populat Hlth Res Inst, Hamilton, ON, Canada
[6] Hamilton Hlth Sci, Hamilton, ON, Canada
[7] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
[8] NIA, NIH, Bethesda, MD 20892 USA
[9] Columbia Univ Coll Phys & Surg, Dept Neurol, New York, NY 10032 USA
[10] Columbia Univ Coll Phys & Surg, Dept Neurosurg, New York, NY 10032 USA
[11] Hennepin Cty Med Ctr, Dept Med, Minneapolis, MN 55415 USA
[12] Univ Minnesota, Minneapolis, MN USA
[13] NEI, NIH, Bethesda, MD 20892 USA
[14] Univ Wisconsin, Sch Med & Publ Hlth, Dept Ophthalmol & Visual Sci, Madison, WI USA
基金
美国国家卫生研究院;
关键词
RETINAL MICROVASCULAR ABNORMALITIES; WHITE-MATTER LESIONS; ATHEROSCLEROSIS RISK; CEREBRAL ATROPHY; FOLLOW-UP; DECLINE; SIGNS; DETERMINANTS; IMPAIRMENT; RATIONALE;
D O I
10.2337/dc14-0502
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Longitudinal evidence linking diabetic retinopathy with changes in brain structure and cognition is sparse. We used data from the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial to determine whether diabetic retinopathy at baseline predicted changes in brain structure or cognition 40 months later. RESEARCH DESIGN AND METHODS Participants from the ACCORD-MIND and ACCORD-Eye substudies were included in analyses of cognition (n = 1,862) and MRI-derived brain variables (n = 432). Retinopathy was categorized as none, mild nonproliferative, or moderate/severe. Tests of cognition included the Mini-Mental State Examination (MMSE), Digit Symbol Substitution Test (DSST), Rey Auditory Verbal Learning Test, and Stroop test. Primary brain outcomes were gray matter and abnormal white matter volumes. RESULTS Baseline retinopathy was associated with lower gray matter volume (adjusted means of 470, 466, and 461 cm(3) for none, mild, and moderate/severe retinopathy, respectively; P = 0.03). Baseline retinopathy also predicted a greater change in MMSE and DSST scores at 40 months in each retinopathy category (MMSE: 0.20, 0.57, and 0.42, respectively [P = 0.04]; DSST: 1.30, 1.84, and 2.89, respectively [P = 0.01]). CONCLUSIONS Diabetic retinopathy is associated with future cognitive decline in people with type 2 diabetes. Although diabetic retinopathy is not a perfect proxy for diabetes-related brain and cognitive decline, patients with type 2 diabetes and retinopathy represent a subgroup at higher risk for future cognitive decline.
引用
收藏
页码:3244 / 3252
页数:9
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