Differential effects of white matter hyperintensity on geriatric depressive symptoms according to APOE-ε4 status

被引:1
作者
Chang, Ki Jung [1 ]
Hong, Chang Hyung [1 ,9 ,11 ]
Lee, Kang Soo [2 ]
Roh, Hyun Woong [1 ]
Choi, Seong Hye [3 ]
Kim, SeongYoon [4 ]
Na, Duk L. [5 ]
Seo, Sang Won [5 ]
Kim, Do-Kwan [6 ]
Kang, Dae Ryong [7 ]
Kim, Jayoun [7 ]
Lee, Yunhwan [8 ,9 ]
Kim, Si Heon [8 ]
Back, Joung Hwan [10 ]
Chung, Young Ki [1 ]
Lim, Ki Young [1 ]
Noh, Jai Sung [1 ]
Oh, Byung Hoon [12 ]
Son, Sang Joon [1 ]
机构
[1] Ajou Univ, Sch Med, Dept Psychiat, Suwon 443721, South Korea
[2] CHA Univ, Sch Med, Dept Psychiat, CHA Hosp, Bundang, South Korea
[3] Inha Univ, Coll Med, Dept Neurol, Inchon, South Korea
[4] Asan Med Ctr, Dept Psychiat, Seoul, South Korea
[5] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Neurol, Seoul, South Korea
[6] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Psychiat, Seoul, South Korea
[7] Ajou Univ, Sch Med, Dept Biostat, Suwon 443721, South Korea
[8] Ajou Univ, Sch Med, Dept Prevent Med & Publ Hlth, Suwon 443721, South Korea
[9] Ajou Univ, Med Ctr, Inst Aging, Suwon 443721, South Korea
[10] Natl Hlth Insurance Serv, Hlth Insurance Policy Res Inst, Seoul, South Korea
[11] Ajou Univ Hosp, Memory Impairment Ctr, Suwon, South Korea
[12] Yonsei Univ, Sch Med, Dept Psychiat, Seoul 120749, South Korea
关键词
LATE-LIFE DEPRESSION; DEFINED VASCULAR DEPRESSION; APOLIPOPROTEIN-E GENOTYPE; APOE EPSILON-4 ALLELE; CEREBROVASCULAR-DISEASE; RISK-FACTORS; METAANALYSIS; LESIONS; ADULTS; DEEP;
D O I
10.1016/j.jad.2015.08.032
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: We aimed to examine differential effects of WMH on progression of depressive symptoms according to APOE 84 status in the elderly. Methods: We obtained data from elderly Korean subjects (n=707) aged 60 years or older at baseline from the CREDOS study from November 2005 to July 2014. A linear mixed model stratified according to APOE genotype (APOE 84 carrier vs. non-carrier) was constructed using GDS score as a primary outcome and degree of overall, deep, periventricular WMH evaluated by a visual rating scale as a risk factor of interest. We also tested interaction between APOE 84, WMH and time as predictors of clinical progression on GDS scores to examine the moderating effect of APOE 84 allele on the relationship between degree of WMH and progression of geriatric depressive symptoms. Results: The mean (SD) follow-up duration of the participants was 2.0 (0.8) years. Among APOE 84 carriers, a severe degree of overall and deep WMH, but not periventricular WMH, predicted progression of geriatric depressive symptoms (overall WMH: coefficient=0.96, p=0.010; deep WMH: 0.87, p =0.016). There were significant interaction between APOE 84, degree of WMH and time in predicting GDS increase (5df, F=2.28, p = 0.046). Limitations: Only subjects seeking medical attention and with follow-up measurements were enrolled in this study. Specific location of WMH and use of antidepressant were uncontrolled. Conclusions: Considering biological markers such as degree of WMH and APOE 84 status may be clinically relevant to predicting progression of geriatric depressive symptoms. (c) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 34
页数:7
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