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老年抑郁症的脑功能状态和血脂水平及相关心理社会因素研究
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摘要
目的:探讨老年抑郁症脑电及单胺类神经递质和血脂水平变化及相关的心理-社会影响因素的影响,以提高对老年抑郁症的认识,为临床治疗和预防提供可靠的理论依据。
     方法:采用病例-对照研究设计方案。按CCMD-3心境障碍抑郁发作诊断标准,收集30例60岁以上首次发作的抑郁患者(抑郁组),34名健康老年人(对照组)。对入选者先进行研究告知,同意后即开始进行一般情况调查表、生活事件量表(LES)、简易应对方式问卷(SCSQ)、艾森克个性问卷(EPQ)、社会支持评定量表(SSRS)进行评定,用以分析老年抑郁症的个体心理社会因素。其次收集个体近一周血生化检查中的甘油三酯(TG)、血清胆固醇(CHO)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)。再用脑电超慢涨落技术(ET)对脑电、熵值、脑功能状态、单胺类神经递质变化进行检测。把两组的结果进行对比,以分析老年抑郁症的脑功能状态、血脂水平和相关的促发因素。
     结果:1.脑功能方面:(1)抑郁组的脑功能优势涨落平均功率空间的前后功率梯度逆转数明显高于对照组,左右功率梯度逆转数对照组明显高于抑郁组(P<0.001)。(2)抑郁组8Hz优势几率明显高于对照组,10Hz优势几率低于对照组(P<0.05);抑郁组4个脑区的熵值均高于对照组(P<0.01)。(3)抑郁组单胺类神经递质去甲肾上腺素(NE)、5-羟色胺(5-HT)、多巴胺(DA)激活水平均低于对照组(P<0.001,P<0.001,P<0.01)。
     2.生化方面:(1)抑郁组的甘油三酯(TG)水平高于对照组(P<0.01),血清胆固醇(CHO)及低密度脂蛋白胆固醇(LDL-C)水平低于对照组(P<0.05, P<0.001),高密度脂蛋白胆固醇(HDL-C)水平两组无显著性差异(P>0.05)。(2)抑郁组单胺类神经递质与血脂水平之间的关系:CHO水平与NE值正相关(r=0.509, P<0.05),CHO水平与5-HT值正相关(r=0.454, P<0.05)。
     3.认知和应对方面:(1)抑郁组认知(MMSE)总分显著低于对照组(P<0.001),因子即刻回忆和延迟回忆分也显著低于对照组(P<0.01,P<0.001)。(2)在应对方式中,抑郁组积极应对维度小于对照组(P<0.001),消极应对维度多于对照组(P<0.01)。
     4.受社会因素影响方面:(1)抑郁组生活事件数量、强度总分及负性生活事件数量、强度值均显著高于对照组(P<0.001)。(2)SSRS评定显示抑郁组社会支持总分、对支持的利用度及主观支持分低于对照组(P<0.001,P<0.001,P<0.01)。
     5.个性因素影响方面:抑郁组神经质、精神质得分高于对照组(P<0.01,P<0.001)。
     结论:(1)老年抑郁症患者脑功率的逆转率高于对照组;α波慢化、认知参量10Hz明显减少、脑有序性降低;其脑功能状态是混沌的。(2)老年抑郁症患者血脂异常,其中低浓度血清胆固醇与老年抑郁症具有相关性。(3)老年抑郁症组存在着较高的认知功能异常:即刻回忆及延迟回忆能力低于对照组;负性生活事件和社会支持少在老年抑郁症的发生中起着重要作用;高精神质和高神经质的老年人更易患抑郁症。(4)老年抑郁症状是神经生物学因素和社会心理学因素共同作用的结果,即心理社会因素、生化代谢异常、大脑功能三方面相互联系,相互影响。
Objective: This study attempted to explore brain electrobiological activity, monoamine neurotransmitters, serum lipids and relative psychosocial factors of elderly depressed patents so as to deepen the understanding of the elderly depression and provide reliably a theoretical basis for treatment and prevention.
     Methods: The method adopted in this paper was case-controlled design. 30 elderly depressive people (aged over 60) (depression group) with the first episode of depression diagnosed according to CCMD-3, and 34 elderly healthy people (aged over 60) (control group) were investigated. All subjects were informed and agreed and then they were interviewed in self-designed general information questionnaire, HAMD, HAMA, MMSE, LES, SCSQ, SSRS and EPQ to analyze the psychosocial factors of elderly depressed people. Secondly, all subjects were collected plasma triglyceride (TG), serum cholesterol (CHO), serum high density lipoprotein-cholesterol (HDL-C) and low density lipoprotein-cholesterol (LDL-C) for nearly a week. Thirdly, the electrobiological activity, entropy value, brain function state and the change of monoamine neurotransmitters of subjects were detected by encephalof luctuography technology (ET).Then comparison of two groups were carried out to analyze the brain function, serum lipids and relative factors of elderly depressed patents,
     Results: 1. Brain fuction:(1)The anterior-posterior reversal rates of dominant power in encephalofluctuograph were higher in depression group than those of control group and the left-right reversal rates were higher in control group than those of depression group(P<0.001).(2)The depression group showed significantly more 8Hz activity than that of control (P<0.05) . The depression group showed significantly less 10Hz activity than that of control group (P<0.05). The entropy value of the depression group showed higher than that of the control group(P<0.01).(3) The monoamine neurotransmitters value (NE, 5-HT and DA) in depression group were lower than those of control group(P<0.001,P<0.001,P<0.01).
     2. Biochemistry:(1)Triacylglycerol (TG) in depression group was higher than that in control group(P<0.01), cholesterol (CHO) and low density lipoprotein-cholesterol(LDL-C) in depression group were lower than those in control group(P<0.05, P<0.001),and serum high density lipoprotein-cholesterol (HDL-C)in two groups showed no statistical significant deviation(P>0.05). (2) The relationship between monoamine neurotransmitters and serum lipids: significantly positive correlations existed in elderly depressed group between CHO and NE(r=0.509, P<0.05),CHO and 5-HT levels respectively(r=0.454, P<0.05).
     3. Cognition and Coping:(1) The scores of MMSE were significantly lower in depression group than control group(P<0.001), the scores of immediate recall and long-delayed recall were significantly lower in depression group than those in control group(P<0.01,P<0.001). (2) The scores of positive coping were significantly lower in depression group than those in control group(P<0.001),The scores of passive coping were significantly higher in depression group than those in control group(P<0.01).
     4. Social factors: (1) The account of life events, the scores of life events, the account of negative life events and the scores of negative life events were significantly higher in depression group than those in control group(P<0.001). (2)There were lower scores of social support and its use ,subjective support in depression group than those in control group(P<0.001, P<0.001, P<0.01).
     5. Personality factors: The scores of neuroticism and psychoticism were significantly higher in depression group than those in control group.
     Conclusion: (1) The brain function of elderly depressed patients was chaos: cerebral power reversed, more slow alpha waves, the orderliness decreased. (2) The serum lipids of elderly depressed patients changed, there was significant relationship between low serum cholesterol and elderly depression. (3) Elderly depressed patients had more severe cognitive impairment, negative life events and poorer social support played an important role in the occurrence of elderly depression, elderly people with higher neuroticism and psychoticism were likelier to develop depression. (4) The elderly depression resulted from the reaction between neurobiological and psychosocial factors, and it was interactive among psychosocial factors, the change of Biochemical Metabolism and brain function.
引文
[1] Newman SC, Sheldon CT, Bland RC. Prevalence of depression in an elderly community sample: a comparison of GMS-AGECAT and DSM-Ⅳdiagnostic criteria [J]. Psychol Med, 1998, 28(6):1339-1345.
    [2] 王世忠, 杨向东, 朱秀琳. 老年抑郁症及相关问题 [J]. 中国误诊学杂志, 2001, 1(9):1372-1374.
    [3] Holley C, Murrell SA, Mast BT. Psychosocial and vascular risk factors for depression in the elderly [J]. Am J Geriatr Psychiatry. 2006, 14(1):84-90.
    [4] Monfort JC. The difficult elderly patient: cureable hostile depression or personality disorder [J]? Int Psychogeriatr, 1995, 7(Suppl):95-111.
    [5] Heun R, Hein S. Risk factors of major depression in the elderly [J]. Eur Psychiatry, 2005, 20(3):199-204.
    [6] Syed A, Chatfield M, Matthews F, et al. Depression in the elderly: pathological study of raphe and locus ceruleus [J]. Neuropathol Appl Neurobiol, 2005, 31(4):405-413.
    [7] Drevets WC. Functional neuroimaging studies of depression: the anatomy of melancholia [J]. Annu Rev Med, 1998, 49:341- 361.
    [8] Soares JC, Mann JJ. The functional neuroanatomy of mood disorders [J]. J Psychiatr Res, 1997, 31(4):393-432.
    [9] Soares JC, Mann JJ. The anatomy of mood disorders--review of structural neuroimaging studies [J]. Biol Psychiatry, 1997, 41(1): 86- 106.
    [10] Rogers MA, Bradshaw JL, Pantelis C, et al. Frontostriatal deficits in unipolar major depression [J]. Brain Res Bull, 1998, 47(4):297- 310.
    [11] Kim JS, Choi- Kwon S. Poststroke depression and emotional incontinence: correlation with lesion location [J]. Neurology, 2000, 54(9):1805-1810.
    [12] Rogers MA, Kasai K, Koji M, et al. Executive and prefrontal dysfunction in unipolar depression: a review of neuropsychological and imaging evidence [J]. Neurosci Res, 2004, 50(1):1-11.
    [13] Barnhart WJ, Makela EH, Latocha. MJ. SSRI-induced apathy syndrome: a clinical review [J]. J Psychiatr Pract, 2004, 10(3):196-199.
    [14] Yatham LN, Liddle PF, Shiah Is, et al. Brain serotonin2 receptors in major depression: a positron emission tomography study [J]. Arch Gen Psychiatry, 2000, 57(9):850-8.
    [15] Dubini A, Bosc M, Polin V. Do noradrenaline and serotonin differentially affect socialmotivation and behaviour [J]? Eur Neuropsychopharmacol, 1997(Suppl):49-55.
    [16] Olusi SO, Fido AA.Serum lipid concentrations in patients with major depressive disorder [J].Biol Psychiatry, 1996, 40(11):1128-31.
    [17] Aijanseppa S, Kivinen P, Helkala EL, et a1.Serum cholesterol and depressive symptoms in elderly Finnish men [J]. Int J Geriatr Psychiatry, 2002, 17(7):629-34.
    [18] Maes M, Smith R, Christophe A, et a1. Lower serum high-density lipoprotein cholesterol (HDL-C) in major depression and in depressed men with serious suicidal attempts: relationship with immune-inflanmmtroy markers [J].Acta Psychiatr Scand, 1997, 95(3):212-21.
    [19] Baldwin RC, Tomenson B. Depression in later life. A comparison of symptoms and risk factors in early and late onset cases [J]. Br J Psychiatry, 1995, 167(5): 649 - 652.
    [20] 梅磊. ET--脑功能研究新技术 [M]. 北京: 国防工业出版社, 1995:288— 300; 356— 362.
    [21] 张明园主编 . 精神科评定量表手册 [M]. 湖南:湖南科学技术出版社 , 1998:184-188.
    [22] Greenwald BS , Kramer-Ginsberg E , Bogerts B, et al. Qualitative magnetic resonance imaging findings in geriatric depression. Possible link between later-onset depression and Alzheimer’s disease [J]? Psychol Med, 1997, 27 (2):421-31.
    [23] Motomura E, Inui K, Nakase S, et al. Late-onset depression: can EEG abnormalities help in clinical sub-typing [J]? J Affect Disord, 2002,68(1):73-9.
    [24] 周传岱, 翟怡娟, 刘月红, 等.261名歼击飞行员脑波α频段涨落图特征的研究[J], 航天医学与医学工程. 1998, 11(1):1l一15.
    [25] 陈康宁, 陈胜利, 罗芳, 等. 脑涨落图中神经递质变化与脑卒中后抑郁障碍[J]. 中国临床康复, 2005, 9(16):118-119.
    [26] Rabasseda X. Duloxetine: A new serotonin/noradrenaline reuptake inhibitor for the treatment of depression [J]. Drugs Today, 2004, 40(9):773-90.
    [27] Bunney WE Jr, Davis JM. Norepinephrine in depressive reactions. A review [J]. Arch Gen Psychiatry, 1965, 13(6):483-494.
    [28] Ressler KJ, Nemeroff CB. Role of serotogergic and noradrenergic systems in the pathophysiology of depression and anxiety disorders [J]. Depress Anxiety, 2000, 12(suppl l):2-19.
    [29] Goodwin FK, Jamison KR. Manic-depressive illness [M]. New York: Oxford University Press, 1990:416-441.
    [30] Siever LJ, Uhde TW, Silberman EK, et al. Evaluation of alpha-adrenergic responsiveness to clonidine challenge and noradrenergic metabolism in the affective disorders and their treatment [J]. Psychopharmacol Bull, 1982, 18(4):118-119.
    [31] Esler M, Turbott J, Schwarz R, et al. The peripheral kinetics of norepinephrine in depressive illness [J]. Arch Gen Psychiatry, 1982, 39(3):295-300.
    [32] Coppen A, Shaw DM. Mineral metabolism in melancholia [J]. Br Med J. 1963, 2(5370):1439-44.
    [33] Sarnyai Z, Sibille EL, Pavlides C, et al. Impaired hippocampal-dependent learning and functional abnormalities in the hippocampus in mice lacking serotonin (1A) receptors [J]. Proc Natl Acad Sci USA, 2000, 97(26):14731-14736.
    [34] Wu J, Kramer GL, Kram M, et al. Serotonin and learned helplessness: a regional study of 5-HT1A, 5-HT2A receptors and the serotonin transport site in rat brain [J]. J Psychiatr Res, 1999, 33(1):17-22
    [35] Sheline YI, Mintun MA, Barch DM, et al. Decreased hippocampal 5-HT (2A) receptor binding in older depressed patients using [18F] altanserin positron emission tomography [J]. Neuropsychopharmacology, 2004, 29(12):2235-2241.
    [36] Molander L, Randrup A. Effects of thymoleptics on behaviour associated with changes in brain dopamine. I. Potentiation of dopa-induced gnawing of mice [J]. Psychopharmacologia, 1976, 45(3):261-5.
    [37] Schwaninger M, Schofl C, Blume R, et al. Inhibition by antidepressant drugs of cyclic AMP response element-binding protein/cyclic AMP response element-directed gene transcription [J]. Mol Pharmacol. 1995, 47(6):1112-8.
    [38] Huang TL, Wu SC, Chiang YS, et al. Correlation between serum lipid, lipoprotein concentrations and anxious state, depressive state or major depressive disorder [J]. Psychiatry Res, 2003, 118(2):147-53.
    [39] Ledochowski M, Murr C, Sperner-Unterweger B, et al. Association between increased serum cholesterol and signs of depressive mood [J]. Clin Chem Lab Med, 2003, 41(6):821-4.
    [40] Beasley CL, Honer WG, Bergmann K, et al. Reductions in cholesterol and synaptic markers in association cortex in mood disorders [J]. Bipolar Disord, 2005, 7(5):449-55.
    [41] Reveley MA. Cholesterol and mental disorder [J]. Br J Psychiatry, 1996, 169(6): 682-9.
    [42] Engelberg H. Low cholesterol and suicide [J]. Lancet, 1992, 339(8795):727-9.
    [43] Terao T, Yoshimura R, Ohmori O, et al. Effect of serum cholesterol levels on meta-chlorophenylpiperazine-evoked neuroendocrine responses in healthy subjects [J]. Biol Psychiatry, 1997, 41(9):974-8.
    [44] Van Heeringen K. The neurobiology of suicide and suicidality [J]. Can J Psychiatry, 2003, 48(5): 292-300.
    [45] Cole MG, Dendukuri N. Risk factors for depression among elderly community subjects: a systematic review and meta-analysis [J]. Am J Psychiatry, 2003, 160(6):1147-1156.
    [46] Steffens DC, Skoog I, Norton MC, et al. Prevalence of depression and its treatment in an elderly population: the Cache County Study [J]. Arch Gen Psychiatry, 2000, 57(6):601-607.
    [47] Unverzagt FW, Gao S, Baiyewu O, et al. Prevalence of cognitive impairment: data from the Indianapolis Study of Health and Aging [J]. Neurology, 2001, 57(9):1655-1662.
    [48] Bassuk S, Berkman LF, Wypij D. Depressive symptomatology and incident cognitive decline in an elderly community sample [J]. Arch Gen Pschiatry, 1998, 55(12):1073-1081.
    [49] Geerlings MI, Schoevers RA, Beekman AT, et al. Depression and risk of cognitive decline and Alzheimer’s disease. Result of two prospective community-based studies in The Netherlands [J]. Br J Psychiatry, 2000, 176:568-575.
    [50] Paterniti S, Verdier-Taillefer MH, Dufouil C, et al. Depressive symptoms and cognitive decline in elderly people. Longitudinal study [J]. Br J Psychiatry, 2002, 181:406-410.
    [51] Vinkers DJ, Gussekloo J, Stek ML, et al. Temporal relation between depression and cognitive impairment in old age: prospective population based study [J]. BMJ, 2004, 329(7471):881.
    [52] Belanoff JK, Kalehzan M, Sund B, et al. Cortisol activity and cognitive changes in psychotic major depression [J]. Am J Psychiatry, 2001, 158 (10): 1612 – 1616.
    [53] Papps BP, Shajahan PM, Ebmeier KP, et al. The effects of noradrenergic re-uptake inhibition on memory encoding in man [J]. Psychopharmacology, 2002, 159 (3): 311 – 318.
    [54] Dalgard OS, Bjork S, Tambs K. Social support, negative life events and mental health [J]. Br J Psychiatry, 1995, 166(1):29-34.
    [55] Margitics F. Role of protective factors in the development of depression [J]. PsychiatrHung, 2005, 20(3):224-37.
    [56] 蔡焯基主编. 抑郁症基础与临床[M]. 第2版, 北京:科学技术出版社, 2001:85.
    [57] Kuehner C, Buerger C.Determinants of subjective quality of life in depressed patients: the role of self-esteem, response styles, and social support [J]. J Affect Disord, 2005, 86(2-3):205-213.
    [58] 吕永良 , 吴爱勤 . 老年抑郁症的研究进展 [J]. 临床精神医学杂志 , 2003, 13(5):306-307.
    [59] Kobasa SC. Stressful life events, personality, and health: an inquiry into hardiness [J]. J Pers Soc Psychol, 1979, 37(1):1-11.
    [60] Cooke DJ. Psychosocial variables and the life event/anxiety-depression link. A community study [J]. Acta Psychiatr Scand, 1986, 74(3):281-291.
    [61] Ormel J, Oldehinkel AJ, Brilman EI. The interplay and etiological continuity of neuroticism, difficulties , and life events in the etiology of major and subsyndromal , first and recurrent depressive episodes in later life [J]. Am J Psychiatry, 2001, 158(6):885-91.
    [62] Mojtabai R, Olfson M. Major depression in community-dwelling middle-aged and older adults: prevalence and 2-and 4-year follow-up symptoms [J]. Psychol Med, 2004, 34(4):623-634.
    [63] Djernes JK. Prevalence and predictors of depression in population of elderly: a review [J]. Acta Psychiatr Scand, 2006, 113(5):372-387.
    [1] World Health Organization. The World Health Report 2002: Reducing Risks, Promoting Health Life[R]. Geneva, Switzerland: World Health Organization, 2002.
    [2] Alexpoulos GS. Depression in the elderly [J]. The Lancet, 2005, 1965(4):1961-1970.
    [3] Van den Berg MD, Oldehinkel AJ, Bouhuys AL, et al. Depression in later life: three etiologically different subgroups [J]. J Affect Disord, 2001, 65(1):16-29.
    [4] 沈渔村主编. 精神病学[M]. 第3 版, 北京:人民卫生出版社, 1994:631.
    [5] 全国情感障碍亚型家系研究协作组. 单相抑郁与双相情感障碍遗传效应及方式的对照研究 [J]. 中华精神科杂志, 1997, 30(4):199-202.
    [6] Holmes C, Russ C, Kirov G, et al. Apolipoprotein E: Depressive illness, depressive symptoms, and Alzheimer’s disease [J]. Biol Psychiatry, 1998, 43(3): 159-164.
    [7] Healy D, Leonard BE. Monoamine transport in depression: kinetics and dynamics [J]. J Affect Disord, 1987, 12(2):91-103.
    [8] Manji HK, Moore GJ, Rajkowska G. Neuroplasticity and cellular resilience in mood disorders [J]. Mol Psychiatry, 2000,5(6):578-593.
    [9] Lanfumey L, Mannoury La Cour C, Frogger N, et al. 5-HT-HPA interaction in two models of transgenic mice relevant to major depression [J]. Neurochem Res, 2000, 25(9-10):1199-1206.
    [10] Rupniak NM, Kramer MS. Discovery of the antidepressant and anti-emetic efficacy of substance P receptor (NK1) antagonists [J]. Trends Pharmacol Sci, 1999, 20(12):485-490.
    [11] 代 英 杰 , 范 骏 , 孟 昭 义 . 抑 郁症的 神经生化特征及进 展 [J]. 中 国 临 床 康复,7(30):4126-4127.
    [12] Bunney WE Jr, Davis JM. Norepinephrine in depressive reactions. A review [J]. Arch Gen Psychiatry, 1965, 13(6):483-494.
    [13] Ressler KJ, Nemeroff CB. Role of serotogergic and noradrenergic systems in the pathophysiology of depression and anxiety disorders [J]. Depress Anxiety, 2000, 12(Suppl 1):2-19.
    [14] Goodwin FK, Jamison KR. Manic-depressive illness [M]. New York: Oxford University Press, 1990:416-441.
    [15] Siever LJ, Uhde TW, Silberman EK, et al. Evaluation of alpha-adrenergic responsiveness to clonidine challenge and noradrenergic metabolism in the affectivedisorders and their treatment [J]. Psychopharmacol Bull, 1982, 18(4):118-119.
    [16] Esler M, Turbott J, Schwarz R, et al. The peripheral kinetics of norepinephrine in depressive illness [J]. Arch Gen Psychiatry, 1982, 39(3):295-300.
    [17] Coppen A, Shaw DM. Mineral metabolism in melancholia [J]. Br Med J. 1963, 2(5370):1439-44.
    [18] Sarnyai Z, Sibille EL, Pavlides C, et al. Impaired hippocampal-dependent learning and functional abnormalities in the hippocampus in mice lacking serotonin (1A) receptors [J]. Proc Natl Acad Sci USA, 2000, 97(26):14731-6.
    [19] Wu J, Kramer GL, Kram M, et al. Serotonin and learned helplessness: a regional study of 5-HT1A, 5-HT2A receptors and the serotonin transport site in rat brain [J]. J Psychiatr Res, 1999, 33(1):17-22.
    [20] Olusi SO, Fido AA. Serum lipid concentrations in patients with major depressive disorder [J]. Biol Psychiatry, 1996, 40(11):1128-31.
    [21] Aijanseppa S, Kivinen P, Helkala EL, et a1. Serum cholesterol and depressive symptoms in elderly Finnish men [J]. Int J Geriatr Psychiatry, 2002, 17(7):629-34.
    [22] Maes M, Smith R, Christophe A, et a1. Lower serum high-density lipoprotein cholesterol (HDL-C) in major depression and in depressed men with serious suicidal attempts: relalonship with immune-inflanmmtroy markers [J]. Acta Psychiatr Scand, 1997, 95(3):212-21.
    [23] Seidel A, Arolt V, Hunstiger M, et al. Cytokine production and serum proteins in depression [J]. Scand J Immunol, 1995, 41(6):534-8.
    [24] Dentino AN , Pieper CF, Rao MK, et al. Association of interleukin-6 and other biologic variables with depression in older people living in the community [J]. J Am Geriatr Soc, 1999, 47(1): 6-11.
    [25] Owen BM, Eccleston D, Ferrier IN, et al. Raised levels of plasma interleukin-1beta in majo r and postviral depression [J]. Acta Psychiatr Scand, 2000, 103(3):226-8.
    [26] Patten SB. Exogenous corticosteroids and major depression in the general population [J]. J Psychosom Res, 2000, 49(6): 447-9.
    [27] McCleery JM, Goodwin GM. H igh and low neuroticism predict different cortisol responses to the combined dexamethasone--CRH test [J]. Biol Psychiatry, 2001, 49(5): 410-5.
    [28] Coplan JD, Wolk SI, Goetz RR, et al. Nocturnal growth hormone secretion studies in adolescents with or without major depression re-examined: integration of adult clinical follow-up data [J]. Biol Psychiatry, 2000, 47(7):594-604.
    [29] Birmaher B, Dahl RE, Williamson DE, et al. Growth hormone secretion in children and adolescents at high risk for major depressive disorder [J]. Arch Gen Psychiatry, 2000, 57(9):867-72.
    [30] Drevets WC. Functional neuroimaging studies of depression: the anatomy of melancholia [J]. Annu Rev Med, 1998, 49:341-61.
    [31] Soares JC, Mann JJ. The functional neuroanatomy of mood disorders [J]. J Psychiatr Res, 1997, 31(4):393-432.
    [32] Soares JC, Mann JJ. The anatomy of mood disorders--review of structural neuroimaging studies [J]. Biol Psychiatry, 1997, 41(1): 86-106.
    [33] Rogers MA, Bradshaw JL, Pantelis C, et al. Frontostriatal deficits in unipolar major depression [J]. Brain Res Bull, 1998, 47(4):297- 310.
    [34] Kim JS, Choi- Kwon S. Poststroke depression and emotional incontinence: correlation with lesion location [J]. Neurology, 2000, 54(9):1805-10.
    [35] Harrison PJ. The neuropathology of primary mood disorder [J]. Brain, 2002, 125: 1428-49.
    [36] Thomas, AJ, O'Brien JT, Davis S, et al. Ischemic basis for deep white matter hyperintensities in major depression: a neuropathological study [J]. Arch Gen Psychiatry, 2002, 59(9):785-92.
    [37] Taylor WD, MacFall JR Payne ME, et al: Late-life depression and microstructural abnosmalities in dorsolateral prefrontal cortex white matter [J]. Am J Psychiatry, 2004, 161(7): 1293-6.
    [38] Nebes RD, Vora IJ, Meltzer CC, et al. Relationship of deep white matter hyperintensities and apolipoprotein E genotype to depressive symptoms in older adults without clinical depression [J]. Am J Psychiatry, 2001, 158(6):878-84.
    [39] Lesser IM, Boone KB, Mehringer CM, et al. cognition and white matter hyperintensities in older depressed patients [J]. Am J psychiatry, 1996, 153(10):1280 - 7.
    [40] Kalayam B, Alexopoulos GS. Prefrontal dysfunction and treatment response in geriatric depression [J]. Arch Gen Psychiatry, 1999, 56(8): 713-8.
    [41] Baldwin RC, Tomenson B. Depression in later life. A comparison of symptoms and risk factors in early and late onset cases [J]. Br J Psychiatry, 1995, 167(5): 649-52.
    [1] Nakasto YR, Carnes BA. Health promotion in older adults. Promoting successful aging in primary care settings [J]. Geriatrics, 2006, 61(4):27-31.
    [2] Monfort JC. The difficult elderly patients: Curable hostile depression or personality disorder [J]? Int Psychogeriatr, 1995, 7(Suppl):95-111.
    [3] 宁自衡, Jose F, 林中宝, 等. 澳门老年人抑郁症状及其影响因素调查分析 [J].中国心理卫生杂志, 2001, 15(5):331—334.
    [4] 孟琛, 项曼君. 北京老年人的抑郁状况调查及CES-D的结构分析[J]. 中国心理卫生杂志, 1997, 11 (1):55—58.
    [5] Djernes JK. Prevalence and predictors of depression in population of elderly: a review [J]. Acta Psychair Scand, 2006, 113(5):372-87.
    [6] 范振国, 陈加美, 卢胜利, 等. 湖州市城区老年抑郁症的流行病学调查 [J]. 中华老年医学杂志, 1994, 13(2):73—75.
    [7] Fuhrer R, Dufouil C, Antonucci TC, et al. Psychological disorder and mortality in French older adults: do social relations modify the association [J]? Am J Epidemiol, 1999, 149(2):116-26.
    [8] 王红, 周铌, 左俊荚, 等. 老年抑郁症的心理社会因素研究进展 [J]. 老年医学与保健,2005, 11(3):184-186.
    [9] Bruce ML. Psychosocial risk factors for depressive disorders in late life [J]. Biol Psychiatry, 2002, 52(3):175-84.
    [10] Heide W, Kompf D. Combined deficits of saccades and visuo-spatial orientation after cortical lesions [J]. Exp Brain Res, 1998, l23 (1-2):164-71.
    [11] Ormel J, Oldehinkel AJ, Brilman EI. The interplay and etiological continuity of neuroticism, difficulties, and life events in the etiology of major and subsyndroma1, first and recurrent depressive episodes in later life [J] . Am J Psychiatry, 2001, 158(6):885-91.
    [12] Ormel J, Wohlfarth T. How neuroticism, long-term difficulties, and life situation change influence psychological distress: a longitudinal mode1 [J]. J Pers Soc Psychol, 1991, 60(5):744-55.
    [13] van Grootheest DS, Beekman AT, Broese van Groenou MI, et al. Sex difference in depression after widowhood. Do men suffer more [J]? Soc Psychiatry Psychiar Epidemiol, 1999, 34(7):391-98.
    [14] 张明园. 生活事件量表[J]. 上海精神医学,1990:60.
    [15] Lawhorne L. Depression in the older adult [J]. Prim Care, 2005, 32(3):777-92.
    [16] Naqvi TZ, Naqvi SS, Merz CN. Gender differences in the link between depression and cardiovascular disease [J]. Psychosom Med, 2005, 67(Suppl 1):S15-8.
    [17] 于欣, 田运华, 沈渔村. 抑郁症与心脏疾病[J]. 中国心理卫生杂志, 1996(增刊): 22-24.
    [18] Musselman DL, Evans DL, Nemeroff CB. The relationship of depression to cardiovascular disease: epidemiology, biology, and treatment [J]. Arch Gen Psychiatry, 1998, 55(7):580-92.
    [19] 黄佐, 樊民, 吴宗贵. 冠心病患者抑郁症状与冠状动脉病变的关系[J]. 中华心血管病杂志, 2003, 31(5):329.
    [20] Glassman AH, Shapiro PA. Depression and course of coronary artery disease [J]. Am J Psychiatry, 1998, 155(1):4-11.
    [21] Davies SJ, Jackson PR, Potokar J, et al. Treatment of anxiety and depressive disorders in patients with cardiovascular disease [J]. BMJ, 2004, 328(7445):939-43.
    [22] Eng PM, Fitzmautice G, Rimm EB, et al. Anger expression and risk of stroke and coronary heart disease among male health professionals [J]. Psychosom Med, 2003, 65(1):100-10.
    [23] Gitay EJ, Geleijnse JM, Zitman FG., et al. Dispositional optimism and all-cause and cardiovascular mortality in a prospective cohort of elderly dutch men and women [J]. Arch Gen Psychiatry, 2004, 61(11):1126-35.
    [24] Barefoot JC , Brummett BH , Clapp-Channning NE , et al. Moderators of the effect of social support on depressive symptoms in cardiac patients[J ] . Am J Cardiol, 2000, 86(4):438-42.
    [25] Charney DS, Menkes DB, Heninger GR. Receptor sensitivity and the mechanism of action of antidepressant treatment [J]. Arch Gen Psychiatry, 1981, 38(10):1160-80.
    [26] Murck H, Held K. The renin-angiotensin-aldosterone system in patients with depression compared to controls-a sleep endocrine study [J]. BMC Psychiatry, 2003, 3:15-18.
    [27] Cole MG, Dendukuri N. Risk factors for depression among elderly community subjects: a systematic review and meta-analysis [J]. Am J Psychiatry, 2003, 160(6):1147-56.
    [28] Sleight AJ, Boess FG, Bos M, et al. The putative 5-ht6 receptor: localization and function [J]. Ann N Y Acad Sci, 1998, 861:91-6.
    [29] 刘欣,刘振东. 抑郁症患者认知功能障碍的比较研究[J]. 中国临床康复,2004, 5760-1.
    [30] Steffens DC, Skoog I, Norton MC, et al. Prevalence of depression and its treatment in an elderly population: the Cache County Study [J]. Arch Gen Psychiatry, 2000, 57(6):601-7.
    [31] Unverzagt FW, Gao S, Baiyewu O, et al. Prevalence of cognitive impairment: data from the Indianapolis Study of Health and Aging [J]. Neurology, 2001, 57(9):1655-62.
    [32] Bassuk S, Berkman L, Wypij D. Depressive symptomatology and incident cognitive decline in an elderly community sample [J]. Arch Genl Pschiatry, 1998, 55(12):1073-81.
    [33] Geerlings MI, Schoevers RA, Beekman AT, et al. Depression and risk of cognitive decline and Alzheimer’s disease. Results of two prospective community-based studies in The Netherlands [J]. Br J Psychiatry, 2000, 176:568-75.
    [34] Paterniti S, Verdier-Taillefer MH, Dufouil C, et al. Depression symptoms and cognitive decline in elderly people. Longitudinal study [J]. Br J Psychiatry, 2002, 181:406-10.
    [35] Comijs HC, van Tilburg T, Geerlings SW, et al. Do severity and duration of depressive symptoms predict cognitive decline in older persons? Results of the Longitudinal Aging Study Amsterdam [J]. Aging Clin Exp Res, 2004, 16(3):226-32.
    [36] Vinkers DJ, Gussekloo J, Stek ML, et al. Temporal relation between depression and cognitive impairment in old age: prospective population based study [J]. BMJ, 2004, 329(74741):881.
    [37] Green RC, Cupples LA, Kurz A, et al. Depression as a risk factor for Alzheimer’s disease: the MIRAGE Study [J]. Arch Neurol, 2003, 60(5):753-9.
    [38] Olin JT, Schneider LS, Katz IR, et al. Provisional diagnostic criteria for depression of Alzheimer disease [J]. Am J Geriatr Psychiatry, 2002, 10(2):125-8.

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