Abstract
Purpose of Review
This review aims to examine the current evidence for vascular contributions to late life depression (LLD).
Recent Findings
White matter hyperintensities (WMHs) are very common in the elderly. Greater WMH severity is consistently associated with LLD. High levels of endothelial plasma soluble intercellular adhesion molecule-1, indicating vascular endothelial dysfunction, are associated with LLD. Chronic ischemic lesions, which are visualized as WMHs on T2-weighted or fluid-attenuated inversion recovery image of MRI, may disrupt frontal-subcortical-limbic networks. These disruptions can then be detected on diffusion tensor imaging. Vascular diseases (stroke, cardiovascular disease, diabetes mellitus, and homocysteinemia) and hemodynamic dysfunction are also established risk factors for LLD.
Summary
Convergent evidence indicates that vascular depression is a useful construct accounting for vascular contributions to LLD. Comprehensive understanding of vascular contributions to LLD will not only inform preventive strategies for LLD but also provide guidance on developing innovative treatments for ameliorating specific vascular risk factors.
Similar content being viewed by others
References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
Blazer D. Major depression in later life. Hosp Pract (Off Ed). 1989;24(9A):69–76. 9
Lebowitz BD, Pearson JL, Schneider LS, Reynolds CF 3rd, Alexopoulos GS, Bruce ML, et al. Diagnosis and treatment of depression in late life. Consensus statement update. JAMA. 1997;278(14):1186–90.
Park JH, Kim KW, Kim MH, Kim MD, Kim BJ, Kim SK, et al. A nationwide survey on the prevalence and risk factors of late life depression in South Korea. J Affect Disord. 2012;138(1–2):34–40.
Park JH, Lee JJ, Lee SB, Huh Y, Choi EA, Youn JC, et al. Prevalence of major depressive disorder and minor depressive disorder in an elderly Korean population: results from the Korean Longitudinal Study on Health and Aging (KLoSHA). J Affect Disord. 2010;125(1–3):234–40.
United Nations. Dept. of economic and social affairs. Population division. World population prospects : the 2006 revision. New York: United Nations; 2007.
Taylor WD. Clinical practice. Depression in the elderly. N Engl J Med. 2014;371(13):1228–36.
Sonnenberg CM, Beekman AT, Deeg DJ, An Tilburg V. Drug treatment in depressed elderly in the Dutch community. Int J Geriatr Psychiatry. 2003;18(2):99–104.
Beekman AT, Deeg DJ, Braam AW, Smit JH, Van Tilburg W. Consequences of major and minor depression in later life: a study of disability, well-being and service utilization. Psychol Med. 1997;27(6):1397–409.
• Johnson AD, McQuoid DR, Steffens DC, Payne ME, Beyer JL, Taylor WD. Effects of stressful life events on cerebral white matter hyperintensity progression. Int J Geriatr Psychiatry. 2016. This work supports that stress exposure has a significant effect on the progression of WMHs, independent of depression diagnosis.
•• Park JH, Lee SB, Lee JJ, Yoon JC, Han JW, Kim TH, et al. Epidemiology of MRI-defined vascular depression: a longitudinal, community-based study in Korean elders. J Affect Disord. 2015;180:200–6. This study provides the notion that greater WMHs severity is a crucial factor predicting future depression risk, which supports the previous vascular depression hypothesis.
• van Sloten TT, Sigurdsson S, van Buchem MA, Phillips CL, Jonsson PV, Ding J, et al. Cerebral small vessel disease and association with higher incidence of depressive symptoms in a general elderly population: the AGES-Reykjavik study. Am J Psychiatry. 2015;172(6):570–8. Most markers of progression of cerebral small vessel disease (CSVD) over time and some markers of baseline CSVD are associated with concurrently developing new depressive symptoms, supporting the vascular depression hypothesis.
Paranthaman R, Greenstein AS, Burns AS, Cruickshank JK, Heagerty AM, Jackson A, et al. Vascular function in older adults with depressive disorder. Biol Psychiatry. 2010;68(2):133–9.
• Taylor WD, Aizenstein HJ, Alexopoulos GS. The vascular depression hypothesis: mechanisms linking vascular disease with depression. Mol Psychiatry. 2013;18(9):963–74. This study reviews data testing the vascular depression hypothesis with a focus on identifying potential underlying vascular mechanisms.
Thomas AJ, Perry R, Barber R, Kalaria RN, O’Brien JT. Pathologies and pathological mechanisms for white matter hyperintensities in depression. Ann N Y Acad Sci. 2002;977:333–9.
Thomas AJ, O’Brien JT, Davis S, Ballard C, Barber R, Kalaria RN, et al. Ischemic basis for deep white matter hyperintensities in major depression: a neuropathological study. Arch Gen Psychiatry. 2002;59(9):785–92.
Liao D, Cooper L, Cai J, Toole JF, Bryan NR, Hutchinson RG, et al. Presence and severity of cerebral white matter lesions and hypertension, its treatment, and its control. The ARIC study. Atherosclerosis risk in communities study. Stroke. 1996;27(12):2262–70.
de Leeuw FE, de Groot JC, Achten E, Oudkerk M, Ramos LM, Heijboer R, et al. Prevalence of cerebral white matter lesions in elderly people: a population based magnetic resonance imaging study. The Rotterdam scan study. J Neurol Neurosurg Psychiatry. 2001;70(1):9–14.
Launer LJ, Berger K, Breteler MM, Dufouil C, Fuhrer R, Giampaoli S, et al. Regional variability in the prevalence of cerebral white matter lesions: an MRI study in 9 European countries (CASCADE). Neuroepidemiology. 2006;26(1):23–9.
Dalby RB, Chakravarty MM, Ahdidan J, Sorensen L, Frandsen J, Jonsdottir KY, et al. Localization of white-matter lesions and effect of vascular risk factors in late-onset major depression. Psychol Med. 2010;40(8):1389–99.
•• Taylor WD, Zhao Z, Ashley-Koch A, Payne ME, Steffens DC, Krishnan RR, et al. Fiber tract-specific white matter lesion severity findings in late-life depression and by AGTR1 A1166C genotype. Hum Brain Mapp. 2013;34(2):295–303. This study provides preliminary evidence that genetic differences related to vascular disease may increase lesion vulnerability differentially across fiber tracts.
• Wen MC, Steffens DC, Chen MK, Zainal NH. Diffusion tensor imaging studies in late-life depression: systematic review and meta-analysis. Int J Geriatr Psychiatry. 2014;29(12):1173–84. This review provides the finding that diffusion tensor imaging studies of LLD consistently show reduced anisotropy in the DLPFC and UF of patients with LLD.
Krishnan KR, Taylor WD, McQuoid DR, MacFall JR, Payne ME, Provenzale JM, et al. Clinical characteristics of magnetic resonance imaging-defined subcortical ischemic depression. Biol Psychiatry. 2004;55(4):390–7.
•• Krishnan KR, Hays JC, Blazer DG. MRI-defined vascular depression. Am J Psychiatry. 1997;154(4):497–501. This study characterizes the clinical and demographic feature of vascular depression.
Taylor WD, MacFall JR, Payne ME, McQuoid DR, Steffens DC, Provenzale JM, et al. Greater MRI lesion volumes in elderly depressed subjects than in control subjects. Psychiatry Res. 2005;139(1):1–7.
Steffens DC, Krishnan KR, Crump C, Burke GL. Cerebrovascular disease and evolution of depressive symptoms in the cardiovascular health study. Stroke. 2002;33(6):1636–44.
• Taylor WD, Steffens DC, MacFall JR, McQuoid DR, Payne ME, Provenzale JM, et al. White matter hyperintensity progression and late-life depression outcomes. Arch Gen Psychiatry. 2003;60(11):1090–6. This study provides evidence that greater progression of WMH volume is associated with poor outcomes in geriatric depression.
Stevenson SF, Doubal FN, Shuler K, Wardlaw JM. A systematic review of dynamic cerebral and peripheral endothelial function in lacunar stroke versus controls. Stroke. 2010;41(6):e434–42.
•• van Agtmaal MJM, Houben A, Pouwer F, Stehouwer CDA, Schram MT. Association of microvascular dysfunction with late-life depression: a systematic review and meta-analysis. JAMA Psychiatry. 2017. This meta-analysis shows that both the peripheral and cerebral forms of microvascular dysfunction are associated with higher odds of (incident) late-life depression.
Basile AM, Pantoni L, Pracucci G, Asplund K, Chabriat H, Erkinjuntti T, et al. Age, hypertension, and lacunar stroke are the major determinants of the severity of age-related white matter changes. The LADIS (Leukoaraiosis and Disability in the Elderly) study. Cerebrovasc Dis. 2006;21(5–6):315–22.
Pantoni L, Garcia JH. The significance of cerebral white matter abnormalities 100 years after Binswanger’s report. A Rev Stroke. 1995;26(7):1293–301.
Dichgans M, Filippi M, Bruning R, Iannucci G, Berchtenbreiter C, Minicucci L, et al. Quantitative MRI in CADASIL: correlation with disability and cognitive performance. Neurology. 1999;52(7):1361–7.
•• Park JH, Jeon BH, Lee JS, Newhouse PA, Taylor WD, Boyd BD, et al. CADASIL as a useful medical model and genetic form of vascular depression. Am J Geriatr Psychiatry. 2017;25(7):719–27. This study demonstrates that WMHs are closely associated with depression in patients with CADASIL and CADASIL is a useful medical model and genetic form of vascular depression.
Dufouil C, Chalmers J, Coskun O, Besancon V, Bousser MG, Guillon P, et al. Effects of blood pressure lowering on cerebral white matter hyperintensities in patients with stroke: the PROGRESS (Perindopril Protection Against Recurrent Stroke Study) magnetic resonance imaging substudy. Circulation. 2005;112(11):1644–50.
Fujita S, Kawaguchi T, Uehara T, Fukushima K. Progress of leukoaraiosis is inhibited by correction of platelet hyper-aggregability. Int Psychogeriatr. 2005;17(4):689–98.
Cavalieri M, Schmidt R, Chen C, Mok V, de Freitas GR, Song S, et al. B vitamins and magnetic resonance imaging-detected ischemic brain lesions in patients with recent transient ischemic attack or stroke: the VITAmins TO Prevent Stroke (VITATOPS) MRI-substudy. Stroke. 2012;43(12):3266–70.
Le Bihan D. Looking into the functional architecture of the brain with diffusion MRI. Nat Rev Neurosci. 2003;4(6):469–80.
O’Sullivan M, Summers PE, Jones DK, Jarosz JM, Williams SC, Markus HS. Normal-appearing white matter in ischemic leukoaraiosis: a diffusion tensor MRI study. Neurology. 2001;57(12):2307–10.
•• Charlton RA, Lamar M, Zhang A, Yang S, Ajilore O, Kumar A. White-matter tract integrity in late-life depression: associations with severity and cognition. Psychol Med. 2014;44(7):1427–37. This study shows that white-matter tract integrity is lower in LLD than healthy controls and is associated with depression severity across all participants.
Aizenstein HJ, Andreescu C, Edelman KL, Cochran JL, Price J, Butters MA, et al. fMRI correlates of white matter hyperintensities in late-life depression. Am J Psychiatry. 2011;168(10):1075–82.
Venkatraman VK, Aizenstein H, Guralnik J, Newman AB, Glynn NW, Taylor C, et al. Executive control function, brain activation and white matter hyperintensities in older adults. NeuroImage. 2010;49(4):3436–42.
Alexopoulos GS, Buckwalter K, Olin J, Martinez R, Wainscott C, Krishnan KR. Comorbidity of late life depression: an opportunity for research on mechanisms and treatment. Biol Psychiatry. 2002;52(6):543–58.
Zimmerman JA, Mast BT, Miles T, Markides KS. Vascular risk and depression in the Hispanic Established Population for the Epidemiologic Study of the Elderly (EPESE). Int J Geriatr Psychiatry. 2009;24(4):409–16.
• Lyness JM, King DA, Conwell Y, Cox C, Caine ED. Cerebrovascular risk factors and 1-year depression outcome in older primary care patients. Am J Psychiatry. 2000;157(9):1499–501. This study demonstrates that the severity of initial cumulative cerebrovascular risk factors is significantly independently associated with 1-year depressive symptoms and diagnoses.
•• Valkanova V, Ebmeier KP. Vascular risk factors and depression in later life: a systematic review and meta-analysis. Biol Psychiatry. 2013;73(5):406–13. This study provides convincing evidence of a strong relationship between key diseases and depression (cardiovascular disease, diabetes, and stroke) and between composite vascular risk and depression but not between some vascular risk factors (hypertension, smoking, dyslipidemia) and depression.
Hackett ML, Yapa C, Parag V, Anderson CS. Frequency of depression after stroke: a systematic review of observational studies. Stroke. 2005;36(6):1330–40.
Whyte EM, Mulsant BH. Post stroke depression: epidemiology, pathophysiology, and biological treatment. Biol Psychiatry. 2002;52(3):253–64.
Whyte EM, Mulsant BH, Vanderbilt J, Dodge HH, Ganguli M. Depression after stroke: a prospective epidemiological study. J Am Geriatr Soc. 2004;52(5):774–8.
Cumming TB, Churilov L, Skoog I, Blomstrand C, Linden T. Little evidence for different phenomenology in poststroke depression. Acta Psychiatr Scand. 2010;121(6):424–30.
Santos M, Kovari E, Gold G, Bozikas VP, Hof PR, Bouras C, et al. The neuroanatomical model of post-stroke depression: towards a change of focus? J Neurol Sci. 2009;283(1–2):158–62.
Ali S, Stone MA, Peters JL, Davies MJ, Khunti K. The prevalence of co-morbid depression in adults with type 2 diabetes: a systematic review and meta-analysis. Diabet Med. 2006;23(11):1165–73.
Li C, Ford ES, Strine TW, Mokdad AH. Prevalence of depression among U.S. adults with diabetes: findings from the 2006 behavioral risk factor surveillance system. Diabetes Care. 2008;31(1):105–7.
Anderson RJ, Freedland KE, Clouse RE, Lustman PJ. The prevalence of comorbid depression in adults with diabetes: a meta-analysis. Diabetes Care. 2001;24(6):1069–78.
Hare DL, Toukhsati SR, Johansson P, Jaarsma T. Depression and cardiovascular disease: a clinical review. Eur Heart J. 2014;35(21):1365–72.
Krishnan KR. Broken heart: depression in cardiovascular disease. Dialogues Clin Neurosci. 2003;5(2):167–74.
Freedland KE, Rich MW, Skala JA, Carney RM, Davila-Roman VG, Jaffe AS. Prevalence of depression in hospitalized patients with congestive heart failure. Psychosom Med. 2003;65(1):119–28.
Perk J, De Backer G, Gohlke H, Graham I, Reiner Z, Verschuren WM, et al. European guidelines on cardiovascular disease prevention in clinical practice (version 2012): The Fifth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of nine societies and by invited experts). Atherosclerosis. 2012;223(1):1–68.
Folstein M, Liu T, Peter I, Buell J, Arsenault L, Scott T, et al. The homocysteine hypothesis of depression. Am J Psychiatry. 2007;164(6):861–7.
Almeida OP, McCaul K, Hankey GJ, Norman P, Jamrozik K, Flicker L. Homocysteine and depression in later life. Arch Gen Psychiatry. 2008;65(11):1286–94.
Li Z, Li Y, Chen L, Chen P, Hu Y. Prevalence of depression in patients with hypertension: a systematic review and meta-analysis. Medicine (Baltimore). 2015;94(31):e1317.
Vevera J, Fisar Z, Kvasnicka T, Zdenek H, Starkova L, Ceska R, et al. Cholesterol-lowering therapy evokes time-limited changes in serotonergic transmission. Psychiatry Res. 2005;133(2–3):197–203.
Sjogren B, Hamblin MW, Svenningsson P. Cholesterol depletion reduces serotonin binding and signaling via human 5-HT(7(a)) receptors. Eur J Pharmacol. 2006;552(1–3):1–10.
Fiedorowicz JG, Haynes WG. Cholesterol, mood, and vascular health: untangling the relationship: does low cholesterol predispose to depression and suicide, or vice versa? Curr Psychiatr Ther. 2010;9(7):17-A.
Tedders SH, Fokong KD, McKenzie LE, Wesley C, Yu L, Zhang J. Low cholesterol is associated with depression among US household population. J Affect Disord. 2011;135(1–3):115–21.
Bove M, Carnevali L, Cicero AF, Grandi E, Gaddoni M, Noera G, et al. Psychosocial factors and metabolic parameters: is there any association in elderly people? The Massa Lombarda project. Aging Ment Health. 2010;14(7):801–6.
Rice MC, Katzel LI, Waldstein SR. Sex-specific associations of depressive symptoms and cardiovascular risk factors in older adults. Aging Ment Health. 2010;14(4):405–10.
Yang CC, Jick SS, Jick H. Lipid-lowering drugs and the risk of depression and suicidal behavior. Arch Intern Med. 2003;163(16):1926–32.
Almeida OP, Yeap BB, Hankey GJ, Golledge J, Flicker L. HDL cholesterol and the risk of depression over 5 years. Mol Psychiatry. 2014;19(6):637–8.
Meyer JS, Terayama Y, Takashima S. Cerebral circulation in the elderly. Cerebrovasc Brain Metab Rev. 1993;5(2):122–46.
de la Torre JC. Cerebral hemodynamics and vascular risk factors: setting the stage for Alzheimer’s disease. J Alzheimers Dis. 2012;32(3):553–67.
De Ciuceis C, Amiri F, Brassard P, Endemann DH, Touyz RM, Schiffrin EL. Reduced vascular remodeling, endothelial dysfunction, and oxidative stress in resistance arteries of angiotensin II-infused macrophage colony-stimulating factor-deficient mice: evidence for a role in inflammation in angiotensin-induced vascular injury. Arterioscler Thromb Vasc Biol. 2005;25(10):2106–13.
Dandona P, Aljada A. Endothelial dysfunction in patients with type 2 diabetes and the effects of thiazolidinedione antidiabetic agents. J Diabetes Complicat. 2004;18(2):91–102.
Tiemeier H, Bakker SL, Hofman A, Koudstaal PJ, Breteler MM. Cerebral haemodynamics and depression in the elderly. J Neurol Neurosurg Psychiatry. 2002;73(1):34–9.
Direk N, Koudstaal PJ, Hofman A, Ikram MA, Hoogendijk WJ, Tiemeier H. Cerebral hemodynamics and incident depression: the Rotterdam study. Biol Psychiatry. 2012;72(4):318–23.
Bakker SL, de Leeuw FE, de Groot JC, Hofman A, Koudstaal PJ, Breteler MM. Cerebral vasomotor reactivity and cerebral white matter lesions in the elderly. Neurology. 1999;52(3):578–83.
Moody DM, Bell MA, Challa VR. Features of the cerebral vascular pattern that predict vulnerability to perfusion or oxygenation deficiency: an anatomic study. AJNR Am J Neuroradiol. 1990;11(3):431–9.
Matsushita K, Kuriyama Y, Nagatsuka K, Nakamura M, Sawada T, Omae T. Periventricular white matter lucency and cerebral blood flow autoregulation in hypertensive patients. Hypertension. 1994;23(5):565–8.
Molina C, Sabin JA, Montaner J, Rovira A, Abilleira S, Codina A. Impaired cerebrovascular reactivity as a risk marker for first-ever lacunar infarction: a case-control study. Stroke. 1999;30(11):2296–301.
Petrica L, Petrica M, Vlad A, Bob F, Gluhovschi C, Gluhovschi G, et al. Cerebrovascular reactivity is impaired in patients with non-insulin-dependent diabetes mellitus and microangiopathy. Wien Klin Wochenschr. 2007;119(11–12):365–71.
Markus HS, Lythgoe DJ, Ostegaard L, O’Sullivan M, Williams SC. Reduced cerebral blood flow in white matter in ischaemic leukoaraiosis demonstrated using quantitative exogenous contrast based perfusion MRI. J Neurol Neurosurg Psychiatry. 2000;69(1):48–53.
Brickman AM, Zahra A, Muraskin J, Steffener J, Holland CM, Habeck C, et al. Reduction in cerebral blood flow in areas appearing as white matter hyperintensities on magnetic resonance imaging. Psychiatry Res. 2009;172(2):117–20.
Vardi N, Freedman N, Lester H, Gomori JM, Chisin R, Lerer B, et al. Hyperintensities on T2-weighted images in the basal ganglia of patients with major depression: cerebral perfusion and clinical implications. Psychiatry Res. 2011;192(2):125–30.
Nitschke JB, Mackiewicz KL. Prefrontal and anterior cingulate contributions to volition in depression. Int Rev Neurobiol. 2005;67:73–94.
Rabbitt P, Scott M, Thacker N, Lowe C, Jackson A, Horan M, et al. Losses in gross brain volume and cerebral blood flow account for age-related differences in speed but not in fluid intelligence. Neuropsychology. 2006;20(5):549–57.
Butters MA, Whyte EM, Nebes RD, Begley AE, Dew MA, Mulsant BH, et al. The nature and determinants of neuropsychological functioning in late-life depression. Arch Gen Psychiatry. 2004;61(6):587–95.
Terborg C, Gora F, Weiller C, Rother J. Reduced vasomotor reactivity in cerebral microangiopathy: a study with near-infrared spectroscopy and transcranial Doppler sonography. Stroke. 2000;31(4):924–9.
Matthews SC, Nelesen RA, Dimsdale JE. Depressive symptoms are associated with increased systemic vascular resistance to stress. Psychosom Med. 2005;67(4):509–13.
Hamer M, Tanaka G, Okamura H, Tsuda A, Steptoe A. The effects of depressive symptoms on cardiovascular and catecholamine responses to the induction of depressive mood. Biol Psychol. 2007;74(1):20–5.
Dawood T, Schlaich M, Brown A, Lambert G. Depression and blood pressure control: all antidepressants are not the same. Hypertension. 2009;54(1):e1. author reply e2
Stein PK, Kleiger RE. Insights from the study of heart rate variability. Annu Rev Med. 1999;50:249–61.
Carney RM, Blumenthal JA, Stein PK, Watkins L, Catellier D, Berkman LF, et al. Depression, heart rate variability, and acute myocardial infarction. Circulation. 2001;104(17):2024–8.
Guinjoan SM, Bernabo JL, Cardinali DP. Cardiovascular tests of autonomic function and sympathetic skin responses in patients with major depression. J Neurol Neurosurg Psychiatry. 1995;59(3):299–302.
Bouzinova EV, Norregaard R, Boedtkjer DM, Razgovorova IA, Moeller AM, Kudryavtseva O, et al. Association between endothelial dysfunction and depression-like symptoms in chronic mild stress model of depression. Psychosom Med. 2014;76(4):268–76.
Puzserova A, Kopincova J, Slezak P, Balis P, Bernatova I. Endothelial dysfunction in femoral artery of the hypertensive rats is nitric oxide independent. Physiol Res. 2013;62(6):615–29.
Alexopoulos GS, Meyers BS, Young RC, Campbell S, Silbersweig D, Charlson M. “Vascular depression” hypothesis. Arch Gen Psychiatry. 1997;54(10):915–22.
Alexopoulos GS, Meyers BS, Young RC, Kakuma T, Silbersweig D, Charlson M. Clinically defined vascular depression. Am J Psychiatry. 1997;154(4):562–5.
Fazekas F, Chawluk JB, Alavi A, Hurtig HI, Zimmerman RA. MR signal abnormalities at 1.5 T in Alzheimer’s dementia and normal aging. AJR Am J Roentgenol. 1987;149(2):351–6.
Sneed JR, Rindskopf D, Steffens DC, Krishnan KR, Roose SP. The vascular depression subtype: evidence of internal validity. Biol Psychiatry. 2008;64(6):491–7.
•• Pimontel MA, Reinlieb ME, Johnert LC, Garcon E, Sneed JR, Roose SP. The external validity of MRI-defined vascular depression. Int J Geriatr Psychiatry. 2013;28(11):1189–96. This study support the notion that MRI-defined vascular depression represents a unique and valid subtype of late-life depression.
Coffey CE, Figiel GS, Djang WT, Cress M, Saunders WB, Weiner RD. Leukoencephalopathy in elderly depressed patients referred for ECT. Biol Psychiatry. 1988;24(2):143–61.
Fujikawa T, Yamawaki S, Touhouda Y. Incidence of silent cerebral infarction in patients with major depression. Stroke. 1993;24(11):1631–4.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of Interest
The author has nothing to declare.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.
Additional information
This article is part of the Topical Collection on Geropsychiatry & Cognitive Disorders of Late Life
Rights and permissions
About this article
Cite this article
Park, J.H. Vascular Contributions to Late Life Depression. Curr Behav Neurosci Rep 4, 291–298 (2017). https://doi.org/10.1007/s40473-017-0128-3
Published:
Issue Date:
DOI: https://doi.org/10.1007/s40473-017-0128-3