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Subcortical ischemic depression

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187: 547: 219:‘severe’ demonstrate the strongest association with depression. These white matter lesions also predict future depression risk in individuals that are not currently depressed: non-depressed participants with identified white matter lesions were eight times more likely to develop depression within the next three years compared to those without these lesions. Although the location of these lesions has been studied in connection to late-life depression, more research is needed to determine location's role in the presentation of vascular depression. 166:. Individuals with vascular depression also tend to have more deficits in self-initiation and concentration, higher cardiac illness burden and cerebrovascular risk factors, cognitive impairment (as associated with the severity of white matter lesions in the brain), and increased treatment resistance. Those with vascular depression have also reported increased lassitude, which is described as a difficulty getting started in the morning and may be related to 270:
factors, and it may likely be both. White matter lesions, proposed to be a causal risk factor, are common in the elderly and are associated with age. Depression and cerebrovascular risk factors are also common in later life. These factors make it difficult to determine what is the causal factor and to tease apart normal functioning from abnormal in the elderly population.
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factors. These two mechanisms parallel the differences between MRI and clinically defined vascular depression, yet do not necessarily represent contradictory mechanisms. These brain changes are thought to be reflected in the white matter lesions identified by MRI. Cerebrovascular risk factors for vascular depression include
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of vascular depression which provides initial support for its classification as a unique subtype. The most distinctive symptoms of vascular depression compared to non-vascular depression include increased cognitive and executive impairment, proposed to be associated with cerebrovascular risk factors.
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Several studies show that the lesions associated with vascular depression are linked to poor depression treatment outcomes. A limitation of these studies is that they lack a measurement of cerebrovascular risk factors before and after the experimental interventions. Therefore, it is unknown if these
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Studies have not yet been conducted using this set of criteria, so it is unclear whether it provides an advantage over current standards. Some aspects of the criteria are not always necessary to diagnose individuals. For example, one study found that late-onset depression, executive dysfunction, and
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A second critique of vascular depression relates to the ambiguity about the causal direction between risk factors and depressive symptoms. It is very difficult to determine if cerebrovascular risk factors cause depressive symptoms or if depressive symptoms instead lead to a worsening of these risk
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A final challenge facing the vascular depression hypothesis is its lack of a formal definition. This makes the disorder fundamentally more difficult to study, especially considering that there is still no agreement on diagnostic criteria. Furthermore, some researchers have found that there is no
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placements have been shown to be effective treatments for some individuals with vascular depression. Individuals treated with TMS have reported decreased depressive symptoms. However, in one of these studies the results were based on clinically defined vascular depression. When participants were
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Research has found that white matter lesions are particularly important in predicting future depression. Increasing severity, or magnitude, of these lesions predicts an increase in depression over time (as studied in individuals who were already depressed). Additionally, lesions classified as
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Researchers hypothesize that vascular depression disrupts processes in certain parts of the brain to put individuals at risk for developing depression. Two primary mechanisms have been proposed: one associates white matter lesions (attributed to cardiovascular burden) and cerebrovascular risk
38:. Thus, it is difficult to determine if vascular depression can be considered a distinct sub-type of major depressive disorder (MDD). However, with current criteria, some studies estimate that vascular depression may account for over half of the cases of MDD in the elderly. 82:
Alternatively, clinically defined criteria as proposed initially by Alexopoulos and colleagues (1997) includes dimensions of depressive symptoms, disability, and cognitive impairment. Specifically, DED syndrome has been characterized by a loss of interest in activities,
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lesions. The most severe lesion in an individual is scored based on predefined criteria and considered in combination with two measures of depressive symptomology. These white matter lesions are thought to disrupt emotional and cognitive functioning.
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There is inadequate evidence to support vascular depression as a distinct subtype of major depressive disorder due to mixed results. Specifically, it is difficult to differentiate a diagnosis of vascular depression from similar diagnoses, such as
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Fabre, I., Galinowski, A., Oppenheim, C., Gallarda, T., Meder, J. F., de Montigny, C., … Poirier, M. F. (2004). Antidepressant efficacy and cognitive effects of repetitive transcranial magnetic stimulation in vascular depression: An open trial.
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Narushima, K., McCormick, L. M., Yamada, T., Thatcher, R. W., & Robinson, R. G. (2010). Subgenual Cingulate Theta Activity Predicts Treatment Response of Repetitive Transcranial Magnetic Stimulation in Participants With Vascular Depression.
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to develop vascular depression. Some research claims that vascular brain disease is sufficient (but not necessary) for the development of depression, but others have found that ischemic disease may not even be a sufficient causal factor.
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There are several criticisms regarding the theory of vascular depression. One critique is with regard to the distinction between sufficient and necessary causes for vascular depression. A cause is considered sufficient if its presence is
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compared to both nondepressed individuals with vascular disease and healthy control participants. This provides support that these symptoms may be a result of vascular depression specifically and not solely individuals’ vascular disease.
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Simpson, S., Baldwin, R. C., Jackson, A., & Burns, A. S. (1998). Is subcortical disease associated with a poor response to antidepressants ? Neurological, neuropsychological and neuroradiological findings in late-life depression.
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Additionally, studies have reported that when compared to individuals with non-vascular depression, those diagnosed with vascular depression tend to be older, have a lower family history of mental illness, and have a history of
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and focuses on the link between clinical symptoms of cardiovascular risk and depressive symptoms. Both of these competing definitions are supported in the literature and provide a strategy to diagnose vascular depression.
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Naarding, P., Tiemeier, H., Breteler, M. M. B., Schoevers, R. A., Jonker, C., Koudstaal, P. J., & Beekman, A. T. F. (2007). Clinically defined vascular depression in the general population.
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Aizenstein and colleagues (2016) proposed diagnostic criteria for vascular depression that incorporate elements of both clinical and MRI-definitions. These diagnostic criteria are:
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There is no formal and accepted definition of vascular depression and the hypothesis requires further research to support the causal link between these vascular lesions and
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depression symptom profile specific to those with vascular risk factors, calling into question vascular depression's distinction from other depressive disorders.
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compared according to MRI defined vascular depression, there was no difference in antidepressant outcomes between those fitting this definition and those not.
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Taylor, W. D., Steffens, D. C., & Krishnan, K. R. (2006). Psychiatric Disease in the Twenty-First Century: The Case for Subcortical Ischemic Depression.
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Krishnan, K. Ranga Rama; Taylor, Warren D.; McQuoid, Douglas R.; MacFall, James R.; Payne, Martha E.; Provenzale, James M.; Steffens, David C. (2004-02-15).
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Jorge, R. E., Moser, D. J., Acion, L., & Robinson, R. G. (2008). Treatment of Vascular Depression Using Repetitive Transcranial Magnetic Stimulation 3.
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Bella, R., Ferri, R., Cantone, M., Pennisi, M., Lanza, G., Malaguarnera, G., … Pennisi, G. (2011). Motor cortex excitability in vascular depression.
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Alexopoulos, G. S., Meyers, B. S., Young, R. C., Kakuma, T., Silbersweig, D., & Charlson, M. (1997). Clinically defined vascular depression.
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subcortical gray lesions in individuals were useful for identifying vascular depression, but only the presence of deep white matter lesions was
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Armstrong, Nicole M.; Meoni, Lucy A.; Carlson, Michelle C.; Xue, Qian-Li; Bandeen-Roche, Karen; Gallo, Joseph J.; Gross, Alden L. (May 2017).
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Alexopoulos, GS; Meyers, BS; Young, RC; Campbell, S; Silbersweig, D; Charlson, M (October 1997). "'Vascular depression' hypothesis".
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Dufouil, C.; de Kersaint-Gilly, A.; Besançon, V.; Levy, C.; Auffray, E.; Brunnereau, L.; Alpérovitch, A.; Tzourio, C. (2001-04-10).
215:. However, these factors do not account for all cerebrovascular changes in individuals as genetics may play a large role as well. 27:. Subcortical ischemic depression refers to vascular depression specifically due to lesions and restricted blood flow, known as 728:"Cardiovascular risk factors and risk of incident depression throughout adulthood among men: The Johns Hopkins Precursors Study" 425:
Baldwin, RC (January 2005). "Is vascular depression a distinct sub-type of depressive disorder? A review of causal evidence".
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treatments are targeting these factors specifically or the more general categorization of late-onset geriatric depression.
31:, in certain parts of the brain. However, the disorder is typically described as vascular depression in the literature. 468:
Alexopoulos, George S.; Kiosses, Dimitris N.; Klimstra, Sibel; Kalayam, Balkrishna; Bruce, Martha L. (January 2002).
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An additional study found that individuals with vascular depression reported greater executive dysfunction and
150:. Some researchers suggest that vascular depression may be too restricted in its definition and proposed 897: 47: 50:(MRI) or clinically defined criteria. MRI-defined vascular depression is more commonly referred to as 24: 546: 286:
can put individuals at risk for the development or increase of depressive symptoms in older adults.
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The criteria for MRI-defined vascular depression focus on the presence and severity of either deep
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Vascular depression was defined in 1997 by Alexopoulos and colleagues, who theorized that
8: 386: 186: 760: 727: 708: 653: 470:"Clinical presentation of the "depression-executive dysfunction syndrome" of late life" 450: 347: 320: 102:
Evidence of vascular pathology in elderly subjects with or without cognitive impairment
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Absence of previous depressive episodes preceding obvious cerebrovascular disease
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Proposed mechanism of vascular depression adapted from Aizenstein et al., 2016
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to lead to vascular depression, yet it is considered necessary if it is
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in the brain and depressive symptoms. An alternative definition is
54:(SID) and emphasizes the relationship between MRI identification of 880: 151: 119: 88: 28: 467: 92: 55: 23:, is a medical condition most commonly seen in older people with 114:
Clinical symptoms characteristic of vascular depression such as
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Co-incidence of depression with cerebrovascular risk factors
321:"Vascular depression consensus report - a critical update" 319:
Aizenstein, HJ; Baskys, A; et al. (3 November 2016).
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The Journal of Neuropsychiatry and Clinical Neurosciences
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Vascular depression is typically diagnosed using either
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Brunoni, AR; Benseñor, IM; Alves, TC (December 2011).
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Neuroimaging data confirming cerebrovascular disease
839:https://doi.org/10.1001/archgenpsychiatry.2007.45 368: 366: 314: 312: 310: 308: 306: 304: 302: 300: 298: 889: 133:to classify individuals as having the disorder. 60:depression executive dysfunction (DED) syndrome 816:https://doi.org/10.1016/j.biopsych.2006.05.028 802: 800: 363: 295: 873:International Journal of Geriatric Psychiatry 553: 427:International Journal of Geriatric Psychiatry 474:The American Journal of Geriatric Psychiatry 797: 70:lesions, often referred to as white matter 781: 779: 574: 572: 137:Distinction from Major Depressive Disorder 843: 759: 600:International Journal of Psychophysiology 588:https://doi.org/10.1017/S0033291706009196 529: 507: 505: 503: 420: 418: 416: 414: 412: 410: 408: 406: 404: 346: 336: 860:https://doi.org/10.1176/jnp.2010.22.1.75 825: 823: 185: 108:Presence of cerebrovascular risk factors 776: 569: 424: 890: 500: 401: 864: 820: 565:https://doi.org/10.1176/ajp.154.4.562 592: 387:10.1001/archpsyc.1997.01830220033006 118:, decrease in processing speed, and 157:However, there is some evidence of 13: 14: 909: 518:Revista Brasileira de Psiquiatria 233:transcranial magnetic stimulation 881:https://doi.org/10.1002/gps.1172 545: 719: 664: 531:10.1590/S1516-44462011000400015 52:subcortical ischemic depression 17:Subcortical ischemic depression 831:Archives of General Psychiatry 732:Journal of Affective Disorders 689:10.1016/j.biopsych.2003.08.014 609: 561:American Journal of Psychiatry 461: 375:Archives of General Psychiatry 251: 1: 289: 222: 41: 7: 10: 914: 277: 48:magnetic resonance imaging 744:10.1016/j.jad.2017.03.004 338:10.1186/s12916-016-0720-5 25:major depressive disorder 181: 284:cerebrovascular disease 85:psychomotor retardation 788:Psychological Medicine 580:Psychological Medicine 231:Keeping this in mind, 209:coronary heart disease 191: 808:Biological Psychiatry 677:Biological Psychiatry 189: 116:executive dysfunction 634:10.1212/wnl.56.7.921 148:late-life depression 563:, 154(4), 562–565. 197:high blood pressure 95:and visual naming. 21:vascular depression 192: 898:Depression (mood) 814:(12), 1299–1303. 201:diabetes mellitus 159:internal validity 74:, or subcortical 905: 883: 868: 862: 847: 841: 827: 818: 804: 795: 783: 774: 773: 763: 723: 717: 716: 668: 662: 661: 613: 607: 596: 590: 576: 567: 557: 551: 550: 549: 543: 533: 509: 498: 497: 465: 459: 458: 439:10.1002/gps.1255 422: 399: 398: 370: 361: 360: 350: 340: 316: 72:hyperintensities 19:, also known as 913: 912: 908: 907: 906: 904: 903: 902: 888: 887: 886: 869: 865: 848: 844: 828: 821: 805: 798: 784: 777: 724: 720: 669: 665: 614: 610: 597: 593: 577: 570: 558: 554: 544: 510: 501: 466: 462: 423: 402: 371: 364: 317: 296: 292: 280: 254: 225: 213:tobacco smoking 184: 139: 44: 12: 11: 5: 911: 901: 900: 885: 884: 879:(9), 833–842. 863: 842: 837:(3), 268–276. 819: 796: 775: 718: 683:(4): 390–397. 663: 628:(7): 921–926. 608: 591: 586:(3), 383–392. 568: 552: 499: 460: 400: 381:(10): 915–22. 362: 293: 291: 288: 279: 276: 253: 250: 224: 221: 205:hyperlipidemia 183: 180: 138: 135: 126: 125: 122: 112: 109: 106: 103: 43: 40: 9: 6: 4: 3: 2: 910: 899: 896: 895: 893: 882: 878: 874: 867: 861: 857: 853: 846: 840: 836: 832: 826: 824: 817: 813: 809: 803: 801: 793: 789: 782: 780: 771: 767: 762: 757: 753: 749: 745: 741: 737: 733: 729: 722: 714: 710: 706: 702: 698: 694: 690: 686: 682: 678: 674: 667: 659: 655: 651: 647: 643: 639: 635: 631: 627: 623: 619: 612: 606:(3), 248–253. 605: 601: 595: 589: 585: 581: 575: 573: 566: 562: 556: 548: 541: 537: 532: 527: 523: 519: 515: 508: 506: 504: 495: 491: 487: 483: 480:(1): 98–106. 479: 475: 471: 464: 456: 452: 448: 444: 440: 436: 432: 428: 421: 419: 417: 415: 413: 411: 409: 407: 405: 396: 392: 388: 384: 380: 376: 369: 367: 358: 354: 349: 344: 339: 334: 330: 327:(Editorial). 326: 322: 315: 313: 311: 309: 307: 305: 303: 301: 299: 294: 287: 285: 275: 271: 267: 264: 260: 249: 246: 245:carotid stent 242: 238: 234: 229: 220: 216: 214: 210: 206: 202: 198: 188: 179: 176: 171: 169: 165: 160: 155: 153: 149: 145: 134: 132: 123: 121: 117: 113: 110: 107: 104: 101: 100: 99: 96: 94: 90: 86: 80: 77: 73: 69: 64: 61: 57: 53: 49: 39: 37: 32: 30: 26: 22: 18: 876: 872: 866: 858:(1), 75–84. 855: 851: 845: 834: 830: 811: 807: 794:, 1015–1026. 791: 787: 735: 731: 721: 680: 676: 666: 625: 621: 611: 603: 599: 594: 583: 579: 560: 555: 524:(4): 400–9. 521: 517: 477: 473: 463: 430: 426: 378: 374: 328: 325:BMC Medicine 324: 281: 272: 268: 262: 258: 255: 230: 226: 217: 193: 172: 164:hypertension 156: 140: 130: 127: 97: 81: 68:white matter 65: 59: 51: 45: 33: 20: 16: 15: 433:(1): 1–11. 252:Controversy 144:post-stroke 76:grey matter 331:(1): 161. 290:References 241:citalopram 237:nimodipine 223:Management 36:depression 752:1573-2517 738:: 60–66. 697:0006-3223 642:0028-3878 622:Neurology 486:1064-7481 131:necessary 42:Diagnosis 892:Category 770:28284097 713:29802787 705:14960292 658:25407657 650:11294930 540:22189931 494:11790640 455:19083813 447:15578670 357:27806704 263:required 152:etiology 120:lethargy 89:paranoia 29:ischemia 761:5405441 395:9337771 348:5093970 278:History 235:(TMS), 168:fatigue 93:fluency 56:lesions 768:  758:  750:  711:  703:  695:  656:  648:  640:  538:  492:  484:  453:  445:  393:  355:  345:  259:enough 243:, and 211:, and 175:apathy 709:S2CID 654:S2CID 451:S2CID 182:Cause 766:PMID 748:ISSN 701:PMID 693:ISSN 646:PMID 638:ISSN 536:PMID 490:PMID 482:ISSN 443:PMID 391:PMID 353:PMID 756:PMC 740:doi 736:214 685:doi 630:doi 526:doi 435:doi 383:doi 343:PMC 333:doi 146:or 894:: 877:19 875:, 856:22 854:, 835:65 833:, 822:^ 812:60 810:, 799:^ 792:28 790:, 778:^ 764:. 754:. 746:. 734:. 730:. 707:. 699:. 691:. 681:55 679:. 675:. 652:. 644:. 636:. 626:56 624:. 620:. 604:82 602:, 584:37 582:, 571:^ 534:. 522:33 520:. 516:. 502:^ 488:. 478:10 476:. 472:. 449:. 441:. 431:20 429:. 403:^ 389:. 379:54 377:. 365:^ 351:. 341:. 329:14 323:. 297:^ 239:, 207:, 203:, 199:, 170:. 154:. 87:, 772:. 742:: 715:. 687:: 660:. 632:: 542:. 528:: 496:. 457:. 437:: 397:. 385:: 359:. 335::

Index

major depressive disorder
ischemia
depression
magnetic resonance imaging
lesions
white matter
hyperintensities
grey matter
psychomotor retardation
paranoia
fluency
executive dysfunction
lethargy
post-stroke
late-life depression
etiology
internal validity
hypertension
fatigue
apathy

high blood pressure
diabetes mellitus
hyperlipidemia
coronary heart disease
tobacco smoking
transcranial magnetic stimulation
nimodipine
citalopram
carotid stent

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