Show simple item record

Domainâ specific impairment in cognitive control among remitted youth with a history of major depression

dc.contributor.authorPeters, Amy T.
dc.contributor.authorJacobs, Rachel H.
dc.contributor.authorCrane, Natania A.
dc.contributor.authorRyan, Kelly A.
dc.contributor.authorWeisenbach, Sara L.
dc.contributor.authorAjilore, Olusola
dc.contributor.authorLamar, Melissa
dc.contributor.authorKassel, Michelle T.
dc.contributor.authorGabriel, Laura B.
dc.contributor.authorWest, Amy E.
dc.contributor.authorZubieta, Jon‐kar
dc.contributor.authorLangenecker, Scott A.
dc.date.accessioned2017-10-05T18:20:11Z
dc.date.available2019-01-07T18:34:38Zen
dc.date.issued2017-10
dc.identifier.citationPeters, Amy T.; Jacobs, Rachel H.; Crane, Natania A.; Ryan, Kelly A.; Weisenbach, Sara L.; Ajilore, Olusola; Lamar, Melissa; Kassel, Michelle T.; Gabriel, Laura B.; West, Amy E.; Zubieta, Jon‐kar ; Langenecker, Scott A. (2017). "Domainâ specific impairment in cognitive control among remitted youth with a history of major depression." Early Intervention in Psychiatry 11(5): 383-392.
dc.identifier.issn1751-7885
dc.identifier.issn1751-7893
dc.identifier.urihttps://hdl.handle.net/2027.42/138407
dc.description.abstractAimImpairment in neuropsychological functioning is common in major depressive disorder (MDD), but it is not clear to what degree these deficits are related to risk (e.g. trait), scar, burden or state effects of MDD. The objective of this study was to use neuropsychological measures, with factor scores in verbal fluency, processing speed, attention, setâ shifting and cognitive control in a unique population of young, remitted, unmedicated, early course individuals with a history of MDD in hopes of identifying putative trait markers of MDD.MethodsYouth aged 18â 23 in remission from MDD (rMDD; n = 62) and healthy controls (HC; n = 43) were assessed with neuropsychological tests at two time points. These were from four domains of executive functioning, consistent with previous literature as impaired in MDD: verbal fluency and processing speed, conceptual reasoning and setâ shifting, processing speed with interference resolution, and cognitive control.ResultsrMDD youth performed comparably to HCs on verbal fluency and processing speed, processing speed with interference resolution, and conceptual reasoning and setâ shifting, reliably over time. Individuals with rMDD demonstrated relative decrements in cognitive control at Time 1, with greater stability than HC participants.ConclusionMDD may be characterized by regulatory difficulties that do not pertain specifically to active mood state or fluctuations in symptoms. Deficient cognitive control may represent a trait vulnerability or early course scar of MDD that may prove a viable target for secondary prevention or early remediation.
dc.publisherWiley Periodicals, Inc.
dc.subject.otherdepression
dc.subject.otherexecutive functioning
dc.subject.otherneuropsychology
dc.subject.otherremission
dc.subject.otheryouth
dc.titleDomainâ specific impairment in cognitive control among remitted youth with a history of major depression
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelPsychiatry
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/138407/1/eip12253_am.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/138407/2/eip12253.pdf
dc.identifier.doi10.1111/eip.12253
dc.identifier.sourceEarly Intervention in Psychiatry
dc.identifier.citedreferenceRund BR, Sundet K, Asbjornsen A et al. Neuropsychological test profiles in schizophrenia and nonâ psychotic depression. Acta Psychiatr Scand 2006; 113: 350 â 359.
dc.identifier.citedreferenceNurnberger JI Jr, Blehar MC, Kaufmann CA et al. Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative. Arch Gen Psychiatry 1994; 51: 849 â 859, discussion 63â 4.
dc.identifier.citedreferenceHamilton M. The assessment of anxiety states by rating. Br J Med Psychol 1959; 32: 50 â 55.
dc.identifier.citedreferenceStoelting GC. Stroop Color and Word Test. Chicago; 1978.
dc.identifier.citedreferenceRuff RM, Light RH, Parker SB, Levin HS. Benton controlled oral word association test: reliability and updated norms. Arch Clin Neuropsychol 1996; 11: 329 â 338.
dc.identifier.citedreferenceWechsler D. Wechsler Adult Intelligence Scaleâ Fourth Edition (WAISâ IV). San Antonio, TX: NCS Pearson; 2008.
dc.identifier.citedreferenceReitan RM. Validity of the Trail Making Test as an indicator of organic brain damage. Percept Mot Skills 1958; 8: 271 â 276.
dc.identifier.citedreferenceLangenecker SA, Zubieta JK, Young EA, Akil H, Nielson KA. A task to manipulate attentional load, setâ shifting, and inhibitory control: convergent validity and testâ retest reliability of the Parametric Go/Noâ Go Test. J Clin Exp Neuropsychol 2007; 29: 842 â 853.
dc.identifier.citedreferenceVotruba KL, Langenecker SA. Factor structure, construct validity, and ageâ and educationâ based normative data for the Parametric Go/Noâ Go Test. J Clin Exp Neuropsychol 2013; 35: 132 â 146.
dc.identifier.citedreferenceBleiberg J, Kane RL, Reeves DL, Garmoe WS, Halpern E. Factor analysis of computerized and traditional tests used in mild brain injury research. Clin Neuropsychol 2000; 14: 287 â 294.
dc.identifier.citedreferenceRyan KA, Vederman AC, McFadden EM et al. Differential executive functioning performance by phase of bipolar disorder. Bipolar Disord 2012; 14: 527 â 536.
dc.identifier.citedreferenceLangenecker SA, Saunders EF, Kade AM, Ransom MT, McInnis MG. Intermediate: cognitive phenotypes in bipolar disorder. J Affect Disord 2010; 122: 285 â 293.
dc.identifier.citedreferenceLaird NM, Ware JH. Randomâ effects models for longitudinal data. Biometrics 1982; 38: 963 â 974.
dc.identifier.citedreferenceLangenecker SA, Saunders EFH, Kade AM, Ransom MT, McInnis MG. Intermediate cognitive phenotypes in bipolar disorder. J Affect Disord 2010; 122: 285 â 293.
dc.identifier.citedreferenceBinder LM, Iverson GL, Brooks BL. To err is human: â abnormalâ neuropsychological scores and variability are common in healthy adults. Arch Clin Neuropsychol 2009; 24: 31 â 46.
dc.identifier.citedreferenceSchretlen DJ, Testa SM, Winicki JM, Pearlson GD, Gordon B. Frequency and bases of abnormal performance by healthy adults on neuropsychological testing. J Int Neuropsychol Soc 2008; 14: 436 â 445.
dc.identifier.citedreferenceCastaneda AE, Tuulioâ Henriksson A, Marttunen M, Suvisaari J, Lonnqvist J. A review on cognitive impairments in depressive and anxiety disorders with a focus on young adults. J Affect Disord 2008; 106: 1 â 27.
dc.identifier.citedreferenceLuna B. Developmental changes in cognitive control through adolescence. Adv Child Dev Behav 2009; 37: 233 â 278.
dc.identifier.citedreferenceBlakemore SJ, Choudhury S. Development of the adolescent brain: implications for executive function and social cognition. J Child Psychol Psychiatry 2006; 47: 296 â 312.
dc.identifier.citedreferenceDe Luca CR, Wood SJ, Anderson V et al. Normative data from the CANTAB. I: development of executive function over the lifespan. J Clin Exp Neuropsychol 2003; 25: 242 â 254.
dc.identifier.citedreferenceTaylor SJ, Barker LA, Heavey L, McHale S. The typical developmental trajectory of social and executive functions in late adolescence and early adulthood. Dev Psychol 2013; 49: 1253 â 1265.
dc.identifier.citedreferenceRubia K, Russell T, Overmeyer S et al. Mapping motor inhibition: conjunctive brain activations across different versions of go/noâ go and stop tasks. Neuroimage 2001; 13: 250 â 261.
dc.identifier.citedreferenceBuchsbaum BR, Greer S, Chang WL, Berman KF. Metaâ analysis of neuroimaging studies of the Wisconsin cardâ sorting task and component processes. Hum Brain Mapp 2005; 25: 35 â 45.
dc.identifier.citedreferenceMacDonald AW 3rd, Cohen JD, Stenger VA, Carter CS. Dissociating the role of the dorsolateral prefrontal and anterior cingulate cortex in cognitive control. Science 2000; 288: 1835 â 1838.
dc.identifier.citedreferenceMiller EK, Cohen JD. An integrative theory of prefrontal cortex function. Annu Rev Neurosci 2001; 24: 167 â 202.
dc.identifier.citedreferenceHolmes AJ, MacDonald A 3rd, Carter CS, Barch DM, Andrew Stenger V, Cohen JD. Prefrontal functioning during context processing in schizophrenia and major depression: an eventâ related fMRI study. Schizophr Res 2005; 76: 199 â 206.
dc.identifier.citedreferenceWagner G, Sinsel E, Sobanski T et al. Cortical inefficiency in patients with unipolar depression: an eventâ related FMRI study with the Stroop task. Biol Psychiatry 2006; 59: 958 â 965.
dc.identifier.citedreferenceMatthews S, Simmons A, Strigo I, Gianaros P, Yang T, Paulus M. Inhibitionâ related activity in subgenual cingulate is associated with symptom severity in major depression. Psychiatry Res 2009; 172: 1 â 6.
dc.identifier.citedreferenceJoormann J, Quinn ME. Cognitive processes and emotion regulation in depression. Depress Anxiety 2014; 31: 308 â 315.
dc.identifier.citedreferenceCalkins AW, McMorran KE, Siegle GJ, Otto MW. The effects of computerized cognitive control training on community adults with depressed mood. Behav Cogn Psychother 2014; 3: 1 â 12.
dc.identifier.citedreferenceJaeger J, Berns S, Uzelac S, Davisâ Conway S. Neurocognitive deficits and disability in major depressive disorder. Psychiatry Res 2006; 145: 39 â 48.
dc.identifier.citedreferenceMcCall WV, Dunn AG. Cognitive deficits are associated with functional impairment in severely depressed patients. Psychiatry Res 2003; 121: 179 â 184.
dc.identifier.citedreferenceNaismith SL, Longley WA, Scott EM, Hickie IB. Disability in major depression related to selfâ rated and objectivelyâ measured cognitive deficits: a preliminary study. BMC Psychiatry 2007; 7: 32.
dc.identifier.citedreferencePorter RJ, Gallagher P, Thompson JM, Young AH. Neurocognitive impairment in drugâ free patients with major depressive disorder. Br J Psychiatry 2003; 182: 214 â 220.
dc.identifier.citedreferenceCohen R, Lohr I, Paul R, Boland R. Impairments of attention and effort among patients with major affective disorders. J Neuropsychiatry Clin Neurosci 2001; 13: 385 â 395.
dc.identifier.citedreferenceKoetsier GC, Volkers AC, Tulen JH, Passchier J, van den Broek WW, Bruijn JA. CPT performance in major depressive disorder before and after treatment with imipramine or fluvoxamine. J Psychiatr Res 2002; 36: 391 â 397.
dc.identifier.citedreferenceKeilp JG, Gorlyn M, Oquendo MA, Burke AK, Mann JJ. Attention deficit in depressed suicide attempters. Psychiatry Res 2008; 159: 7 â 17.
dc.identifier.citedreferenceLandro NI, Stiles TC, Sletvold H. Neuropsychological function in nonpsychotic unipolar major depression. Neuropsychiatry Neuropsychol Behav Neurol 2001; 14: 233 â 240.
dc.identifier.citedreferenceRavnkilde B, Videbech P, Clemmensen K, Egander A, Rasmussen NA, Rosenberg R. Cognitive deficits in major depression. Scand J Psychol 2002; 43: 239 â 251.
dc.identifier.citedreferenceLampe IK, Sitskoorn MM, Heeren TJ. Effects of recurrent major depressive disorder on behavior and cognitive function in female depressed patients. Psychiatry Res 2004; 125: 73 â 79.
dc.identifier.citedreferenceLangenecker SA, Caveney AF, Giordani B et al. The sensitivity and psychometric properties of a brief computerâ based cognitive screening battery in a depression clinic. Psychiatry Res 2007; 152: 143 â 154.
dc.identifier.citedreferenceHammar A, Lund A, Hugdahl K. Selective impairment in effortful information processing in major depression. J Int Neuropsychol Soc 2003; 9: 954 â 959.
dc.identifier.citedreferenceSingh MK, DelBello MP, Fleck DE, Shear PK, Strakowski SM. Inhibition and attention in adolescents with nonmanic mood disorders and a high risk for developing mania. J Clin Exp Neuropsychol 2009; 31: 1 â 7.
dc.identifier.citedreferenceAsthana HS, Mandal MK, Khurana H, Haqueâ Nizamie S. Visuospatial and affect recognition deficit in depression. J Affect Disord 1998; 48: 57 â 62.
dc.identifier.citedreferenceFossati P, Coyette F, Ergis AM, Allilaire JF. Influence of age and executive functioning on verbal memory of inpatients with depression. J Affect Disord 2002; 68: 261 â 271.
dc.identifier.citedreferenceVythilingam M, Vermetten E, Anderson GM et al. Hippocampal volume, memory, and cortisol status in major depressive disorder: effects of treatment. Biol Psychiatry 2004; 56: 101 â 112.
dc.identifier.citedreferenceNaismith SL, Hickie IB, Turner K et al. Neuropsychological performance in patients with depression is associated with clinical, etiological and genetic risk factors. J Clin Exp Neuropsychol 2003; 25: 866 â 877.
dc.identifier.citedreferenceLangenecker SA, Kennedy SE, Guidotti LM et al. Frontal and limbic activation during inhibitory control predicts treatment response in major depressive disorder. Biol Psychiatry 2007; 62: 1272 â 1280.
dc.identifier.citedreferenceElderkinâ Thompson V, Moody T, Knowlton B, Hellemann G, Kumar A. Explicit and implicit memory in lateâ life depression. Am J Geriatr Psychiatry 2011; 19: 364 â 373.
dc.identifier.citedreferenceBasso M, Combs D, Purdie R, Candilis P, Bornstein R. Neuropsychological correlates of symptom dimensions in inpatients with major depressive disorder. Psychiatry Res 2013; 207: 61 â 67.
dc.identifier.citedreferenceDunkin JJ, Leuchter AF, Cook IA, Kaslâ Godley JE, Abrams M, Rosenbergâ Thompson S. Executive dysfunction predicts nonresponse to fluoxetine in major depression. J Affect Disord 2000; 60: 13 â 23.
dc.identifier.citedreferenceMohr DC, Epstein L, Luks TL et al. Brain lesion volume and neuropsychological function predict efficacy of treatment for depression in multiple sclerosis. J Consult Clin Psychol 2003; 71: 1017 â 1024.
dc.identifier.citedreferencePotter GG, Kittinger JD, Wagner HR, Steffens DC, Krishnan KR. Prefrontal neuropsychological predictors of treatment remission in lateâ life depression. Neuropsychopharmacology 2004; 29: 2266 â 2271.
dc.identifier.citedreferenceRoiser JP, Elliott R, Sahakian BJ. Cognitive mechanisms of treatment in depression. Neuropsychopharmacology 2012; 37: 117 â 136.
dc.identifier.citedreferenceDouglas KM, Porter RJ, Knight RG, Maruff P. Neuropsychological changes and treatment response in severe depression. Br J Psychiatry 2011; 198: 115 â 122.
dc.identifier.citedreferenceMcClintock SM, Husain MM, Greer TL, Cullum CM. Association between depression severity and neurocognitive function in major depressive disorder: a review and synthesis. Neuropsychology 2010; 24: 9 â 34.
dc.identifier.citedreferenceTrivedi MH, Greer TL. Cognitive dysfunction in unipolar depression: implications for treatment. J Affect Disord 2014; 152â 154: 19 â 27.
dc.identifier.citedreferenceBaune BT, Fuhr M, Air T, Hering C. Neuropsychological functioning in adolescents and young adults with major depressive disorderâ a review. Psychiatry Res 2014; 218: 261 â 271.
dc.identifier.citedreferenceSnyder HR. Major depressive disorder is associated with broad impairments on neuropsychological measures of executive function: a metaâ analysis and review. Psychol Bull 2013; 139: 81 â 132.
dc.identifier.citedreferenceMoylan S, Maes M, Wray NR, Berk M. The neuroprogressive nature of major depressive disorder: pathways to disease evolution and resistance, and therapeutic implications. Mol Psychiatry 2013; 18: 595 â 606.
dc.identifier.citedreferenceHasler G, Drevets WC, Manji HK, Charney DS. Discovering endophenotypes for major depression. Neuropsychopharmacology 2004; 29: 1765 â 1781.
dc.identifier.citedreferenceHasselbalch BJ, Knorr U, Kessing LV. Cognitive impairment in the remitted state of unipolar depressive disorder: a systematic review. J Affect Disord 2011; 134: 20 â 31.
dc.identifier.citedreferenceDouglas KM, Porter RJ. Longitudinal assessment of neuropsychological function in major depression. Aust N Z J Psychiatry 2009; 43: 1105 â 1117.
dc.identifier.citedreferenceNebes RD, Pollock BG, Houck PR et al. Persistence of cognitive impairment in geriatric patients following antidepressant treatment: a randomized, doubleâ blind clinical trial with nortriptyline and paroxetine. J Psychiatr Res 2003; 37: 99 â 108.
dc.identifier.citedreferenceBhalla RK, Butters MA, Mulsant BH et al. Persistence of neuropsychologic deficits in the remitted state of lateâ life depression. Am J Geriatr Psychiatry 2006; 14: 419 â 427.
dc.identifier.citedreferenceLee JS, Potter GG, Wagner HR, Welshâ Bohmer KA, Steffens DC. Persistent mild cognitive impairment in geriatric depression. Int Psychogeriatr 2007; 19: 125 â 135.
dc.identifier.citedreferencePortella MJ, Marcos T, Rami L, Navarro V, Gasto C, Salamero M. Residual cognitive impairment in lateâ life depression after a 12â month period followâ up. Int J Geriatr Psychiatry 2003; 18: 571 â 576.
dc.identifier.citedreferenceHamilton M. A rating scale for depression. J Neurol Neurosurg Psychiatry 1960; 23: 56 â 62.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.