Hostname: page-component-8448b6f56d-jr42d Total loading time: 0 Render date: 2024-04-24T02:47:20.343Z Has data issue: false hasContentIssue false

Cognition and autonomic function in schizophrenia: Inferior cognitive test performance in electrodermal and niacin skin flush non-responders

Published online by Cambridge University Press:  15 April 2020

B.M. Nilsson*
Affiliation:
Department of Neuroscience, Psychiatry, Uppsala University, SE-751 85Uppsala, Sweden
G Holm
Affiliation:
Department of Neuroscience, Psychiatry, Uppsala University, SE-751 85Uppsala, Sweden
C.M. Hultman
Affiliation:
Department of Medical Epidemiology and Biostatistics, Karolinska Institute, SE-17177Stockholm, Sweden
L. Ekselius
Affiliation:
Department of Neuroscience, Psychiatry, Uppsala University, SE-751 85Uppsala, Sweden
*
*Corresponding author. Department of Neuroscience, Psychiatry, Uppsala University Hospital, SE-75185 Uppsala, Sweden. Tel.: +46767248848/46706144489. E-mail address:bjorn.nilsson@neuro.uu.se, bjorn.nilsson@akademiska.se (B.M. Nilsson).
Get access

Abstract

Background:

Patients with schizophrenia suffer from a broad range of cognitive disturbances. The impact in terms of functional outcome is significant. There are also several reports of disturbed autonomic regulation in the disease. The present study examined cognitive function as well as psychophysiological parameters in patients with schizophrenia and healthy controls.

Methods:

Twenty-five patients and 14 controls were investigated with electrodermal activity (EDA), an oral niacin skin flush test and a comprehensive neurocognitive test program including the Wechsler battery (WAIS-R), Fingertapping Test, Trail Making Test, Verbal Fluency, Benton Visual Retention Test, Wisconsin Card Sorting Test and Rey Auditory Verbal Learning Test.

Results:

The patients generally had inferior test results compared to controls. Further analysis revealed that the EDA non-responding patient group explained this variation with significant lower test results than controls. On executive tests, EDA non-responders also performed significantly worse than EDA responding patients. The small group of niacin non-responding patients exhibited an even lower overall test performance. Delayed niacin flush also correlated inversely with psychomotor function and IQ in the patients.

Conclusion:

The findings support the hypothesis of a neurodevelopment disturbance affecting both autonomic function and higher cortical function in schizophrenia.

Type
Original article
Copyright
Copyright © Elsevier Masson SAS 2015

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bar, KJ, Letzsch, A, Jochum, T, Wagner, G, Greiner, W, Sauer, H. Loss of efferent vagal activity in acute schizophrenia. J Psychiatr Res 2005;39:519527.CrossRefGoogle ScholarPubMed
Boden, R, Lindstrom, L, Rautaharju, P, Sundstrom, J. Electrocardiographic signs of autonomic imbalance in medicated patients with first-episode schizophrenia spectrum disorders--relations to first treatment discontinuation and five-year remission status. Eur Psychiatry 2012;27:213218.CrossRefGoogle ScholarPubMed
Bosveld-van Haandel, L, Knegtering, R, Kluiter, H, van den Bosch, RJ. Niacin skin flushing in schizophrenic and depressed patients and healthy controls. Psychiatry Res 2006;143:303306.CrossRefGoogle ScholarPubMed
Brekke, JS, Raine, A, Ansel, M, Lencz, T, Bird, L. Neuropsychological and psychophysiological correlates of psychosocial functioning in schizophrenia. Schizophr Bull 1997;23:1928.CrossRefGoogle Scholar
Brekke, JS, Raine, A, Thomson, C. Cognitive and psychophysiological correlates of positive, negative, and disorganized symptoms in the schizophrenia spectrum. Psychiatry Res 1995;57:241250.CrossRefGoogle ScholarPubMed
Chang, SS, Liu, CM, Lin, SH, Hwu, HG, Hwang, TJ, Liu, SK, et al.Impaired flush response to niacin skin patch among schizophrenia patients and their nonpsychotic relatives: the effect of genetic loading. Schizophr Bull 2009;35:213221.CrossRefGoogle ScholarPubMed
Chouinard, G, Margolese, HC. Manual for the Extrapyramidal Symptom Rating Scale (ESRS). Schizophr Res 2005;76:247265.CrossRefGoogle Scholar
Dawson, ME, Nuechterlein, KH. Psychophysiological dysfunctions in the developmental course of schizophrenic disorders. Schizophr Bull 1984;10:204232.CrossRefGoogle ScholarPubMed
Dawson, ME, Nuechterlein, KH, Schell, AM, Gitlin, M, Ventura, J. Autonomic abnormalities in schizophrenia. State or trait indicators?. Arch Gen Psychiatry 1994;51:813824.CrossRefGoogle ScholarPubMed
Dawson, ME, Schell, AM. What does electrodermal activity tell us about prognosis in the schizophrenia spectrum?. Schizophr Res 2002;54:8793.CrossRefGoogle ScholarPubMed
Drummond, PD, Lance, JW. Facial flushing and sweating mediated by the sympathetic nervous system. Brain 1987;110(Pt 3)793803.CrossRefGoogle ScholarPubMed
Drummond, PD, Lazaroo, D. The effect of niacin on facial blood flow in people with an elevated fear of negative evaluation. Eur Neuropsychopharmacol 2012;22:200204.CrossRefGoogle ScholarPubMed
Fuentes, I, Garcia Merita, M, Miquel, M, Rojo, J. Relationships between electrodermal activity and symptomatology in schizophrenia. Psychopathology 1993;26:4752.CrossRefGoogle Scholar
Glen, AI, Cooper, SJ, Rybakowski, J, Vaddadi, K, Brayshaw, N, Horrobin, DF. Membrane fatty acids, niacin flushing and clinical parameters. Prostaglandins Leukot Essent Fatty Acids 1996;55:915.CrossRefGoogle ScholarPubMed
Gruzelier, JH, Venables, PH. Skin conductance orienting activity in a heterogeneous sample of schizophrenics. J Nerv Ment Dis 1972;155:277287.CrossRefGoogle Scholar
Horrobin, DF, Glen, AI, Vaddadi, K. The membrane hypothesis of schizophrenia. Schizophr Res 1994;13:195207.CrossRefGoogle ScholarPubMed
Hudson, CJ, Lin, A, Cogan, S, Cashman, F, Warsh, JJ. The niacin challenge test: clinical manifestation of altered transmembrane signal transduction in schizophrenia?. Biol Psychiatry 1997;41:507513.CrossRefGoogle Scholar
Hultman, CM, Ohlund, LS, Wieselgren, IM, Ohman, A, Ost, LG. Electrodermal activity and social network as predictors of outcome of episodes in schizophrenia. J. Abnorm Psychol 1996;105:626636.CrossRefGoogle Scholar
Ikezawa, S, Corbera, S, Liu, J, Wexler, BE. Empathy in electrodermal responsive and nonresponsive patients with schizophrenia. Schizophr Res 2012;142:7176.CrossRefGoogle ScholarPubMed
Israel, AK, Seeck, A, Boettger, MK, Rachow, T, Berger, S, Voss, A, et al.Peripheral endothelial dysfunction in patients suffering from acute schizophrenia: a potential marker for cardiovascular morbidity?. Schizophr Res 2011;128:4450.CrossRefGoogle ScholarPubMed
Kamanna, VS, Ganji, SH, Kashyap, ML. The mechanism and mitigation of niacin-induced flushing. Int J Clin Pract 2009;63:13691377.CrossRefGoogle ScholarPubMed
Kay, SR, Fiszbein, A, Opler, LA. The positive and negative syndrome scale (PANSS) for schizophrenia. Schizophr Bull 1987;13:261276.CrossRefGoogle Scholar
Kim, DK, Shin, YM, Kim, CE, Cho, HS, Kim, YS. Electrodermal responsiveness, clinical variables, and brain imaging in male chronic schizophrenics. Biol Psychiatry 1993;33:786793.Google ScholarPubMed
Levinson, DF, Edelberg, R. Scoring criteria for response latency and habituation in electrodermal research: a critique. Psychophysiology 1985;22:417426.CrossRefGoogle ScholarPubMed
Lezak, MDNeuropsychological assessment, Third edition, New York: Oxford University Press; 1995.Google Scholar
Lin, SH, Liu, CM, Chang, SS, Hwu, HG, Liu, SK, Hwang, TJ, et al.Familial aggregation in skin flush response to niacin patch among schizophrenic patients and their nonpsychotic relatives. Schizophr Bull 2007;33:174182.CrossRefGoogle ScholarPubMed
Lindstrom, LHClinical and biological markers for outcome in schizophrenia: a review of a longitudinal follow-up study in Uppsala schizophrenia research project. Neuropsychopharmacology 1996;14:23S26S.CrossRefGoogle ScholarPubMed
Liu, CM, Chang, SS, Liao, SC, Hwang, TJ, Shieh, MH, Liu, SK, et al.Absent response to niacin skin patch is specific to schizophrenia and independent of smoking. Psychiatry Res 2007;152:181187.CrossRefGoogle ScholarPubMed
Lysaker, PH, Bryson, GJ, Lancaster, RS, Evans, JD, Bell, MDInsight in schizophrenia: associations with executive function and coping style. Schizophr Res 2003;59:4147.CrossRefGoogle ScholarPubMed
Mathewson, KJ, Jetha, MK, Goldberg, JO, Schmidt, LAAutonomic regulation predicts performance on Wisconsin Card Sorting Test (WCST) in adults with schizophrenia. Biol Psychol 2012;91:389399.CrossRefGoogle ScholarPubMed
Messamore, ENiacin subsensitivity is associated with functional impairment in schizophrenia. Schizophr Res 2012;137:180184.CrossRefGoogle Scholar
Messamore, E, Hoffman, WF, Janowsky, AThe niacin skin flush abnormality in schizophrenia: a quantitative dose-response study. Schizophr Res 2003;62:251258.CrossRefGoogle ScholarPubMed
Messamore, E, Hoffman, WF, Yao, JKNiacin sensitivity and the arachidonic acid pathway in schizophrenia. Schizophr Res 2010;122:248256.CrossRefGoogle Scholar
Montgomery, P, Burton, JR, Sewell, RP, Spreckelsen, TF, Richardson, AJLow blood long chain omega-3 fatty acids in UK children are associated with poor cognitive performance and behavior: a cross-sectional analysis from the DOLAB study. PLoS ONE 8 2013 e66697.CrossRefGoogle ScholarPubMed
Morrow, JD, Parsons, WG 3rd WG, Roberts, LJ 2nd LJ. Release of markedly increased quantities of prostaglandin D2 in vivo in humans following the administration of nicotinic acid. Prostaglandins 1989;38:263274.CrossRefGoogle ScholarPubMed
Nadalin, S, Giacometti, J, Jonovska, S, Tomljanovic, D, Buretic-Tomljanovic, AThe impact of PLA2G4A and PTGS2 gene polymorphisms, and red blood cell PUFAs deficit on niacin skin flush response in schizophrenia patients. Prostaglandins Leukot Essent Fatty Acids 2013;88:185190.CrossRefGoogle ScholarPubMed
Nilsson, BM, Hultman, CM, Ekselius, LTest-retest stability of the oral niacin test and electrodermal activity in patients with schizophrenia. Prostaglandins Leukot Essent Fatty Acids 2009;81:367372.CrossRefGoogle ScholarPubMed
Nilsson, BM, Hultman, CM, Wiesel, FANiacin skin-flush response and electrodermal activity in patients with schizophrenia and healthy controls. Prostaglandins Leukot Essent Fatty Acids 2006;74:339346.CrossRefGoogle ScholarPubMed
Ohman, AElectrodermal activity and vulnerability to schizophrenia: a review. Biol Psychol 1981;12:87145.CrossRefGoogle ScholarPubMed
Ohman, A, Ohlund, LS, Alm, T, Wieselgren, IM, Ost, LG, Lindstrom, LHElectrodermal nonresponding, premorbid adjustment, and symptomatology as predictors of long-term social functioning in schizophrenics. J Abnorm Psychol 1989;98:426435.CrossRefGoogle ScholarPubMed
Parson, HK, Harati, H, Cooper, D, Vinik, AIThe role of prostaglandin D2 and the autonomic nervous system on niacin induced flushing. J Diabetes 2012.Google Scholar
Puri, BK, Easton, T, Das, I, Kidane, L, Richardson, AJThe niacin skin flush test in schizophrenia: a replication study. Int J Clin Pract 2001;55:368370.Google ScholarPubMed
Ross, BM, Hughes, B, Turenne, S, Seeman, M, Warsh, JJReduced vasodilatory response to methylnicotinate in schizophrenia as assessed by laser Doppler flowmetry. Eur Neuropsychopharmacol 2004;14:191197.CrossRefGoogle ScholarPubMed
Schaefer, J, Giangrande, E, Weinberger, DR, Dickinson, DThe global cognitive impairment in schizophrenia: consistent over decades and around the world. Schizophr Res 2013;150:4250.CrossRefGoogle ScholarPubMed
Schell, AM, Dawson, ME, Nuechterlein, KH, Subotnik, KL, Ventura, JThe temporal stability of electrodermal variables over a one-year period in patients with recent-onset schizophrenia and in normal subjects. Psychophysiology 2002;39:124132.CrossRefGoogle Scholar
Schell, AM, Dawson, ME, Rissling, A, Ventura, J, Subotnik, KL, Gitlin, MJ, et al.Electrodermal predictors of functional outcome and negative symptoms in schizophrenia. Psychophysiology 2005;42:483492.CrossRefGoogle Scholar
Shah, SH, Vankar, GK, Peet, M, Ramchand, CNUnmedicated schizophrenic patients have a reduced skin flush in response to topical niacin. Schizophr Res 2000;43:163164.Google ScholarPubMed
Smesny, S, Berger, G, Rosburg, T, Riemann, S, Riehemann, S, McGorry, P, et al.Potential use of the topical niacin skin test in early psychosis -- a combined approach using optical reflection spectroscopy and a descriptive rating scale. J Psychiatr Res 2003;37:237247.CrossRefGoogle Scholar
Smesny, S, Rosburg, T, Riemann, S, Baur, K, Rudolph, N, Berger, G, et al.Impaired niacin sensitivity in acute first-episode but not in multi-episode schizophrenia. Prostaglandins Leukot Essent Fatty Acids 2005;72:393402.CrossRefGoogle ScholarPubMed
Strauss, JS, Carpenter, WT Jr.The prediction of outcome in schizophrenia. I. Characteristics of outcome. Arch Gen Psychiatry 1972;27:739746.CrossRefGoogle Scholar
Tavares, H, Yacubian, J, Talib, LL, Barbosa, NR, Gattaz, WFIncreased phospholipase A2 activity in schizophrenia with absent response to niacin. Schizophr Res 2003;61:16.CrossRefGoogle ScholarPubMed
Ward, PE, Sutherland, J, Glen, EM, Glen, AINiacin skin flush in schizophrenia: a preliminary report. Schizophr Res 1998;29:269274.CrossRefGoogle ScholarPubMed
Weinberger, DRImplications of normal brain development for the pathogenesis of schizophrenia. Arch Gen Psychiatry 1987;44:660669.CrossRefGoogle ScholarPubMed
Submit a response

Comments

No Comments have been published for this article.