Differences in course of illness between patients with bipolar II disorder with and without epileptiform discharges or other sharp activity on electroencephalograms: a cross-sectional study

O K Drange, S G Sæther, P I Finseth, G Morken, A E Vaaler, V Arntsen, O Henning, O A Andreassen, T Elvsåshagen, U F Malt, E Bøen, O K Drange, S G Sæther, P I Finseth, G Morken, A E Vaaler, V Arntsen, O Henning, O A Andreassen, T Elvsåshagen, U F Malt, E Bøen

Abstract

Background: A diagnosis of bipolar II disorder requires that the symptoms cannot be better explained by a medical condition. Epilepsy is in some cases associated with an affective syndrome mimicking an unstable bipolar II disorder. Epileptiform discharges on electroencephalograms (EEGs) are typical, but not pathognomonic, for epilepsy. A previous study has found a high frequency of epileptiform discharges and other sharp activity among patients with bipolar disorder. The aim of the study was to identify if epileptic discharges or other sharp activity per se are associated with an altered course of illness among patients with bipolar II disorder.

Methods: Eighty six patients diagnosed with bipolar II disorder at two psychiatric departments were interviewed about prior course of illness and assessed with EEGs. The patients were split into two groups based on the presence (n = 12) or absence (n = 74) of epileptiform discharges or other sharp activity. Wilcoxon rank sum test, Fisher's exact test, and Pearson's chi squared test were used to assess differences between the groups on six variables of course of illness.

Results: Patients with epileptiform discharges or other sharp activity had a history of more hypomanic episodes per year (median (interquartile range (IQR)) 1.5 (3.2) vs. 0.61 (1.1), p = 0.0090) and a higher hypomania:depression ratio (median (IQR) 3.2 (16) vs. 1.0 (1.0), p = 0.00091) as compared to patients without. None of the patients with epileptiform discharges or other sharp activity had self-reported epileptic seizures in their history.

Conclusions: Epileptiform discharges or other sharp activity on EEGs are associated with more hypomanic episodes and an increased hypomania:depression ratio. Our results warrant replication in prospective studies, but suggest that EEG findings could be of prognostic importance for patients diagnosed with bipolar II disorder in psychiatric care.

Trial registration: ClinicalTrials.gov ( NCT00201526 ).

Keywords: Bipolar disorder; Electroencephalography; Epileptiform discharges; Sharp activity.

Conflict of interest statement

OKD, SGS, PIF, GM, AEV, VA, and UFM declare that they have no competing interests. OAA has received speaker’s fees from Lundbeck, and is a consultant to HealthLytix. OH has received speaker’s fees from UCB, Livanova, and Eisai. TE has received speaker’s fees from Lundbeck and Janssen Cilag. EB has received speaker’s fees from Lundbeck.

Figures

Fig. 1
Fig. 1
Frequency and ratio of depressive and hypomanic episodes among patients with and without epileptiform discharges or other sharp activity. Data are presented as violin plots with individual level data points at logarithmic y-axes. A small horizontal and vertical jitter is added to better discriminate overlying data points

References

    1. American Psychiatric Association . Diagnostic and statistical manual of mental disorders: diagnostic and statistical manual of mental disorders. 5. Arlington: American Psychiatric Association; 2013.
    1. Merikangas KR, Jin R, He JP, Kessler RC, Lee S, Sampson NA, et al. Prevalence and correlates of bipolar spectrum disorder in the world mental health survey initiative. Arch Gen Psychiatry. 2011;68:241–251. doi: 10.1001/archgenpsychiatry.2011.12.
    1. Merikangas KR, Akiskal HS, Angst J, Greenberg PE, Hirschfeld RM, Petukhova M, et al. Lifetime and 12-month prevalence of bipolar spectrum disorder in the National Comorbidity Survey replication. Arch Gen Psychiatry. 2007;64:543–552. doi: 10.1001/archpsyc.64.5.543.
    1. Regeer EJ, Kupka RW, ten Have M, Vollebergh W, Nolen WA. Low self-recognition and awareness of past hypomanic and manic episodes in the general population. Int J Bipolar Disord. 2015;3:22. doi: 10.1186/s40345-015-0039-8.
    1. Jackson AF, Bolger DJ. The neurophysiological bases of EEG and EEG measurement: a review for the rest of us. Psychophysiology. 2014;51:1061–1071. doi: 10.1111/psyp.12283.
    1. Beniczky S, Aurlien H, Brøgger JC, Fuglsang-Frederiksen A, Martins-Da-Silva A, Trinka E, et al. Standardized Computer-based Organized Reporting of EEG: SCORE. Epilepsia. 2013;54:Appendix S4. doi: 10.1111/epi.12228.
    1. Kane N, Acharya J, Benickzy S, Caboclo L, Finnigan S, Kaplan PW, et al. A revised glossary of terms most commonly used by clinical electroencephalographers and updated proposal for the report format of the EEG findings. Revision 2017. Clin Neurophysiol Pract. 2017;2:170–185. doi: 10.1016/j.cnp.2017.07.002.
    1. Fisher RS, Acevedo C, Arzimanoglou A, Bogacz A, Cross JH, Elger CE, et al. ILAE official report: a practical clinical definition of epilepsy. Epilepsia. 2014;55:475–482. doi: 10.1111/epi.12550.
    1. Krishnamoorthy E, Trimble M, Blumer D. The classification of neuropsychiatric disorders in epilepsy: a proposal by the ILAE commission on psychobiology of epilepsy. Epilepsy Behav. 2007;10:349–353. doi: 10.1016/j.yebeh.2006.10.002.
    1. Knott S, Forty L, Craddock N, Thomas RH. Epilepsy and bipolar disorder. Epilepsy Behav. 2015;52:267–274. doi: 10.1016/j.yebeh.2015.07.003.
    1. Mula M. The clinical spectrum of bipolar symptoms in epilepsy: a critical reappraisal. Postgrad Med. 2010;122:17–23. doi: 10.3810/pgm.2010.07.2171.
    1. Pillai J, Sperling MR. Interictal EEG and the diagnosis of epilepsy. Epilepsia. 2006;47(Suppl. 1):14–22. doi: 10.1111/j.1528-1167.2006.00654.x.
    1. Gregory RP, Oates T, Merry RTG. Electroencephalogram epileptiform abnormalities in candidates for aircrew training. Electroencephalogr Clin Neurophysiol. 1993;86:75–77. doi: 10.1016/0013-4694(93)90069-8.
    1. Seidel S, Pablik E, Aull-Watschinger S, Seidl B, Pataraia E. Incidental epileptiform discharges in patients of a tertiary Centre. Clin Neurophysiol. 2016;127:102–107. doi: 10.1016/j.clinph.2015.02.056.
    1. Small JG, Milstein V, Medlock CE. Clinical EEG findings in mania. Clin Electroencephalogr. 1997;28:229–235. doi: 10.1177/155005949702800408.
    1. Levy AB, Drake ME, Shy KE. EEG evidence of epileptiform paroxysms in rapid cycling bipolar patients. J Clin Psychiatry. 1988;49:232–234.
    1. Cole AJ, Scott J, Ferrier IN, Eccleston D. Patterns of treatment resistance in bipolar affective disorder. Acta Psychiatr Scand. 1993;88:121–123. doi: 10.1111/j.1600-0447.1993.tb03424.x.
    1. First MB, Spitzer R, Gibbon M, Williams JB. Structured clinical interview for DSM–IV – patient version. Washington, DC: Am Psychiatr Press; 1997.
    1. Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, Weiller E, et al. The mini-international neuropsychiatric interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. 1998;59(Suppl 2):22–33.
    1. Angst J, Adolfsson R, Benazzi F, Gamma A, Hantouche E, Meyer TD, et al. The HCL-32: towards a self-assessment tool for hypomanic symptoms in outpatients. J Affect Disord. 2005;88:217–233. doi: 10.1016/j.jad.2005.05.011.
    1. Leverich GS, Nolen WA, Rush AJ, McElroy SL, Keck PE, Denicoff KD, et al. The Stanley Foundation bipolar treatment outcome network: I. Longitudinal methodology. J Affeect Disord. 2001;67:33–44. doi: 10.1016/S0165-0327(01)00430-X.
    1. Rush AJ, Gullion CM, Basco MR, Jarrett RB, Trivedi MH. The inventory of depressive symptomatology (IDS): psychometric properties. Psychol Med. 1996;26:477–486. doi: 10.1017/S0033291700035558.
    1. Young RC, Biggs JT, Ziegler VE, Meyer DA. A rating scale for mania: reliability, Validity and Sensitivity. Br J Psychiatry. 1978;133:429–435. doi: 10.1192/bjp.133.5.429.
    1. Core Team R. R: a language and environment for statistical computing. Vienna: R Foundation for oStatistical Computing; 2019.
    1. RStudio Team . RStudio: integrated development for R. Boston: RStudio, Inc.; 2015.
    1. Shukla S, Cook BL, Mukherjee S, Godwin C, Miller MG. Mania following head trauma. Am J Psychiatry. 1987;144:93–96. doi: 10.1176/ajp.144.10.1379.
    1. Tondo L, Vazquez G, Baldessarini R. Depression and mania in bipolar disorder. Curr Neuropharmacol. 2017;15:353–358. doi: 10.2174/1570159X14666160606210811.
    1. Drange OK, Vaaler AE, Morken G, Andreassen OA, Malt UF, Finseth PI. Clinical characteristics of patients with bipolar disorder and premorbid traumatic brain injury: a cross-sectional study. Int J Bipolar Disord. 2018;6:19. doi: 10.1186/s40345-018-0128-6.
    1. Pettersson E, Lichtenstein P, Larsson H, Song J, Agrawal A, Børglum AD, et al. Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls. Psychol Med. 2018;49:1166–73. doi: 10.1017/S0033291718002039.
    1. Kjeldsen MJ, Corey LA, Christensen K, Friis ML. Epileptic seizures and syndromes in twins: the importance of genetic factors. Epilepsy Res. 2003;55:137–146. doi: 10.1016/S0920-1211(03)00117-7.
    1. Sucksdorff D, Brown AS, Chudal R, Jokiranta-Olkoniemi E, Leivonen S, Suominen A, et al. Parental and comorbid epilepsy in persons with bipolar disorder. J Affect Disord. 2015;188:107–111. doi: 10.1016/j.jad.2015.08.051.
    1. Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, et al. Analysis of shared heritability in common disorders of the brain. Science. 2018;360:6395.
    1. Smeland OB, Frei O, Shadrin A, O’Connell K, Fan C-C, Bahrami S, et al. Discovery of shared genomic loci using the conditional false discovery rate approach. Hum Genet. 2020;139:85–94. doi: 10.1007/s00439-019-02060-2.
    1. Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, et al. Genomewide association study identifies 30 loci associated with bipolar disorder. Nat Genet. 2019;51:793–803. doi: 10.1038/s41588-019-0397-8.
    1. Lopez AY, Wang X, Xu M, Maheshwari A, Curry D, Lam S, et al. Ankyrin-G isoform imbalance and interneuronopathy link epilepsy and bipolar disorder. Mol Psychiatry. 2017;22:1464–1472. doi: 10.1038/mp.2016.233.
    1. Allen AS, Berkovic SF, Cossette P, Delanty N, Dlugos D, Eichler EE, et al. De novo mutations in epileptic encephalopathies. Nature. 2013;501:217–221. doi: 10.1038/nature12439.
    1. Baldin E, Hauser WA, Buchhalter JR, Hesdorffer DC, Ottman R. Yield of epileptiform electroencephalogram abnormalities in incident unprovoked seizures: a population-based study. Epilepsia. 2014;55:1389–1398. doi: 10.1111/epi.12720.

Source: PubMed

3
Předplatit