RSS-Feed abonnieren
DOI: 10.1055/s-0038-1667412
Functional Dissociation between Cognitive Estimation and Object Naming in Focal Temporal and Frontal Lobe Epilepsies
Funding This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. Declarations of interest: None.Publikationsverlauf
Publikationsdatum:
12. August 2018 (online)
Abstract
Purpose This study addresses specific impairments of cognitive estimation and object naming in patients with focal temporal lobe epilepsy (TLE) and frontal lobe epilepsy (FLE). It was investigated whether selective impairments can be explained by differences in lesion localization and functional hemispheric specialization.
Materials and Methods Seventy-eight patients (39 females, 39 males) with FLE and TLE were investigated using the German “Test zum Kognitiven Schätzen” and the “Boston Naming Test” to assess cognitive estimation abilities and visual object naming.
Questions According to theoretical models that support a distinct hemispheric dominance for estimation and naming, it was expected that epilepsy localization in the right hemisphere would result in impairments of cognitive estimation, whereas patients with left epileptogenic foci would show deficits in object naming.
Results In comparison to a healthy control group, a significant impairment in estimation performance was present in patients with right temporal mesial and right frontal epilepsy. A significant impairment of naming performance was found in patients with left temporal mesial, right temporal mesial, left temporal neocortical, and left frontal epilepsy. Overall, localization-dependent deficits were detected in patients with hippocampal sclerosis (cognitive estimation and object naming), right frontal epilepsy (cognitive estimation), and left temporal neocortical/left frontal epilepsy (object naming). In patients with right temporal neocortical epilepsy, no functional deficits were found.
Conclusion It is hypothesized that there is a functional dissociation between cognitive estimation processes and object naming due to different functional specialization of the left and right hemispheres, respectively.
-
References
- 1 Smith ML, Milner B. Differential effects of frontal-lobe lesions on cognitive estimation and spatial memory. Neuropsychologia 1984; 22 (06) 697-705
- 2 Lewis PA, Miall RC. A right hemispheric prefrontal system for cognitive time measurement. Behav Processes 2006; 71 (02) (03) 226-234
- 3 Morin C, Guigot J, Manai R. et al. Impairment in clock-time estimation following right hemisphere ischemic damage. Brain Res Cogn Brain Res 2005; 22 (02) 305-307
- 4 Tsujii T, Sakatani K, Masuda S, Akiyama T, Watanabe S. Evaluating the roles of the inferior frontal gyrus and superior parietal lobule in deductive reasoning: an rTMS study. Neuroimage 2011; 58 (02) 640-646
- 5 Evans JS. Dual-processing accounts of reasoning, judgment, and social cognition. Annu Rev Psychol 2008; 59: 255-278
- 6 Osherson D, Perani D, Cappa S, Schnur T, Grassi F, Fazio F. Distinct brain loci in deductive versus probabilistic reasoning. Neuropsychologia 1998; 36 (04) 369-376
- 7 Upton D, Thompson PJ. General neuropsychological characteristics of frontal lobe epilepsy. Epilepsy Res 1996; 23 (02) 169-177
- 8 Maquet P, Lejeune H, Pouthas V. et al. Brain activation induced by estimation of duration: a PET study. Neuroimage 1996; 3 (02) 119-126
- 9 Woods AJ, Mennemeier M, Garcia-Rill E. et al. Bias in magnitude estimation following left hemisphere injury. Neuropsychologia 2006; 44 (08) 1406-1412
- 10 Rubia K, Schuri U, von Cramon DY, Poeppel E. Time estimation as a neuronal network property: a lesion study. Neuroreport 1997; 8 (05) 1273-1276
- 11 Wassermann EM, Blaxton TA, Hoffman EA. et al. Repetitive transcranial magnetic stimulation of the dominant hemisphere can disrupt visual naming in temporal lobe epilepsy patients. Neuropsychologia 1999; 37 (05) 537-544
- 12 Moore CJ, Price CJ. Three distinct ventral occipitotemporal regions for reading and object naming. Neuroimage 1999; 10 (02) 181-192
- 13 Oyegbile TO, Dow C, Jones J. et al. The nature and course of neuropsychological morbidity in chronic temporal lobe epilepsy. Neurology 2004; 62 (10) 1736-1742
- 14 Seidenberg M, Geary E, Hermann B. Investigating temporal lobe contribution to confrontation naming using MRI quantitative volumetrics. J Int Neuropsychol Soc 2005; 11 (04) 358-366
- 15 Bonelli SB, Powell R, Thompson PJ. et al. Hippocampal activation correlates with visual confrontation naming: fMRI findings in controls and patients with temporal lobe epilepsy. Epilepsy Res 2011; 95 (03) 246-254
- 16 Hermann BP, Perrine K, Chelune GJ. et al. Visual confrontation naming following left anterior temporal lobectomy: a comparison of surgical approaches. Neuropsychology 1999; 13 (01) 3-9
- 17 Davies KG, Bell BD, Bush AJ, Hermann BP, Dohan Jr FC, Jaap AS. Naming decline after left anterior temporal lobectomy correlates with pathological status of resected hippocampus. Epilepsia 1998; 39 (04) 407-419
- 18 Bell BD, Hermann BP, Woodard AR. et al. Object naming and semantic knowledge in temporal lobe epilepsy. Neuropsychology 2001; 15 (04) 434-443
- 19 Obler LK, Rykhlevskaia E, Schnyer D. et al. Bilateral brain regions associated with naming in older adults. Brain Lang 2010; 113 (03) 113-123
- 20 Damasio AR, Tranel D. Nouns and verbs are retrieved with differently distributed neural systems. Proc Natl Acad Sci U S A 1993; 90 (11) 4957-4960
- 21 Daniele A, Giustolisi L, Silveri MC, Colosimo C, Gainotti G. Evidence for a possible neuroanatomical basis for lexical processing of nouns and verbs. Neuropsychologia 1994; 32 (11) 1325-1341
- 22 Vihla M, Laine M, Salmelin R. Cortical dynamics of visual/semantic vs. phonological analysis in picture confrontation. Neuroimage 2006; 33 (02) 732-738
- 23 Tomaszewki FariasS, Harrington G, Broomand C, Seyal M. Differences in functional MR imaging activation patterns associated with confrontation naming and responsive naming. Am J Neuroradiol 2005; 26 (10) 2492-2499
- 24 Springer JA, Binder JR, Hammeke TA. et al. Language dominance in neurologically normal and epilepsy subjects: a functional MRI study. Brain 1999; 122 (Pt 11) 2033-2046
- 25 Liljeström M, Tarkiainen A, Parviainen T. et al. Perceiving and naming actions and objects. Neuroimage 2008; 41 (03) 1132-1141
- 26 Abrahams S, Goldstein LH, Simmons A. et al. Functional magnetic resonance imaging of verbal fluency and confrontation naming using compressed image acquisition to permit overt responses. Hum Brain Mapp 2003; 20 (01) 29-40
- 27 Brand M, Kalbe E, Kessler J. Test zum kognitiven Schätzen: TKS. Göttingen: Beltz Test; 2002: 3-28
- 28 Kaplan E, Goodglass H, Weintraub S. Boston Naming Test. Philadelphia, PA: Lea & Febiger; 1983: 1-4
- 29 Pedraza O, Sachs BC, Ferman TJ, Rush BK, Lucas JA. Difficulty and discrimination parameters of Boston naming test items in a consecutive clinical series. Arch Clin Neuropsychol 2011; 26 (05) 434-444
- 30 Raymer AM, Foundas AL, Maher LM. et al. Cognitive neuropsychological analysis and neuroanatomic correlates in a case of acute anomia. Brain Lang 1997; 58 (01) 137-156
- 31 Sawrie SM, Martin RC, Gilliam FG. et al. Visual confrontation naming and hippocampal function: a neural network study using quantitative (1)H magnetic resonance spectroscopy. Brain 2000; 123 (Pt 4) 770-780
- 32 Smith ML, Milner B. Right hippocampal impairment in the recall of spatial location: encoding deficit or rapid forgetting?. Neuropsychologia 1989; 27 (01) 71-81
- 33 Hermann B, Loring DW, Wilson S. Paradigm shifts in the neuropsychology of epilepsy. J Int Neuropsychol Soc 2017; 23 (09) (10) 791-805