Selective disruption of hippocampus-mediated recognition memory processes after episodes of transient global amnesia

Transient global amnesia (TGA) is characterized by the abrupt onset of severe amnesia without concomitant focal neurological symptoms. Recent studies revealed that small and punctate MR-signal diffusion-weighted imaging (DWI) lesions can be found within the hippocampus of TGA patients during the pos...

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Hauptverfasser: Jäger, Theodor (VerfasserIn) , Szabo, Kristina (VerfasserIn) , Griebe, Martin (VerfasserIn) , Bäzner, Hansjörg (VerfasserIn) , Möller, Johanna (VerfasserIn) , Hennerici, Michael G. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: [2009]
In: Neuropsychologia
Year: 2008, Jahrgang: 47, Heft: 1, Pages: 70-76
ISSN:1873-3514
DOI:10.1016/j.neuropsychologia.2008.08.019
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.neuropsychologia.2008.08.019
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0028393208003540
Volltext
Verfasserangaben:Theodor Jäger, Kristina Szabo, Martin Griebe, Hansjörg Bäzner, Johanna Möller, Michael G. Hennerici

MARC

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520 |a Transient global amnesia (TGA) is characterized by the abrupt onset of severe amnesia without concomitant focal neurological symptoms. Recent studies revealed that small and punctate MR-signal diffusion-weighted imaging (DWI) lesions can be found within the hippocampus of TGA patients during the post-acute phase. On the basis of dual-process models of recognition memory, the present study examined the hypothesis that hippocampal dysfunction as suggested by these DWI lesions disrupts hippocampus-mediated recollection in patients with TGA, whereas familiarity-based recognition memory that is assumed to be supported by extra-hippocampal brain regions should be unaffected. We administered a recognition memory task for faces and words to eleven TGA patients during the post-acute phase and to eleven matched controls. Receiver operating characteristics (ROCs) were obtained in order to derive estimates of familiarity and recollection by applying a formal dual-process model of recognition memory. Analyses of ROC curves revealed a disruption of recollection in TGA patients’ memory for words [t(20)=2.70, p<.05], but no difference in familiarity-based recognition memory between patients and controls [t(20)=−1.10, p=.284]. Post hoc analyses indicated that the deficit in recollection is more pronounced in TGA patients who show visible hippocampal lesions on diffusion-weighted MR imaging compared to those without detectable hippocampal lesions. In conclusion, consistent with recent neuroanatomical dual-process models of recognition memory, hippocampal dysfunction in patients with TGA is associated with a selective effect on specific recognition memory subprocesses. 
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