Subarachnoid hemorrhage is followed by temporomesial volume loss: MRI volumetric study

Neurology

Volumn 67, Issue 4, 2006, Pages 575-582

  Bendel, P ^a   Koivisto, T ^a   Hanninen T ^a   Kolehmainen, A ^a   Kononen M ^a   Hurskainen, H ^a   Pennanen, C ^b   Vanninen, R ^a  

^a KUOPIO UNIVERSITY HOSPITAL   (Finland)

^b Kuopio University Hospital ^*

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; AMYGDALOID NUCLEUS; ARTICLE; BLOOD VOLUME; BRAIN ARTERY ANEURYSM; BRAIN ARTERY ANEURYSM RUPTURE; BRAIN SIZE; COGNITION; CONTROLLED STUDY; CORRELATION ANALYSIS; ENDOVASCULAR SURGERY; FEMALE; HIPPOCAMPUS; HUMAN; MAJOR CLINICAL STUDY; MALE; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SUBARACHNOID HEMORRHAGE; TREATMENT OUTCOME;

ATROPHY; FEMALE; FINLAND; HUMANS; IMAGING, THREE-DIMENSIONAL; INCIDENCE; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; PROGNOSIS; RISK ASSESSMENT; RISK FACTORS; SUBARACHNOID HEMORRHAGE; TEMPORAL LOBE; TREATMENT OUTCOME;

EID: 33747637130     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000230221.95670.bf     Document Type: Article

References (31)

1. Geuze E, Vermetten E, Bremner JD. MR-based in vivo hippocampal volumetrics: 2. Findings in neuropsychiatric disorders. Mol Psychiatry 2005;10:160-184.
2. Vanninen R, Koivisto T, Saari T, Hernesniemi J, Vapalahti M. Ruptured intracranial aneurysms: acute endovascular treatment with electrolytically detachable coils: a prospective randomized study. Radiology 1999;211:325-336.
3. Koivisto T, Vanninen R, Hurskainen H, Saari T, Hernesniemi J, Vapalahti M. Outcomes of early endovascular versus surgical treatment of ruptured cerebral aneurysms: a prospective randomized study. Stroke 2000;31:2369-2377.
4. Martin J. Neuroanatomy text and atlas. 2nd ed. Stanford: Appleton & Lange, 1996.
5. Watson C, Andermann F, Gloor P, et al. Anatomic basis of amygdaloid and hippocampal volume measurement by magnetic resonance imaging. Neurology 1992;42:1743-1750.
6. Laakso MP, Soininen H, Partanen K, et al. MRI of the hippocampus in Alzheimer's disease: sensitivity, specificity, and analysis of the incorrectly classified subjects. Neurobiol Aging 1998;19:23-31.
7. Pennanen C, Kivipelto M, Tuomainen S, et al. Hippocampus and entorhinal cortex in mild cognitive impairment and early AD. Neurobiol Aging 2004;25:303-310.
8. Wechsler D. Wechsler Adult Intelligence Scale-Revised. New York: The Psychological Corporation, 1981.
9. Lezak M. Neuropsychological assessment. New York: Oxford University Press, 1995.
10. Borkowski J, Benton A, Spreen O. Word fluency and brain damage. Neuropsychologia 1967;5:135-140.
11. Wechsler D. Wechsler Memory Scale manual. San Antonio: The Psychological Corporation, 1974.
12. Golden C. Stroop Color and Word Tests. Chicago: Stoerting, 1978.
13. Reitan R. Validity of the Trail Making tests as an indicator of organic brain damage. Percept Mot Skills 1958;8:271-276.
14. Vilkki J, Holst P, Ohman J, Servo A, Heiskanen O. Cognitive deficits related to computed tomographic findings after surgery for a ruptured intracranial aneurysm. Neurosurgery 1989;25:166-172.
15. Guglielmi G, Vinuela F, Dion J, Duckwiler G. Electrothrombosis of saccular aneurysms via endovascular approach: Part 2. Preliminary clinical experience. J Neurosurg 1991;75:8-14.
16. Brilstra EH, Rinkel GJ, van der Graaf Y, van Rooij WJ, Algra A. Treatment of intracranial aneurysms by embolization with coils: a systematic review. Stroke 1999;30:470-476.
17. Molyneux A, Kerr R, Stratton I, et al. International Subarachnoid Aneurysm Trial (ISAT) of neurosurgical clipping versus endovascular coiling in 2143 patients with ruptured intracranial aneurysms: a randomised trial. Lancet 2002;360:1267-1274.
18. Molyneux AJ, Kerr RS, Yu LM, et al. International subarachnoid aneurysm trial (ISAT) of neurosurgical clipping versus endovascular coiling in 2143 patients with ruptured intracranial aneurysms: a randomised comparison of effects on survival, dependency, seizures, rebleeding, subgroups, and aneurysm occlusion. Lancet 2005;366:809-817.
19. Hadjivassiliou M, Tooth CL, Romanowski CA, et al. Aneurysmal SAH: cognitive outcome and structural damage after clipping or coiling. Neurology 2001;56:1672-1677.
20. Kalviainen R, Salmenpera T, Partanen K, Vainio P, Riekkinen P, Pitkanen A. Recurrent seizures may cause hippocampal damage in temporal lobe epilepsy. Neurology 1998;50:1377-1382.
21. Convit A, De Leon MJ, Tarshish C, et al. Specific hippocampal volume reductions in individuals at risk for Alzheimer's disease. Neurobiol Aging 1997;18:131-138.
22. Stein MB, Koverola C, Hanna C, Torchia MG, McClarty B. Hippocampal volume in women victimized by childhood sexual abuse. Psychol Med 1997;27:951-959.
23. Bogerts B, Lieberman JA, Ashtari M, et al. Hippocampus-amygdala volumes and psychopathology in chronic schizophrenia. Biol Psychiatry 1993;33:236-246.
24. Villarreal G, Hamilton DA, Petropoulos H, et al. Reduced hippocampal volume and total white matter volume in posttraumatic stress disorder. Biol Psychiatry 2002;52:119-125.
25. Campbell S, Marriott M, Nahmias C, MacQueen GM. Lower hippocampal volume in patients suffering from depression: a meta-analysis. Am J Psychiatry 2004;161:598-607.
26. Fujioka M, Nishio K, Miyamoto S, et al. Hippocampal damage in the human brain after cardiac arrest. Cerebrovasc Dis 2000;10:2-7.
27. Geuze E, Vermetten E, Bremner JD. MR-based in vivo hippocampal volumetrics: 1. Review of methodologies currently employed. Mol Psychiatry 2005;10:147-159.
28. Ljunggren B, Sonesson B, Saveland H, Brandt L. Cognitive impairment and adjustment in patients without neurological deficits after aneurysmal SAH and early operation. J Neurosurg 1985;62:673-679.
29. Mu Q, Xie J, Wen Z, Weng Y, Shuyun Z. A quantitative MR study of the hippocampal formation, the amygdala, and the temporal horn of the lateral ventricle in healthy subjects 40 to 90 years of age. AJNR Am J Neuroradiol 1999;20:207-211.
30. Squire LR, Stark CE, Clark RE. The medial temporal lobe. Annu Rev Neurosci 2004;27:279-306.
31. McGaugh JL. The amygdala modulates the consolidation of memories of emotionally arousing experiences. Annu Rev Neurosci 2004;27:1-28.