Skip to main content
Top
Published in: Neurocritical Care 2/2020

01-04-2020 | Magnetic Resonance Imaging | Original Work

Brain Volume Changes in Patients with Acute Brain Dysfunction Due to Sepsis

Authors: Günseli Orhun, Erdem Tüzün, Başar Bilgiç, Perihan Ergin Özcan, Serra Sencer, Mehmet Barburoğlu, Figen Esen

Published in: Neurocritical Care | Issue 2/2020

Login to get access

Abstract

Background

Sepsis-induced brain dysfunction (SIBD) is often encountered in sepsis patients and is related to increased morbidity. No specific tests are available for SIBD, and neuroimaging findings are often normal. In this study, our aim was to analyze the diagnostic value of volumetric analysis of the brain structures and to find out its significance as a prognostic measure.

Methods

In this prospective observational study, brain magnetic resonance imaging (MRI) sections of 25 consecutively enrolled SIBD patients (17 with encephalopathy and 8 with coma) and 22 healthy controls underwent volumetric evaluation by an automated segmentation method.

Results

Ten SIBD patients had normal MRI, and 15 patients showed brain lesions or atrophy. The most prominent volume reduction was found in cerebral and cerebellar white matter, cerebral cortex, hippocampus, and amygdala, whereas deep gray matter regions and cerebellar cortex were relatively less affected. SIBD patients with normal MRI showed significantly reduced volumes in hippocampus and cerebral white matter. Caudate nuclei, putamen, and thalamus showed lower volume values in non-survivor SIBD patients, and left putamen and right thalamus showed a more pronounced volume reduction in coma patients.

Conclusions

Volumetric analysis of the brain appears to be a sensitive measure of volumetric changes in SIBD. Volume reduction in specific deep gray matter regions might be an indicator of unfavorable outcome.
Literature
1.
go back to reference Iacobone E, Bailly-Salin J, Polito A, et al. Sepsis-associated encephalopathy and its differential diagnosis. Crit Care Med. 2009;37(10):S331–6.PubMedCrossRef Iacobone E, Bailly-Salin J, Polito A, et al. Sepsis-associated encephalopathy and its differential diagnosis. Crit Care Med. 2009;37(10):S331–6.PubMedCrossRef
2.
go back to reference Girard TD, Jackson JC, Pandharipande PP, et al. Delirium as a predictor of long-term cognitive impairment in survivors of critical illness. Crit Care Med. 2010;38(7):1513.PubMedPubMedCentralCrossRef Girard TD, Jackson JC, Pandharipande PP, et al. Delirium as a predictor of long-term cognitive impairment in survivors of critical illness. Crit Care Med. 2010;38(7):1513.PubMedPubMedCentralCrossRef
3.
go back to reference Ely EW, Shintani A, Truman B, et al. Delirium as a predictor of mortality in mechanically ventilated patients in the intensive care unit. JAMA. 2004;291(14):1753–62.CrossRefPubMed Ely EW, Shintani A, Truman B, et al. Delirium as a predictor of mortality in mechanically ventilated patients in the intensive care unit. JAMA. 2004;291(14):1753–62.CrossRefPubMed
4.
go back to reference Iwashyna TJ, Ely EW, Smith DM, Langa KM. Long-term cognitive impairment and functional disability among survivors of severe sepsis. JAMA. 2010;304(16):1787–94.PubMedPubMedCentralCrossRef Iwashyna TJ, Ely EW, Smith DM, Langa KM. Long-term cognitive impairment and functional disability among survivors of severe sepsis. JAMA. 2010;304(16):1787–94.PubMedPubMedCentralCrossRef
5.
go back to reference Hopkins RO, Weaver LK, Collingridge D, et al. Two-year cognitive, emotional, and quality-of-life outcomes in acute respiratory distress syndrome. Am J Respir Crit Care Med. 2005;171(4):340–7.PubMedCrossRef Hopkins RO, Weaver LK, Collingridge D, et al. Two-year cognitive, emotional, and quality-of-life outcomes in acute respiratory distress syndrome. Am J Respir Crit Care Med. 2005;171(4):340–7.PubMedCrossRef
6.
8.
go back to reference Bartynski WS, Boardman JF, Zeigler ZR, Shadduck RK, Lister J. Posterior reversible encephalopathy syndrome in infection, sepsis, and shock. AJNR Am J Neuroradiol. 2006;27(10):2179–90.PubMedPubMedCentral Bartynski WS, Boardman JF, Zeigler ZR, Shadduck RK, Lister J. Posterior reversible encephalopathy syndrome in infection, sepsis, and shock. AJNR Am J Neuroradiol. 2006;27(10):2179–90.PubMedPubMedCentral
9.
go back to reference Suchyta MR, Jephson A, Hopkins RO. Neurologic changes during critical illness: brain imaging findings and neurobehavioral outcomes. Brain Imaging Behav. 2010;4(1):22–34.PubMedCrossRef Suchyta MR, Jephson A, Hopkins RO. Neurologic changes during critical illness: brain imaging findings and neurobehavioral outcomes. Brain Imaging Behav. 2010;4(1):22–34.PubMedCrossRef
10.
go back to reference Orhun G, Tüzün E, Özcan PE, et al. Association between inflammatory markers and cognitive outcome in patients with acute brain dysfunction due to sepsis. Arch Neuropsychiatry. 2019;56(1):63. Orhun G, Tüzün E, Özcan PE, et al. Association between inflammatory markers and cognitive outcome in patients with acute brain dysfunction due to sepsis. Arch Neuropsychiatry. 2019;56(1):63.
11.
go back to reference Orhun G, Esen F, Ozcan PE, et al. Neuroimaging findings in sepsis-induced brain dysfunction: association with clinical and laboratory findings. Neurocrit Care. 2019;30(1):106–17.PubMedCrossRef Orhun G, Esen F, Ozcan PE, et al. Neuroimaging findings in sepsis-induced brain dysfunction: association with clinical and laboratory findings. Neurocrit Care. 2019;30(1):106–17.PubMedCrossRef
12.
go back to reference Semmler A, Widmann CN, Okulla T, et al. Persistent cognitive impairment, hippocampal atrophy and EEG changes in sepsis survivors. J Neurol Neurosurg Psychiatry. 2013;84(1):62–9.PubMedCrossRef Semmler A, Widmann CN, Okulla T, et al. Persistent cognitive impairment, hippocampal atrophy and EEG changes in sepsis survivors. J Neurol Neurosurg Psychiatry. 2013;84(1):62–9.PubMedCrossRef
14.
go back to reference Dellinger RP, Levy MM, Rhodes A, et al. Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock, 2012. Intensive Care Med. 2013;39(2):165–228.PubMedCrossRefPubMedCentral Dellinger RP, Levy MM, Rhodes A, et al. Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock, 2012. Intensive Care Med. 2013;39(2):165–228.PubMedCrossRefPubMedCentral
15.
go back to reference Sutter R, Chalela JA, Leigh R, et al. Significance of parenchymal brain damage in patients with critical illness. Neurocrit Care. 2015;23(2):243–52.PubMedCrossRef Sutter R, Chalela JA, Leigh R, et al. Significance of parenchymal brain damage in patients with critical illness. Neurocrit Care. 2015;23(2):243–52.PubMedCrossRef
16.
go back to reference Ely EW, Inouye SK, Bernard GR, et al. Delirium in mechanically ventilated patients: validity and reliability of the confusion assessment method for the intensive care unit (CAM-ICU). JAMA. 2001;286(21):2703–10.CrossRefPubMed Ely EW, Inouye SK, Bernard GR, et al. Delirium in mechanically ventilated patients: validity and reliability of the confusion assessment method for the intensive care unit (CAM-ICU). JAMA. 2001;286(21):2703–10.CrossRefPubMed
17.
go back to reference Sessler CN, Gosnell MS, Grap MJ, et al. The Richmond Agitation–Sedation Scale: validity and reliability in adult intensive care unit patients. Am J Respir Crit Care Med. 2002;166(10):1338–44.PubMedCrossRef Sessler CN, Gosnell MS, Grap MJ, et al. The Richmond Agitation–Sedation Scale: validity and reliability in adult intensive care unit patients. Am J Respir Crit Care Med. 2002;166(10):1338–44.PubMedCrossRef
18.
go back to reference Posner JB, Plum F, Saper CB, Schiff N. Plum and Posner’s diagnosis of stupor and coma, vol. 17. Oxford: OUP USA; 2007. Posner JB, Plum F, Saper CB, Schiff N. Plum and Posner’s diagnosis of stupor and coma, vol. 17. Oxford: OUP USA; 2007.
19.
go back to reference Fischl B, Salat DH, Busa E, et al. Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain. Neuron. 2002;33(3):341–55.PubMedCrossRef Fischl B, Salat DH, Busa E, et al. Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain. Neuron. 2002;33(3):341–55.PubMedCrossRef
20.
go back to reference Gunther ML, Morandi A, Krauskopf E, et al. The association between brain volumes, delirium duration, and cognitive outcomes in intensive care unit survivors: the VISIONS cohort magnetic resonance imaging study*. Crit Care Med. 2012;40(7):2022–32.PubMedPubMedCentralCrossRef Gunther ML, Morandi A, Krauskopf E, et al. The association between brain volumes, delirium duration, and cognitive outcomes in intensive care unit survivors: the VISIONS cohort magnetic resonance imaging study*. Crit Care Med. 2012;40(7):2022–32.PubMedPubMedCentralCrossRef
21.
go back to reference Finke C, Kopp UA, Pajkert A, et al. Structural hippocampal damage following anti-N-methyl-d-aspartate receptor encephalitis. Biol Psychiatry. 2016;79(9):727–34.PubMedCrossRef Finke C, Kopp UA, Pajkert A, et al. Structural hippocampal damage following anti-N-methyl-d-aspartate receptor encephalitis. Biol Psychiatry. 2016;79(9):727–34.PubMedCrossRef
22.
go back to reference Finke C, Pruss H, Heine J, et al. Evaluation of cognitive deficits and structural hippocampal damage in encephalitis with leucine-rich, glioma-inactivated 1 antibodies. JAMA Neurol. 2017;74(1):50–9.PubMedCrossRef Finke C, Pruss H, Heine J, et al. Evaluation of cognitive deficits and structural hippocampal damage in encephalitis with leucine-rich, glioma-inactivated 1 antibodies. JAMA Neurol. 2017;74(1):50–9.PubMedCrossRef
23.
go back to reference Yoneda Y, Mori E, Yamashita H, Yamadori A. MRI volumetry of medial temporal lobe structures in amnesia following herpes simplex encephalitis. Eur Neurol. 1994;34(5):243–52.PubMedCrossRef Yoneda Y, Mori E, Yamashita H, Yamadori A. MRI volumetry of medial temporal lobe structures in amnesia following herpes simplex encephalitis. Eur Neurol. 1994;34(5):243–52.PubMedCrossRef
24.
go back to reference Anderson VM, Fisniku LK, Khaleeli Z, et al. Hippocampal atrophy in relapsing-remitting and primary progressive MS: a comparative study. Mult Scler. 2010;16(9):1083–90.PubMedCrossRef Anderson VM, Fisniku LK, Khaleeli Z, et al. Hippocampal atrophy in relapsing-remitting and primary progressive MS: a comparative study. Mult Scler. 2010;16(9):1083–90.PubMedCrossRef
25.
go back to reference Semmler A, Hermann S, Mormann F, et al. Sepsis causes neuroinflammation and concomitant decrease of cerebral metabolism. J Neuroinflammation. 2008;5:38.PubMedPubMedCentralCrossRef Semmler A, Hermann S, Mormann F, et al. Sepsis causes neuroinflammation and concomitant decrease of cerebral metabolism. J Neuroinflammation. 2008;5:38.PubMedPubMedCentralCrossRef
26.
go back to reference Peng QY, Wang YM, Chen CX, et al. Inhibiting the CD38/cADPR pathway protected rats against sepsis associated brain injury. Brain Res. 2018;1678:56–63.PubMedCrossRef Peng QY, Wang YM, Chen CX, et al. Inhibiting the CD38/cADPR pathway protected rats against sepsis associated brain injury. Brain Res. 2018;1678:56–63.PubMedCrossRef
27.
go back to reference Fu Q, Wu J, Zhou X-Y, et al. NLRP3/Caspase-1 pathway-induced pyroptosis mediated cognitive deficits in a mouse model of sepsis-associated encephalopathy. Inflammation. 2019;42:306–18.PubMedCrossRef Fu Q, Wu J, Zhou X-Y, et al. NLRP3/Caspase-1 pathway-induced pyroptosis mediated cognitive deficits in a mouse model of sepsis-associated encephalopathy. Inflammation. 2019;42:306–18.PubMedCrossRef
28.
go back to reference Zaghloul N, Addorisio ME, Silverman HA, et al. Forebrain cholinergic dysfunction and systemic and brain inflammation in murine sepsis survivors. Front Immunol. 2017;8:1673.PubMedPubMedCentralCrossRef Zaghloul N, Addorisio ME, Silverman HA, et al. Forebrain cholinergic dysfunction and systemic and brain inflammation in murine sepsis survivors. Front Immunol. 2017;8:1673.PubMedPubMedCentralCrossRef
29.
go back to reference Femminella GD, Ninan S, Atkinson R, et al. Does microglial activation influence hippocampal volume and neuronal function in Alzheimer’s disease and Parkinson’s Disease dementia? J Alzheimers Dis. 2016;51(4):1275–89.PubMedCrossRef Femminella GD, Ninan S, Atkinson R, et al. Does microglial activation influence hippocampal volume and neuronal function in Alzheimer’s disease and Parkinson’s Disease dementia? J Alzheimers Dis. 2016;51(4):1275–89.PubMedCrossRef
30.
go back to reference Kondo A, Sugiura C, Fujii Y, et al. Fulminant sepsis-associated encephalopathy in two children: serial neuroimaging findings and clinical course. Neuropediatrics. 2009;40(4):157–61.PubMedCrossRef Kondo A, Sugiura C, Fujii Y, et al. Fulminant sepsis-associated encephalopathy in two children: serial neuroimaging findings and clinical course. Neuropediatrics. 2009;40(4):157–61.PubMedCrossRef
Metadata
Title
Brain Volume Changes in Patients with Acute Brain Dysfunction Due to Sepsis
Authors
Günseli Orhun
Erdem Tüzün
Başar Bilgiç
Perihan Ergin Özcan
Serra Sencer
Mehmet Barburoğlu
Figen Esen
Publication date
01-04-2020
Publisher
Springer US
Published in
Neurocritical Care / Issue 2/2020
Print ISSN: 1541-6933
Electronic ISSN: 1556-0961
DOI
https://doi.org/10.1007/s12028-019-00759-8

Other articles of this Issue 2/2020

Neurocritical Care 2/2020 Go to the issue