2012
DOI: 10.1016/j.genhosppsych.2011.08.008
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Catatonia as a manifestation of tacrolimus-induced neurotoxicity in organ transplant patients: a case series

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Cited by 27 publications
(17 citation statements)
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“…Our patient had underlying hypertension, diabetes mellitus type 2, thyroid dysfunction and a right adrenal adenoma. Interestingly, her tacrolimus levels were at therapeutic levels, but severe neurotoxicity seemed to not be related to tacrolimus levels, similarly as seen in the study by Veroux et al 6 Based on the FK506 consensus reports by Jusko et al 7 and Wong, 8 tacrolimus therapeutic ranges in kidney transplanted patients should be 10-15 µg/L in the first 6 months of treatment; [8][9][10][11][12] µg/L in the following semester; and 5-10 µg/L as maintenance therapy after one year. Bottiger et al 9 reported neurotoxicity in 10% of patients with drug levels between 10 g/ml and 30 g/mL, while this incidence rises up to more than 20% in patients with a level >30 g/ml.…”
Section: Discussionmentioning
confidence: 57%
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“…Our patient had underlying hypertension, diabetes mellitus type 2, thyroid dysfunction and a right adrenal adenoma. Interestingly, her tacrolimus levels were at therapeutic levels, but severe neurotoxicity seemed to not be related to tacrolimus levels, similarly as seen in the study by Veroux et al 6 Based on the FK506 consensus reports by Jusko et al 7 and Wong, 8 tacrolimus therapeutic ranges in kidney transplanted patients should be 10-15 µg/L in the first 6 months of treatment; [8][9][10][11][12] µg/L in the following semester; and 5-10 µg/L as maintenance therapy after one year. Bottiger et al 9 reported neurotoxicity in 10% of patients with drug levels between 10 g/ml and 30 g/mL, while this incidence rises up to more than 20% in patients with a level >30 g/ml.…”
Section: Discussionmentioning
confidence: 57%
“…This molecule can cross the intact blood brain barrier and probably attaches to myelin, which is rich in lipids, permitting tacrolimus to exert a direct toxic effect through nitrous oxide production. 10 Tacrolimus has downstream regulatory effects on both dopaminergic and N-Methyl-Daspartate receptor systems 2,11 which may be another factor. Another postulated hypothesis relates to hypertensive encephalopathy, which corresponds to white matter changes observed in the parietal and occipital lobes.…”
Section: Discussionmentioning
confidence: 99%
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“…4,9,10 Various tacrolimusassociated behavioural abnormalities have been reported: catatonia or akinetic mutism, paranoid and fugue-like states, psychotic symptoms, and mania. 7,[11][12][13][14] To our knowledge, it does appear that there has not been any earlier report of tacrolimus-induced schizophrenia-like disorder.…”
Section: Discussionmentioning
confidence: 78%
“…Tacrolimus, a potent calcineurin inhibitor exhibits neuroprotection actions in several experimental models of central nervous system trauma, including stroke and improved neurological recovery following peripheral and spinal cord injuries [2][3][4][5][6]. However, some side effects from oral and intravenous administration of Tacrolimus in clinical case studies have been reported which include nephrotoxicity [7], lung damage [8], various neuropsychiatric problems, neurotoxic effects such as akinetic mutism and catatonic mutism [9,10]. On the contrary, in experimental studies, Tacrolimus improves the functional outcome of spinal cord injury [5,11,12] and has an in vivo neurotrophic action whereby it enhances the rate of axon regeneration leading to more rapid neurological recovery [13][14][15][16].…”
Section: Introductionmentioning
confidence: 99%