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MRI in seven cases of tacrolimus (FK-506) encephalopathy: utility of FLAIR and diffusion-weighted imaging
1Department of Radiology, Yamaguchi University School of Medicine, Ube, Japan.
Abstract:
We assessed the utility of fluid-attenuated inversion-recovery (FLAIR) and diffusion-weighted (DWI) images in investigation of tacrolimus (FK-506) encephalopathy, and to see whether we could predict its cause from clinical and imaging data. In seven patients with presumed FK-506 toxicity the areas involved on MRI were similar to those in cyclosporin A (CsA) toxicity. The abnormal signal was most evident on FLAIR in all cases. In three of four patients who underwent DWI, no diffusion abnormalities were detected; in the remaining patient, increased diffusion was seen in the deep white matter bilaterally on the apparent diffusion coefficient map, consistent with the findings on T2-weighted spin-echo and FLAIR images. Five of the six patients for whom we had clinical data showed sudden changes in electrolyte or fluid equilibrium due to diarrhoea, a polyuria or oliguria one day before or on the day of onset of the central nervous system disturbances. We speculate that FK-506 encephalopathy is triggered by the disturbance of the electrolyte and/or fluid equilibrium, given a certain serum level of FK-506.
Insights
Tacrolimus (FK-506) encephalopathy shows similar MRI findings to cyclosporin A toxicity, with FLAIR imaging being most sensitive. Electrolyte or fluid imbalance may trigger FK-506 encephalopathy in patients with sufficient drug levels.
Area of Science:
- Neuroimaging
- Toxicology
- Nephrology
Background:
- Tacrolimus (FK-506) is an immunosuppressant frequently used in organ transplantation.
- FK-506 toxicity can manifest as encephalopathy, a serious neurological complication.
- Understanding the imaging characteristics and potential triggers of FK-506 encephalopathy is crucial for patient management.
Purpose of the Study:
- To evaluate the utility of fluid-attenuated inversion-recovery (FLAIR) and diffusion-weighted imaging (DWI) in diagnosing tacrolimus (FK-506) encephalopathy.
- To determine if clinical and imaging data can predict the cause of FK-506 encephalopathy.
- To compare imaging findings in FK-506 encephalopathy with those of cyclosporin A (CsA) toxicity.
Main Methods:
- Retrospective analysis of MRI scans (FLAIR and DWI) in seven patients with suspected FK-506 toxicity.
- Correlation of imaging findings with clinical data, including serum FK-506 levels and electrolyte/fluid balance.
- Comparison of MRI findings with historical data from cyclosporin A (CsA) toxicity.
Main Results:
- Areas affected by FK-506 toxicity on MRI were similar to those seen in CsA toxicity.
- Abnormal signals were most consistently detected on FLAIR sequences in all patients.
- Diffusion abnormalities were detected in only one of four patients who underwent DWI, showing increased diffusion in deep white matter.
- Five of six patients with available clinical data experienced sudden electrolyte or fluid equilibrium disturbances preceding or coinciding with neurological symptoms.
Conclusions:
- FLAIR MRI is highly sensitive for detecting abnormalities in FK-506 encephalopathy.
- Imaging findings in FK-506 encephalopathy resemble those of CsA toxicity.
- Disturbances in electrolyte and/or fluid equilibrium may act as a trigger for FK-506 encephalopathy in individuals with adequate tacrolimus serum levels.
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