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Tryptophan and serotonin metabolism in familial erythrophagocytic lymphohistiocytosis

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Journal of Inherited Metabolic Disease

Summary

Reduced concentrations of tryptophan and 5-hydroxyindoleacetic acid (the major CSF metabolite of serotonin) were found in the cerebrospinal fluid of two children with familial erythrophagocytic lymphohistiocytosis. This was associated with elevated cerebrospinal fluid neopterin concentrations indicating increased macrophage activity within the central nervous system. In one child, cytotoxic therapy induced a complete clinical remission and an increase of tryptophan and 5-hydroxyindoleacetic acid concentrations to normal; during a subsequent relapse, concentrations of these analytes again fell below normal. In the other child, in whom therapy produced only a transient improvement, tryptophan and 5-hydroxyindoleacetic acid concentrations remained low and the child died. It is likely that increased activity of indoleamine 2,3-dioxygenase induced by the activation of macrophages was responsible for the disturbance in serotonin and tryptophan homeostasis within the brain. Excessive tryptophan catabolism and the disturbance of serotonin turnover may play a role in the aetiology of the neurological symptoms seen in familial erythrophagocytic lymphohistiocytosis.

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Howells, D.W., Hyland, K., Smith, I. et al. Tryptophan and serotonin metabolism in familial erythrophagocytic lymphohistiocytosis. J Inherit Metab Dis 15, 891–897 (1992). https://doi.org/10.1007/BF01800228

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  • DOI: https://doi.org/10.1007/BF01800228

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