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Department of Neurology,
Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne, UK
Correspondence to: Department of Neurology, Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne NE1 4LP, UK. Telephone 0044 191 232 5131, extension 25974; fax 0044 191 261 0881.
Received 18 December 1998 and in revised form 1 June 1998;
Accepted 3 June 1998
Renal failure is relatively common, but except in association
with spina bifida or paraplegia it is unlikely to occur as a result of
disease of the CNS. Renal failure, however, commonly affects the
nervous system. The effects of kidney failure on the nervous system are
more pronounced when failure is acute. In addition to the important
problems related to renal failure there are both acquired and
genetically determined diseases which may affect the kidney and the
brain. Those acquired diseases include the vasculitides, the
paraproteinaemias, and various granulomatous conditions (considered in
other chapters of Neurology and Medicine). In two of the
most commonly encountered genetically determined diseases, Von
Hippel-Lindau disease and polycystic kidney disease, location of
pathogenic mutations will provide improved screening programmes and,
possibly, allow therapeutic intervention. Uraemia may affect both the
central and peripheral nervous systems. Whereas the clinical features
of uraemia are well documented, the pathophysiology is less well
understood and probably multifactorial. Uraemic encephalopathy, which
classically fluctuates, is associated with problems in cognition and
memory and may progress to delirium, convulsions, and coma. The
encephalopathy may initially worsen with periods of dialysis and almost
certainly relates to altered metabolic states in association with ionic
changes and possibly impaired synaptic function. Renal failure may
affect the peripheral nervous system, resulting in a neuropathy which
shows a predilection for large diameter axons. This may be reversed by
dialysis and transplantation. The myopathy seen in renal failure, often
associated with bone pain and tenderness, is similar to that
encountered in primary hyperparathyroidism and osteomalacia.
Dialysis itself is associated with neurological syndromes including
the dysequilibrium syndrome, subdural haematoma, and Wernicke's
encephalopathy. Dialysis dementia, which was prevalent during the
1970s, has reduced in frequency with the use of aluminium free
dialysate. With the introduction of transplantation and the concomitant use of powerful immunosuppressive drugs, the pattern of
neurological problems encountered in renal replacement therapy has
shifted. Five per cent of patients develop nerve injuries during renal
transplantation, and up to 40% of patients experience neurological
side effects from cyclosporine. Furthermore, CNS infections, often
fungal in type, have been reported in up to 45% of transplant patients
coming to postmortem. The nature of the involvement of
neurologists with their nephrology colleagues is
therefore evolving.
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