Tropical distal renal tubular acidosis: clinical and epidemiological studies in 78 patients

• Published in: QJM : An International Journal of Medicine Vol. 105; no. 9; pp. 861 - 877
• Main Authors: KHOSITSETH, S, BRUCE, L. J, KINGWATANAKUL, P, SUMBOONNANONDA, A, VASUVATTAKUL, S, YENCHITSOMANUS, P, WRONG, O, WALSH, S. B, BAWAZIR, W. M, OGLE, G. D, UNWIN, R. J, THONG, M.-K, SINHA, R, CHOO, K. E, CHARTAPISAK, W
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01-09-2012
• Subjects: Acidosis, Renal Tubular - epidemiology; Acidosis, Renal Tubular - genetics; Anion Exchange Protein 1, Erythrocyte - genetics; Anion Exchange Protein 1, Erythrocyte - metabolism; Asia - epidemiology; Biological and medical sciences; Child; Child, Preschool; Consanguinity; Epidemiology; Erythrocytes, Abnormal - metabolism; Erythrocytes, Abnormal - physiology; Female; General aspects; Hematologic Diseases - epidemiology; Hematologic Diseases - genetics; Heterozygote; Homozygote; Humans; Infant; Malaria - genetics; Male; Medical sciences; Mutation - genetics; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Papua New Guinea - epidemiology; Pedigree; Phenotype; Philippines - epidemiology; Public health. Hygiene; Public health. Hygiene-occupational medicine; Thailand - epidemiology; Tubulopathies; Papua New Guinea; Thailand; Asia; Philippines; Malaysia; Kidney disease; Human; Urinary system disease; Tubulopathy; Patient; Epidemiology; Kidney; Medicine; Symptomatology; Renal tubule; Urinary system; Distal; Public health
• ISSN: 1460-2725; 1460-2393
• DOI: 10.1093/qjmed/hcs139

Distal renal tubular acidosis (dRTA) caused by mutations of the SLC4A1 gene encoding the erythroid and kidney isoforms of anion exchanger 1 (AE1 or band 3) has a high prevalence in some tropical countries, particularly Thailand, Malaysia, the Philippines and Papua New Guinea (PNG). Here the disease is almost invariably recessive and can result from either homozygous or compound heterozygous SLC4A1 mutations.
We have collected and reviewed our own and published data on tropical dRTA to provide a comprehensive series of clinical and epidemiological studies in 78 patients.
Eight responsible SLC4A1 mutations have been described so far, four of them affecting multiple unrelated families. With the exception of the mutation causing South-East Asian ovalocytosis (SAO), none of these mutations has been reported outside the tropics, where dRTA caused by SLC4A1 mutations is much rarer and almost always dominant, resulting from mutations that are quite different from those found in the tropics. SLC4A1 mutations, including those causing dRTA, may cause morphological red cell changes, often with excess haemolysis. In dRTA, these red cell changes are usually clinically recessive and not present in heterozygotes. The high tropical prevalence of dRTA caused by SLC4A1 mutations is currently unexplained.
A hypothesis suggesting that changes in red cell metabolism caused by these mutations might protect against malaria is put forward to explain the phenomenon, and a possible mechanism for this effect is proposed.