The renal tubular acidoses

Journal of the Royal Society of Medicine

Volumn 94, Issue 5, 2001, Pages 221-225

  Unwin, Robert J ^a   Capasso, Giovambattista ^b  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BICARBONATE; THIAZIDE DIURETIC AGENT; VITAMIN D; VITAMIN K GROUP;

BICARBONATE BLOOD LEVEL; HUMAN; HYPOKALEMIA; KIDNEY ACIDIFYING CAPACITY; KIDNEY CALCIFICATION; KIDNEY TUBULE ACIDOSIS; LONG TERM CARE; MEDULLARY SPONGE KIDNEY; PATHOPHYSIOLOGY; REVIEW; URINALYSIS; URINARY EXCRETION; URINE PH; VITAMIN SUPPLEMENTATION;

EID: 0034997782     PISSN: 01410768     EISSN: None     Source Type: Journal    
DOI: 10.1177/014107680109400506     Document Type: Review

References (30)

1. 1 Madias NE, Kraut JA. Uremic acidosis. In Seldin DW, Giebisch G, eds. The Regulation of Acid-Base Balance. New York: Raven Press, 1989: 285-317
2. 2 Kamel KS, Briceno LF, Sanchez MI, et al. A new classification for renal defects in net acid excretion. Am J Kidney Dis 1997;29:136-46
3. 3 Boron WF. Chemistry of buffer equilibria in blood plasma. In Seldin DW, Giebisch G, eds. The Regulation of Acid-Base Balance. New York: Raven Press, 1989: 3-32
4. 4 DuBose TDJ. Hyperkalemic metabolic acidosis. Am J Kidney Dis 1999; 33:XLV-XLVIII
5. 5 Alpern RJ. Cell mechanisms of proximal tubule acidification. Physiol Rev 1990;70:79-114
6. 6 Amemiya M, Loffing J, Lotscher M, et al. Expression of NHE-3 in the apical membrane of rat renal proximal tubule and thick ascending limb. Kidney Int 1995;48:1206-15
7. 7 Wang T, Yang CL, Abbiati T, et al. Mechanism of proximal tubule bicarbonate absorption in NHE3 null mice. Am J Physiol 1999; 277:F297-F302
8. +ATPase. Annu Rev Physiol 1996;58:427-45
9. 9 Cohen EP, Bastani B, Cohen MR, Kolner S, Hemken P, Gluck SL. Absence of H(+)ATPase in cortical collecting tubules of a patient with Sjogren's syndrome and distal renal tubular acidosis. J Am Soc Nephrol 1992;3:264-71
10. + ATPase in kidney transplant rejection. J Lab Clin Med 1996; 127:310-14
11. +-ATPase cause renal tubular acidosis with sensorineural deafness. Nat Genet 1999;21:84-90
12. 12 Smith AN, Skaug J, Choate KA, et al. Mutations in ATP6NIB, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing. Nat Genet 2000;26:71-5
13. 13 Karet FE, Gainza FJ, Gyory AZ, et al. Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis. Proc Natl Acad Sci USA 1998;95:6337-42
14. 14 Bruce LJ, Cope DL, Jones GK, et al. Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene. J Clin Invest 1997;100:1693-707
15. 15 Jarolim P, Shayakul C, Prabakaran D, et al. Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3-exchanger. J Biol Chim 1998;273:6380-8
16. 16 Tamphaichitr VS, Sumboonnanonda A, Ideguchi H, et al. Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A. J Clin Invest 1998;102:2173-9
17. 17 Igarashi T, Inatomi J, Sekine T, et al. Mutations in SLC4A4 cause permanent isolated proximal renal tubular acidosis with ocular abnormalities. Nat Genet 1999;23:264-6
18. 18 Sly WS, Hewett-Emmett D, Whyte MP, Yu YS, Tashian RE. Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcificatioin. Proc Natl Acad Sci USA 1983;80: 2752-6
19. 19 Soriano JR, Boichis H, Edelmann CM, Jr. Bicarbonate reabsorption and hydrogen ion excretion in children with renal tubular acidosis. J Pediatr 1967;71:802-13
20. 20 Wrong OM, Feest TG. The natural history of distal renal tubular acidosis. Contrib Nephrol 1980;21:137-44
21. 21 Wrong O, Davies HEF. The excretion of acid in renal disease. Q J Med 1959;28:259-313
22. 22 Walter SJ, Shirley DG, Unwin RJ, Wrong OM. Assessment of urinary acidification. Kidney Int 1999;55:2092A
23. 23 Wrong O, Nephrocalcinosis. In: Cameron S, Davison AM, Grunefeld J-P, Kerr DS, Ritz E, eds. Oxford Textbook of Nephrology. Oxford: Oxford University Press, 1998: 1375-96
24. 24 DeFranco PE, Haragsim L, Schmitz PG, Bastania B. Absence of vacuolar H(+)-ATPase pump in the collecting duct of a patient with hypokalemic distal renal tubular acidosis and Sjögren's syndrome. J Am Soc Nephrol 1995;6:295-301
25. 25 Hamm LL. Renal handling of citrate. Kidney Int 1990;38:728-35
26. 26 Richards P, Chamberlain MJ, Wrong OM. Treatment of osteomalacia of renal tubular acidosis by sodium bicarbonate alone. Lancet 1972; ii:994-7
27. 27 Lloyd SE, Pearce SH, Fisher SE, et al. A common molecular basis for three inherited kidney stone diseases. Nature 1996;379: 445-9
28. 28 Nielsen S, Kwon TH, Christensen BM, Promeneur D, Frokiaer J, Marples D. Physiology and pathophysiology of renal aquaporins. J Am Soc Nephrol 1999;10:647-63
29. 29 Lai LW, Chan DM, Erickson RP, Hsu SJ, Lien YH. Correction of renal tubular acidosis in carbonic anhydrase II-deficient mice with gene therapy. J Clin Invest 1998;101:1320-5
30. 30 Lien YH, Lai LW. Liposome-mediated gene transfer into the tubules. Exp Nephrol 1997;5:132-6