Literature DB >> 32399606

Are conventional stone analysis techniques reliable for the identification of 2,8-dihydroxyadenine kidney stones? A case series.

Hrafnhildur L Runolfsdottir1,2, Tzu-Ling Lin3, David S Goldfarb4, John A Sayer5,6,7, Mini Michael8, David Ketteridge9, Peter R Rich10, Vidar O Edvardsson11,12, Runolfur Palsson13,14.   

Abstract

We have recently encountered patients incorrectly diagnosed with adenine phosphoribosyltransferase (APRT) deficiency due to misidentification of kidney stones as 2,8-dihydroxyadenine (DHA) stones. The objective of this study was to examine the accuracy of stone analysis for identification of DHA. Medical records of patients referred to the APRT Deficiency Research Program of the Rare Kidney Stone Consortium in 2010-2018 with a diagnosis of APRT deficiency based on kidney stone analysis were reviewed. The diagnosis was verified by measurement of APRT enzyme activity or genetic testing. Attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectra of pure crystalline DHA and a kidney stone obtained from one of the confirmed APRT deficiency cases were generated. The ATR-FTIR spectrum of the kidney stone matched the crystalline DHA spectrum and was used for comparison with available infrared spectra of stone samples from the patients. Of 17 patients referred, 14 had sufficient data available to be included in the study. In all 14 cases, the stone analysis had been performed by FTIR spectroscopy. The diagnosis of APRT deficiency was confirmed in seven cases and rejected in the remaining seven cases. Comparison of the ATR-FTIR spectrum of the DHA stone with the FTIR spectra from three patients who did not have APRT deficiency showed no indication of DHA as a stone component. Misidentification of DHA as a kidney stone component by clinical laboratories appears common among patients referred to our program. Since current clinical protocols used to interpret infrared spectra for stone analysis cannot be considered reliable for the identification of DHA stones, the diagnosis of APRT deficiency must be confirmed by other methods.

Entities:  

Keywords:  APRT deficiency; Infrared spectroscopy; Kidney stone composition; Misdiagnosis; Nephrolithiasis

Mesh:

Substances:

Year:  2020        PMID: 32399606      PMCID: PMC7395965          DOI: 10.1007/s00240-020-01187-6

Source DB:  PubMed          Journal:  Urolithiasis        ISSN: 2194-7228            Impact factor:   3.436


  25 in total

1.  2,8-Dihydroxyadenine urolithiasis, an underdiagnosed disease.

Authors:  I Ceballos-Picot; J L Perignon; M Hamet; M Daudon; P Kamoun
Journal:  Lancet       Date:  1992-04-25       Impact factor: 79.321

Review 2.  EAU Guidelines on Diagnosis and Conservative Management of Urolithiasis.

Authors:  Christian Türk; Aleš Petřík; Kemal Sarica; Christian Seitz; Andreas Skolarikos; Michael Straub; Thomas Knoll
Journal:  Eur Urol       Date:  2015-08-28       Impact factor: 20.096

3.  Clinical study of ammonium acid urate urolithiasis.

Authors:  Yii-Her Chou; Chun-Nung Huang; Wei-Ming Li; Shu-Pin Huang; Wen-Jeng Wu; Chia-Chun Tsai; Ai-Wen Chang; Szu-Miao Chen; Yu-Ling Lin; Yi-Pin Lin
Journal:  Kaohsiung J Med Sci       Date:  2012-02-22       Impact factor: 2.744

4.  Medical management of kidney stones: AUA guideline.

Authors:  Margaret S Pearle; David S Goldfarb; Dean G Assimos; Gary Curhan; Cynthia J Denu-Ciocca; Brian R Matlaga; Manoj Monga; Kristina L Penniston; Glenn M Preminger; Thomas M T Turk; James R White
Journal:  J Urol       Date:  2014-05-20       Impact factor: 7.450

Review 5.  Clinical value of crystalluria and quantitative morphoconstitutional analysis of urinary calculi.

Authors:  Michel Daudon; Paul Jungers
Journal:  Nephron Physiol       Date:  2004

6.  2,8-Dihydroxyadenine lithiasis.

Authors:  H A Simmonds
Journal:  Clin Chim Acta       Date:  1986-10-31       Impact factor: 3.786

7.  Genetic and clinical studies on 19 families with adenine phosphoribosyltransferase deficiencies.

Authors:  N Kamatani; C Terai; S Kuroshima; K Nishioka; K Mikanagi
Journal:  Hum Genet       Date:  1987-02       Impact factor: 4.132

Review 8.  [2,8-dihydroxyadenine nephrolithiasis: from diagnosis to therapy].

Authors:  H Bouzidi; B Lacour; M Daudon
Journal:  Ann Biol Clin (Paris)       Date:  2007 Nov-Dec       Impact factor: 0.459

Review 9.  2,8-Dihydroxyadenine urolithiasis: a not so rare inborn error of purine metabolism.

Authors:  Irène Ceballos-Picot; Michel Daudon; Jérôme Harambat; Albert Bensman; Bertrand Knebelmann; Guillaume Bollée
Journal:  Nucleosides Nucleotides Nucleic Acids       Date:  2014       Impact factor: 1.381

10.  Recurrent 2,8-dihydroxyadenine nephropathy: a rare but preventable cause of renal allograft failure.

Authors:  M Zaidan; R Palsson; E Merieau; E Cornec-Le Gall; A Garstka; U Maggiore; P Deteix; M Battista; E-R Gagné; I Ceballos-Picot; J-P Duong Van Huyen; C Legendre; M Daudon; V O Edvardsson; B Knebelmann
Journal:  Am J Transplant       Date:  2014-10-10       Impact factor: 8.086

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