TY - JOUR
T1 - Net acid excretion and urinary organic anions in idiopathic uric acid nephrolithiasis
AU - Bobulescu, I. Alexandru
AU - Park, Sun K.
AU - Richie Xu, L. H.
AU - Blanco, Francisco
AU - Poindexter, John
AU - Adams-Huet, Beverley
AU - Davidson, Taylor L.
AU - Sakhaee, Khashayar
AU - Maalouf, Naim M.
AU - Moe, Orson W.
N1 - Funding Information:
This work was supported by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Grants R01-DK113377 (to I.A.B.), R01-DK081423 (to K.S. and O.W.M.), and R01-DK091392 (to O.W.M.); NIDDK O’Brien Kidney Research Center Grant P30-DK07938; and Endowed Professors Collaborative Research Support Grant (to K.S. and O.W.M.) from the Charles and Jane Pak Foundation. The University of Texas Southwestern Clinical Research Unit is supported in part by National Institutes of Health Grant UL1-TR001105.
Funding Information:
I.A.B. and N.M.M. received research funding from Takeda Pharmaceutical Company Ltd via the Investigator-Initiated Sponsored Research mechanism for research unrelated to this article. There was no funding or involvement from Takeda Pharmaceutical Company Ltd or any other commercial entity in any aspect of this article, including no involvement in study design, conduct, analysis, manuscript preparation, or decision to publish.
Funding Information:
Theauthorsaregrateful for theassistanceof theresearchnursingand technical staff at the Charles and Jane Pak Center for Mineral Metabolismand Clinical Research, the MineralMetabolismLaboratory, and the Clinical and Translational Research Center at the University of Texas Southwestern. We thank Drs. Lawrence Sweetman and Erland Arning(CenterofMetabolomics,Baylor Institute ofMetabolicDisease, Dallas, TX) for assistance with urine metabolomics service. This work was supported by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Grants R01-DK113377 (to I.A.B.), R01-DK081423 (toK.S. andO.W.M.), andR01-DK091392 (to O.W.M.); NIDDK O’Brien Kidney Research Center Grant P30- DK07938; and Endowed Professors Collaborative Research Support Grant (to K.S. and O.W.M.) from the Charles and Jane Pak Foundation. The University of Texas Southwestern Clinical Research Unit is supported in part by National Institutes of Health Grant UL1-TR001105.
Publisher Copyright:
© 2019 by the American Society of Nephrology.
PY - 2019/3/7
Y1 - 2019/3/7
N2 - Background and objectives Idiopathic uric acid nephrolithiasis, which is closely associated with obesity and the metabolic syndrome, is increasing in prevalence. Unduly acidic urine pH, the quintessential pathophysiologic feature of this disease, is in part explained by inadequate excretion of the principal urinary buffer ammonium. The role of net acid excretion in the pathogenesis of uric acid nephrolithiasis is incompletely understood. Design, setting, participants, & measurements We compared acid-base parameters of patients with idiopathic uric acid nephrolithiasis with matched control subjects under controlled diets in an inpatient metabolic unit. Measurements included fasting blood and 24-hour urine chemistries and 24-hour urine metabolomic analysis. Comparisons between groups included analysis of covariance models controlling for urine pH or body mass index. Results Subjects with idiopathic uric acid nephrolithiasis had lower urine pH (5.5 versus 5.9; P<0.001) and higher net acid excretion (60 versus 43 mEq/24 h; P,0.001), with the excess H+ carried by nonammonium buffers. In all subjects, there was a positive relationship of net acid excretion with higher body mass index in spite of strictly controlled equivalent dietary acid intake. This relationship was most evident among control subjects (r=0.36; P=0.03). It was attenuated in patients with idiopathic uric acid nephrolithiasis whose net acid excretion remained fixedly high and ammonium excretion remained low relative to net acid excretion, resulting in low urine pH over a wide body mass index range. Urinary metabolomics was performed to attempt to identify excess organic acids presented to the kidney in idiopathic uric acid nephrolithiasis. Among the tricarboxylic acid cycle intermediates and amino acid and lipid metabolites analyzed, 26 organic anions with acid dissociation constants values in the range of urine pH showed greater protonation. However, protons carried by the identified organic acids did not entirely account for the higher titratable acidity seen in idiopathic uric acid nephrolithiasis. Conclusions Higher acid load to the kidney, resulting in higher urinary net acid excretion, is an important factor in the pathogenesis of idiopathic uric acid nephrolithiasis.
AB - Background and objectives Idiopathic uric acid nephrolithiasis, which is closely associated with obesity and the metabolic syndrome, is increasing in prevalence. Unduly acidic urine pH, the quintessential pathophysiologic feature of this disease, is in part explained by inadequate excretion of the principal urinary buffer ammonium. The role of net acid excretion in the pathogenesis of uric acid nephrolithiasis is incompletely understood. Design, setting, participants, & measurements We compared acid-base parameters of patients with idiopathic uric acid nephrolithiasis with matched control subjects under controlled diets in an inpatient metabolic unit. Measurements included fasting blood and 24-hour urine chemistries and 24-hour urine metabolomic analysis. Comparisons between groups included analysis of covariance models controlling for urine pH or body mass index. Results Subjects with idiopathic uric acid nephrolithiasis had lower urine pH (5.5 versus 5.9; P<0.001) and higher net acid excretion (60 versus 43 mEq/24 h; P,0.001), with the excess H+ carried by nonammonium buffers. In all subjects, there was a positive relationship of net acid excretion with higher body mass index in spite of strictly controlled equivalent dietary acid intake. This relationship was most evident among control subjects (r=0.36; P=0.03). It was attenuated in patients with idiopathic uric acid nephrolithiasis whose net acid excretion remained fixedly high and ammonium excretion remained low relative to net acid excretion, resulting in low urine pH over a wide body mass index range. Urinary metabolomics was performed to attempt to identify excess organic acids presented to the kidney in idiopathic uric acid nephrolithiasis. Among the tricarboxylic acid cycle intermediates and amino acid and lipid metabolites analyzed, 26 organic anions with acid dissociation constants values in the range of urine pH showed greater protonation. However, protons carried by the identified organic acids did not entirely account for the higher titratable acidity seen in idiopathic uric acid nephrolithiasis. Conclusions Higher acid load to the kidney, resulting in higher urinary net acid excretion, is an important factor in the pathogenesis of idiopathic uric acid nephrolithiasis.
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U2 - 10.2215/CJN.10420818
DO - 10.2215/CJN.10420818
M3 - Article
C2 - 30745301
AN - SCOPUS:85062635924
SN - 1555-9041
VL - 14
SP - 411
EP - 420
JO - Clinical Journal of the American Society of Nephrology
JF - Clinical Journal of the American Society of Nephrology
IS - 3
ER -