Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, Texas.
Department of Internal Medicine.
Clin J Am Soc Nephrol. 2019 Mar 7;14(3):411-420. doi: 10.2215/CJN.10420818. Epub 2019 Feb 11.
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.
Subjects with idiopathic uric acid nephrolithiasis had lower urine pH (5.5 versus 5.9; <0.001) and higher net acid excretion (60 versus 43 mEq/24 h; <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 (=0.36; =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.
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.
特发性尿酸肾结石与肥胖和代谢综合征密切相关,其发病率正在上升。尿液 pH 值过低,是这种疾病的典型病理生理特征,部分原因是主要尿缓冲物铵的排泄不足。净酸排泄在尿酸肾结石发病机制中的作用尚不完全清楚。
设计、设置、参与者和测量:我们在住院代谢病房中,比较了特发性尿酸肾结石患者和匹配对照者在控制饮食下的酸碱参数。测量包括空腹血液和 24 小时尿液化学和 24 小时尿液代谢组学分析。组间比较包括协方差分析模型,控制尿液 pH 值或体重指数。
特发性尿酸肾结石患者的尿 pH 值较低(5.5 比 5.9;<0.001),净酸排泄量较高(60 比 43 mEq/24 h;<0.001),多余的 H 由非铵缓冲剂携带。在所有受试者中,尽管严格控制了相同的饮食酸摄入量,但净酸排泄量与较高的体重指数呈正相关。在对照组中,这种关系最为明显(=0.36;=0.03)。在特发性尿酸肾结石患者中,这种关系减弱,因为净酸排泄量高而铵排泄量相对低,导致在广泛的体重指数范围内尿 pH 值较低。进行尿液代谢组学分析,试图确定特发性尿酸肾结石患者肾脏中存在的过量有机酸。在所分析的三羧酸循环中间产物、氨基酸和脂质代谢物中,26 种具有尿液 pH 值范围内酸解离常数值的有机阴离子表现出更大的质子化。然而,在所鉴定的有机酸中携带的质子并不能完全解释特发性尿酸肾结石中所见的更高可滴定酸度。
更高的肾脏酸负荷导致更高的尿净酸排泄,是特发性尿酸肾结石发病机制的一个重要因素。