尿
基础(拓扑)
铵
医学
内科学
化学
数学
有机化学
数学分析
作者
Samuel L. Svendsen,Amalie Quist Rousing,Rasmus Carlsen,Dinah Sherzad Khatir,Donna E. Jensen,Nikita Misella Hansen,Louise Salomo,Henrik Birn,Niels Henrik Buus,Jens Leipziger,Mads V. Sørensen,Peder Berg
出处
期刊:Journal of The American Society of Nephrology
日期:2024-07-17
标识
DOI:10.1681/asn.0000000000000447
摘要
Key Points This study developed a urine acid/base score to assess tubular acid excretion capacity and identify early acid retention in CKD. The results show that early signs of acid retention (a low acid/base score) are associated with a higher risk for CKD progression. Future research should address if a low urine acid/base score can be improved and if this translates into clinically meaningful effects. Background Acidosis is associated with exacerbated loss of kidney function in CKD. Currently, acid/base status is assessed by plasma measures, although organ-damaging covert acidosis, subclinical acidosis, may be present before reflected in plasma. Low urine NH 4 + excretion associates with poor kidney outcomes in CKD and is proposed as a marker for subclinical acidosis. However, low NH 4 + excretion could result from either a low capacity or a low demand for acid excretion. We hypothesized that a urine acid/base score reflecting both the demand and capacity for acid excretion would better predict CKD progression. Methods Twenty-four–hour urine collections were included from three clinical studies of patients with CKD stage 3 and 4: a development cohort ( N =82), a variation cohort ( N =58), and a validation cohort ( N =73). A urine acid/base score was derived and calculated from urinary pH and [NH 4 + ]. Subclinical acidosis was defined as an acid/base score below the lower limit of the 95% prediction interval of healthy controls. The main outcomes were change in measured GFR after 18 months and CKD progression (defined as ≥50% decline in eGFR, initiation of long-term dialysis, or kidney transplantation) during up to 10 years of follow-up. Results Subclinical acidosis was prevalent in all cohorts ( n =54/82, 48/73, and 40/58, respectively, approximately 67%). Subclinical acidosis was associated with an 18% (95% confidence interval [CI], 2 to 32) larger decrease of measured GFR after 18 months. During a median follow-up of 6 years, subclinical acidosis was associated with a higher risk of CKD progression. Adjusted hazard ratios were 9.88 (95% CI, 1.27 to 76.7) in the development cohort and 11.1 (95% CI, 2.88 to 42.5) in the validation cohort. The acid/base score had a higher predictive value for CKD progression than NH 4 + excretion alone. Conclusions Subclinical acidosis, defined by a new urine acid/base score, was associated with a higher risk of CKD progression in patients with CKD stage 3 and 4.
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