Magni Giulia, Unwin Robert J, Moochhala Shabbir H
Department of Renal Medicine. Royal Free Hospital Trust and University College London (UCL). London. UK.
Arch Esp Urol. 2021 Jan;74(1):123-128.
Renal tubular acidosis (RTA) is a set of raredis orders in which the renal tubule is unable to excreteacid normally and there by maintain normal acid-basebalance, resulting in a complete or incomplete metabolicacidosis. In distal RTA (dRTA, also known as classicalor type 1 RTA), there is a defect in excreting H+ ionsalong the distal nephron (distal tubule and collectingduct), leading to an alkaline urinary pH with calcium phosphate precipitation and stones. Causes of dRTAinclude genetic mutations, autoimmune disease, and some drugs.Clinical manifestations of the genetic forms of dRTA typically occur during childhood and may vary from mildclinical symptoms, such as a mild metabolic acidosis, hypokalaemia,and incidental detection of kidney stones, to more serious manifestations such as failure to thrive,severe metabolic acidosis, rickets and nephrocalcinosis.Progressive hearing loss may develop in patients withrecessive dRTA, which, depending the causative genemutation, can be present at birth or develop later in adolescence or early adulthood. Diagnosis of dRTA can be challenging, since it requires a high index of suspicion and/or measurement of urinary pH after an acid load, usually in the form of oral ammonium chloride; this should normally acidify the urine to pH below 5.3. In dRTA, urinary citrate levels a real so low and patients are at increased risk of for mingkidney stones from a combination of alkaline urine and low citrate. Ideally, affected patients need regular outpatient follow-up by a urologist and nephrologist. Thus, any patient found to have a calcium phosphate kidney stone, low urinary citrate, and raised urinary pH, especially with an early morning pH >5.5, should be evaluated for underlying dRTA. Patients with complete dRTA will have a low (<20 mmol/L) plasma or serum bicarbonate concentration, whereas in those with incomplete dRTA, bicarbonate levels are usually normal. Oral alkali as potassiumcitrate is still the mainstay of treatment in dRTA.
肾小管酸中毒(RTA)是一组罕见的病症,其中肾小管无法正常排泄酸,从而维持正常的酸碱平衡,导致完全或不完全的代谢性酸中毒。在远端肾小管酸中毒(dRTA,也称为经典型或1型RTA)中,远端肾单位(远端小管和集合管)排泄氢离子存在缺陷,导致尿液pH呈碱性,伴有磷酸钙沉淀和结石。dRTA的病因包括基因突变、自身免疫性疾病和一些药物。dRTA遗传形式的临床表现通常发生在儿童期,症状可能从轻度临床症状,如轻度代谢性酸中毒、低钾血症和偶然发现肾结石,到更严重的表现,如生长发育迟缓、严重代谢性酸中毒、佝偻病和肾钙质沉着症。隐性dRTA患者可能会出现进行性听力丧失,根据致病基因突变的不同,听力丧失可能在出生时就存在,或在青春期后期或成年早期出现。dRTA的诊断可能具有挑战性,因为它需要高度的怀疑指数和/或在酸负荷后测量尿液pH值,通常以口服氯化铵的形式进行;正常情况下,这应使尿液酸化至pH值低于5.3。在dRTA中,尿柠檬酸盐水平也很低,由于碱性尿液和低柠檬酸盐的共同作用,患者形成肾结石的风险增加。理想情况下,受影响的患者需要泌尿外科医生和肾内科医生定期门诊随访。因此,任何发现有磷酸钙肾结石、低尿柠檬酸盐和尿液pH值升高,尤其是晨尿pH值>5.5的患者,都应评估是否存在潜在的dRTA。完全性dRTA患者的血浆或血清碳酸氢盐浓度较低(<20 mmol/L),而不完全性dRTA患者的碳酸氢盐水平通常正常。口服碱性药物如柠檬酸钾仍然是dRTA治疗的主要方法。