Sheffler Rachel, Karpf Stephanie, Rebolloso Sarah, Miksicek Vicki, Buchweitz John P, Puschner Birgit
Department of Pathobiology and Diagnostic Investigation, College of Veterinary Medicine, Michigan State University, Lansing, MI, USA.
Veterinary Diagnostic Laboratory, Nutrition and Toxicology Section, College of Veterinary Medicine, Michigan State University, Lansing, MI, USA.
BMC Vet Res. 2025 May 8;21(1):327. doi: 10.1186/s12917-025-04788-8.
Control of circulating phosphorus concentrations in patients with chronic kidney disease is a mainstay of treatment and may include use of aluminum hydroxide as an intestinal phosphate binder. Serious complications of excess aluminum reported in dogs and man include encephalopathy, microcytic anemia, osteomalacia, and regional myopathy at serum concentrations exceeding 100 ng/mL. Reports of aluminum toxicosis are not available for cats receiving aluminum hydroxide and circulating aluminum concentrations are poorly characterized. The aim of this study is to establish therapeutic and toxic serum aluminum concentrations in cats and apply this data to an intoxication case.
Of cats with CKD who received aluminum hydroxide, 9/21 serum samples exceeded aluminum concentrations of 100 ng/mL. After removal of outliers, 18 cats with kidney disease who received aluminum hydroxide had mean serum aluminum concentrations of 69 ng/mL [95% CI: 42-97 ng/mL], which was significantly higher than mean aluminum concentrations in cats not receiving aluminum hydroxide (p = 0.0034). The mean aluminum concentration of 141 feline serum samples not receiving aluminum hydroxide was 29 ng/mL [95% CI: 24-33 ng/mL]. Of the 141 samples, 16 cats presenting for wellness or dental procedures had mean concentrations of 36 ng/mL [95% CI: 15-56 ng/mL]. This data was applied to a case of a 16-year-old spayed female domestic shorthair with IRIS stage 2 chronic kidney disease with a 7-month history of mild hindlimb weakness and intermittent right forelimb myoclonus. The patient received oral aluminum hydroxide, and the serum contained 376 ng/mL of aluminum suggestive of toxicosis. Resolution of clinical signs was noted following a switch to an aluminum-free phosphate binding medication, and, at 5-month follow-up, the serum aluminum concentration was 71 ng/mL.
Our data suggest that serum aluminum concentrations in cats exceeding 86 ng/mL can result in clinical aluminum toxicosis and is comparable to the 100 ng/mL toxic threshold described in humans. The data provided facilitate the diagnostic assessment of cats receiving aluminum hydroxide supplementation. Veterinarians must recognize the toxic effects of aluminum and pursue diagnostic testing in suspect cases to mitigate invasive and costly workup for aluminum-associated clinical signs or euthanasia due to deterioration of these patients.
控制慢性肾脏病患者循环血磷浓度是治疗的关键,可能包括使用氢氧化铝作为肠道磷结合剂。在犬类和人类中,过量铝摄入的严重并发症包括脑病、小细胞性贫血、骨软化症以及血清浓度超过100 ng/mL时出现的局部肌病。目前尚无关于接受氢氧化铝治疗的猫发生铝中毒的报道,且循环铝浓度的特征尚不明确。本研究的目的是确定猫的治疗性和中毒性血清铝浓度,并将该数据应用于一例中毒病例。
在接受氢氧化铝治疗的慢性肾脏病猫中,21份血清样本中有9份超过了100 ng/mL的铝浓度。去除异常值后,18只接受氢氧化铝治疗的肾病猫的血清铝平均浓度为69 ng/mL [95%置信区间:42 - 97 ng/mL],显著高于未接受氢氧化铝治疗的猫的平均铝浓度(p = 0.0034)。141份未接受氢氧化铝治疗的猫血清样本的平均铝浓度为29 ng/mL [95%置信区间:24 - 33 ng/mL]。在这141份样本中,16只进行健康检查或牙科手术的猫的平均浓度为36 ng/mL [95%置信区间:15 - 56 ng/mL]。该数据应用于一例16岁绝育雌性家猫,其患有国际肾脏病学会(IRIS)2期慢性肾脏病,有7个月轻度后肢无力和间歇性右前肢肌阵挛病史。该患者接受了口服氢氧化铝治疗,血清中铝含量为376 ng/mL,提示铝中毒。改用无铝磷结合药物后,临床症状得到缓解,在5个月的随访中,血清铝浓度为71 ng/mL。
我们的数据表明,猫血清铝浓度超过86 ng/mL可导致临床铝中毒,这与人类描述的100 ng/mL中毒阈值相当。所提供的数据有助于对接受氢氧化铝补充治疗的猫进行诊断评估。兽医必须认识到铝的毒性作用,并在疑似病例中进行诊断检测,以避免因这些患者病情恶化而进行侵入性且昂贵的检查或安乐死。