Castro Victor M, Roberson Ashlee M, McCoy Thomas H, Wiste Anna, Cagan Andrew, Smoller Jordan W, Rosenbaum Jerrold F, Ostacher Michael, Perlis Roy H
Center for Experimental Drugs and Diagnostics, Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
Partners Research Information Systems and Computing, Partners HealthCare System, One Constitution Center, Boston, MA, USA.
Neuropsychopharmacology. 2016 Mar;41(4):1138-43. doi: 10.1038/npp.2015.254. Epub 2015 Aug 21.
Although lithium preparations remain first-line treatment for bipolar disorder, risk for development of renal insufficiency may discourage their use. Estimating such risk could allow more informed decisions and facilitate development of prevention strategies. We utilized electronic health records from a large New England health-care system between 2006 and 2013 to identify patients aged 18 years or older with a lithium prescription. Renal insufficiency was identified using the presence of renal failure by ICD9 code or laboratory-confirmed glomerular filtration rate below 60 ml/min. Logistic regression was used to build a predictive model in a random two-thirds of the cohort, which was tested in the remaining one-third. Risks associated with aspects of pharmacotherapy were also examined in the full cohort. We identified 1445 adult lithium-treated patients with renal insufficiency, matched by risk set sampling 1 : 3 with 4306 lithium-exposed patients without renal insufficiency. In regression models, features associated with risk included older age, female sex, history of smoking, history of hypertension, overall burden of medical comorbidity, and diagnosis of schizophrenia or schizoaffective disorder (p<0.01 for all contrasts). The model yielded an area under the ROC curve exceeding 0.81 in an independent testing set, with 74% of renal insufficiency cases among the top two risk quintiles. Use of lithium more than once daily, lithium levels greater than 0.6 mEq/l, and use of first-generation antipsychotics were independently associated with risk. These results suggest the possibility of stratifying risk for renal failure among lithium-treated patients. Once-daily lithium dosing and maintaining lower lithium levels where possible may represent strategies for reducing risk.
尽管锂制剂仍是双相情感障碍的一线治疗药物,但发生肾功能不全的风险可能会阻碍其使用。评估此类风险有助于做出更明智的决策,并促进预防策略的制定。我们利用2006年至2013年间来自新英格兰一个大型医疗保健系统的电子健康记录,确定年龄在18岁及以上且有锂处方的患者。通过国际疾病分类第九版(ICD9)代码诊断的肾衰竭或实验室确认的肾小球滤过率低于60毫升/分钟来确定肾功能不全。在队列中随机抽取三分之二的数据用于构建逻辑回归预测模型,并在其余三分之一的数据中进行测试。还在整个队列中研究了与药物治疗相关的风险因素。我们确定了1445名接受锂治疗的成年肾功能不全患者,通过风险集抽样以1:3的比例与4306名未发生肾功能不全的锂暴露患者进行匹配。在回归模型中,与风险相关的特征包括年龄较大、女性、吸烟史、高血压史、总体医疗合并症负担以及精神分裂症或分裂情感性障碍的诊断(所有对比的p<0.01)。该模型在独立测试集中的ROC曲线下面积超过0.81,在前两个风险五分位数中,74%为肾功能不全病例。每日多次使用锂、锂水平大于0.6毫当量/升以及使用第一代抗精神病药物与风险独立相关。这些结果表明,在接受锂治疗的患者中有可能对肾衰竭风险进行分层。每日一次服用锂并尽可能维持较低的锂水平可能是降低风险的策略。