Rej Soham, Pira Shamira, Marshe Victoria, Do André, Elie Dominique, Looper Karl J, Herrmann Nathan, Müller Daniel J
Campbell Family Research Institute, Centre for Addiction and Mental Health, University of Toronto, Toronto, ON, Canada.
Department of Psychiatry, Sunnybrook Health Sciences Centre, University of Toronto, 2075 Bayview Avenue, Toronto, ON, M4N 3M5, Canada.
Int Urol Nephrol. 2016 Nov;48(11):1843-1853. doi: 10.1007/s11255-016-1352-6. Epub 2016 Jun 29.
Lithium is an essential treatment in bipolar disorder and treatment-resistant depression; however, its use has been limited by concerns regarding its renal adverse effects. An improved understanding of potential molecular mechanisms can help develop prevention and treatment strategies for lithium-associated renal disease.
We conducted a systematic literature search using MEDLINE, Embase, and PsychINFO including English-language original research articles published prior to November 2015 that specifically investigated lithium's effects on nephrogenic diabetes insipidus (NDI) and chronic kidney disease (CKD), using molecular markers.
From a total of 3510 records, 71 pre-clinical studies and two relevant clinical studies were identified. Molecular alterations were reported in calcium signaling, inositol monophosphate, extracellular-regulated, prostaglandin, sodium/solute transport, G-protein-coupled receptors, nitric oxide, vasopressin/aquaporin, and inflammation-related pathways in lithium-associated renal disease. The majority of studies found that these mechanisms were implicated in NDI, while few studies had examined CKD.
Future studies will have to focus on (1) validating the present findings in human subjects and (2) examining CKD, which is the most clinically relevant lithium-associated renal effect. This will improve our understanding of lithium's biological effects, as well as inform a personalized medicine approach, which could lead to safer lithium prescribing and less renal adverse events.
锂是双相情感障碍和难治性抑郁症的重要治疗药物;然而,其使用因对肾脏不良反应的担忧而受到限制。更好地理解潜在的分子机制有助于制定锂相关肾脏疾病的预防和治疗策略。
我们使用MEDLINE、Embase和PsychINFO进行了系统的文献检索,纳入了2015年11月之前发表的英文原创研究文章,这些文章使用分子标记物专门研究了锂对肾性尿崩症(NDI)和慢性肾脏病(CKD)的影响。
从总共3510条记录中,确定了71项临床前研究和两项相关临床研究。在锂相关肾脏疾病中,钙信号传导、肌醇单磷酸、细胞外调节、前列腺素、钠/溶质转运、G蛋白偶联受体、一氧化氮、血管加压素/水通道蛋白和炎症相关途径中均有分子改变的报道。大多数研究发现这些机制与NDI有关,而很少有研究探讨CKD。
未来的研究将不得不聚焦于(1)在人类受试者中验证目前的发现,以及(2)研究CKD,这是临床上与锂相关的最主要肾脏效应。这将增进我们对锂生物学效应的理解,并为个性化医疗方法提供依据,从而实现更安全的锂处方并减少肾脏不良事件。