Waller D G, Edwards J G, Naik R, Polak A
Q J Med. 1984 Summer;53(211):369-79.
Renal function tests were performed in 101 unselected patients who had been on lithium for two weeks to 12 years. None had a recorded episode of lithium intoxication. The glomerular filtration rate (GFR), was not correlated with the cumulative dose of lithium or the duration of use of other psychotropic drugs. Nine patients had creatinine clearances lower than predicted; in six of these, no cause was identified and the small reductions in GFR may have been related to lithium use. Urinary concentrating ability (Umax) declined with age, and total dose of lithium received. Although the concurrent use of neuroleptics did not significantly reduce the Umax, the total duration of treatment with these drugs showed a negative correlation. The results suggest that prolonged use of neuroleptics, particularly in patients treated with lithium, may be responsible for an irreversible reduction in urine concentrating ability. Microalbuminuria was present in 40 per cent of the patients, although the rate of albumin excretion was not correlated with duration of use of psychotropic drugs. beta 2 microglobulin excretion was only raised in nine of these patients, suggesting that increased glomerular permeability rather than impaired proximal tubular protein reabsorption was responsible for the proteinuria. The urinary excretion of beta 2 microglobulin and N-acetyl-beta-glucosaminidase were slightly increased in small numbers of patients, indicating little evidence for proximal tubular damage. Increased NAG excretion did not correlate with reduced distal tubular function. However, there was a tendency to higher urinary beta 2 microglobulin excretion in patients with a reduced Umax.
对101例未经过挑选、服用锂盐两周至12年的患者进行了肾功能测试。无一例有锂中毒的记录事件。肾小球滤过率(GFR)与锂盐的累积剂量或其他精神药物的使用时长无关。9例患者的肌酐清除率低于预期;其中6例未发现病因,肾小球滤过率的小幅降低可能与锂盐使用有关。尿浓缩能力(Umax)随年龄和所接受锂盐的总剂量下降。尽管同时使用抗精神病药物并未显著降低Umax,但这些药物的总治疗时长呈负相关。结果表明,长期使用抗精神病药物,尤其是在接受锂盐治疗的患者中,可能导致尿浓缩能力不可逆下降。40%的患者存在微量白蛋白尿,尽管白蛋白排泄率与精神药物的使用时长无关。这些患者中仅有9例β2微球蛋白排泄升高,提示蛋白尿是由肾小球通透性增加而非近端肾小管蛋白重吸收受损所致。少数患者的β2微球蛋白和N - 乙酰 - β - 氨基葡萄糖苷酶的尿排泄略有增加,表明近端肾小管损伤的证据很少。NAG排泄增加与远端肾小管功能降低无关。然而,Umax降低的患者尿β2微球蛋白排泄有升高的趋势。