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锂。精神疾病的当前状况。

Lithium. Current status in psychiatric disorders.

作者信息

Peet M, Pratt J P

机构信息

Northern General Hospital, Sheffield, England.

出版信息

Drugs. 1993 Jul;46(1):7-17. doi: 10.2165/00003495-199346010-00002.

DOI:10.2165/00003495-199346010-00002
PMID:7691509
Abstract

Lithium is the recommended treatment for the prophylaxis of bipolar affective disorder. The drug is also effective in the prophylactic treatment of recurrent unipolar depression, although many psychiatrists prefer to use antidepressant drugs for this indication. The efficacy of lithium is well established in the short term treatment of mania, although neuroleptic drugs are required at the start of treatment for more severely disturbed patients. Lithium augmentation of antidepressant drugs is increasingly popular for the treatment of resistant depression. It is now common practice to maintain serum lithium concentrations in the range 0.5 to 0.8 mmol/L, which is generally as effective as higher concentrations while reducing the incidence of adverse effects and intoxication. Some individuals may nevertheless require higher serum concentrations. Most adverse effects such as tremor and gastrointestinal upset are usually minor and often transient. There is no good evidence of nephrotoxicity with long term treatment, but persistent polyuria can occur. Hypothyroidism, with or without goitre, can occur uncommonly during long term lithium therapy. Prescribers should be alert to, and patients should be educated about, the predisposing factors and early symptoms relating to lithium intoxication. Specialist mood disorder clinics can facilitate safer and more effective lithium treatment.

摘要

锂盐是预防双相情感障碍的推荐治疗药物。该药物对复发性单相抑郁的预防性治疗也有效,尽管许多精神科医生更倾向于使用抗抑郁药物来治疗这一适应症。锂盐在躁狂症的短期治疗中疗效已得到充分证实,尽管对于病情更严重的患者在治疗开始时需要使用抗精神病药物。锂盐增强抗抑郁药物治疗难治性抑郁症越来越普遍。目前的常见做法是将血清锂浓度维持在0.5至0.8 mmol/L范围内,这通常与更高浓度一样有效,同时可降低不良反应和中毒的发生率。不过,有些人可能需要更高的血清浓度。大多数不良反应,如震颤和胃肠道不适,通常较轻且往往是短暂的。长期治疗没有充分证据表明会出现肾毒性,但可能会发生持续性多尿。长期锂盐治疗期间,甲状腺功能减退症(无论有无甲状腺肿)可能罕见发生。开处方者应警惕锂盐中毒的诱发因素和早期症状,并应对患者进行相关教育。专业的情绪障碍诊所可以促进更安全、更有效的锂盐治疗。

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1
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Is There Justification to Treat Neurodegenerative Disorders by Repurposing Drugs? The Case of Alzheimer's Disease, Lithium, and Autophagy.通过重新利用药物治疗神经退行性疾病是否合理?以阿尔茨海默病、锂和自噬为例。
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本文引用的文献

1
Lithium salts in the treatment of psychotic excitement.锂盐治疗精神病性兴奋。
Med J Aust. 1949 Sep 3;2(10):349-52. doi: 10.1080/j.1440-1614.1999.06241.x.
2
The treatment of manic psychoses by the administration of lithium salts.通过锂盐给药治疗躁狂性精神病。
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Lithium induces rapid relief of depression in tricyclic antidepressant drug non-responders.
Br J Psychiatry. 1981 Mar;138:252-6. doi: 10.1192/bjp.138.3.252.
锂诱导的肾性尿崩症的蛋白质组学分析:水通道蛋白2下调和细胞增殖的机制
Proc Natl Acad Sci U S A. 2008 Mar 4;105(9):3634-9. doi: 10.1073/pnas.0800001105. Epub 2008 Feb 22.
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Mood Disorders in Family Practice: Beyond Unipolarity to Bipolarity.家庭医疗中的情绪障碍:从单相到双相
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5
Tol1, a fission yeast phosphomonoesterase, is an in vivo target of lithium, and its deletion leads to sulfite auxotrophy.Tol1是一种裂殖酵母磷酸单酯酶,是锂在体内的作用靶点,其缺失会导致亚硫酸盐营养缺陷。
J Bacteriol. 2000 Jul;182(13):3619-25. doi: 10.1128/JB.182.13.3619-3625.2000.
6
Lithium does not alter the choline/creatine ratio in the temporal lobe of human volunteers as measured by proton magnetic resonance spectroscopy.通过质子磁共振波谱测量发现,锂不会改变人类志愿者颞叶中的胆碱/肌酸比率。
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Long term treatment of bipolar disorder.双相情感障碍的长期治疗。
Drugs. 1996 Mar;51(3):367-82. doi: 10.2165/00003495-199651030-00003.
8
Lithium-induced downregulation of aquaporin-2 water channel expression in rat kidney medulla.锂诱导大鼠肾髓质水通道蛋白-2水通道表达下调。
J Clin Invest. 1995 Apr;95(4):1838-45. doi: 10.1172/JCI117863.
4
Lithium and chlorpromazine in psychotic inpatients.锂盐与氯丙嗪用于精神病住院患者的情况
Psychiatry Res. 1982 Aug;7(1):69-81. doi: 10.1016/0165-1781(82)90054-3.
5
Lithium carbonate and imipramine in the prophylaxis of unipolar and bipolar II illness: a prospective, placebo-controlled comparison.碳酸锂和丙咪嗪预防单相和双相II型疾病:一项前瞻性、安慰剂对照比较研究。
Arch Gen Psychiatry. 1982 Sep;39(9):1065-9. doi: 10.1001/archpsyc.1982.04290090053011.
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Recurrence of affective illness after withdrawal of long-term lithium treatment.长期锂盐治疗停药后情感性疾病的复发
Acta Psychiatr Scand. 1983 Aug;68(2):126-33. doi: 10.1111/j.1600-0447.1983.tb06990.x.
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Lithium-carbamazepine neurotoxicity and risk factors.
Am J Psychiatry. 1984 Dec;141(12):1604-6. doi: 10.1176/ajp.141.12.1604.
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Drug therapy in the prevention of recurrences in unipolar and bipolar affective disorders. Report of the NIMH Collaborative Study Group comparing lithium carbonate, imipramine, and a lithium carbonate-imipramine combination.预防单相和双相情感障碍复发的药物治疗。美国国立精神卫生研究所协作研究小组比较碳酸锂、丙咪嗪及碳酸锂 - 丙咪嗪联合用药的报告。
Arch Gen Psychiatry. 1984 Nov;41(11):1096-104. doi: 10.1001/archpsyc.1983.01790220086014.
9
Decreasing lithium dosage reduces morbidity and side-effects during prophylaxis.在预防期间减少锂盐剂量可降低发病率和副作用。
J Affect Disord. 1983 Nov;5(4):353-62. doi: 10.1016/0165-0327(83)90026-5.
10
Continuation therapy with lithium and amitriptyline in unipolar depressive illness: a randomized, double-blind, controlled trial.锂盐与阿米替林用于单相抑郁障碍的延续治疗:一项随机、双盲、对照试验
Psychol Med. 1984 Feb;14(1):37-50. doi: 10.1017/s0033291700003068.