Service d'endocrinologie, CHU de Bordeaux, 33000 Bordeaux, France.
CHU de Lille, endocrinology, diabetology, metabolism and nutrition, 59000 Lille, France; Inserm U1190, 59000 Lille, France; Université de Lille, 59000 Lille, France.
Ann Endocrinol (Paris). 2022 Aug;83(4):219-225. doi: 10.1016/j.ando.2022.01.001. Epub 2022 Jan 21.
Lithium is an efficient treatment of bipolar disorder. Besides renal insufficiency, many endocrine side effects are described such as the occurrence of thyroid disorders, hypercalcaemia and nephrogenic diabetes insipidus. Lithium inhibits the secretion of thyroid hormones. The prevalence of goiter is 4 times more common in Lithium-treated patients compared as to the general population. Hypothyroidism (8-20%) is more frequent in women and in case of pre-existing thyroid autoimmunity. Grave's disease and other hyperthyroidisms are sometimes reported. Lithium stimulates the proliferation of parathyroid cells by activating the Wnt pathway. An increase in serum calcium and PTH is described in patients treated with Lithium with a 4 to 6-fold higher risk of primary hyperparathyroidism than in the general population. Nevertheless, 24-hour urine calcium is not often increased, and the phenotype can mimic a hypercalcemia-hypocalciuria syndrome that may regress with Lithium discontinuation. Surgery should be cautious since parathyroid hyperplasia is more common than parathyroid adenoma. Nephrogenic diabetes insipidus is frequently reported and may be debilitating, sometimes intricated with severe dehydration, hypernatremia, and acute renal insufficiency. Nephrogenic diabetes insipidus is not generally reversible after Lithium discontinuation, especially in patients who have chronic kidney disease due to interstitial tubule nephritis. In conclusion, clinical assessment (goiter, diuresis) and biological monitoring of serum calcium, sodium creatinine, TSH and lithium are recommended in patients receiving Lithium therapy. The risk of Lithium discontinuation in case of side effects should be weighed against the psychological risk, and must be discussed with the psychiatrist.
锂是治疗双相情感障碍的有效方法。除了肾功能不全外,还描述了许多内分泌副作用,如甲状腺疾病、高钙血症和肾性尿崩症的发生。锂抑制甲状腺激素的分泌。与普通人群相比,锂治疗患者甲状腺肿的患病率高 4 倍。甲状腺功能减退症(8-20%)在女性和存在自身免疫性甲状腺疾病时更为常见。Graves 病和其他甲状腺功能亢进症有时也有报道。锂通过激活 Wnt 通路刺激甲状旁腺细胞的增殖。锂治疗患者的血清钙和 PTH 增加,原发性甲状旁腺功能亢进的风险比普通人群高 4 到 6 倍。然而,24 小时尿钙并不经常增加,表型可能模仿高钙血症-低钙尿综合征,停用锂后可能会消退。由于甲状旁腺增生比甲状旁腺瘤更为常见,因此手术应谨慎进行。肾性尿崩症经常报道,可能使人虚弱,有时伴有严重脱水、高钠血症和急性肾功能不全。锂停药后,肾性尿崩症通常不会逆转,尤其是在因间质性小管肾炎导致慢性肾脏病的患者中。总之,建议在接受锂治疗的患者中进行临床评估(甲状腺肿、利尿)和血清钙、钠、肌酐、TSH 和锂的生物学监测。应权衡因副作用而停用锂的风险与心理风险,并与精神科医生讨论。