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In Whom Does Lithium Work?

To the Editor: In the January issue, Nierenberg et al. (1) try to answer an important question: Does lithium provide mood stabilization to a population of patients with lifetime bipolar I or II disorder who have chronic mood problems? According to the description of the sample, participants experienced an average of eight episodes per year, and although depressive episodes were fewer in number than manic or hypomanic episodes, patient scores on the Mini International Neuropsychiatric Interview at intake suggest that depression rather than mania accounted for more of their difficulties. Improvement in “mood” (it was not specified which mood) was the metric used to ascertain lithium’s success.

These results were contrasted to those of Gelenberg et al. (2), whose study sample consisted of patients with bipolar I disorder who had been euthymic for 2 months before intake so that relapse into mania or depression (not just mood improvement) could be determined. Moreover, those with four or more episodes were excluded from the study. In other words, the sample assessed by Nierenberg et al. would not have been in the Gelenberg et al. study, whose participants, granted, represented only a minority of mood-disordered patients (157 of 1,200). The comparison, therefore, is between apples and oranges.

While the Nierenberg et al. study is important in addressing what may be the majority of people with a diagnosis of bipolar I or II disorder (i.e., chronically mood unstable and primarily depressed [3]), it does not provide evidence to disprove lithium’s efficacy in the population for whom it was originally shown to be effective for prophylaxis and treatment: individuals with a positive family history, an interval course with a manic episode followed by a depressive episode and then a symptom-free episode, and fewer episodes (4, 5). In fact, the sample in the Nierenberg et al. study includes precisely those in whom we would not have expected a lithium response. The sample distinction is important; it is also important to remind clinicians that lithium was never touted as a panacea for general mood dysregulation.

From the Departments of Psychiatry, Pediatrics, and Child and Adolescent Psychiatry, Stony Brook University School of Medicine, Stony Brook, N.Y.

Dr. Carlson has received research funding from GlaxoSmithKline, Merck, NIMH, Otsuka, and Pfizer.

References

1 Nierenberg AA, Friedman ES, Bowden CL, Sylvia LG, Thase ME, Ketter T, Ostacher MJ, Leon AC, Reilly-Harrington N, Iosifescu DV, Pencina M, Severe JB, Calabrese JR: Lithium Treatment Moderate-Dose Use Study (LiTMUS) for bipolar disorder: a randomized comparative effectiveness trial of optimized personalized treatment with and without lithium. Am J Psychiatry 2013; 170:102–110LinkGoogle Scholar

2 Gelenberg AJ, Kane JM, Keller MB, Lavori P, Rosenbaum JF, Cole K, Lavelle J: Comparison of standard and low serum levels of lithium for maintenance treatment of bipolar disorder. N Engl J Med 1989; 321:1489–1493Crossref, MedlineGoogle Scholar

3 Judd LL, Akiskal HS, Schettler PJ, Endicott J, Maser J, Solomon DA, Leon AC, Rice JA, Keller MB: The long-term natural history of the weekly symptomatic status of bipolar I disorder. Arch Gen Psychiatry 2002; 59:530–537Crossref, MedlineGoogle Scholar

4 Abou-Saleh MT: Who responds to prophylactic lithium therapy? Br J Psychiatry Suppl 1993; 163:20–26CrossrefGoogle Scholar

5 Maj M: The effect of lithium in bipolar disorder: a review of recent research evidence. Bipolar Disord 2003; 5:180–188Crossref, MedlineGoogle Scholar