Controversies regarding lithium-associated weight gain: case-control study of real-world drug safety data.

Greil, Waldemar; de Bardeci, Mateo; Müller-Oerlinghausen, Bruno; Nievergelt, Nadja; Stassen, Hans; Hasler, Gregor; Erfurth, Andreas; Cattapan, Katja; Rüther, Eckart; Seifert, Johanna; Toto, Sermin; Bleich, Stefan; Schoretsanitis, Georgios (2023). Controversies regarding lithium-associated weight gain: case-control study of real-world drug safety data. International journal of bipolar disorders, 11(1), p. 34. Springer 10.1186/s40345-023-00313-8

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BACKGROUND

The impact of long-term lithium treatment on weight gain has been a controversial topic with conflicting evidence. We aim to assess reporting of weight gain associated with lithium and other mood stabilizers compared to lamotrigine which is considered free of metabolic adverse drug reactions (ADRs).

METHODS

We conducted a case/non-case pharmacovigilance study using data from the AMSP project (German: "Arzneimittelsicherheit in der Psychiatrie"; i.e., Drug Safety in Psychiatry), which collects data on ADRs from patients treated in psychiatric hospitals in Germany, Austria, and Switzerland. We performed a disproportionality analysis of reports of weight gain (> 10% of baseline body weight) calculating reporting odds ratio (ROR). We compared aripiprazole, carbamazepine, lithium, olanzapine, quetiapine, risperidone, and valproate to lamotrigine. Additional analyses related to different mood stabilizers as reference medication were performed. We also assessed sex and age distributions of weight-gain reports.

RESULTS

We identified a total of 527 cases of severe drug-induced weight gain representing 7.4% of all severe ADRs. The ROR for lithium was 2.1 (95%CI 0.9-5.1, p > 0.05), which did not reach statistical significance. Statistically significant disproportionate reporting of weight gain was reported for olanzapine (ROR: 11.5, 95%CI 4.7-28.3, p < 0.001), quetiapine (ROR: 3.4, 95%CI 1.3-8.4, p < 0.01), and valproate (ROR: 2.4, 95%CI 1.1-5.0, p = 0.03) compared to lamotrigine. Severe weight gain was more prevalent in non-elderly (< 65 years) than in elderly patients, with an ROR of 7.6 (p < 0.01) in those treated with lithium, and an ROR of 14.7 (p < 0.01) in those not treated with lithium.

CONCLUSIONS

Our findings suggest that lithium is associated with more reports of severe weight gain than lamotrigine, although this difference did not reach statistical significance. However, lithium use led to fewer reports of severe weight gain than some alternative drugs for long-term medication (olanzapine, quetiapine, and valproate), which is consistent with recent studies. Monitoring of weight gain and metabolic parameters remains essential with lithium and its alternatives.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > University Psychiatric Services > University Hospital of Psychiatry and Psychotherapy > Translational Research Center
04 Faculty of Medicine > University Psychiatric Services > University Hospital of Psychiatry and Psychotherapy

UniBE Contributor:

Cattapan-Ludewig, Katja

Subjects:

600 Technology > 610 Medicine & health

ISSN:

2194-7511

Publisher:

Springer

Language:

English

Submitter:

Pubmed Import

Date Deposited:

16 Oct 2023 12:13

Last Modified:

17 Oct 2023 10:12

Publisher DOI:

10.1186/s40345-023-00313-8

PubMed ID:

37840048

Uncontrolled Keywords:

Adverse drug reaction (ADR) Case–control study Drug safety Lithium Mood stabilizer Pharmacovigilance Weight gain

BORIS DOI:

10.48350/187213

URI:

https://boris.unibe.ch/id/eprint/187213

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