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Peer-reviewedCC BYCureus

Lithium Toxicity Following Initiation of Semaglutide in a Patient With Bipolar Disorder: A Case Report

4 affiliations
  1. 1Medicine, Rush University Medical Center, Chicago, USA
  2. 2Psychiatry, Bergen New Bridge Medical Center, Paramus, USA
  3. 3Medicine, St. George's University, St. George's, GRD
  4. 4Academy for Advancement of Science and Technology, Bergen County Academies, Hackensack, USA

Abstract

Glucagon-like peptide-1 (GLP-1) receptor agonists are increasingly prescribed for type 2 diabetes mellitus and obesity, including among patients with severe mental illness. Their effects on gastrointestinal motility, oral intake, and volume status raise concern for interactions with drugs with narrow therapeutic indices that are cleared almost entirely by the kidney, such as lithium. We describe a 69-year-old woman with bipolar disorder, stable for several years on lithium, who presented with acute confusion, dysarthria, and expressive aphasia. A stroke protocol was activated, and noncontrast head CT, CT angiography of the head and neck, and MRI of the brain showed no acute infarct or hemorrhage. Semaglutide had been initiated approximately one month earlier for weight management, and she had experienced substantial weight loss with persistent nausea, intermittent vomiting, and reduced oral intake. Serum lithium was elevated above the reference range, accompanied by a reduced estimated glomerular filtration rate and biochemical findings suggestive of volume depletion. Lithium was held, and intravenous fluids were administered; renal function improved and the neurologic deficits resolved. Lithium was subsequently resumed at a reduced dose without recurrence. In this patient, initiation of semaglutide was temporally associated with lithium toxicity in the setting of gastrointestinal intolerance, reduced oral intake, and suspected volume depletion. Although a single case cannot establish causality, this observation supports closer lithium monitoring when initiating GLP-1 receptor agonists and during dose escalation.

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BibTeX
@article{dhingra2026lithium,
  title = {{Lithium Toxicity Following Initiation of Semaglutide in a Patient With Bipolar Disorder: A Case Report}},
  author = {Annika Dhingra and Charissa M Nichols and Ezekiel Sanchez and Anurag Ayyagari and Yashvi Rateshwar and Nina Narvaez},
  journal = {Cureus},
  year = {2026},
  month = sep,
  doi = {10.7759/cureus.117235},
  url = {https://europepmc.org/article/PMC/PMC13722138},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Lithium Toxicity Following Initiation of Semaglutide in a Patient With Bipolar Disorder: A Case Report
AU  - Annika Dhingra
AU  - Charissa M Nichols
AU  - Ezekiel Sanchez
AU  - Anurag Ayyagari
AU  - Yashvi Rateshwar
AU  - Nina Narvaez
PY  - 2026
DA  - 2026/09/30
JO  - Cureus
DO  - 10.7759/cureus.117235
UR  - https://europepmc.org/article/PMC/PMC13722138
AB  - Glucagon-like peptide-1 (GLP-1) receptor agonists are increasingly prescribed for type 2 diabetes mellitus and obesity, including among patients with severe mental illness. Their effects on gastrointestinal motility, oral intake, and volume status raise concern for interactions with drugs with narrow therapeutic indices that are cleared almost entirely by the kidney, such as lithium. We describe a 69-year-old woman with bipolar disorder, stable for several years on lithium, who presented with acute confusion, dysarthria, and expressive aphasia. A stroke protocol was activated, and noncontrast head CT, CT angiography of the head and neck, and MRI of the brain showed no acute infarct or hemorrhage. Semaglutide had been initiated approximately one month earlier for weight management, and she had experienced substantial weight loss with persistent nausea, intermittent vomiting, and reduced oral intake. Serum lithium was elevated above the reference range, accompanied by a reduced estimated glomerular filtration rate and biochemical findings suggestive of volume depletion. Lithium was held, and intravenous fluids were administered; renal function improved and the neurologic deficits resolved. Lithium was subsequently resumed at a reduced dose without recurrence. In this patient, initiation of semaglutide was temporally associated with lithium toxicity in the setting of gastrointestinal intolerance, reduced oral intake, and suspected volume depletion. Although a single case cannot establish causality, this observation supports closer lithium monitoring when initiating GLP-1 receptor agonists and during dose escalation.
SN  - 2168-8184
ER  -