Evidence map›Paper›PMID 41321428›Full record

ReviewBiological psychiatry global open science2026

Clinical Insights Into the Mechanistic Crossroads of Lamotrigine and Therapeutic Ketosis in Bipolar Depression.

Dina N Ali, Iain H Campbell, Jonathan G Leung, Tamahara Gonzalez Campos, Duan Liu, Mete Ercis, Matej Markota, Deniz Ceylan, Kyla Lara-Breitinger, Francisco Lopez-Jimenez and 4 more

Abstract readReview
In one paragraph

Review in Biological psychiatry global open science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Dina N AliDepartment of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.
Iain H CampbellDivision of Psychiatry, Centre for Clinical Brain Sciences, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, United Kingdom.
Jonathan G LeungDepartment of Pharmacy Services, Mayo Clinic, Rochester, Minnesota.
Tamahara Gonzalez CamposDepartment of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.
Duan LiuDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota.
Mete ErcisDepartment of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.
Matej MarkotaDepartment of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.
Deniz CeylanDepartment of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.
Kyla Lara-BreitingerDepartment of Cardiology, Mayo Clinic, Rochester, Minnesota.
Francisco Lopez-JimenezDepartment of Cardiology, Mayo Clinic, Rochester, Minnesota.
Adam S AndersonDepartment of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.
Aysegul OzerdemDepartment of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.
Stacey J WinhamDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota.
Mark A FryeDepartment of Psychiatry & Psychology, Mayo Clinic, Rochester, Minnesota.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are substantial care gaps in optimizing treatment response for bipolar depression given, at best, a modicum of benefit from antidepressant treatment and, in contrast, a substantial cardiometabolic burden associated with regulatory-approved antipsychotic treatment. Lamotrigine (LGT) is an anticonvulsant with an evidence base in both epilepsy and bipolar disorder (BD), in particular bipolar depression "stabilizing from down under." There is a well-established bidirectional relationship between BD and epilepsy. Recognizing the complex interplay between mood, diet, and energy metabolism, lifestyle interventions have emerged as an adjunctive therapeutic approach in BD. Among these, therapeutic ketosis, with century-old evidence base in epilepsy, has regained new interest as a promising adjunctive treatment for mood and metabolic comorbidities. LGT and therapeutic ketosis both target neurobiological pathways that regulate energy metabolism and promote neuronal stability-key processes implicated in mood regulation and neuronal protection. This alignment suggests the possibility of synergistic effects in BD. In this review, we explore the overlapping mechanisms of LGT and therapeutic ketosis and provide clinical insights into their combined use in BD, offering a comprehensive perspective on this innovative treatment strategy.

Indexed as

Bipolar disorderEpilepsyKetogenic dietLamotrigineMitochondriaNeuroinflammation

Identifiers

PMID41321428
PMCPMC12663626

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.