Evidence map›Paper›PMID 27226264›Full record

ArticleBipolar disorders2016

Hypothyroidism risk compared among nine common bipolar disorder therapies in a large US cohort.

Christophe G Lambert, Aurélien J Mazurie, Nicolas R Lauve, Nathaniel G Hurwitz, S Stanley Young, Robert L Obenchain, Nicolas W Hengartner, Douglas J Perkins, Mauricio Tohen, Berit Kerner

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Bipolar disorders, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
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

16 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
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  9. Women's issues.Epileptic disorders : international epilepsy journal with videotape · 2020
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  14. Medical Comorbidities in Bipolar Disorder.Current psychiatry reports · 2018
    Review
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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

10 authors at 5 institutions in 1 country.

Christophe G LambertCenter for Global Health, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Aurélien J MazurieBioinformatics Core, Montana State University, Bozeman, MT, USA.
Nicolas R LauveDepartment of Computer Science, University of New Mexico, Albuquerque, NM, USA.
Nathaniel G HurwitzNew Mexico Behavioral Health Institute, Las Vegas, NM, USA.
S Stanley YoungCGStat, LLC, Raleigh, NC, USA.
Robert L ObenchainRisk Benefit Statistics, LLC, Bella Vista, CA, USA.
Nicolas W HengartnerLos Alamos National Laboratory, Los Alamos, NM, USA.
Douglas J PerkinsCenter for Global Health, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Mauricio TohenDepartment of Psychiatry and Behavioral Sciences, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.
Berit KernerSemel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Center for Global Health · USUniversity of New Mexico · USLos Alamos National Laboratory · USMontana State University · USUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThyroid abnormalities in patients with bipolar disorder (BD) have been linked to lithium treatment for decades, yet other drugs have been less well studied. Our objective was to compare hypothyroidism risk for lithium versus the anticonvulsants and second-generation antipsychotics commonly prescribed for BD.

methodsAdministrative claims data on 24,574 patients with BD were analyzed with competing risk survival analysis. Inclusion criteria were (i) one year of no prior hypothyroid diagnosis nor BD drug treatment, (ii) followed by at least one thyroid test during BD monotherapy on lithium carbonate, mood-stabilizing anticonvulsants (lamotrigine, valproate, oxcarbazepine, or carbamazepine) or antipsychotics (aripiprazole, olanzapine, risperidone, or quetiapine). The outcome was cumulative incidence of hypothyroidism per drug, in the presence of the competing risk of ending monotherapy, adjusted for age, sex, physician visits, and thyroid tests.

resultsAdjusting for covariates, the four-year cumulative risk of hypothyroidism for lithium (8.8%) was 1.39-fold that of the lowest risk therapy, oxcarbazepine (6.3%). Lithium was non-statistically significantly different from quetiapine. While lithium conferred a higher risk when compared to all other treatments combined as a group, hypothyroidism risk error bars overlapped for all drugs. Treatment (p = 3.86e-3), age (p = 6.91e-10), sex (p = 3.93e-7), and thyroid testing (p = 2.79e-87) affected risk. Patients taking lithium were tested for hypothyroidism 2.26-3.05 times more frequently than those on other treatments.

conclusionsThyroid abnormalities occur frequently in patients with BD regardless of treatment. Therefore, patients should be regularly tested for clinical or subclinical thyroid abnormalities on all therapies and treated as indicated to prevent adverse effects of hormone imbalances on mood.

Indexed as

AdultAnticonvulsantsAntimanic AgentsAntipsychotic AgentsBipolar DisorderCohort StudiesFemaleHumansHypothyroidismLithium CompoundsMaleRiskSurvival AnalysisAnticonvulsantsAntimanic AgentsAntipsychotic AgentsLithium Compoundsanticonvulsantsantipsychoticsbipolar disordercompeting riskshypothyroidismlithium

Identifiers

PMID27226264
PMCPMC5089566
OpenAlexW2398293230

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.