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Related Concept Videos

Bipolar Disorder01:30

Bipolar Disorder

Bipolar disorder is a chronic mental health condition marked by significant mood fluctuations, including episodes of mania and depression. Elevated energy levels, heightened mood or irritability, impulsive behavior, reduced sleep needs, rapid speech, racing thoughts, inflated self-esteem, and distractibility characterize mania. Individuals with bipolar disorder often alternate between depressive and manic states, with periods of emotional stability lasting an average of six months to a year.
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu01:29

Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu

Genetic variations significantly influence drug response through pharmacokinetics, receptor interactions, and biologic milieu modifications. Pharmacokinetic alterations impact drug metabolism and clearance, affecting efficacy and toxicity. Variants in drug-metabolizing enzymes, such as CYP2C9 and CYP2C19, alter drug activation and elimination. For example, CYP2C9 loss-of-function variants require lower warfarin doses to prevent excessive bleeding, while CYP2C19 variants reduce clopidogrel...
Mania and Antimanic Drugs: Overview01:24

Mania and Antimanic Drugs: Overview

Mania, a psychological condition characterized by elevated mood, increased energy, and reduced sleep need, is part of the bipolar disorder cycle. The exact cause of mania isn't entirely known, but it is thought to be a combination of genetic, environmental, and neurological factors. Bipolar disorder involves alternating manic and depressive episodes. Mood stabilizers like lithium, antipsychotics, and anticonvulsants help manage these episodes. Lithium carbonate is particularly effective as a...
Principles of Pharmacogenetics: Types of Genetic Variants01:27

Principles of Pharmacogenetics: Types of Genetic Variants

The human genome is over 99.9% identical between individuals, yet genetic differences exist at millions of bases. The human genome contains approximately 3 million variant positions per individual, many of which are heterozygous, contributing to genetic diversity and individual traits. Genetic variations include single-nucleotide polymorphisms (SNPs), insertions, deletions, and copy number variations (CNVs).SNPs, the most common variation, involve single-base changes in DNA. These can be...
Human Genetics01:28

Human Genetics

Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
Pharmacogenomics: Identification of New Drug Targets01:29

Pharmacogenomics: Identification of New Drug Targets

Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...

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Related Experiment Video

Updated: Jul 10, 2026

Robotically Delivered fMRI-Guided Personalized Transcranial Magnetic Stimulation Therapy for Treatment-Resistant Depression
13:18

Robotically Delivered fMRI-Guided Personalized Transcranial Magnetic Stimulation Therapy for Treatment-Resistant Depression

Published on: April 10, 2026

Genetic Variants Associated With Treatment Response in Bipolar Disorder: A Systematic Review.

Ana Luiza da Silva Selani1, Beatriz Cristina Betarelli, Marília Aparecida Batista Dos Santos

  • 1Department of Drugs and Medicines, School of Pharmaceutical Sciences, São Paulo State University, Araraquara, Brazil.

Journal of Clinical Psychopharmacology
|July 9, 2026
PubMed
Summary

Genetic variants influence bipolar disorder treatment response, with BDNF showing consistent associations. Other gene findings are inconsistent due to study variations.

Keywords:
affective disordersmood disorderspersonalized medicinepharmacogenetics variantspharmacogenomicstreatment outcome

Related Experiment Videos

Last Updated: Jul 10, 2026

Robotically Delivered fMRI-Guided Personalized Transcranial Magnetic Stimulation Therapy for Treatment-Resistant Depression
13:18

Robotically Delivered fMRI-Guided Personalized Transcranial Magnetic Stimulation Therapy for Treatment-Resistant Depression

Published on: April 10, 2026

Area of Science:

  • Pharmacogenomics
  • Neuroscience
  • Psychiatry

Background:

  • Bipolar disorder (BD) treatment response varies significantly among individuals.
  • Identifying genetic factors influencing treatment efficacy is crucial for personalized medicine.

Purpose of the Study:

  • To systematically review and identify genetic variants associated with pharmacological treatment response in bipolar disorder patients.

Main Methods:

  • A comprehensive systematic review of multiple databases (PubMed, Scopus, PsycINFO, SciELO, LILACS) was performed.
  • Inclusion criteria focused on studies examining genetic variants and treatment response in BD.
  • Data extraction and quality assessment were conducted by two independent reviewers.

Main Results:

  • 69 studies involving 31,760 participants were included.
  • BDNF gene variants, particularly Val66Met (rs6265), showed consistent associations with treatment response.
  • Findings for other genes (GSK3β, SLC6A4, COMT, CREB1, DRD2, 5-HT2A) were heterogeneous.

Conclusions:

  • Genetic variations play a role in bipolar disorder pharmacological treatment response.
  • Consistent evidence supports associations for a subset of genes, notably BDNF.
  • Methodological heterogeneity across studies contributes to inconsistent findings for other genetic variants.