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Supportive Care in Cancer

, Volume 27, Issue 2, pp 351–371 | Cite as

Systematic review of genetic polymorphisms associated with psychoneurological symptoms in breast cancer survivors

  • Gee Su YangEmail author
  • Sreelakshmy Kumar
  • Susan G. Dorsey
  • Angela R. Starkweather
  • Debra Lynch Kelly
  • Debra E. Lyon
Review Article
  • 191 Downloads

Abstract

Purpose

Psychoneurological (PN) symptoms, such as anxiety, cognitive impairment, depression, fatigue, sleep disturbances, and pain, are highly prevalent in breast cancer patients undergoing cancer treatment. Emerging evidence suggests that genetic polymorphisms may contribute to differential symptom susceptibility. We aimed to systematically review associations between genetic polymorphisms and PN symptoms during or after cancer treatment for early-stage breast cancer.

Methods

Twenty-six eligible articles published until October 2017 were identified in PubMed, PsycINFO, Web of Science, and additional records. Information on study characteristics, genetic polymorphisms, and PN symptoms was extracted. Study quality was evaluated by the STrengthening the REporting of Genetic Association (STREGA) guideline. Genes included in the analysis were categorized by biological pathways based on the Reactome database.

Results

A total of 54 single nucleotide polymorphisms and haplotypes that are significantly associated with PN symptoms were identified; half of them were associated with increased severity of PN symptoms, while the other half contributed to the decrease of PN symptoms. Pain has the known highest number of associated genetic polymorphisms reported, followed by fatigue, cognitive impairment, depressive symptoms, sleep disturbances, and anxiety. The majority of genetic polymorphisms were involved in immune system and neuronal system pathways. Most studies were unsuccessful in meeting the STREGA guideline, which requires transparent reporting of methods and results.

Conclusions

This review provides comprehensive evidence of genetic polymorphisms underlying PN symptoms, which may pave the way for the development of personalized therapeutics targeting these symptoms. More well-designed genome-wide association studies are required to validate and replicate these findings.

Keywords

Breast cancer Psychoneurological symptoms Genetic polymorphism Single nucleotide polymorphism Systematic review 

Notes

Acknowledgements

We would like to thank Ms. Debra McDonald for proofreading.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflicts of interest.

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  • Gee Su Yang
    • 1
    Email author
  • Sreelakshmy Kumar
    • 1
  • Susan G. Dorsey
    • 2
  • Angela R. Starkweather
    • 3
  • Debra Lynch Kelly
    • 1
  • Debra E. Lyon
    • 1
  1. 1.Department of Biobehavioral Nursing Science, College of NursingUniversity of FloridaGainesvilleUSA
  2. 2.Department of Pain and Translational Symptom Science, School of NursingUniversity of MarylandBaltimoreUSA
  3. 3.School of NursingUniversity of ConnecticutStorrsUSA

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