2023
DOI: 10.1016/j.jad.2023.03.007
|View full text |Cite
|
Sign up to set email alerts
|

Genetic predisposition to depression and inflammation impacts symptom burden and survival in patients with head and neck cancer: A longitudinal study

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
3

Relationship

1
2

Authors

Journals

citations
Cited by 3 publications
(3 citation statements)
references
References 37 publications
0
3
0
Order By: Relevance
“…In general, radiotherapy is reasonably well tolerated. Acute and delayed potential radiotherapy-related toxicities are those that occur within the first 6 months post-treatment and beyond ( 86 ). Skin reactions, from redness to ulceration, can be the first sign of acute toxicity ( 87 ).…”
Section: Radiotherapymentioning
confidence: 99%
“…In general, radiotherapy is reasonably well tolerated. Acute and delayed potential radiotherapy-related toxicities are those that occur within the first 6 months post-treatment and beyond ( 86 ). Skin reactions, from redness to ulceration, can be the first sign of acute toxicity ( 87 ).…”
Section: Radiotherapymentioning
confidence: 99%
“…22 We computed a polygenic risk score for depression (PRS-D) based on a genome-wide association study of depression, 23 using the PRSoS software. 24 The same P value thresholding approach for calculating PRS-D, as described in Henry et al, 25 was used in this study. Specifically, we used the PRS-D at a P value threshold of P = .01, which demonstrated the greatest model fit for the association with symptom burden in this cohort (see Henry et al 25 ).…”
Section: Genotyping and Polygenic Risk Score Computation For Depressionmentioning
confidence: 99%
“…24 The same P value thresholding approach for calculating PRS-D, as described in Henry et al, 25 was used in this study. Specifically, we used the PRS-D at a P value threshold of P = .01, which demonstrated the greatest model fit for the association with symptom burden in this cohort (see Henry et al 25 ). A low PRS-D suggests that the individual has a low polygenic risk for depression relative to the sample population, and vice versa for a high PRS-D.…”
Section: Genotyping and Polygenic Risk Score Computation For Depressionmentioning
confidence: 99%