Evidence map›Paper›PMID 39441826›Full record

SynthesisJNCI cancer spectrum2024

Systematic review of associations between anxiety, depression, and functional/biological aging among cancer survivors.

Brennan Parmelee Streck, Dilorom Sass, Rachelle Brick, Leah Fisk, Alicia A Livinski, Jennifer L Guida

Abstract readSystematic Review
In one paragraph

Synthesis in JNCI cancer spectrum, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Brennan Parmelee StreckBasic Biobehavioral and Psychological Sciences Branch, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD 20850, United States.ORCID 0000-0001-7033-1372
Dilorom SassNeurooncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20814, United States.
Rachelle BrickBasic Biobehavioral and Psychological Sciences Branch, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD 20850, United States.
Leah FiskSchool of Health and Rehabilitation Sciences, Department of Occupational Therapy, The University of Pittsburgh, Pittsburgh, PA 15219, United States.
Alicia A LivinskiNational Institutes of Health Library, Office of Research Services, Office of the Director, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-7201-3500
Jennifer L GuidaBasic Biobehavioral and Psychological Sciences Branch, Division of Cancer Control and Population Sciences, National Cancer Institute, Rockville, MD 20850, United States.ORCID 0000-0001-5590-5286

Funding

National Cancer Institute's Intramural Continuing Umbrella for Research Experiences
6 · The paper itself

Abstract

backgroundEvidence suggests a mind-body component to aging through which psychological distress from anxiety and depression drives molecular changes that promote early decline (ie, accelerated aging). Cancer survivors experience particularly high rates of anxiety and depression. Some survivors also have accelerated aging, though the relationships between anxiety and depression and aging are not clear. A synthesis of evidence is needed to understand the state of the science and impending priorities.

methodsPubMed, Embase, CINAHL, Web of Science, and PsycNet databases were searched for studies that measured associations between depression, anxiety, and nonchronological aging in cancer survivors (2012-2022). Data were methodologically evaluated.

resultsSurvivorship studies were included if they were peer reviewed, published in English from 2012 to 2022, and measured associations between anxiety and depression and aging. In total, 51 studies were included. Just over half were cross-sectional (53%). Foci included functional (n = 35 [69%]) and biological (n = 16 [31%]). Functional aging measures included frailty, sarcopenia, geriatric assessment, and cognition. Biological aging measures included telomere length, telomerase, age-related inflammatory blood-based biomarkers, renal insufficiency, anemia, and DNA methylation. We tested 223 associations. Associations between anxiety, depression, and aging were generally positive, though with varying strengths. Most compelling were associations between functional aging and depression. There were concerns for selection and measurement biases.

conclusionsFindings suggest positive associations between anxiety, depression, and aging among cancer survivors. Future work is needed to clarify temporality, develop a consensus on the measurement of aging, and diversify cohorts.

Indexed as

AgingAnxietyCancer SurvivorsDepressionAgedBiomarkersCognitionCross-Sectional StudiesDNA MethylationFemaleFrailtyGeriatric AssessmentHumansMaleMiddle AgedNeoplasmsBiomarkersTelomerase

Identifiers

PMID39441826
PMCPMC11631420

What OpenQuestion holds

Textmetadata
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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.