Abstract 7415: Association between sleep traits and risk of non-Hodgkin's lymphoma subtypes: a mendelian randomization study in the International Lymphoma Epidemiology (InterLymph) Consortium
Abstract Introduction: With over 80, 000 new cases of non-Hodgkin's lymphoma (NHL) diagnosed annually, modifiable risk factors remain unclear. Circadian disruption, linked to cancers like breast and prostate, affects immune cells (e.g., natural killer cells and T-helper cells) by altering their trafficking and proliferation. Some studies (PMID: 30566672, 27611440) suggest long sleep may increase overall NHL risk, including a Mendelian randomization (MR) study (PMID: 32895918). However, no research has examined the causal relationship between sleep traits, including long sleep, and NHL risk, by subtypes. We hypothesize that sleep traits are causally associated with NHL subtypes in European populations, testing this using MR with data from the International Lymphoma Epidemiology Consortium (InterLymph). Methods: We conducted two-sample MR using genome-wide association studies (GWAS) summary data for sleep traits and NHL subtypes. Only independent, genome-wide significant (p < 5×10-8) Single Nucleotide Polymorphisms (SNPs) were selected as valid instruments, sourced from the UK Biobank. Sleep traits included chronotype (153 SNPs), insomnia (48 SNPs), sleep duration (78 SNPs), excessive daytime sleepiness (37 SNPs), short sleep (27 SNPs), and long sleep (8 SNPs). NHL subtype data were from InterLymph: follicular lymphoma (6, 508 cases / 64, 183 controls), mantle cell lymphoma (1, 169 cases / 61, 603 controls), Waldenstrom macroglobulinemia/lymphoplasmacytic lymphoma (WM/LPL: 1, 697 cases / 59, 333 controls), and chronic lymphocytic leukemia (8, 522 cases / 67, 653 controls). The primary analysis used inverse-variance weighted (IVW) random-effects, with MR-Egger for pleiotropy adjustment. Results: Using the IVW method, we did not identify any statistically significant causal association between sleep traits and the risk of NHL subtypes, but did yield several intriguing trends. Long sleep (sleep duration >= 9 h per night) showed a marginally increased NHL risk [Odds ratio (OR) range: 1.51 - 247.9] across each subtype. Short sleep (sleep duration < 7 h per night) showed a similar trend [OR range: 1.25 - 1.81], except for WM/LPL, where we noticed a negative trend. The confidence limit for long sleep was imprecise due to the small number of variants. We did not notice any significant directional horizontal pleiotropy or weak instrument bias. Conclusions: We found no conclusive evidence of a relationship between sleep traits and four NHL subtypes. However, we see suggestive trends of long and short sleep associated with higher risk of some NHL subtypes. These findings align with the previous studies, which showed long sleep was associated with higher risk of NHL overall. Future directions include expanding our analysis to additional NHL subtypes, generating polygenic risk scores, and conducting stratified analyses. Citation Format: Pankhil Shah, Brittany Crawford, Anwar Merchant, Brenda Birmann, Angelica Macauda, Michelle A. Hildebrandt, Aaron Norman, Neil E. Caporaso, Meredith Yeager, Michael Dean, Immaculata De Vivo, Lynn Goldin, Nicola J. Camp, Rosalie Griffin, Delphine Casabonne, Federico Canzian, Pelin Unal, Elad Ziv, Catherine R. Marinac, Alexandra Nieters, Stephen J. Chanock, Mitchell J. Machiela, Michael Conry, Charlie Zhong, Hanla A. Park, Simon Cheah, Jonathan N. Hofmann, Elizabeth E. Brown, Celine Vachon, Susan Slager, Sonja Berndt, Sophia S. Wang, Vijai Joseph, James McKay, Henrik Hjalgrim, Lara Sucheston-Campbell, Karl Smith-Byrne, Alyssa Clay-Gilmour. Association between sleep traits and risk of non-Hodgkin's lymphoma subtypes: a mendelian randomization study in the International Lymphoma Epidemiology (InterLymph) Consortium [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 7415.
Authors
- Hanla A. Park (ORCID: https://orcid.org/0000-0001-8055-3729)
- Federico Canzian (ORCID: https://orcid.org/0000-0002-4261-4583)
- Angelica Macauda (ORCID: https://orcid.org/0000-0001-6895-6269)
- Joseph Vijai (ORCID: https://orcid.org/0000-0002-7933-151X)
- Aaron D. Norman (ORCID: https://orcid.org/0000-0002-4208-2708)
- Delphine Casabonne (ORCID: https://orcid.org/0000-0002-7874-3707)
- Brittany Crawford
- Brenda M. Birmann (ORCID: https://orcid.org/0000-0002-7550-5498)
- Anwar T. Merchant (ORCID: https://orcid.org/0000-0003-1045-5079)
- Sophia Wang (ORCID: https://orcid.org/0000-0003-2597-9393)
- Simon Cheah (ORCID: https://orcid.org/0000-0002-0352-1165)
- Michael Conry (ORCID: https://orcid.org/0000-0003-1904-8947)
- Karl Smith-Byrne (ORCID: https://orcid.org/0000-0002-1932-7463)
- Elad Ziv (ORCID: https://orcid.org/0000-0002-2324-2884)
- Immaculata De Vivo (ORCID: https://orcid.org/0000-0002-7185-7402)
- Jonathan N. Hofmann (ORCID: https://orcid.org/0000-0002-1043-5812)
- Alyssa Clay‐Gilmour (ORCID: https://orcid.org/0000-0001-9998-4879)
- Celine M. Vachon
- Sonja I. Berndt (ORCID: https://orcid.org/0000-0001-5230-0652)
- Susan L. Slager (ORCID: https://orcid.org/0000-0002-5173-4712)
- Pelin Gürkan Ünal (ORCID: https://orcid.org/0000-0001-8141-5627)
- Nicola J. Camp (ORCID: https://orcid.org/0000-0002-4788-1998)
- Charlie Zhong (ORCID: https://orcid.org/0000-0001-6973-887X)
- Lynn R. Goldin (ORCID: https://orcid.org/0000-0001-7350-446X)
- Pankhil Shah
- Henrik Hjalgrim
- Catherine R. Marinac (ORCID: https://orcid.org/0000-0002-9128-3012)
- Rosalie Griffin (ORCID: https://orcid.org/0000-0001-9437-8861)
- James McKay (ORCID: https://orcid.org/0000-0002-1787-3874)
- Michael Dean
- Elizabeth E. Brown (ORCID: https://orcid.org/0009-0007-5427-3425)
- Michelle A.T. Hildebrandt
- Alexandra Nieters
- Neil E. Caporaso
- Stephen J. Chanock
- Mitchell J. Machiela
- Lara Sucheston‐Campbell
- Meredith Yeager
Institutions
- Statens Serum Institut (DK)
- University of Copenhagen (DK)
- Brigham and Women's Hospital (US)
- American Cancer Society (US)
- National Institutes of Health (US)
- Memorial Sloan Kettering Cancer Center (US)
- The University of Texas MD Anderson Cancer Center (US)
- Harvard University (US)
- University of South Carolina (US)
- University of Freiburg (DE)
- The University of Melbourne (AU)
- German Cancer Research Center (DE)
- University of California, San Francisco (US)
- Wayne State University (US)
- Cancer Council Victoria (AU)
- University of Utah (US)
- Heidelberg University (DE)
- Rigshospitalet (DK)
- University of Alabama at Birmingham (US)
- Kettering University (US)
- City of Hope (US)
- Dana-Farber Cancer Institute (US)
- Mayo Clinic in Arizona (US)
- Danish Cancer Society (DK)
- Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (ES)
- UCSF Helen Diller Family Comprehensive Cancer Center (US)
- Centre international de recherche sur le cancer (FR)
Publication Details
- Journal
- Cancer Research
- Published
- 2025-04-21
- DOI
- https://doi.org/10.1158/1538-7445.am2025-7415
- Primary Topic
- Lymphoma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00