Abstract
Few epidemiological studies have examined the relationship between dietary fat, which may affect immune function and risk of Hodgkin lymphoma (HL). The aim of this study was to test the hypothesis that high dietary intake of fat and specific subtypes of fat is associated with the risk of HL among 486 HL cases and 630 population-based controls recruited between 1997 and 2000 in Connecticut and Massachusetts. Unconditional logistic regression was used to calculate odds ratios (ORs) and 95 % confidence intervals (CIs) stratified by age and gender. Among younger adults, HL risk was significantly and positively associated with higher intake of saturated fat [ORs for increasing quartiles = 1.3, 1.8, and 2.1; p trend = 0.04] and negatively associated with higher intake of monounsaturated fat [ORs for increasing quartiles = 0.5, 0.5, and 0.4; p trend = 0.03), after adjustment for potential confounders including lifestyle and other dietary factors. The associations with saturated fat (ORs for increasing quartile = 2.4, 3.2, and 4.4; p trend < 0.01] and monounsaturated fat (ORs for increasing quartile = 0.3, 0.6, and 0.3; p trend = 0.04) were most apparent in younger women, whereas there was no significant association between intake of total fat or any type of fat and risk of HL in older females or younger or older males. These findings show that the associations between dietary fat and risk of HL may vary by gender and age and require confirmation in other populations.
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References
Kelley DS, Bendich A (1996) Essential nutrients and immunologic functions. Am J Clin Nutr 63:994S–996S
Cameron RG, Armstrong D, Clandinin MT, Cinader B (1986) Changes in lymphoma development in female SJL/J mice as a function of the ratio in low polyunsaturated/high polyunsaturated fat diet. Cancer Lett 30:175–180
Jose DG, Good RA (1973) Quantitative effects of nutritional essential amino acid deficiency upon immune responses to tumors in mice. J Exp Med 137:1–9
Wallace FA, Miles EA, Evans C, Stock TE, Yaqoob P, Calder PC (2001) Dietary fatty acids influence the production of Th1—but not Th2-type cytokines. J Leukoc Biol 69:449–457
Skibola CF (2007) Obesity, diet and risk of non-Hodgkin lymphoma. Cancer Epidemiol Biomarkers Prev 16:392–395
Kelley DS, Dougherty RM, Branch LB, Taylor PC, Iacono JM (1992) Concentration of dietary N-6 polyunsaturated fatty acids and the human immune status. Clin Immunol Immunopathol 62:240–244
Polesel J, Talamini R, Montella M et al (2006) Linoleic acid, vitamin D and other nutrient intakes in the risk of non-Hodgkin lymphoma: an Italian case–control study. Ann Oncol 17:713–718
Zheng T, Holford TR, Leaderer B et al (2004) Diet and nutrient intakes and risk of non-Hodgkin’s lymphoma in Connecticut women. Am J Epidemiol 159:454–466
Purdue MP, Bassani DG, Klar NS, Sloan M, Kreiger N (2004) Dietary factors and risk of non-Hodgkin lymphoma by histologic subtype: a case–control analysis. Cancer Epidemiol Biomarkers Prev 13:1665–1676
Zhang S, Hunter DJ, Rosner BA et al (1999) Dietary fat and protein in relation to risk of non-Hodgkin’s lymphoma among women. J Natl Cancer Inst 91:1751–1758
Chiu BC, Cerhan JR, Folsom AR et al (1996) Diet and risk of non-Hodgkin lymphoma in older women. JAMA 275:1315–1321
Cross AJ, Ward MH, Schenk M et al (2006) Meat and meat-mutagen intake and risk of non-Hodgkin lymphoma: results from a NCI-SEER case–control study. Carcinogenesis 27:293–297
Franceschi S, Serraino D, Carbone A, Talamini R, La Vecchia C (1989) Dietary factors and non-Hodgkin’s lymphoma: a case–control study in the northeastern part of Italy. Nutr Cancer 12:333–341
Tavani A, Pregnolato A, Negri E et al (1997) Diet and risk of lymphoid neoplasms and soft tissue sarcomas. Nutr Cancer 27:256–260
Chang ET, Zheng T, Lennette ET et al (2004) Heterogeneity of risk factors and antibody profiles in Epstein–Barr virus genome-positive and -negative Hodgkin lymphoma. J Infect Dis 189:2271–2281
Bohlke K, Harlow BL, Cramer DW, Spiegelman D, Mueller NE (1999) Evaluation of a population roster as a source of population controls: the Massachusetts Resident Lists. Am J Epidemiol 150:354–358
US Census Bureau (2002) 2000 Census of population and housing, summary file 3[Connecticut]. US Census Bureau, Washington, DC
Chang ET, Zheng T, Weir EG et al (2004) Childhood social environment and Hodgkin’s lymphoma: new findings from a population-based case–control study. Cancer Epidemiol Biomarkers Prev 13:1361–1370
Chang ET, Zheng T, Weir EG et al (2004) Aspirin and the risk of Hodgkin’s lymphoma in a population-based case–control study. J Natl Cancer Inst 96:305–315
Morton LM, Turner JJ, Cerhan JR et al (2007) Proposed classification of lymphoid neoplasms for epidemiologic research from the Pathology Working Group of the International Lymphoma Epidemiology Consortium (InterLymph). Blood 110:695–708
Ambinder RF, Mann RB (1994) Epstein–Barr-encoded RNA in situ hybridization: diagnostic applications. Hum Pathol 25:602–605
Gulley ML, Glaser SL, Craig FE et al (2002) Guidelines for interpreting EBER in situ hybridization and LMP1 immunohistochemical tests for detecting Epstein–Barr virus in Hodgkin lymphoma. Am J Clin Pathol 117:259–267
Willett WC, Sampson L, Stampfer MJ et al (1985) Reproducibility and validity of a semiquantitative food frequency questionnaire. Am J Epidemiol 122:51–65
Willett WC, Howe GR, Kushi LH (1997) Adjustment for total energy intake in epidemiologic studies. Am J Clin Nutr 65:1220S–1228S discussion 9S–31S
Greenland S (1989) Modeling and variable selection in epidemiologic analysis. Am J Public Health 79:340–349
Glaser SL (1986) Recent incidence and secular trends in Hodgkin’s disease and its histologic subtypes. J Chronic Dis 39:789–798
Glaser SL, Swartz WG (1990) Time trends in Hodgkin’s disease incidence. The role of diagnostic accuracy. Cancer 66:2196–2204
Medeiros LJ, Greiner TC (1995) Hodgkin’s disease. Cancer 75:357–369
Howlader NNA, Krapcho M, Neyman N, Aminou R, Altekruse SF, Kosary CL, Ruhl J, Tatalovich Z, Cho H, Mariotto A, Eisner MP, Lewis DR, Chen HS, Feuer EJ, Cronin KA (2012) SEER cancer statistics review, 1975–2009 (Vintage 2009 Populations). National Cancer Institute, Bethesda
Chen YT, Zheng T, Chou MC, Boyle P, Holford TR (1997) The increase of Hodgkin’s disease incidence among young adults. Experience in Connecticut, 1935–1992. Cancer 79:2209–2218
Glaser SL, Clarke CA, Stearns CB, Dorfman RF (2001) Age variation in Hodgkin’s disease risk factors in older women: evidence from a population-based case–control study. Leuk Lymphoma 42:997–1004
Glaser SL, Clarke CA, Nugent RA, Stearns CB, Dorfman RF (2002) Social class and risk of Hodgkin’s disease in young–adult women in 1988–94. Int J Cancer 98:110–117
Turner JJ, Morton LM, Linet MS et al (2010) InterLymph hierarchical classification of lymphoid neoplasms for epidemiologic research based on the WHO classification (2008): update and future directions. Blood 116:e90–e98
Zurier RB (1993) Fatty acids, inflammation and immune responses. Prostaglandins Leukot Essent Fatty Acids 48:57–62
Carroll KK, Braden LM, Bell JA, Kalamegham R (1986) Fat and cancer. Cancer 58:1818–1825
Vitale JJ, Broitman SA (1981) Lipids and immune function. Cancer Res 41:3706–3710
Cinader B, Clandinin MT, Hosokawa T, Robblee NM (1983) Dietary fat alters the fatty acid composition of lymphocyte membranes and the rate at which suppressor capacity is lost. Immunol Lett 6:331–337
Biggar RJ, Jaffe ES, Goedert JJ, Chaturvedi A, Pfeiffer R, Engels EA (2006) Hodgkin lymphoma and immunodeficiency in persons with HIV/AIDS. Blood 108:3786–3791
Landgren O, Engels EA, Pfeiffer RM et al (2006) Autoimmunity and susceptibility to Hodgkin lymphoma: a population-based case–control study in Scandinavia. J Natl Cancer Inst 98:1321–1330
Vajdic CM, McDonald SP, McCredie MR et al (2006) Cancer incidence before and after kidney transplantation. JAMA 296:2823–2831
Engels EA, Pfeiffer RM, Fraumeni JF Jr et al (2011) Spectrum of cancer risk among US solid organ transplant recipients. JAMA 306:1891–1901
Pollak M (2000) Insulin-like growth factor physiology and cancer risk. Eur J Cancer 36:1224–1228
Bianchini F, Kaaks R, Vainio H (2002) Overweight, obesity, and cancer risk. Lancet Oncol 3:565–574
Khandwala HM, McCutcheon IE, Flyvbjerg A, Friend KE (2000) The effects of insulin-like growth factors on tumorigenesis and neoplastic growth. Endocr Rev 21:215–244
Jones JI, Clemmons DR (1995) Insulin-like growth factors and their binding proteins: biological actions. Endocr Rev 16:3–34
Acknowledgments
This work was supported by Public Health Service grants P01 CA069266-01A1 (N. E. Mueller) and T32 CA09001-24 (E. T. Chang) from the National Cancer Institute, National Institutes of Health, Department of Health and Human Services, and by Fogarty training grants D43TW 008323 and D43TW 007864-01 from the National Institutes of Health (T. Zheng).
The authors thank Kathryn Trainor, Patricia Morey, and Karen Pawlish (Harvard School of Public Health) for their thorough management of the project and its databases. In addition, we thank Mary Fronk (Harvard School of Public Health) for her capable administrative support. Judith Fine, Rajni Mehta, and Patricia Owens (Yale University Rapid Case Ascertainment and School of Medicine); and Dan Friedman (Massachusetts Cancer Registry).
In Massachusetts, participating case patients were identified from the following sources with institutional review board approval: AtlantiCare Medical Center, Beth Israel Deaconess Medical Center, Beverly Hospital, Boston Medical Center, Brigham and Women’s Hospital, Brockton Hospital, Brockton VA/West Roxbury Hospital, Cambridge Hospital, Caritas Southwood Hospital, Carney Hospital, Children’s Hospital Boston, Dana-Farber Cancer Institute, Deaconess Glover Memorial Hospital, Deaconess Waltham Hospital, Emerson Hospital, Faulkner Hospital, Good Samaritan Medical Center, Harvard Vanguard, Holy Family Hospital and Medical Center, Jordan Hospital, Lahey Hitchcock Medical Center, Lawrence General Hospital, Lawrence Memorial Hospital of Medford, Lowell General Hospital, Massachusetts Cancer Registry, Massachusetts Eye and Ear Infirmary, Massachusetts General Hospital, Melrose-Wakefield Hospital, MetroWest Medical Center, Morton Hospital, Mount Auburn Hospital, New England Baptist Hospital, New England Medical Center, Newton-Wellesley Hospital, North Shore Medical Center, Norwood Hospital, Quincy Hospital, Saint’s Memorial Hospital, South Shore Hospital, St. Elizabeth’s Hospital, Sturdy Memorial Hospital, University of Massachusetts Medical Center, and Winchester Hospital.
In Connecticut, participating case patients were identified from the following sources with institutional review board approval: Bridgeport Hospital, Bristol Hospital, Charlotte Hungerford Hospital, Connecticut Department of Public Health Human Investigation Committee, Danbury Hospital, Day-Kimball Hospital, Greenwich Hospital, Griffin Hospital, Hartford Hospital, Johnson Memorial Hospital, Lawrence and Memorial Hospital, Manchester Memorial Hospital, MidState Medical Center, Middlesex Memorial Hospital, Milford Hospital, New Britain General Hospital, New Milford Hospital, Norwalk Hospital, Rockville General Hospital, Sharon Hospital, St. Francis Hospital and Medical Center, St. Mary’s Hospital, St. Raphael’s Hospital, St. Vincent’s Hospital, Stamford Hospital, WW Backus Hospital, Waterbury Hospital, Windham Hospital, and Yale-New Haven Hospital.
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Gao, Y., Li, Q., Bassig, B.A. et al. Subtype of dietary fat in relation to risk of Hodgkin lymphoma: a population-based case–control study in Connecticut and Massachusetts. Cancer Causes Control 24, 485–494 (2013). https://doi.org/10.1007/s10552-012-0136-2
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DOI: https://doi.org/10.1007/s10552-012-0136-2