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Association between pre-diagnostic circulating lipid metabolites and colorectal cancer risk: a nested case-control study in the European Prospective Investigation into Cancer and Nutrition (EPIC).
Harewood, Rhea; Rothwell, Joseph A; Besevic, Jelena; Viallon, Vivian; Achaintre, David; Gicquiau, Audrey; Rinaldi, Sabina; Wedekind, Roland; Prehn, Cornelia; Adamski, Jerzy; Schmidt, Julie A; Jacobs, Inarie; Tjønneland, Anne; Olsen, Anja; Severi, Gianluca; Kaaks, Rudolf; Katzke, Verena; Schulze, Matthias B; Prada, Marcela; Masala, Giovanna; Agnoli, Claudia; Panico, Salvatore; Sacerdote, Carlotta; Jakszyn, Paula Gabriela; Sánchez, Maria-Jose; Castilla, Jesús; Chirlaque, María-Dolores; Atxega, Amaia Aizpurua; van Guelpen, Bethany; Heath, Alicia K; Papier, Keren; Tong, Tammy Y N; Summers, Scott A; Playdon, Mary; Cross, Amanda J; Keski-Rahkonen, Pekka; Chajès, Véronique; Murphy, Neil; Gunter, Marc J.
Afiliación
  • Harewood R; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France. Electronic address: harewoodr@iarc.who.int.
  • Rothwell JA; Centre for Epidemiology and Population Health (U1018), Exposome and Heredity Team, Faculté de Médecine, Université Paris-Saclay, UVSQ, INSERM, Gustave Roussy, F-94805, Villejuif, France.
  • Besevic J; Clinical Trial Service Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Viallon V; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France.
  • Achaintre D; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France; School of Plant Sciences and Food Security, Faculty of Biology, Tel-Aviv University, Tel Aviv-Yafo, Israel.
  • Gicquiau A; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France.
  • Rinaldi S; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France.
  • Wedekind R; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France.
  • Prehn C; Metabolomics and Proteomics Core, Helmholtz Zentrum München, 85764, Neuherberg, Germany.
  • Adamski J; Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, 8 Medical Drive, Singapore, 117597; Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Ingolstädter Landstraße 1, 85764, Neuherberg, Germany; In
  • Schmidt JA; Department of Clinical Medicine, Department of Clinical Epidemiology, Aarhus University and Aarhus University Hospital, Olof Palmes Allé 43-45, 8200 Aarhus N, Denmark.
  • Jacobs I; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France.
  • Tjønneland A; Danish Cancer Society Research Center, Diet, Cancer and Health, Strandboulevarden 49, DK-2100, Copenhagen, Denmark; Department of Public Health, University of Copenhagen, Copenhagen, Denmark.
  • Olsen A; Danish Cancer Society Research Center, Diet, Cancer and Health, Strandboulevarden 49, DK-2100, Copenhagen, Denmark; The Department of Public Health, University of Aarhus, Aarhus, Denmark.
  • Severi G; Centre for Epidemiology and Population Health (U1018), Exposome and Heredity Team, Faculté de Médecine, Université Paris-Saclay, UVSQ, INSERM, Gustave Roussy, F-94805, Villejuif, France; Department of Statistics, Computer Science, Applications "G. Parenti", University of Florence, Florence, Italy.
  • Kaaks R; German Cancer Research Center (DKFZ), Division of Cancer Epidemiology, Heidelberg, Germany.
  • Katzke V; German Cancer Research Center (DKFZ), Division of Cancer Epidemiology, Heidelberg, Germany.
  • Schulze MB; Department of Molecular Epidemiology, German Institute of Human Nutrition Potsdam-Rehbruecke, Arthur-Scheunert-Allee 114-116, 14558, Nuthetal, Germany; Institute of Nutritional Science, University of Potsdam, Nuthetal, Germany.
  • Prada M; Department of Molecular Epidemiology, German Institute of Human Nutrition Potsdam-Rehbruecke, Arthur-Scheunert-Allee 114-116, 14558, Nuthetal, Germany.
  • Masala G; Institute for Cancer Research, Prevention and Clinical Network (ISPRO), Florence, Italy.
  • Agnoli C; Epidemiology and Prevention Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Venezian, 1, 20133, Milan, Italy.
  • Panico S; Dipartimento Di Medicina Clinica E Chirurgia Federico Ii University, Naples, Italy.
  • Sacerdote C; Unit of Cancer Epidemiology, Città della Salute e della Scienza University-Hospital and Center for Cancer Prevention (CPO), Via Santena 7, 10126, Turin, Italy.
  • Jakszyn PG; Unit of Nutrition and Cancer, Cancer Epidemiology Research Programme, Catalan Institute of Oncology (ICO-IDIBELL), Barcelona, Spain; Blanquerna School of Health Sciences, Ramon Llull University, Barcelona, Spain.
  • Sánchez MJ; Escuela Andaluza de Salud Pública (EASP), 18011, Granada, Spain; Instituto de Investigación Biosanitaria ibs.GRANADA, 18012, Granada, Spain; Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), 28029, Madrid, Spain; Department of Preventive Medicine and Public Health
  • Castilla J; Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), 28029, Madrid, Spain; Instituto de Salud Pública de Navarra - IdiSNA, Pamplona, Spain.
  • Chirlaque MD; Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), 28029, Madrid, Spain; Department of Epidemiology, Regional Health Council, IMIB-Arrixaca, Murcia University, Murcia, Spain.
  • Atxega AA; Ministry of Health of the Basque Government, Sub Directorate for Public Health and Addictions of Gipuzkoa, San Sebastian, Spain; Biodonostia Health Research Institute, Epidemiology of Chronic and Communicable Diseases Group, San Sebastián, Spain.
  • van Guelpen B; Department of Radiation Sciences, Oncology, Umeå University, Umeå, Sweden; Wallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden.
  • Heath AK; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
  • Papier K; Cancer Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Tong TYN; Cancer Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Summers SA; Department of Nutrition and Integrative Physiology and the Diabetes and Metabolism Research Center, University of Utah, Salt Lake City, Utah, USA.
  • Playdon M; Department of Nutrition and Integrative Physiology and the Diabetes and Metabolism Research Center, University of Utah, Salt Lake City, Utah, USA; Cancer Control and Population Sciences, Huntsman Cancer Institute, Salt Lake City, Utah, USA.
  • Cross AJ; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
  • Keski-Rahkonen P; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France.
  • Chajès V; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France.
  • Murphy N; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France.
  • Gunter MJ; International Agency for Research on Cancer (IARC), 25 Av. Tony Garnier, 69007, Lyon, France; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
EBioMedicine ; 101: 105024, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38412638
ABSTRACT

BACKGROUND:

Altered lipid metabolism is a hallmark of cancer development. However, the role of specific lipid metabolites in colorectal cancer development is uncertain.

METHODS:

In a case-control study nested within the European Prospective Investigation into Cancer and Nutrition (EPIC), we examined associations between pre-diagnostic circulating concentrations of 97 lipid metabolites (acylcarnitines, glycerophospholipids and sphingolipids) and colorectal cancer risk. Circulating lipids were measured using targeted mass spectrometry in 1591 incident colorectal cancer cases (55% women) and 1591 matched controls. Multivariable conditional logistic regression was used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for associations between concentrations of individual lipid metabolites and metabolite patterns with colorectal cancer risk.

FINDINGS:

Of the 97 assayed lipids, 24 were inversely associated (nominally p < 0.05) with colorectal cancer risk. Hydroxysphingomyelin (SM (OH)) C222 (ORper doubling 0.60, 95% CI 0.47-0.77) and acylakyl-phosphatidylcholine (PC ae) C343 (ORper doubling 0.71, 95% CI 0.59-0.87) remained associated after multiple comparisons correction. These associations were unaltered after excluding the first 5 years of follow-up after blood collection and were consistent according to sex, age at diagnosis, BMI, and colorectal subsite. Two lipid patterns, one including 26 phosphatidylcholines and all sphingolipids, and another 30 phosphatidylcholines, were weakly inversely associated with colorectal cancer.

INTERPRETATION:

Elevated pre-diagnostic circulating levels of SM (OH) C222 and PC ae C343 and lipid patterns including phosphatidylcholines and sphingolipids were associated with lower colorectal cancer risk. This study may provide insight into potential links between specific lipids and colorectal cancer development. Additional prospective studies are needed to validate the observed associations.

FUNDING:

World Cancer Research Fund (reference 2013/1002); European Commission (FP7 BBMRI-LPC; reference 313010).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Límite: Female / Humans / Male Idioma: En Revista: EBioMedicine Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Límite: Female / Humans / Male Idioma: En Revista: EBioMedicine Año: 2024 Tipo del documento: Article
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