Visceral Obesity and Metabolic Syndrome Are Associated with Well-Differentiated Gastroenteropancreatic Neuroendocrine Tumors

The determinants for gastroenteropancreatic neuroendocrine tumors (GEP-NET) recent burden are matters of debate. Obesity and metabolic syndrome (MetS) are well established risks for several cancers even though no link with GEP-NETs was yet established. Our aim in this study was to investigate whethe...

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Main Authors: Ana P. Santos, Ana C. Santos, Clara Castro, Luís Raposo, Sofia S. Pereira, Isabel Torres, Rui Henrique, Helena Cardoso, Mariana P. Monteiro
Format: Article
Language:English
Published: MDPI AG 2018-08-01
Series:Cancers
Subjects:
Online Access:http://www.mdpi.com/2072-6694/10/9/293
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spelling doaj-1c89af95cb544d54a47c758d1c5f26152020-11-25T00:41:46ZengMDPI AGCancers2072-66942018-08-0110929310.3390/cancers10090293cancers10090293Visceral Obesity and Metabolic Syndrome Are Associated with Well-Differentiated Gastroenteropancreatic Neuroendocrine TumorsAna P. Santos0Ana C. Santos1Clara Castro2Luís Raposo3Sofia S. Pereira4Isabel Torres5Rui Henrique6Helena Cardoso7Mariana P. Monteiro8Department of Endocrinology of Portuguese Oncology Institute of Porto (IPO-Porto) & Clinical Research Unit—Research Center of IPO-Porto, 4200-072 Porto, PortugalDepartment of Public Health and Forensic Sciences and Medical Education, Unit of Clinical Epidemiology, Predictive Medicine and Public Health, University of Porto Medical School, 4200-319 Porto, PortugalEPIUnit—Instituto de Saúde Pública, Universidade do Porto, 4050-600 Porto, PortugalEPIUnit—Instituto de Saúde Pública, Universidade do Porto, 4050-600 Porto, PortugalEndocrine, Cardiovascular & Metabolic Research, Unit for Multidisciplinary Research in Biomedicine (UMIB), University of Porto, 4050-313 Porto, PortugalDepartment of Endocrinology of Portuguese Oncology Institute of Porto (IPO-Porto) & Clinical Research Unit—Research Center of IPO-Porto, 4200-072 Porto, PortugalDepartment of Pathology of Portuguese Oncology Institute of Porto (IPO-Porto) & Cancer Biology and Epigenetics Group—Research Center of IPO-Porto, 4200-072 Porto, PortugalEndocrine, Cardiovascular & Metabolic Research, Unit for Multidisciplinary Research in Biomedicine (UMIB), University of Porto, 4050-313 Porto, PortugalEndocrine, Cardiovascular & Metabolic Research, Unit for Multidisciplinary Research in Biomedicine (UMIB), University of Porto, 4050-313 Porto, PortugalThe determinants for gastroenteropancreatic neuroendocrine tumors (GEP-NET) recent burden are matters of debate. Obesity and metabolic syndrome (MetS) are well established risks for several cancers even though no link with GEP-NETs was yet established. Our aim in this study was to investigate whether well-differentiated GEP-NETs were associated with obesity and MetS. Patients with well-differentiated GEP-NETs (n = 96) were cross-matched for age, gender, and district of residence with a control group (n = 96) derived from the general population in a case-control study. Patients presented gastro-intestinal (75.0%) or pancreatic (22.9%) tumors, grade G1 (66.7%) or G2 (27.1%) with localized disease (31.3%), regional metastasis (16.7%) or distant metastasis (43.8%) at diagnosis, and 45.8% had clinical hormonal syndromes. MetS was defined according to Joint Interim Statement (JIS) criteria. Well-differentiated GEP-NETs were associated with MetS criteria as well as the individual components’ waist circumference, fasting triglycerides, and fasting plasma glucose (p = 0.003, p = 0.002, p = 0.011 and p < 0.001, respectively). The likelihood of the association was higher when the number of individual MetS components was greater than four. MetS and some individual MetS components including visceral obesity, dyslipidemia, and increased fasting glucose are associated with well-differentiated GEP-NET. This data provides a novel insight in unraveling the mechanisms leading to GEP-NET disease.http://www.mdpi.com/2072-6694/10/9/293gastroenteropancreatic neuroendocrine tumorabdominal obesitymetabolic syndromeglucose abnormalities
collection DOAJ
language English
format Article
sources DOAJ
author Ana P. Santos
Ana C. Santos
Clara Castro
Luís Raposo
Sofia S. Pereira
Isabel Torres
Rui Henrique
Helena Cardoso
Mariana P. Monteiro
spellingShingle Ana P. Santos
Ana C. Santos
Clara Castro
Luís Raposo
Sofia S. Pereira
Isabel Torres
Rui Henrique
Helena Cardoso
Mariana P. Monteiro
Visceral Obesity and Metabolic Syndrome Are Associated with Well-Differentiated Gastroenteropancreatic Neuroendocrine Tumors
Cancers
gastroenteropancreatic neuroendocrine tumor
abdominal obesity
metabolic syndrome
glucose abnormalities
author_facet Ana P. Santos
Ana C. Santos
Clara Castro
Luís Raposo
Sofia S. Pereira
Isabel Torres
Rui Henrique
Helena Cardoso
Mariana P. Monteiro
author_sort Ana P. Santos
title Visceral Obesity and Metabolic Syndrome Are Associated with Well-Differentiated Gastroenteropancreatic Neuroendocrine Tumors
title_short Visceral Obesity and Metabolic Syndrome Are Associated with Well-Differentiated Gastroenteropancreatic Neuroendocrine Tumors
title_full Visceral Obesity and Metabolic Syndrome Are Associated with Well-Differentiated Gastroenteropancreatic Neuroendocrine Tumors
title_fullStr Visceral Obesity and Metabolic Syndrome Are Associated with Well-Differentiated Gastroenteropancreatic Neuroendocrine Tumors
title_full_unstemmed Visceral Obesity and Metabolic Syndrome Are Associated with Well-Differentiated Gastroenteropancreatic Neuroendocrine Tumors
title_sort visceral obesity and metabolic syndrome are associated with well-differentiated gastroenteropancreatic neuroendocrine tumors
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2018-08-01
description The determinants for gastroenteropancreatic neuroendocrine tumors (GEP-NET) recent burden are matters of debate. Obesity and metabolic syndrome (MetS) are well established risks for several cancers even though no link with GEP-NETs was yet established. Our aim in this study was to investigate whether well-differentiated GEP-NETs were associated with obesity and MetS. Patients with well-differentiated GEP-NETs (n = 96) were cross-matched for age, gender, and district of residence with a control group (n = 96) derived from the general population in a case-control study. Patients presented gastro-intestinal (75.0%) or pancreatic (22.9%) tumors, grade G1 (66.7%) or G2 (27.1%) with localized disease (31.3%), regional metastasis (16.7%) or distant metastasis (43.8%) at diagnosis, and 45.8% had clinical hormonal syndromes. MetS was defined according to Joint Interim Statement (JIS) criteria. Well-differentiated GEP-NETs were associated with MetS criteria as well as the individual components’ waist circumference, fasting triglycerides, and fasting plasma glucose (p = 0.003, p = 0.002, p = 0.011 and p < 0.001, respectively). The likelihood of the association was higher when the number of individual MetS components was greater than four. MetS and some individual MetS components including visceral obesity, dyslipidemia, and increased fasting glucose are associated with well-differentiated GEP-NET. This data provides a novel insight in unraveling the mechanisms leading to GEP-NET disease.
topic gastroenteropancreatic neuroendocrine tumor
abdominal obesity
metabolic syndrome
glucose abnormalities
url http://www.mdpi.com/2072-6694/10/9/293
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