Effect of Metabolic Syndrome and Individual Components on Colon Cancer Characteristics and Prognosis

被引:8
作者
Silva, Ana [1 ,2 ]
Pereira, Sofia S. [3 ]
Monteiro, Mariana P. [3 ,4 ]
Araujo, Antonio [5 ,6 ]
Faria, Gil [7 ,8 ,9 ]
机构
[1] Ctr Hosp Univ Porto, Pharm Dept, Porto, Portugal
[2] Polytech Porto, Sch Hlth, Polytech Inst Porto, Porto, Portugal
[3] Univ Porto, Endocrine Cardiovasc & Metab Res, Unit Multidisciplinary Biomed Res UMIB, Inst Biomed Sci Abel Salazar ICBAS, Porto, Portugal
[4] UCL, Ctr Obes Res, London, England
[5] Univ Porto, Unit Oncobiol Res, Unit Multidisciplinary Biomed Res UMIB, Inst Biomed Sci Abel Salazar ICBAS, Porto, Portugal
[6] Ctr Hosp Univ Porto, Med Oncol Dept, Porto, Portugal
[7] Ctr Res Hlth Technol & Informat Syst, iGo Dept, CINTESIS, Porto, Portugal
[8] Hosp Pedro Hispano, Unidade Local Saude Matosinhos, Gen Surg, Senhora Da Hora, Portugal
[9] Univ Porto, Fac Med, Dept Surg, Porto, Portugal
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
关键词
colon cancer; metabolic syndrome; tumor staging; survival; lymph node ratio;
D O I
10.3389/fonc.2021.631257
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metabolic syndrome (MS) is recognized as a risk factor for colon cancer (CC). However, whether the cluster of metabolic changes that define MS also influence CC prognosis remains unclear. Thus, our aim was to investigate whether the presence of MS or any of the MS individual components could provide prognostic information on tumor phenotype and survival outcomes. Clinical and pathological data from patients with CC (n = 300) who underwent surgical resection at a single tertiary hospital were retrospectively collected to evaluate presence of MS components and diagnostic criteria, CC phenotype and disease outcomes. Patients were allocated into two groups according to the presence or absence of MS (n = 85 MS vs n = 83 non-MS). The overall prevalence of MS individual components was 82.7% for increased waist-circumference (WC), 61.3% for high blood pressure (BP), 48.8% for low HDL-cholesterol, 39.9% for high fasting glucose, and 33.9% for hypertriglyceridemia. Patients in the MS group presented smaller tumors (p = 0.006) with lower T-stage (p = 0.002). High BP (p = 0.029) and hypertriglyceridemia (p = 0.044) were associated with a smaller tumor size, while low-HDL (p = 0.008) was associated with lower T-stage. After propensity score matching using age, tumor size and staging as covariates high-BP (p = 0.020) and WC (p = 0.003) were found to influence disease-free survival, but not overall survival. In conclusion, despite MS being an established risk factor for CC, our data does not support the hypothesis that MS components have a negative impact on disease extension or prognosis. Nevertheless, a protective role of BP and lipid lowering drugs cannot be excluded.
引用
收藏
页数:10
相关论文
共 36 条
  • [1] The metabolic syndrome and risk of incident colorectal cancer
    Ahmed, Rehana L.
    Schmitz, Kathryn H.
    Anderson, Kristin E.
    Rosamond, Wayne D.
    Folsom, Aaron R.
    [J]. CANCER, 2006, 107 (01) : 28 - 36
  • [2] Harmonizing the Metabolic Syndrome A Joint Interim Statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity
    Alberti, K. G. M. M.
    Eckel, Robert H.
    Grundy, Scott M.
    Zimmet, Paul Z.
    Cleeman, James I.
    Donato, Karen A.
    Fruchart, Jean-Charles
    James, W. Philip T.
    Loria, Catherine M.
    Smith, Sidney C., Jr.
    [J]. CIRCULATION, 2009, 120 (16) : 1640 - 1645
  • [3] Metabolic syndrome - a new world-wide definition. A consensus statement from the international diabetes federation
    Alberti, KGMM
    Zimmet, P
    Shaw, J
    [J]. DIABETIC MEDICINE, 2006, 23 (05) : 469 - 480
  • [4] Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
  • [5] 2-S
  • [6] Clinically Relevant Doses of Candesartan Inhibit Growth of Prostate Tumor Xenografts In Vivo through Modulation of Tumor Angiogenesis
    Alhusban, Ahmed
    Al-Azayzih, Ahmad
    Goc, Anna
    Gao, Fei
    Fagan, Susan C.
    Somanath, Payaningal R.
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2014, 350 (03) : 635 - 645
  • [7] Angiogenesis and Oxidative Stress in Metastatic Tumor Progression: Pathogenesis and Novel Therapeutic Approach of Colon Cancer
    Auyeung, Kathy K.
    Ko, Joshua K.
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2017, 23 (27) : 3952 - 3961
  • [8] Obesity and colorectal cancer
    Bardou, Marc
    Barkun, Alan N.
    Martel, Myriam
    [J]. GUT, 2013, 62 (06) : 933 - 947
  • [9] Prognostic Value of the Lymph Node Ratio in Stage III Colorectal Cancer: A Systematic Review
    Ceelen, W.
    Van Nieuwenhove, Y.
    Pattyn, P.
    [J]. ANNALS OF SURGICAL ONCOLOGY, 2010, 17 (11) : 2847 - 2855
  • [10] Prognostic impact of renin-angiotensin system blockade in esophageal squamous cell carcinoma
    Chen, Yen-Hao
    Huang, Cheng-Hua
    Lu, Hung-I
    Chen, Chang-Han
    Huang, Wan-Ting
    Hsieh, Ming-Jang
    Rau, Kun-Ming
    Chang, Alice Y. W.
    Lin, Wei-Che
    Li, Shau-Hsuan
    [J]. JOURNAL OF THE RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM, 2015, 16 (04) : 1185 - 1192