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Association between Metabolic Syndrome Risk Factors and Immunohistochemical Profile in Women with Breast Cancer

BACKGROUND: The association between metabolic syndrome (MetS) and breast cancer may significantly impact the mortality and incidence of breast cancer. This study aimed to assess the association between MetS risk factors and immunohistochemical (IHC) profiles in women with breast cancer. METHODS: Thi...

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Autores principales: Danesh, Hiva, Anbiaei, Robab, Ziamajidi, Nasrin, Farhadian, Maryam, Barartabar, Zeinab, Abbasalipourkabir, Roghayeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541543/
https://www.ncbi.nlm.nih.gov/pubmed/37786471
http://dx.doi.org/10.30476/IJMS.2022.95039.2673
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author Danesh, Hiva
Anbiaei, Robab
Ziamajidi, Nasrin
Farhadian, Maryam
Barartabar, Zeinab
Abbasalipourkabir, Roghayeh
author_facet Danesh, Hiva
Anbiaei, Robab
Ziamajidi, Nasrin
Farhadian, Maryam
Barartabar, Zeinab
Abbasalipourkabir, Roghayeh
author_sort Danesh, Hiva
collection PubMed
description BACKGROUND: The association between metabolic syndrome (MetS) and breast cancer may significantly impact the mortality and incidence of breast cancer. This study aimed to assess the association between MetS risk factors and immunohistochemical (IHC) profiles in women with breast cancer. METHODS: This cross-sectional study used the medical records of 300 breast cancer patients with an average age of 53.11±12.97 years in the Chemotherapy and Radiation Therapy Clinic of Dr. Anbiai, Tehran, Iran (2020-2021). The cases were divided into five subgroups including luminal A, luminal B (HER-2(-)), luminal B (HER-2(+)), HER-2 overexpressing, and triple negative. RESULTS: There was no difference in the prognostic indicators between the presence and absence of MetS in women with breast cancer. A higher proportion of luminal A tumors (39.3%), luminal B (HER-2(+)) (25%), triple-negative (17%), luminal B (HER-2(-)) (10.7%), HER-2 overexpression (8%) was observed in women with MetS than those without MetS. Multivariate logistic regression analysis showed that patients with MetS had a 41% higher chance of developing luminal A than those without MetS, and patients with a BMI≥30 Kg/m(2) had an 80% higher chance of developing luminal B (HER-2(+)) than those with a BMI<30 Kg/m(2). Moreover, women with a waist circumference higher than 88 cm had a 14 % lower chance of developing Luminal B (HER-2(+)) than those with a waist circumference less than 88 cm. CONCLUSION: There was no difference in prognostic indicators and IHC profile in patients with and without MetS.
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spelling pubmed-105415432023-10-02 Association between Metabolic Syndrome Risk Factors and Immunohistochemical Profile in Women with Breast Cancer Danesh, Hiva Anbiaei, Robab Ziamajidi, Nasrin Farhadian, Maryam Barartabar, Zeinab Abbasalipourkabir, Roghayeh Iran J Med Sci Original Article BACKGROUND: The association between metabolic syndrome (MetS) and breast cancer may significantly impact the mortality and incidence of breast cancer. This study aimed to assess the association between MetS risk factors and immunohistochemical (IHC) profiles in women with breast cancer. METHODS: This cross-sectional study used the medical records of 300 breast cancer patients with an average age of 53.11±12.97 years in the Chemotherapy and Radiation Therapy Clinic of Dr. Anbiai, Tehran, Iran (2020-2021). The cases were divided into five subgroups including luminal A, luminal B (HER-2(-)), luminal B (HER-2(+)), HER-2 overexpressing, and triple negative. RESULTS: There was no difference in the prognostic indicators between the presence and absence of MetS in women with breast cancer. A higher proportion of luminal A tumors (39.3%), luminal B (HER-2(+)) (25%), triple-negative (17%), luminal B (HER-2(-)) (10.7%), HER-2 overexpression (8%) was observed in women with MetS than those without MetS. Multivariate logistic regression analysis showed that patients with MetS had a 41% higher chance of developing luminal A than those without MetS, and patients with a BMI≥30 Kg/m(2) had an 80% higher chance of developing luminal B (HER-2(+)) than those with a BMI<30 Kg/m(2). Moreover, women with a waist circumference higher than 88 cm had a 14 % lower chance of developing Luminal B (HER-2(+)) than those with a waist circumference less than 88 cm. CONCLUSION: There was no difference in prognostic indicators and IHC profile in patients with and without MetS. Shiraz University of Medical Sciences 2023-09 /pmc/articles/PMC10541543/ /pubmed/37786471 http://dx.doi.org/10.30476/IJMS.2022.95039.2673 Text en Copyright: © Iranian Journal of Medical Sciences https://creativecommons.org/licenses/by-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NoDerivatives 4.0 International License. This license allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Original Article
Danesh, Hiva
Anbiaei, Robab
Ziamajidi, Nasrin
Farhadian, Maryam
Barartabar, Zeinab
Abbasalipourkabir, Roghayeh
Association between Metabolic Syndrome Risk Factors and Immunohistochemical Profile in Women with Breast Cancer
title Association between Metabolic Syndrome Risk Factors and Immunohistochemical Profile in Women with Breast Cancer
title_full Association between Metabolic Syndrome Risk Factors and Immunohistochemical Profile in Women with Breast Cancer
title_fullStr Association between Metabolic Syndrome Risk Factors and Immunohistochemical Profile in Women with Breast Cancer
title_full_unstemmed Association between Metabolic Syndrome Risk Factors and Immunohistochemical Profile in Women with Breast Cancer
title_short Association between Metabolic Syndrome Risk Factors and Immunohistochemical Profile in Women with Breast Cancer
title_sort association between metabolic syndrome risk factors and immunohistochemical profile in women with breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541543/
https://www.ncbi.nlm.nih.gov/pubmed/37786471
http://dx.doi.org/10.30476/IJMS.2022.95039.2673
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