Metabolic Syndrome and Breast Cancer Molecular Subtypes: An Observational Patient Study

IF 1.8 Q3 ONCOLOGY
Dafina Ademi-Islami, S. Manxhuka-Kerliu, Dhurata Tarifa-Koroveshi, Rozafa Koliqi, B. Mujaj
{"title":"Metabolic Syndrome and Breast Cancer Molecular Subtypes: An Observational Patient Study","authors":"Dafina Ademi-Islami, S. Manxhuka-Kerliu, Dhurata Tarifa-Koroveshi, Rozafa Koliqi, B. Mujaj","doi":"10.1177/11782234221080555","DOIUrl":null,"url":null,"abstract":"Background: Breast cancer molecular subtypes share various prognostic profiles, and luminal A molecular subtypes have a better prognosis compared with other molecular subtypes. However, whether metabolic syndrome or individual risk factors of metabolic syndrome influence on the development of molecular subtype remains elusive. We aimed to assess the association between metabolic syndrome risk factors and breast cancer molecular subtypes among patients with metabolic syndrome in a clinical setting. Methods: In total, 101 breast cancer patients with mean age, 58.4 ± 8.5 years, and overt metabolic syndrome prospectively were recruited. Immunohistochemistry procedure was used to determine molecular subtypes. Assessment of clinical, biochemical, and anthropometric parameters was performed. Logistic regression analysis was used to assess the relationship between risk factors and breast cancer molecular subtypes categories. A similar approach was used to assess the relation between breast cancer molecular subtypes and menopause. Results: Comparison of metabolic syndrome individual risk factors according to breast cancer molecular subtypes no statistical difference was found for systolic (P = .33) and diastolic blood pressure (P = .17), fasting glucose (P = .77), triglycerides (P = .62), high-density lipoprotein (P = .33), body mass index (P = .87), and waist circumference (P = .81). A positive trend was found between high-density lipoprotein and HER2+. No association was found with other risk factors. Moreover, an association was found between HER2+ categories and menopause. Conclusion: In breast cancer patients with metabolic syndrome, we observed an increased trend between high-density lipoprotein and HER2+ molecular subtype, suggesting that underlying dyslipidemia may favor poor prognosis. HER2+ was associated with menopause which may influence further expression of HER2+ .","PeriodicalId":9163,"journal":{"name":"Breast Cancer : Basic and Clinical Research","volume":"27 1","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2022-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Breast Cancer : Basic and Clinical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/11782234221080555","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 3

Abstract

Background: Breast cancer molecular subtypes share various prognostic profiles, and luminal A molecular subtypes have a better prognosis compared with other molecular subtypes. However, whether metabolic syndrome or individual risk factors of metabolic syndrome influence on the development of molecular subtype remains elusive. We aimed to assess the association between metabolic syndrome risk factors and breast cancer molecular subtypes among patients with metabolic syndrome in a clinical setting. Methods: In total, 101 breast cancer patients with mean age, 58.4 ± 8.5 years, and overt metabolic syndrome prospectively were recruited. Immunohistochemistry procedure was used to determine molecular subtypes. Assessment of clinical, biochemical, and anthropometric parameters was performed. Logistic regression analysis was used to assess the relationship between risk factors and breast cancer molecular subtypes categories. A similar approach was used to assess the relation between breast cancer molecular subtypes and menopause. Results: Comparison of metabolic syndrome individual risk factors according to breast cancer molecular subtypes no statistical difference was found for systolic (P = .33) and diastolic blood pressure (P = .17), fasting glucose (P = .77), triglycerides (P = .62), high-density lipoprotein (P = .33), body mass index (P = .87), and waist circumference (P = .81). A positive trend was found between high-density lipoprotein and HER2+. No association was found with other risk factors. Moreover, an association was found between HER2+ categories and menopause. Conclusion: In breast cancer patients with metabolic syndrome, we observed an increased trend between high-density lipoprotein and HER2+ molecular subtype, suggesting that underlying dyslipidemia may favor poor prognosis. HER2+ was associated with menopause which may influence further expression of HER2+ .
代谢综合征和乳腺癌分子亚型:一项观察性患者研究
背景:乳腺癌分子亚型具有不同的预后特征,其中腔内A分子亚型较其他分子亚型预后更好。然而,代谢综合征或代谢综合征的个体危险因素对分子亚型的发展是否有影响尚不清楚。我们的目的是在临床环境中评估代谢综合征危险因素与乳腺癌分子亚型在代谢综合征患者中的关系。方法:前瞻性纳入101例平均年龄58.4±8.5岁、伴有明显代谢综合征的乳腺癌患者。采用免疫组织化学方法确定分子亚型。进行临床、生化和人体测量参数评估。采用Logistic回归分析评估危险因素与乳腺癌分子亚型分类的关系。一个类似的方法被用来评估乳腺癌分子亚型和更年期之间的关系。结果:代谢综合征个体危险因素按乳腺癌分子亚型比较收缩压(P = 0.33)、舒张压(P = 0.17)、空腹血糖(P = 0.77)、甘油三酯(P = 0.62)、高密度脂蛋白(P = 0.33)、体重指数(P = 0.87)、腰围(P = 0.81)差异无统计学意义。高密度脂蛋白与HER2+呈阳性趋势。未发现与其他危险因素相关。此外,发现HER2+类型与更年期之间存在关联。结论:在乳腺癌代谢综合征患者中,我们观察到高密度脂蛋白和HER2+分子亚型之间的升高趋势,提示潜在的血脂异常可能导致预后不良。HER2+与绝经相关,这可能影响HER2+的进一步表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.10
自引率
3.40%
发文量
22
审稿时长
8 weeks
期刊介绍: Breast Cancer: Basic and Clinical Research is an international, open access, peer-reviewed, journal which considers manuscripts on all areas of breast cancer research and treatment. We welcome original research, short notes, case studies and review articles related to breast cancer-related research. Specific areas of interest include, but are not limited to, breast cancer sub types, pathobiology, metastasis, genetics and epigenetics, mammary gland biology, breast cancer models, prevention, detection, therapy and clinical interventions, and epidemiology and population genetics.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信