Department of Plastic and Breast Surgery, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, Aarhus N, 8200, Denmark.
Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark.
BMC Cancer. 2024 Jul 7;24(1):812. doi: 10.1186/s12885-024-12598-8.
Cancer has become the leading diabetes-related cause of death in high-income countries, and more knowledge is needed to clarify the impact of diabetes on site-specific cancers. The purpose of this study is to assess the association between diabetes and malignant melanoma by conducting a comprehensive systematic review and meta-analysis.
Using predefined eligibility criteria, PubMed, The Cochrane Library and Web of Science were systematically searched up to February 22, 2023. Exposure was defined as diabetes or type 2 diabetes and the outcomes were defined as melanoma incidence, melanoma stage or melanoma-specific mortality. The identified articles were evaluated by two independent reviewers and quality assessment was conducted using the Newcastle-Ottawa Scale for observational studies. Meta-analyses were conducted using RevMan 5.4.1 on melanoma risk using adjusted risk estimates and on melanoma stage using a dichotomous model.
The literature search revealed 20 studies in total eligible for inclusion, 14 for the analysis of melanoma risk, 3 for melanoma thickness and ulceration, and 4 for melanoma-specific survival. According to the meta-analyses, diabetes did not impact the risk of developing melanoma (RR:1.05, 95%CI:0.99-1.12, p = 0.10). However, type 2 diabetes was associated with more advanced melanoma stages at the time of diagnosis (Breslow-thickness > 1 mm: RR 1.35, 95%CI: 1.22-1.49, p = < 0.001) and presence of ulceration (RR 1.30, 95%CI: 1.00-1.68, p = 0.05). A meta-analysis on the association between diabetes and melanoma-specific mortality was not feasible due to diverse study designs.
Our meta-analysis found no association between diabetes and the risk of developing melanoma, but diabetes was associated with increased tumour thickness and the presence of ulceration at the time of diagnosis. Further research is warranted to explore the association between diabetes melanoma stage and prognosis.
PROSPERO ID CRD42023394187.
癌症已成为高收入国家中与糖尿病相关的主要死亡原因,因此需要更多的知识来阐明糖尿病对特定部位癌症的影响。本研究旨在通过全面的系统评价和荟萃分析来评估糖尿病与恶性黑色素瘤之间的关系。
使用预先设定的纳入标准,系统地检索了 PubMed、The Cochrane Library 和 Web of Science,检索时间截至 2023 年 2 月 22 日。暴露定义为糖尿病或 2 型糖尿病,结局定义为黑色素瘤发病率、黑色素瘤分期或黑色素瘤特异性死亡率。由两名独立的评审员评估所识别的文章,并使用纽卡斯尔-渥太华量表对观察性研究进行质量评估。使用 RevMan 5.4.1 对黑色素瘤风险进行荟萃分析,使用调整后的风险估计值,对黑色素瘤分期进行二分类模型分析。
文献检索共发现 20 项符合纳入标准的研究,其中 14 项用于分析黑色素瘤风险,3 项用于分析黑色素瘤厚度和溃疡,4 项用于分析黑色素瘤特异性生存。根据荟萃分析结果,糖尿病并不影响黑色素瘤的发病风险(RR:1.05,95%CI:0.99-1.12,p=0.10)。然而,2 型糖尿病与诊断时更晚期的黑色素瘤分期相关(Breslow 厚度>1mm:RR 1.35,95%CI:1.22-1.49,p<0.001)和溃疡存在(RR 1.30,95%CI:1.00-1.68,p=0.05)。由于研究设计的多样性,对糖尿病与黑色素瘤特异性死亡率之间的关系进行荟萃分析是不可行的。
本荟萃分析未发现糖尿病与黑色素瘤发病风险之间存在关联,但糖尿病与诊断时肿瘤厚度增加和溃疡存在相关。需要进一步研究来探讨糖尿病与黑色素瘤分期和预后之间的关系。
PROSPERO ID CRD42023394187。