Department of Population Health, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Dermatology Research Centre, University of Queensland Diamantina Institute, Brisbane, Queensland, Australia.
JAMA Dermatol. 2020 Dec 1;156(12):1324-1332. doi: 10.1001/jamadermatol.2020.4097.
Keratoacanthoma (KA) is a common and generally benign keratinocyte skin tumor. Reports of the incidence rates of KA are scant. In addition, the risk factors for KA are not well understood, although associations with UV radiation exposure and older age have been described.
To investigate the incidence rate of KA and the risk factors for developing KA.
DESIGN, SETTING, AND PARTICIPANTS: The study included data from 40 438 of 193 344 randomly selected residents of Queensland, Australia, who participated in the QSkin Sun and Health (QSkin) prospective population-based cohort study. All participants completed a baseline survey between 2010 and 2011 and were ages 40 to 69 years at baseline. Histopathologic reports of KA were prospectively collected until June 30, 2014, through data linkage with pathologic records. Cox proportional hazards models were used to identify risk factors associated with KA while controlling for potential confounding variables. Data were analyzed from January 2 to April 8, 2020.
Demographic characteristics, phenotypes, UV radiation exposure, medical history, and lifestyle.
Among 40 438 participants (mean [SD] age, 56 [8] years; 18 240 men [45.1%]), 596 individuals (mean [SD] age, 62 [6] years; 349 men [58.6%]) developed 776 KA tumors during a median follow-up period of 3.0 years (interquartile range, 2.8-3.3 years). The person-based age-standardized incidence rate for KA in the age-restricted cohort was 409 individuals per 100 000 person-years (based on the 2001 Australian population). Risk factors after adjustment for potential confounders were older age (age ≥60 years vs age <50 years; hazard ratio [HR], 6.38; 95% CI, 4.65-8.75), male sex (HR, 1.56; 95% CI, 1.33-1.84), fair skin (vs olive, dark, or black skin; HR, 3.42; 95% CI, 1.66-7.04), inability to tan (vs ability to tan deeply; HR, 1.69; 95% CI, 1.19-2.40), previous excisions of keratinocyte cancers (ever had an excision vs never had an excision; HR, 6.28; 95% CI, 5.03-7.83), current smoking (vs never smoking, HR, 2.02; 95% CI, 1.59-2.57), and high alcohol use (≥14 alcoholic drinks per week vs no alcoholic drinks per week; HR, 1.42; 95% CI, 1.09-1.86).
This is, to date, the first large prospective population-based study to report the incidence rate and risk factors for KA. The high person-based incidence rate (409 individuals per 100 000 person-years) highlights the substantial burden of KA in Queensland, Australia. Furthermore, the study's findings suggest that older age (≥60 years), male sex, UV radiation-sensitive phenotypes, indications of high sun exposure (eg, previous keratinocyte cancer excisions), smoking, and high alcohol use are independent risk factors for the development of KA.
角化棘皮瘤(KA)是一种常见且通常良性的角朊细胞皮肤肿瘤。关于 KA 的发病率报告很少。此外,KA 的风险因素尚不清楚,尽管已经描述了与紫外线辐射暴露和年龄较大的关联。
调查 KA 的发病率和发生 KA 的风险因素。
设计、设置和参与者:该研究包括来自澳大利亚昆士兰州的 193344 名随机选择的居民中的 40438 名参与者的数据,他们参加了 QSkin Sun 和健康(QSkin)前瞻性基于人群的队列研究。所有参与者在基线时年龄为 40 至 69 岁,在 2010 年至 2011 年期间完成了基线调查,并通过与病理记录的数据链接前瞻性地收集 KA 的组织病理学报告。使用 Cox 比例风险模型来确定与 KA 相关的风险因素,同时控制潜在的混杂变量。数据于 2020 年 1 月 2 日至 4 月 8 日进行分析。
人口统计学特征、表型、紫外线辐射暴露、病史和生活方式。
在 40438 名参与者中(平均[标准差]年龄,56[8]岁;18240 名男性[45.1%]),596 名参与者(平均[标准差]年龄,62[6]岁;349 名男性[58.6%])在中位随访期 3.0 年内(四分位距,2.8-3.3 年)发生了 776 例 KA 肿瘤。在年龄受限队列中,KA 的年龄标准化发病率为每 100000 人年 409 例(基于 2001 年澳大利亚人口)。调整潜在混杂因素后的风险因素为年龄较大(年龄≥60 岁与年龄<50 岁;风险比[HR],6.38;95%置信区间[CI],4.65-8.75)、男性(HR,1.56;95%CI,1.33-1.84)、浅色皮肤(与橄榄色、深色或黑色皮肤相比;HR,3.42;95%CI,1.66-7.04)、无法晒黑(与能够深度晒黑相比;HR,1.69;95%CI,1.19-2.40)、以前切除过角化细胞癌(曾切除过 vs 从未切除过;HR,6.28;95%CI,5.03-7.83)、当前吸烟(与从不吸烟相比;HR,2.02;95%CI,1.59-2.57)和高饮酒量(≥14 份含酒精饮料/周与无含酒精饮料/周;HR,1.42;95%CI,1.09-1.86)。
这是迄今为止第一项报告 KA 发病率和风险因素的大型前瞻性基于人群的研究。高人群发病率(每 100000 人年 409 例)突出了澳大利亚昆士兰州 KA 的巨大负担。此外,该研究结果表明,年龄较大(≥60 岁)、男性、紫外线辐射敏感表型、高阳光暴露迹象(例如,以前的角化细胞癌切除)、吸烟和大量饮酒是 KA 发展的独立风险因素。