Dental Core Trainee 2 in Oral and Maxillofacial Surgery, Queen Elizabeth University Hospital, Glasgow, UK.
Speciality Dentist in Oral Medicine, Glasgow Dental Hospital, Glasgow, UK.
Evid Based Dent. 2022 Mar;23(1):38-39. doi: 10.1038/s41432-022-0255-x. Epub 2022 Mar 25.
Data sources Data was from The Health Improvement Network (THIN) database from January 1999 to May 2016.Study selection This was a series of population-based, case-control studies looking to evaluate the association between hydrochlorothiazide (HCTZ) exposure and skin, lip and oral cancer in the UK population.Case/control selection Using the THIN database, patients with the following outcomes were grouped: squamous cell carcinoma (SCC) skin cancer; basal cell carcinoma (BCC) skin cancer; melanoma; lip cancer and oral cancer. Patients within the lip cancer and oral cancer groups were accepted with a history of non-melanoma skin cancer (NMSC). Patients in the SCC and BCC groups were not accepted with a history of cancer. Patients with a history of organ transplantation, human immunodeficiency virus (HIV) or immunosuppressant drug use before the index date were not accepted, due to the risk of predisposition to cancer. Controls were randomly selected using incidence density sampling. Up to 100 controls were randomly selected, matched on sex, exact year of birth and calendar year of cohort entry for lip cancer. However, for the remaining outcomes, only 20 controls were matched as above. Adults with incident NMSC, melanoma, lip cancer and oral cancer were matched to controls. Incidence rate ratios (IRRs) for the aforementioned outcomes were calculated for every cumulative HCTZ exposure.Data analysis Odds ratios were calculated using conditional logistic regression. Associations were presented using a two-year HCTZ exposure lag-time and a five-year HCTZ exposure lag-time. Associations were evaluated using sensitivity analysis, restricted to patients with at least ten years' follow-up. There was adjustment for smoking status and BMI. Published incidence rates were used to calculate the absolute risk estimate for SCC as the incidence of SCC in the cohort was less than expected. For high-dose cumulative HCTZ exposure, the number of patients needed to treat to cause one additional cancer (number needed to harm) per year overall was estimated using rate differences. Analysis was carried out using SAS Enterprise Guidev7.1 and STATAv15.Results Relative incidence of SCC, BCC and lip cancer was significantly elevated with every use of HCTZ. Relative incidence of melanoma and oral cancer was not significantly elevated with HCTZ exposure. Smoking was inversely associated with BCC and melanoma risk, but significantly increased the risk of lip and oral cavity cancers. SCC risk was not strongly associated with smoking. Significantly reduced risk of SCC, BCC melanoma and oral cavity cancer was associated with a BMI ≥30 kg/m2.Conclusions The risk of NMSC and lip cancer in a UK population is increased with cumulative high-dose HCTZ exposure. It is therefore important for dentists to note as it may increase suspicion of lesions in patients taking these medications.
数据来源 数据来源于 1999 年 1 月至 2016 年 5 月的健康改善网络(THIN)数据库。
研究选择 这是一系列基于人群的病例对照研究,旨在评估英国人群中海洛嗪(HCTZ)暴露与皮肤、唇和口腔癌之间的关联。
病例/对照选择 使用 THIN 数据库,将具有以下结局的患者分为以下几类:鳞状细胞癌(SCC)皮肤癌;基底细胞癌(BCC)皮肤癌;黑色素瘤;唇癌和口腔癌。唇癌和口腔癌组的患者接受了非黑色素瘤皮肤癌(NMSC)病史。SCC 和 BCC 组的患者不接受癌症病史。由于有患癌症的倾向,索引日期前接受过器官移植、人类免疫缺陷病毒(HIV)或免疫抑制剂药物治疗的患者不被接受。使用密度抽样法随机选择对照。对于唇癌,最多随机选择 100 名对照,按性别、出生的确切年份和队列入组的日历年份进行匹配。然而,对于其余结局,仅匹配了 20 名上述条件的对照。将新发 NMSC、黑色素瘤、唇癌和口腔癌的成年人与对照相匹配。计算了上述结局的累积 HCTZ 暴露的发病率比(IRR)。使用条件逻辑回归计算了比值比。使用两年 HCTZ 暴露滞后时间和五年 HCTZ 暴露滞后时间呈现关联。使用敏感性分析评估关联,该分析仅限于至少有十年随访的患者。调整了吸烟状况和 BMI。使用公布的发病率计算 SCC 的绝对风险估计值,因为队列中 SCC 的发病率低于预期。对于高剂量累积 HCTZ 暴露,使用率差异估计每年每治疗一例癌症(需要治疗的例数)的风险。使用 SAS Enterprise Guidev7.1 和 STATAv15 进行分析。
结果 SCC、BCC 和唇癌的相对发病率随着 HCTZ 的每次使用而显著升高。HCTZ 暴露与黑色素瘤和口腔癌的相对发病率无显著升高。吸烟与 BCC 和黑色素瘤风险呈负相关,但显著增加唇和口腔癌的风险。SCC 风险与吸烟无明显关联。BMI≥30kg/m2 与 SCC、BCC、黑色素瘤和口腔癌的风险显著降低有关。
结论 在英国人群中,NMSC 和唇癌的风险随着累积高剂量 HCTZ 暴露而增加。因此,牙医注意到这一点很重要,因为这可能会增加对服用这些药物的患者的病变的怀疑。