Department of Internal Medicine I (K.L., K.W., B.H., B.A., S.H.), University Hospital Würzburg, 97080 Würzburg, Germany; Clinical Endocrinology (M.Q.), Charité Campus Mitte, Charité University Medicine Berlin, 10117 Berlin, Germany; Medizinische Klinik und Poliklinik IV (A.S.D., M.R.), University Hospital Munich, 80336 Munich, Germany; Institute of Clinical Chemistry and Laboratory Medicine (H.W., A.H., N.F.), University Medicine Greifswald, 17489 Greifswald, Germany; Private Practice Endocrinology (H.W.), 99084 Erfurt, Germany; Department of Nephrology, Medical Faculty (L.C.R., I.Q.), Heinrich-Heine University Düesseldorf, 40225 Düsseldorf, Germany; and Department of Endocrinology and Metabolism (H.S.W.), Rostock University Medical Center, 18147 Rostock, Germany; Comprehensive Cancer Center Mainfranken & Department of Medicine I (C.T.F.), University of Wuerzburg, 97080 Wuerzburg, Germany.
J Clin Endocrinol Metab. 2016 Apr;101(4):1656-63. doi: 10.1210/jc.2015-3405. Epub 2016 Feb 4.
Primary aldosteronism (PA) is the most common cause of secondary hypertension. Aldosterone excess can cause DNA damage in vitro and in vivo. Single case reports have indicated a coincidence of PA with renal cell carcinoma and other tumors. However, the prevalence of benign and malignant neoplasms in patients with PA has not yet been studied.
In the multicenter MEPHISTO study, the prevalence of benign and malignant tumors was investigated in 335 patients with confirmed PA. Matched hypertensive subjects from the population-based Study of Health in Pomerania cohort served as controls.
Of the 335 PA patients, 119 (35.5%) had been diagnosed with a tumor at any time, and 30 had two or more neoplasms. Lifetime malignancy occurrence was reported in 9.6% of PA patients compared to 6.0% of hypertensive controls (P = .08). PA patients with a history of malignancy had higher baseline aldosterone levels at diagnosis of PA (P = .009), and a strong association between aldosterone levels and the prevalence of malignancies was observed (P = .03). In total, 157 neoplasms were identified in the PA patients; they were benign in 61% and malignant in 25% of the cases (14% of unknown dignity). Renal cell carcinoma was diagnosed in five patients (13% of all malignancies) and was not reported in controls
Compared to hypertensive controls, the prevalence of malignancies was positively correlated with aldosterone levels, tended to be higher in PA patients, but did not differ significantly.
原发性醛固酮增多症(PA)是继发性高血压最常见的原因。醛固酮过多可导致体外和体内的 DNA 损伤。个别病例报告表明,PA 与肾细胞癌和其他肿瘤同时存在。然而,PA 患者的良性和恶性肿瘤的患病率尚未得到研究。
在多中心 MEPHISTO 研究中,研究了 335 例确诊的 PA 患者的良性和恶性肿瘤的患病率。匹配的高血压患者来自基于人群的波美拉尼亚研究队列作为对照组。
在 335 例 PA 患者中,119 例(35.5%)在任何时候都被诊断患有肿瘤,30 例患者有两个或更多的肿瘤。PA 患者的终身恶性肿瘤发生率为 9.6%,而高血压对照组为 6.0%(P =.08)。PA 患者中有恶性肿瘤病史的患者在诊断为 PA 时的醛固酮水平更高(P =.009),并且观察到醛固酮水平与恶性肿瘤的患病率之间存在强烈关联(P =.03)。在 PA 患者中总共发现了 157 个肿瘤;其中 61%为良性,25%为恶性(14%为不确定等级)。5 例患者(所有恶性肿瘤的 13%)被诊断为肾细胞癌,对照组未报告。
与高血压对照组相比,恶性肿瘤的患病率与醛固酮水平呈正相关,在 PA 患者中倾向于更高,但差异无统计学意义。