Prete Alessandro, Subramanian Anuradhaa, Bancos Irina, Chortis Vasileios, Tsagarakis Stylianos, Lang Katharina, Macech Magdalena, Delivanis Danae A, Pupovac Ivana D, Reimondo Giuseppe, Marina Ljiljana V, Deutschbein Timo, Balomenaki Maria, O'Reilly Michael W, Gilligan Lorna C, Jenkinson Carl, Bednarczuk Tomasz, Zhang Catherine D, Dusek Tina, Diamantopoulos Aristidis, Asia Miriam, Kondracka Agnieszka, Li Dingfeng, Masjkur Jimmy R, Quinkler Marcus, Ueland Grethe Å, Dennedy M Conall, Beuschlein Felix, Tabarin Antoine, Fassnacht Martin, Ivović Miomira, Terzolo Massimo, Kastelan Darko, Young William F, Manolopoulos Konstantinos N, Ambroziak Urszula, Vassiliadi Dimitra A, Taylor Angela E, Sitch Alice J, Nirantharakumar Krishnarajah, Arlt Wiebke
The Institute of Metabolism and Systems Research, University of Birmingham, Centre for Endocrinology, Diabetes and Metabolism, Birmingham Health Partners, and Department of Endocrinology, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom (A.P., V.C., K.L.).
Institute of Applied Health Research, University of Birmingham, Birmingham, United Kingdom (A.S.).
Ann Intern Med. 2022 Mar;175(3):325-334. doi: 10.7326/M21-1737. Epub 2022 Jan 4.
Benign adrenal tumors are commonly discovered on cross-sectional imaging. Mild autonomous cortisol secretion (MACS) is regularly diagnosed, but its effect on cardiometabolic disease in affected persons is ill defined.
To determine cardiometabolic disease burden and steroid excretion in persons with benign adrenal tumors with and without MACS.
Cross-sectional study.
14 endocrine secondary and tertiary care centers (recruitment from 2011 to 2016).
1305 prospectively recruited persons with benign adrenal tumors.
Cortisol excess was defined by clinical assessment and the 1-mg overnight dexamethasone-suppression test (serum cortisol: <50 nmol/L, nonfunctioning adrenal tumor [NFAT]; 50 to 138 nmol/L, possible MACS [MACS-1]; >138 nmol/L and absence of typical clinical Cushing syndrome [CS] features, definitive MACS [MACS-2]). Net steroid production was assessed by multisteroid profiling of 24-hour urine by tandem mass spectrometry.
Of the 1305 participants, 49.7% had NFAT ( = 649; 64.1% women), 34.6% had MACS-1 ( = 451; 67.2% women), 10.7% had MACS-2 ( = 140; 73.6% women), and 5.0% had CS ( = 65; 86.2% women). Prevalence and severity of hypertension were higher in MACS-2 and CS than NFAT (adjusted prevalence ratios [aPRs] for hypertension: MACS-2, 1.15 [95% CI, 1.04 to 1.27], and CS, 1.37 [CI, 1.16 to 1.62]; aPRs for use of ≥3 antihypertensives: MACS-2, 1.31 [CI, 1.02 to 1.68], and CS, 2.22 [CI, 1.62 to 3.05]). Type 2 diabetes was more prevalent in CS than NFAT (aPR, 1.62 [CI, 1.08 to 2.42]) and more likely to require insulin therapy for MACS-2 (aPR, 1.89 [CI, 1.01 to 3.52]) and CS (aPR, 3.06 [CI, 1.60 to 5.85]). Urinary multisteroid profiling revealed an increase in glucocorticoid excretion from NFAT over MACS-1 and MACS-2 to CS, whereas androgen excretion decreased.
Cross-sectional design; possible selection bias.
A cardiometabolic risk condition, MACS predominantly affects women and warrants regular assessment for hypertension and type 2 diabetes.
Diabetes UK, the European Commission, U.K. Medical Research Council, the U.K. Academy of Medical Sciences, the Wellcome Trust, the U.K. National Institute for Health Research, the U.S. National Institutes of Health, the Claire Khan Trust Fund at University Hospitals Birmingham Charities, and the Mayo Clinic Foundation for Medical Education and Research.
肾上腺良性肿瘤常在横断面成像检查中被发现。轻度自主性皮质醇分泌(MACS)常被诊断出来,但其对患者心脏代谢疾病的影响尚不明确。
确定有和没有MACS的肾上腺良性肿瘤患者的心脏代谢疾病负担和类固醇排泄情况。
横断面研究。
14个内分泌二级和三级护理中心(2011年至2016年招募)。
1305名前瞻性招募的肾上腺良性肿瘤患者。
通过临床评估和1毫克过夜地塞米松抑制试验定义皮质醇过量(血清皮质醇:<50 nmol/L,无功能肾上腺肿瘤[NFAT];50至138 nmol/L,可能的MACS[MACS-1];>138 nmol/L且无典型临床库欣综合征[CS]特征,明确的MACS[MACS-2])。通过串联质谱法对24小时尿液进行多类固醇分析来评估类固醇净生成。
在1305名参与者中,49.7%患有NFAT(n = 649;64.1%为女性),34.6%患有MACS-1(n = 451;67.2%为女性),10.7%患有MACS-2(n = 140;73.6%为女性),5.0%患有CS(n = 65;86.2%为女性)。MACS-2和CS组高血压的患病率和严重程度高于NFAT组(高血压的调整患病率比[aPRs]:MACS-2为1.15[95%CI,1.04至1.27],CS为1.37[CI,1.16至1.62];使用≥3种抗高血压药物的aPRs:MACS-2为1.31[CI,1.02至1.68],CS为2.22[CI,1.62至3.05])。2型糖尿病在CS组比NFAT组更常见(aPR,1.62[CI,1.08至2.42]),MACS-2组(aPR,1.89[CI,1.01至3.52])和CS组(aPR,3.06[CI,1.60至5.85])更有可能需要胰岛素治疗。尿液多类固醇分析显示,从NFAT到MACS-1、MACS-2再到CS,糖皮质激素排泄增加,而雄激素排泄减少。
横断面设计;可能存在选择偏倚。
心脏代谢风险状况MACS主要影响女性,需要定期评估高血压和2型糖尿病。
英国糖尿病协会、欧盟委员会、英国医学研究理事会、英国医学科学院、惠康信托基金会、英国国家卫生研究院、美国国立卫生研究院、伯明翰大学医院慈善机构的克莱尔·汗信托基金以及梅奥诊所医学教育与研究基金会。