Chevais A, Elfimova A R, Beltsevich D G
Endocrinology Research Centre.
Probl Endokrinol (Mosk). 2023 Jun 30;69(3):58-67. doi: 10.14341/probl13301.
Primary bilateral macronodular adrenal hyperplasia (PBMAH) is characterized by bilateral benign adrenocortical lesions, which in some cases lead to Cushing syndrome (CS). Due to the low detection, non-specific, erased clinical picture and slow, long-term progression, it is difficult to assess the true prevalence of PBMAH. This also leads to fairly limited literature data. A detailed analysis of biochemical, imaging parameters, the clinical presentations, in particular, an assessment of the course of comorbidities (arterial hypertension (AH), diabetes (DM), osteoporosis), is necessary to develop an algorithm for managing patients with PBMAH.
Analysis of clinical and laboratory characteristics of patients with various forms of PBMAH.
A single-center, retrospective, observational, cross-sectional study was carried out. This study included 110 patients with PBMAH who got referred to the National Research Center for Endocrinology in the period from 2013-2023. We carried out comparative and correlation analysis of hormonal (plasma cortisol concentrations after 1 mg dexamethasone (1-mg DST), urinary free cortisol (СКМ), ACTH), biochemical (glycated hemoglobin), radiological data (nodular tissue volume), course of comorbidities (metabolic syndrome, DM, AH, osteoporosis) in three groups of patients: with overt CS, mild autonomous cortisol excess (MACE) and comorbid diseases, and patients with PBMAH without hormonal activity.
Among 110 patients 79.1% were women, median age - 60 [51; 68]. The proportion of hormonally inactive forms of PBMAH was 37.3%, the overt CS and MACE was detected in 25.4 and 37.3% consequently. According to the hormonal -examination data: the cortisol level during 1-mg DST was 173.8 nmol/l [86.0; 441.0], ACTH - 3.35 pg/ml [1.00; 8.00], СКМ - 445.5 [249.0; 900.0]. Statistically significant positive moderate correlations were found between the volume of nodular tissue and the level of cortisol after PDT1 (r=0.40, p<0.001), СКМ (r=0.29, p<0.004), as well as a negative moderate correlation between the volume and the level of ACTH (r=-0.40, p<0.001). When analyzing the prevalence and clinical severity of comorbid conditions, DM was diagnosed in 22 (53.7%), AH in 36 (87.8%), obesity and osteoporosis - 23 (56%) and 3 (7.3%) patients. There was no statistically significant difference in the prevalence of CS-associated diseases among the above groups (p=0.56).
PBMAH is a heterogeneous pathology with different clinical, hormonal, and imaging characteristics. A correlation was found between the volume of nodular tissue and the degree of hormonal activity of PBMAH. The obtained results emphasize the difficulty in determining clear indications for surgical treatment in the group of patients with MACE. The radicality of proposed surgical procedure should be weighed against its potential complications.
原发性双侧大结节性肾上腺增生(PBMAH)的特征是双侧肾上腺皮质良性病变,在某些情况下会导致库欣综合征(CS)。由于其检出率低、临床表现不特异、隐匿以及进展缓慢、病程长,难以评估PBMAH的真实患病率。这也导致相关文献数据相当有限。详细分析生化、影像学参数、临床表现,尤其是评估合并症(动脉高血压(AH)、糖尿病(DM)、骨质疏松症)的病程,对于制定PBMAH患者的管理算法很有必要。
分析不同形式PBMAH患者的临床和实验室特征。
进行了一项单中心、回顾性、观察性横断面研究。该研究纳入了2013年至2023年期间转诊至国家内分泌研究中心的110例PBMAH患者。我们对三组患者的激素(1毫克地塞米松(1-mg DST)后血浆皮质醇浓度、尿游离皮质醇(СКМ)、促肾上腺皮质激素(ACTH))、生化(糖化血红蛋白)、放射学数据(结节组织体积)、合并症病程(代谢综合征、DM、AH、骨质疏松症)进行了比较和相关性分析:明显CS组、轻度自主性皮质醇增多症(MACE)和合并疾病组以及无激素活性的PBMAH患者组。
110例患者中,79.1%为女性,中位年龄为60岁[51;68]。PBMAH无激素活性形式的比例为37.3%,明显CS和MACE的检出率分别为25.4%和37.3%。根据激素检查数据:1-mg DST时皮质醇水平为173.8 nmol/l[86.0;441.0],ACTH为3.35 pg/ml[1.00;8.00],СКМ为445.5[249.0;900.0]。在结节组织体积与PDT1后皮质醇水平(r = 0.40,p<0.001)、СКМ(r = 0.29,p<0.004)之间发现了具有统计学意义的中度正相关,以及在体积与ACTH水平之间发现了中度负相关(r = -0.40,p<0.001)。在分析合并症的患病率和临床严重程度时,22例(53.7%)患者诊断为DM,36例(87.8%)患者诊断为AH,23例(56%)患者诊断为肥胖和骨质疏松症,3例(7.3%)患者诊断为骨质疏松症。上述组间CS相关疾病的患病率无统计学显著差异(p = 0.56)。
PBMAH是一种具有不同临床、激素和影像学特征的异质性疾病。发现结节组织体积与PBMAH的激素活性程度之间存在相关性。所得结果强调了在MACE患者组中确定明确手术治疗指征的困难。应权衡所提议手术的彻底性及其潜在并发症。