Trifanescu Raluca, Carsote Mara, Caragheorgheopol Andra, Hortopan Dan, Dumitrascu Anda, Dobrescu Mariana, Poiana Catalina
"Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania ; "C.I. Parhon" National Institute of Endocrinology, Bucharest, Romania.
"Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
Maedica (Bucur). 2013 Jun;8(2):108-15.
Secondary endocrine hypertension accounts for 5-12% of hypertension's causes. In selected patients (type 2 diabetes mellitus, sleep apnea syndrome with resistant hypertension, sudden deterioration in hypertension control), prevalence could be higher.
To present etiology of endocrine secondary hypertension in a series of patients younger than 40 years at hypertension's onset.
Medical records of 80 patients (39M/41F), aged 30.1 ± 8.2 years (range: 12-40 years), with maximum systolic blood pressure=190.4 ± 29.2 mm Hg, range: 145-300 mm Hg, maximum diastolic blood pressure=107.7 ± 16.9 mm Hg, range: 80-170 mm Hg) referred by cardiologists for endocrine hypertension screening were retrospectively reviewed. Cardiac and renal causes of secondary hypertension were previously excluded. In all patients, plasma catecholamines were measured by ELISA and plasma cortisol by immunochemiluminescence. Orthostatic aldosterone (ELISA) and direct renin (chemiluminescence) were measured in 48 patients.
Secondary endocrine hypertension was confirmed in 16 out of 80 patients (20%). Primary hyperaldosteronism was diagnosed in 7 (4M/3F) out of 48 screened patients (14.6%). i.e. 8.75% from whole group: 5 patients with adrenal tumors (3 left/2 right), 2 patients with bilateral adrenal hyperplasia; all patients were hypokalemic at diagnostic (average nadir K+ levels = 2.5 ± 0.5 mmol/L); four patients were hypokalaemic on diuretic therapy (indapamidum); other 3 patients were hypokalaemic in the absence of diuretic therapy. Cushing's syndrome was diagnosed in 6 patients (7.5%): subclinical Cushing due to 4 cm right adrenal tumour - n = 1, overt ACTH-independent Cushing's syndrome due to: macronodular adrenal hyperplasia associated with primary hyperparathyroidism - n = 1; due to adrenal carcinoma - n = 1; due to adrenal adenomas - n = 2; Cushing's disease - n = 1). Pheochromocytomas were diagnosed in 3 patients (3.75%).
Primary hyperaldosteronism was the most frequent cause of secondary endocrine hypertension in our series, followed by Cushing's syndrome and pheochromocytomas. Screening of young hypertensive patients for secondary causes, especially primary hyperaldosteronism, is mandatory.
继发性内分泌性高血压占高血压病因的5% - 12%。在特定患者(2型糖尿病、伴有顽固性高血压的睡眠呼吸暂停综合征、高血压控制突然恶化)中,患病率可能更高。
阐述一系列高血压发病时年龄小于40岁患者的内分泌性继发性高血压病因。
回顾性分析了80例患者(39例男性/41例女性)的病历,年龄30.1±8.2岁(范围:12 - 40岁),最高收缩压 = 190.4±29.2 mmHg,范围:145 - 300 mmHg,最高舒张压 = 107.7±16.9 mmHg,范围:80 - 170 mmHg),这些患者由心脏病专家转诊来进行内分泌性高血压筛查。继发性高血压的心脏和肾脏病因已预先排除。所有患者均通过酶联免疫吸附测定法(ELISA)检测血浆儿茶酚胺,通过免疫化学发光法检测血浆皮质醇。48例患者检测了立位醛固酮(ELISA)和直接肾素(化学发光法)。
80例患者中有16例(20%)确诊为继发性内分泌性高血压。48例接受筛查的患者中有7例(4例男性/3例女性)诊断为原发性醛固酮增多症(14.6%),即占整个研究组的8.75%:5例患者有肾上腺肿瘤(3例左侧/2例右侧),2例患者为双侧肾上腺增生;所有患者诊断时均为低钾血症(平均最低血钾水平 = 2.5±0.5 mmol/L);4例患者在接受利尿剂(吲达帕胺)治疗时出现低钾血症;其他3例患者在未接受利尿剂治疗时出现低钾血症。6例患者(7.5%)诊断为库欣综合征:因右侧4 cm肾上腺肿瘤导致的亚临床库欣综合征 - 1例;因以下原因导致的显性促肾上腺皮质激素非依赖性库欣综合征:与原发性甲状旁腺功能亢进相关的大结节性肾上腺增生 - 1例;因肾上腺癌 - 1例;因肾上腺腺瘤 - 2例;库欣病 - 1例)。3例患者(3.75%)诊断为嗜铬细胞瘤。
在我们的研究系列中,原发性醛固酮增多症是继发性内分泌性高血压最常见的病因,其次是库欣综合征和嗜铬细胞瘤。对年轻高血压患者进行继发性病因筛查,尤其是原发性醛固酮增多症,是必不可少的。