Prejbisz Aleksander, Postuła Marek, Cybulska Idalia, Dobrucki Tomasz, Kabat Marek, Peczkowska Mariola, Janas Jadwiga, Janaszek-Sitkowska Hanna, Makowiecka-Cieśla Magdalena, Januszkiewicz Andrzej
Department of Hypertension, Institute of Cardiology, Warsaw, Poland.
Kardiol Pol. 2003 Jan;58(1):17-26.
Primary aldosteronism (PA) is a secondary form of hypertension resulting from the autonomous hypersecretion of aldosterone. The recognition of PA has an important impact on clinical management, since the choice of therapy is different - surgical for adenoma and medical for hyperplasia.
To evaluate patients with PA in regard to clinical and biochemical factors differentiating between adenoma of adrenal cortex (APA) and idiopathic adrenal hyperplasia (IHA).
We retrospectively analysed 62 patients with PA (33 females, 29 males, mean age 49.3+/-12.5 years, range 26-78) diagnosed in the Department of Hypertension between 1990-2001. In 37 patients (mean age 47.4+/-12.1 years, 22 females, 15 males) APA was diagnosed whereas in the remaining 26 patients (mean age 52.2+/-12.6 years, 14 males, 11 females) IHA was detected. Clinical manifestation, biochemical, serum aldosterone (SA), plasma renin activity (PRA) as well as echocardiographic parameters and blood pressure (BP) levels were evaluated. Diagnostic accuracy of computed tomography (CT) and scintigraphy was also assessed.
Mean systolic BP was significantly higher in the patients with APA. Both groups had similar mean diastolic BP. Severe hypertension, resistant to three or more medications, was found in 63.3% of all patients. Muscle weakness was reported by 39.7% of patients, polyuria - by 19%, and polydypsia - by 10.3% of patients. Patients with muscle weakness had higher mean systolic BP level and lower plasma potassium level than patients without this complaint. Symptoms suggesting cardiac arrhythmia were reported by 45% of patients. A normal potassium level was found in 25.8% of all patients. The hypokalemic patients were younger, had shorter known duration of hypertension, higher mean systolic BP level and higher SA concentration than the normokalemic patients. Supine SA levels were significantly higher in the APA group than in the IHA group (50.3+/-29.0 ng% vs 30.5+/-14.7 ng%; p<0.001). The SA/PRA ratio higher than 30:1 was found in all patients. Response to postural test with a rise in SA concentration higher than 30% was observed in 40% patients with APA and in 87.5% patients with IHA (p<0.0001). There was a strong correlation between supine and upright SA level, and systolic and diastolic BP level as well as plasma potassium level. Left ventricular hypertrophy was present in 60% of patients. The differentiation between APA and IHA was possible using CT, scintigraphy or both methods in 75%, 89.2% and 100% of patients, respectively.
One quarter of patients with PA were normokalemic. PA should be suspected especially in patients with severe hypertension, resistant to three or more antihypertensive drugs. Changes in SA concentration during the postural tests such as CT and scintigraphy are useful for differentiation between APA and IHA.
原发性醛固酮增多症(PA)是一种由于醛固酮自主分泌过多导致的继发性高血压。PA的诊断对临床治疗有重要影响,因为治疗选择不同——腺瘤采用手术治疗,增生采用药物治疗。
评估PA患者在区分肾上腺皮质腺瘤(APA)和特发性肾上腺增生(IHA)方面的临床和生化因素。
我们回顾性分析了1990年至2001年间在高血压科诊断的62例PA患者(33例女性,29例男性,平均年龄49.3±12.5岁,范围26 - 78岁)。其中37例患者(平均年龄47.4±12.1岁,22例女性,15例男性)诊断为APA,其余26例患者(平均年龄52.2±12.6岁,14例男性,11例女性)诊断为IHA。评估了临床表现、生化指标、血清醛固酮(SA)、血浆肾素活性(PRA)以及超声心动图参数和血压(BP)水平。还评估了计算机断层扫描(CT)和闪烁扫描的诊断准确性。
APA患者的平均收缩压显著更高。两组的平均舒张压相似。所有患者中有63.3%存在重度高血压,对三种或更多药物治疗耐药。39.7%的患者报告有肌肉无力,19%的患者有多尿,10.3% 的患者有多饮。有肌肉无力的患者比无此症状的患者平均收缩压水平更高,血钾水平更低。45%的患者报告有提示心律失常的症状。所有患者中有25.8%血钾水平正常。低钾血症患者比血钾正常患者更年轻,高血压病程更短,平均收缩压水平更高,SA浓度更高。APA组的仰卧位SA水平显著高于IHA组(50.3±29.0 ng% 对30.5±14.7 ng%;p<0.001)。所有患者的SA/PRA比值均高于30:1。40%的APA患者和87.5%的IHA患者在体位试验中SA浓度升高超过30%(p<0.0001)。仰卧位和立位SA水平与收缩压和舒张压水平以及血钾水平之间存在强相关性。60%的患者存在左心室肥厚。分别使用CT、闪烁扫描或两种方法,在75%、89.2%和100%的患者中能够区分APA和IHA。
四分之一的PA患者血钾正常。PA尤其应怀疑在重度高血压、对三种或更多抗高血压药物耐药的患者中。体位试验如CT和闪烁扫描期间SA浓度的变化有助于区分APA和IHA。