Rossi Gian Paolo, Bernini Giampaolo, Caliumi Chiara, Desideri Giovambattista, Fabris Bruno, Ferri Claudio, Ganzaroli Chiara, Giacchetti Gilberta, Letizia Claudio, Maccario Mauro, Mallamaci Francesca, Mannelli Massimo, Mattarello Mee-Jung, Moretti Angelica, Palumbo Gaetana, Parenti Gabriele, Porteri Enzo, Semplicini Andrea, Rizzoni Damiano, Rossi Ermanno, Boscaro Marco, Pessina Achille Cesare, Mantero Franco
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J Am Coll Cardiol. 2006 Dec 5;48(11):2293-300. doi: 10.1016/j.jacc.2006.07.059. Epub 2006 Nov 13.
We prospectively investigated the prevalence of curable forms of primary aldosteronism (PA) in newly diagnosed hypertensive patients.
The prevalence of curable forms of PA is currently unknown, although retrospective data suggest that it is not as low as commonly perceived.
Consecutive hypertensive patients referred to 14 hypertension centers underwent a diagnostic protocol composed of measurement of Na+ and K+ in serum and 24-h urine, sitting plasma renin activity, and aldosterone at baseline and after 50 mg captopril. The patients with an aldosterone/renin ratio >40 at baseline, and/or >30 after captopril, and/or a probability of PA (by a logistic discriminant function) > or =50% underwent imaging tests and adrenal vein sampling (AVS) or adrenocortical scintigraphy to identify the underlying adrenal pathology. An aldosterone-producing adenoma (APA) was diagnosed in patients who in addition to excess autonomous aldosterone secretion showed: 1) lateralized aldosterone secretion at AVS or adrenocortical scintigraphy, 2) adenoma at surgery and pathology, and 3) a blood pressure decrease after adrenalectomy. Evidence of excess autonomous aldosterone secretion without such criteria led to a diagnosis of idiopathic hyperaldosteronism (IHA).
A total of 1,180 patients (age 46 +/- 12 years) were enrolled; a conclusive diagnosis was attained in 1,125 (95.3%). Of these, 54 (4.8%) had an APA and 72 (6.4%) had an IHA. There were more APA (62.5%) and fewer IHA cases (37.5%) at centers where AVS was available (p = 0.002); the opposite occurred where AVS was unavailable.
In newly diagnosed hypertensive patients referred to hypertension centers, the prevalence of APA is high (4.8%). The availability of AVS is essential for an accurate identification of the adrenocortical pathologies underlying PA.
我们前瞻性地调查了新诊断高血压患者中可治愈形式的原发性醛固酮增多症(PA)的患病率。
尽管回顾性数据表明可治愈形式的PA患病率并非如普遍认为的那样低,但目前其确切患病率尚不清楚。
连续转诊至14个高血压中心的高血压患者接受了一项诊断方案,包括测量血清和24小时尿中的Na⁺和K⁺、静息血浆肾素活性以及基线和服用50mg卡托普利后醛固酮水平。基线时醛固酮/肾素比值>40,和/或服用卡托普利后>30,和/或PA发生概率(通过逻辑判别函数)≥50%的患者接受影像学检查和肾上腺静脉采样(AVS)或肾上腺皮质闪烁显像,以确定潜在的肾上腺病变。除自主醛固酮分泌过多外,还具备以下表现的患者被诊断为醛固酮瘤(APA):1)AVS或肾上腺皮质闪烁显像显示醛固酮分泌侧化;2)手术和病理检查发现腺瘤;3)肾上腺切除术后血压下降。无上述标准但有自主醛固酮分泌过多证据的患者被诊断为特发性醛固酮增多症(IHA)。
共纳入1180例患者(年龄46±12岁);1125例(95.3%)获得了明确诊断。其中,54例(4.8%)患有APA,72例(6.4%)患有IHA。在可进行AVS的中心,APA病例更多(62.5%),IHA病例更少(37.5%)(p = 0.002);在无法进行AVS的中心情况则相反。
在转诊至高血压中心的新诊断高血压患者中,APA的患病率较高(4.8%)。AVS对于准确识别PA潜在的肾上腺皮质病变至关重要。