Griffing G T, Dale S L, Holbrook M M, Melby J C
J Clin Endocrinol Metab. 1983 Feb;56(2):218-21. doi: 10.1210/jcem-56-2-218.
Nonaldosterone mineralocorticoids, such as deoxycorticosterone (DOC) and 18-hydroxy-DOC, have been reported to be elevated in some patients with primary aldosteronism (PA). Since DOC is a probable precursor of a more potent mineralocorticoid, 19-nor-deoxycorticosterone (19-nor-DOC), this study evaluated urinary free (UF) 19-nor-DOC excretion in 6 patients with PA and compared the results to those from 11 patients with low renin hypertension (LRH) and 7 normotensive subjects. PA was due to either an aldosterone-producing adenoma (APA; 4 patients) or bilateral adrenal hyperplasia (2 patients) diagnosed by adrenal venous catheterization or surgery. Compared to LRH subjects, patients with PA had a higher mean blood pressure (137 +/- 9 vs. 114 +/- 3 mm Hg), a lower plasma potassium level (3.1 +/- 0.2 vs. 3.9 +/- 0.1 meq/1) and greater renin suppression (0.3 +/- 0.1 vs. 0.6 +/- 0.1 ng angiotensin I/ml . h). UF 19-nor-DOC levels were elevated in PA subjects compared to those in normotensives (3,716 +/- 1,517 vs. 428 +/- 112 ng/day) but not compared to those in LRH patients (1,237 +/- 471). Two patients with APA had distinctly elevated UF 19-nor-DOC levels (11,137 and 7,744 ng/day), but another APA patient had the lowest value (305 ng/day). UF 19-nor-DOC positively correlated with the aldosterone secretion rate in PA (r = 0.75) but not LRH subjects. In conclusion, this study demonstrates that patients with PA may have elevated levels of UF 19-nor-DOC which are proportional to the aldosterone excess and could be a contributing factor to the hypertension, hypokalamia, and excess mineralocorticoid activity of this disease.
据报道,在一些原发性醛固酮增多症(PA)患者中,非醛固酮类盐皮质激素,如脱氧皮质酮(DOC)和18-羟基-DOC会升高。由于DOC可能是一种更强效盐皮质激素19-去甲脱氧皮质酮(19-去甲-DOC)的前体,本研究评估了6例PA患者的尿游离(UF)19-去甲-DOC排泄情况,并将结果与11例低肾素性高血压(LRH)患者和7例血压正常者的结果进行了比较。PA是由肾上腺静脉插管或手术诊断为醛固酮分泌性腺瘤(APA;4例患者)或双侧肾上腺增生(2例患者)所致。与LRH患者相比,PA患者的平均血压更高(137±9 vs. 114±3 mmHg),血浆钾水平更低(3.1±0.2 vs. 3.9±0.1 meq/1),肾素抑制更明显(0.3±0.1 vs. 0.6±0.1 ng血管紧张素I/ml·h)。与血压正常者相比,PA患者的UF 19-去甲-DOC水平升高(3716±1517 vs. 428±112 ng/天),但与LRH患者相比则没有升高(1237±471)。2例APA患者的UF 19-去甲-DOC水平明显升高(11137和7744 ng/天),但另1例APA患者的值最低(305 ng/天)。PA患者的UF 19-去甲-DOC与醛固酮分泌率呈正相关(r = 0.75),而LRH患者则无此相关性。总之,本研究表明,PA患者的UF 19-去甲-DOC水平可能升高,且与醛固酮过量成比例,可能是该疾病高血压、低钾血症和盐皮质激素活性过高的一个促成因素。