Ainslie G M, Benatar S R
Q J Med. 1985 Jun;55(218):253-70.
Serum angiotensin converting enzyme (SACE), despite certain limitations, has been found to be a useful adjunct to the diagnosis, assessment of disease activity, and management of sarcoidosis. The spectrofluorimetric assay was used to measure SACE in 50 normal controls, 76 patients with tuberculosis (42 pulmonary, 16 lymphatic and 18 military cases), 20 patients with cryptogenic fibrosing alveolitis, 50 patients with silicosis, three patients with extrinsic allergic alveolitis, 10 patients with Crohn's disease, two patients with Gaucher's disease, and 128 patients with sarcoidosis on 303 occasions (144 during periods judged as clinically active and 189 inactive). Our results show a normal range (mean +/- 2SD) of 19-54 nmol/ml/min. The false positive rate is 2 per cent in normal controls, 9.2 per cent in tuberculosis (38.9 per cent in military but 0 per cent in the other forms), 48 per cent in silicosis, 100 per cent in Gaucher's disease, and 0 per cent in the other diseases. The sensitivity, specificity, positive and negative predictive values were 58.1, 83.8, 83.8 and 58.1 per cent respectively. The sensitivity rose to 85.9 per cent if only those samples taken from patients in whom sarcoidosis was suspected on initial presentation were included, and 92.1 per cent if only those with clinically active sarcoidosis were included. The sensitivity of SACE as a diagnostic test in sarcoidosis is thus influenced by the relative frequency of active and inactive sarcoidosis. The specificity is influenced by the prevalence of military tuberculosis and silicosis, but is uninfluenced by other common varieties of interstitial lung disease such as cryptogenic fibrosing alveolitis and extrinsic allergic alveolitis, or by other non-pulmonary granulomatous disease. There was no correlation of the SACE level with age, sex, population group, associated other illness or duration of sarcoidosis. Statistically, SACE levels were significantly higher in patients with Types II and III chest radiographs as compared to Type I and 0, and also in those with additional clinically evident extra-thoracic disease e.g. in lymph node, eye and especially multiple systems. SACE also reflected clinical activity with levels being statistically significantly greater in those patients assessed as having active disease, although 7.9 per cent of these had normal levels. Our observations indicate that SACE levels correlate well with disease activity longitudinally, both in relation to spontaneous remission and steroid therapy, and are thus helpful in patient management.
血清血管紧张素转换酶(SACE)尽管存在某些局限性,但已被发现是结节病诊断、疾病活动评估及管理的有用辅助手段。采用荧光分光光度法对50名正常对照者、76例结核病患者(42例肺结核、16例淋巴结核和18例粟粒性结核)、20例隐源性纤维性肺泡炎患者、50例矽肺患者、3例外源性过敏性肺泡炎患者、10例克罗恩病患者、2例戈谢病患者以及128例结节病患者进行了303次检测(144次在临床判断为活动期时进行,189次在非活动期时进行)。我们的结果显示正常范围(均值±2标准差)为19 - 54 nmol/ml/分钟。正常对照者的假阳性率为2%,结核病患者为9.2%(粟粒性结核为38.9%,其他类型为0%),矽肺患者为48%,戈谢病患者为100%,其他疾病患者为0%。敏感性、特异性、阳性预测值和阴性预测值分别为58.1%、83.8%、83.8%和58.1%。若仅纳入初诊时疑似结节病患者的样本,敏感性升至85.9%;若仅纳入临床活动期结节病患者的样本,敏感性则为92.1%。因此,SACE作为结节病诊断试验的敏感性受结节病活动期和非活动期相对频率的影响。特异性受粟粒性结核和矽肺患病率的影响,但不受隐源性纤维性肺泡炎和外源性过敏性肺泡炎等其他常见间质性肺疾病类型或其他非肺部肉芽肿性疾病的影响。SACE水平与年龄、性别、人群组、伴发的其他疾病或结节病病程均无相关性。从统计学角度来看,与I型和0型胸部X线片相比,II型和III型胸部X线片患者以及伴有临床明显胸外疾病(如淋巴结、眼部尤其是多系统受累)的患者SACE水平显著更高。SACE也反映了临床活动情况,在被评估为患有活动期疾病的患者中,其水平在统计学上显著更高,尽管其中7.9%的患者水平正常。我们的观察结果表明,SACE水平在纵向与疾病活动情况密切相关,无论是与自发缓解还是与类固醇治疗相关,因此有助于患者管理。