Galli R, Chavaz A, Balant L, Chatelanat F, Fabre J
Schweiz Med Wochenschr. 1979 Jun 9;109(23):874-80.
Qualitative analysis of urinary proteins is contrasted with histological findings of 45 renal biopsies performed in patients with chronic glomerulonephritis. Compared to electrophoresis on cellulose acetate and immunoelectrophoresis, a method using polyacrylamide gel after sodium dodecylsulfate treatment makes for more refined and objective differentiation of protein abnormalities. On the whole, proteinuria of the selective glomerular or physiological type predominates in the event of minimal change or membranous lesions. The non-selective type is found more frequently with diffuse proliferative or membranoproliferative glomerulonephritis (p less than 0.025). There are, however, too many exceptions to this rule to allow certainty, and a precise diagnosis of the particular type of glomerulonephritis is thus only possible histologically. Each type of histological involvement may cause almost any of the qualitative abnormalities of proteinuria. On the other hand, qualitative analysis of urinary proteins is useful for the detection of glomerulonephritis. A glomerular type of proteinuria may sometimes reveal involvement of kidneys at a time when, quantitatively, there is no proteinuria. In cases of orthostatic proteinuria a persistent glomerular type of tracing in recumbency suggests an organic kidney ailment. All patients in this series had a glomerular type of proteinuria when excretion was pathological, thus allowing a distinction from pure tubular involvement. 10 patients of the group, however, although they clearly had glomerular lesions (3 were diffuse proliferative glomerulonephritis) showed perfectly normal proteinuria both quantitatively and qualitatively. This was the case in systemic lupus erythematosus where kidney biopsy was performed without clinical suspicion of renal involvement. In summary, qualitative abnormalities of proteinuria call attention to underlying glomerulonephritis, although no distinction can be made between the various forms and there may be no detectable abnormality even in the event of major kidney involvement.
对慢性肾小球肾炎患者进行的45例肾活检组织学检查结果与尿蛋白定性分析进行了对比。与醋酸纤维素电泳和免疫电泳相比,十二烷基硫酸钠处理后使用聚丙烯酰胺凝胶的方法能更精细、客观地区分蛋白质异常。总体而言,微小病变或膜性病变时,选择性肾小球性或生理性蛋白尿占主导。非选择性蛋白尿在弥漫性增殖性或膜增生性肾小球肾炎中更常见(p小于0.025)。然而,该规则有太多例外情况,无法确定,因此仅通过组织学检查才能精确诊断特定类型的肾小球肾炎。每种组织学受累类型几乎都可能导致蛋白尿的任何定性异常。另一方面,尿蛋白定性分析有助于肾小球肾炎的检测。有时,肾小球性蛋白尿可能在定量无蛋白尿时揭示肾脏受累。在直立性蛋白尿病例中,卧位时持续的肾小球性追踪提示器质性肾脏疾病。本系列所有患者在排泄病理性时均为肾小球性蛋白尿,从而可与单纯肾小管受累相区分。然而,该组中有10例患者,尽管他们明显有肾小球病变(3例为弥漫性增殖性肾小球肾炎),但定量和定性蛋白尿均完全正常。系统性红斑狼疮患者在未临床怀疑肾脏受累时进行肾活检就是这种情况。总之,蛋白尿的定性异常提示潜在的肾小球肾炎,尽管无法区分各种形式,即使在肾脏严重受累时也可能无可检测到的异常。