Awad Hesham, el-Safty Ibrahim, el-Barbary Mohamed, Imam Safaa
Pediatric Department, Faculty of Medicine, Ain-Shams University, Cairo, Egypt.
Am J Med Sci. 2002 Nov;324(5):261-6. doi: 10.1097/00000441-200211000-00005.
Renal cells are not fully differentiated at birth, representing a major risk in preterm infants. We evaluated glomerular and tubular functional integrity as well as structural integrity of renal tubules among healthy full-term and preterm infants as well as diseased preterm infants.
A total of 50 newborns (10 healthy full-term, 10 healthy preterm, and 30 diseased preterm, at 38.9 +/- 1.10, 34.2 +/- 0.92, and 32 +/- 2.47 weeks gestational age, respectively) were included in the present study. Glomerular function was assessed by measuring urinary levels of both microalbumin and immunoglobulin G as well as serum creatinine levels, whereas the proximal tubular function was investigated by measuring the urinary levels of both alpha1-microglobulin and beta2-microglobulin as well as retinol-binding protein. Also, distal tubular reabsorption capacity was investigated by assessing fractional excretion of sodium. Moreover, the structural integrity of renal proximal tubules was studied by measuring the urinary activities of both the brush-border membrane enzyme leucine-aminopeptidase (LAP) and the lysosomal enzyme N-acetyl-beta-D-glucosaminidase. The preceding investigations were done on both the first and third days of life of all 50 newborns.
Glomerular and tubular function and structure was relatively impaired at birth among both healthy and diseased preterm as well as healthy full-term neonates and improved rapidly thereafter. The diseased preterm neonates showed worse renal function and structure with minimal improvement regardless of the underlying sickness.
Renal insufficiency and renal immaturity could be evaluated using enzymuria and low- and high-molecular-weight proteinuria as noninvasive methods.
肾细胞在出生时并未完全分化,这是早产儿面临的主要风险。我们评估了健康足月儿、早产儿以及患病早产儿的肾小球和肾小管功能完整性以及肾小管的结构完整性。
本研究共纳入50名新生儿(分别为10名健康足月儿、10名健康早产儿和30名患病早产儿,胎龄分别为38.9±1.10周、34.2±0.92周和32±2.47周)。通过测量尿微量白蛋白和免疫球蛋白G水平以及血清肌酐水平来评估肾小球功能,而通过测量尿α1-微球蛋白、β2-微球蛋白以及视黄醇结合蛋白水平来研究近端肾小管功能。此外,通过评估钠的分数排泄来研究远端肾小管重吸收能力。而且,通过测量刷状缘膜酶亮氨酸氨肽酶(LAP)和溶酶体酶N-乙酰-β-D-氨基葡萄糖苷酶的尿活性来研究肾近端小管的结构完整性。上述所有检测均在50名新生儿出生后的第1天和第3天进行。
健康和患病的早产儿以及健康足月儿在出生时肾小球和肾小管的功能及结构均相对受损,此后迅速改善。患病早产儿的肾功能和结构较差,无论潜在疾病如何,改善都很有限。
可使用酶尿以及低分子量和高分子量蛋白尿作为非侵入性方法来评估肾功能不全和肾不成熟。