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Screening for Microalbuminuria: A comparison of single sample methods of collection and techniques of albumin analysis

  1. Steve J Schwab, MD,
  2. Fredrick L Dunn, MD and
  3. Mark N Feinglos
  1. Divisions of Nephrology and Metabolism, Endocrinology, and Nutrition, Department of Medicine, Duke University Medical Center Durham, North Carolina
  1. Address Correspondence and reprint requests to Steve J. Schwab, MD, P.O. Box 3014, Division of Nephrology, Duke University Medical Center, Durham, NC 27710.

Abstract

OBJECTIVE To evaluate single-sample urine collections to determine their ability to screen patients for the presence of microalbuminuria. Microalbuminuria in patients with type I diabetes predicts the development of diabetic renal disease.

RESEARCH DESIGN AND METHODS Cross-sectional analysis of single-sample urine collection techniques (first morning void, random upright void) and methods of albumin analysis (RIA, reagent tablet) were compared with conventional 24-h urine collections (RIA). The study included 94 patients (45 males, 49 females; mean serum creatinine 88 μM) with type I diabetes, selected from a screened population of 301 patients from the University Hospital Subspecialty Clinics.

RESULTS A 24-hour urine collection RIA analysis for albumin revealed 36 normal patients (< 30 mg), 27 with microalbuminuria (30–300 mg), and 31 with albuminuria (> 300 mg). Random upright urine samples were more sensitive (RIA 89%, tablets 78%) for the detection of microalbuminuria than first morning void specimens (RIA 70%, tablets 60%). Specificity was > 80% with both random and first morning voids.

CONCLUSIONS Screening for microalbuminuria can be performed in the clinic by random upright single-sample urine collections. When reagent tablets were used, these results are available immediately. Patients who screen positive should be confirmed by 24-h or other timed urine collections.

  • Received October 2, 1991.
  • Revision received June 18, 1992.
  • Accepted June 18, 1992.
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