Advertisement

No Association of Antibodies to Glutamic Acid Decarboxylase and Diabetic Complications in Patients With IDDM

  1. Ursula Roll,
  2. Axel Nuber, MD,
  3. Anja Schröder,
  4. Evelin Gerlach, MD,
  5. Hans-U Janka, MD and
  6. Anette-G Ziegler, MD
  1. Diabetes Research Institute and Schwabing City Hospital Munich, Germany
  1. Address correspondence and reprint requests to Anette-G. Ziegler, MD, Diabetes Research Institute, Schwabing City Hospital, Koelner Platz 1, 80804 Munich, Germany.

Abstract

OBJECTIVE To evaluate the association of antibodies to glutamic acid decarboxylase (GAD-ab) and diabetic complications (neuropathy, retinopathy, and nephropa-thy) in patients with insulin-dependent diabetes mellitus (IDDM).

RESEARCH DESIGN AND METHODS We examined the prevalence of GAD-ab (immunoprecipitation assay) and islet cell antibodies (ICAs) (indirect immu-nofluorescence) in a representative sample of IDDM patients (n = 146) with different disease duration (2–52 years, median 13.2 years). Of all patients characterized for the existence of diabetic complications, 56 of 146 had peripheral neuropathy, 24 of 142 had autonomie neuropathy, 67 of 141 had retinopathy, and 39 of 146 had nephrop-athy.

RESULTS GAD-ab (>2 SD) were detected more frequently than ICA (>5 Juvenile Diabetes Foundation units) in IDDM patients of different disease duration (GAD-ab+ 37% [54 of 146] vs. ICA+ 22% [32 of 146], P = 0.011; diabetes duration less than median: GAD-ab+ 47% vs. ICA+ 23%, P = 0.0046; diabetes duration greater than median: GAD-ab+ 27% vs. ICA+ 22%, P < 0.05). For GAD-ab and for ICA, respectively, no difference was observed in frequency of positivity or titers between patients with or without diabetic complications.

CONCLUSIONS Both GAD-ab and, to a lesser extent, ICA persist for a long time in several individuals. This persistence is not related to diabetic neuropathy or any other diabetic complication.

  • Received December 20, 1993.
  • Revision received July 21, 1994.
  • Accepted July 21, 1994.
| Table of Contents
Advertisement