May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Circulating Anti–Pericyte Autoantibodies: A Novel Modifier of Risk of Progression of Diabetic Retinopathy?
Author Affiliations & Notes
  • R.C. Nayak
    University of Lund, Lund, Sweden
  • K. Lynch
    University Hospital MAS, Malmö, Sweden
  • C. Gustavsson
    University Hospital MAS, Malmö, Sweden
  • P.J. Farthing–Nayak
    Ophthalmology, University of Arizona, Tucson, AZ
  • C.–D. Agardh
    University Hospital MAS, Malmö, Sweden
  • E. Agardh
    University Hospital MAS, Malmö, Sweden
  • Footnotes
    Commercial Relationships  R.C. Nayak, None; K. Lynch, None; C. Gustavsson, None; P.J. Farthing–Nayak, None; C. Agardh, None; E. Agardh, None.
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 3872. doi:
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    • Get Citation

      R.C. Nayak, K. Lynch, C. Gustavsson, P.J. Farthing–Nayak, C.–D. Agardh, E. Agardh; Circulating Anti–Pericyte Autoantibodies: A Novel Modifier of Risk of Progression of Diabetic Retinopathy? . Invest. Ophthalmol. Vis. Sci. 2006;47(13):3872.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Anti–pericyte autoantibodies (APAA) are present in high frequency among diabetic subjects with and without non–proliferative retinopathy. This study aimed to determine whether progression of retinopathy in type 2 diabetes was associated with the same medical risk factors in APAA positive as in APAA negative subjects.

Methods: : Type 2 diabetic patients with non–proliferative diabetic retinopathy at baseline were followed prospectively for two years monitoring progression of retinopathy. 38/175 (21.7%) patients showed progression in EDTRS grade by >2 steps in at least one eye. Serum APAAs were detected by immunofluorescence on tissue–cultured bovine retinal pericytes.

Results: : Progression of retinopathy was associated with HbA1c (p=0.002), diabetes duration (p=0.03), and albumin creatinine ratio (p=0.02) in APAA negative but not in APAA positive subjects. The association between progression and APAA was strongest in the upper quartile for HbA1c (>8.0%), where 71.4% of patients negative for APAA progressed in retinopathy while only 24.1% of patients positive for APAA progressed (p=0.007).

Conclusions: : The results suggest that APAA is a modifier of risk of progression of retinopathy due to hyperglycemia and that it could be useful as a biochemical marker of risk of progression of diabetic retinopathy in type 2 diabetic patients with poor metabolic control.

Keywords: diabetic retinopathy • clinical (human) or epidemiologic studies: outcomes/complications 
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