Risk factors for development and progression of diabetic retinopathy in Dutch patients with type 1 diabetes mellitus

Abstract Purpose To investigate risk factors for the development and progression of diabetic retinopathy ( DR ) and long‐term visual outcomes in Dutch patients with type 1 diabetes mellitus (T1 DM ). Methods Cumulative incidences were calculated for DR , vision‐threatening DR ( VTDR ), defined as (pre)proliferative DR and diabetic macular oedema, and best‐corrected visual acuity ( BCVA ) <0.5 and <0.3 at the most recent eye examination. The following factors were assessed: duration of diabetes, age of onset of T1 DM , gender, mean HbA1c, HbA1c variability (defined as coefficient of varia... Mehr ...

Verfasser: Schreur, Vivian
van Asten, Freekje
Ng, Heijan
Weeda, Jack
Groenewoud, Joannes M.M.
Tack, Cees J.
Hoyng, Carel B.
de Jong, Eiko K.
Klaver, Caroline C.W.
Jeroen Klevering, B.
Dokumenttyp: Artikel
Erscheinungsdatum: 2018
Reihe/Periodikum: Acta Ophthalmologica ; volume 96, issue 5, page 459-464 ; ISSN 1755-375X 1755-3768
Verlag/Hrsg.: Wiley
Schlagwörter: Ophthalmology / General Medicine
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26690620
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://dx.doi.org/10.1111/aos.13815

Abstract Purpose To investigate risk factors for the development and progression of diabetic retinopathy ( DR ) and long‐term visual outcomes in Dutch patients with type 1 diabetes mellitus (T1 DM ). Methods Cumulative incidences were calculated for DR , vision‐threatening DR ( VTDR ), defined as (pre)proliferative DR and diabetic macular oedema, and best‐corrected visual acuity ( BCVA ) <0.5 and <0.3 at the most recent eye examination. The following factors were assessed: duration of diabetes, age of onset of T1 DM , gender, mean HbA1c, HbA1c variability (defined as coefficient of variation of five separate HbA1c measurements), mean arterial blood pressure, body mass index, albuminuria and lipid profile. We used multivariable Cox regression models to identify factors associated with DR development and progression to VTDR . Results We found 25‐year cumulative incidences of 63% for DR , 21% for VTDR , 2% for BCVA <0.5, and 1% for BCVA <0.3. Mean HbA1c ( HR 1.023, p < 0.001), HbA1c variability ( HR 1.054, p < 0.001), age of onset of T1 DM ( HR 1.024, p < 0.001), HDL cholesterol ( HR 0.502, p = 0.002) and total cholesterol ( HR 1.210, p = 0.029) showed an independent association with faster development of any form of DR . The mean HbA1c ( HR 1.023, p < 0.001) and the presence of albuminuria ( HR 2.940, p = 0.028) were associated with faster progression to VTDR . Conclusion These data show relatively low cumulative incidences of DR , VTDR and visual impairment. Higher mean HbA1c, HbA1c variability, age of onset of T1 DM and total cholesterol were independently associated with the risk of DR development, and a protective association was found for HDL cholesterol in subjects with T1 DM . Mean HbA1c and presence of albuminuria were associated with progression of DR .