PLoS ONE (Jan 2014)

Increased risk of acute angle closure in retinitis pigmentosa: a population-based case-control study.

  • Yu-Chieh Ko,
  • Chia-Jen Liu,
  • De-Kuang Hwang,
  • Tzeng-Ji Chen,
  • Catherine J Liu

DOI
https://doi.org/10.1371/journal.pone.0107660
Journal volume & issue
Vol. 9, no. 9
p. e107660

Abstract

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PurposeTo investigate the association between retinitis pigmentosa (RP) and acute angle closure during a 15-year follow-up period.MethodsUsing the Taiwan Longitudinal Health Insurance Database 2000, we identified 382 RP patients based on the diagnostic code of RP (International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM) 362.74) made during 1996-2010, excluding subjects under age of 20 years at diagnosis or subjects undergoing lens extraction before the index date. The control group included 3820 randomly selected non-RP subjects matched with the RP patients in age, gender and the index date of diagnosis. The incidence of acute angle closure during the study period was observed based on an ICD-9-CM code of 365.22. Cochran-Mantel-Haenszel test was used to determine the odds ratio (OR) of having acute angle closure in RP patients.ResultsThe mean age at the diagnosis of RP was 51.1 years (standard deviation [SD] 16.7). Acute angle closure occurred in 5 RP patients (1.3%) and in 15 controls (0.4%). The mean age with the acute angle closure was 53.3 years (SD 8.0) in RP patients and 64.6 years (SD 8.4) in controls (P = 0.015). After adjusting for age, gender and comorbid disorders, RP patients had 3.64-fold (95% confidence interval [CI], 1.29-10.25, PConclusionsRP patients had increased risk of acute angle closure than controls. Contrary to the fact that angle closure disease is more prevalent in elderly females in general population, acute angle closure attack occurred earlier in life and the risk was higher in males among RP patients.