April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Racial Differences in the Diagnostic Value of IOP Asymmetry
Author Affiliations & Notes
  • Alice L Williams
    Wills Eye Institute, Philadelphia, PA
  • Benjamin Leiby
    Thomas Jefferson University, Philadelphia, PA
  • Cora Wright
    Temple University School of Medicine, Philadelphia, PA
  • Daniela M. de Barros
    Universidade Estadual Paulista, Campos Botucatu, Brazil
  • Iman Fahmy
    Research Institute of Ophthalmology, Cairo, Egypt
  • Suruchi Bhardwaj
    Temple University School of Medicine, Philadelphia, PA
  • Amitava Biswas
    Sunetra Family Eye Care Centre, Kolkata, India
  • Parul Ichhpujani
    Government Medical College and Hospital, Chandigarh, India
  • Jeffrey D Henderer
    Temple University School of Medicine, Philadelphia, PA
  • George L Spaeth
    Wills Eye Institute, Philadelphia, PA
  • Footnotes
    Commercial Relationships Alice Williams, None; Benjamin Leiby, None; Cora Wright, None; Daniela M. de Barros, None; Iman Fahmy, None; Suruchi Bhardwaj, None; Amitava Biswas, None; Parul Ichhpujani, None; Jeffrey Henderer, None; George Spaeth, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 137. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Alice L Williams, Benjamin Leiby, Cora Wright, Daniela M. de Barros, Iman Fahmy, Suruchi Bhardwaj, Amitava Biswas, Parul Ichhpujani, Jeffrey D Henderer, George L Spaeth; Racial Differences in the Diagnostic Value of IOP Asymmetry. Invest. Ophthalmol. Vis. Sci. 2014;55(13):137.

      Download citation file:


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

      ×
  • Supplements
Abstract
 
Purpose
 

We have previously demonstrated that there is a direct relationship between the amount of intraocular pressure (IOP) asymmetry and the probability of having glaucoma. The purpose of the present study is to determine if this relationship varies by race.

 
Methods
 

Collaborative retrospective study of 375 glaucoma patients and 375 controls matched for age, race and gender. The study group was composed of equal numbers of Asian, Black, European, Latino and North African patients. Former Wills Eye Hospital fellows collected single pre-treatment measurements of IOP on patients diagnosed as having definite glaucoma based on characteristic optic nerve damage and confirmatory visual field damage. Patients with a normal eye examination who had normal-appearing optic discs and no apparent glaucoma, or who had a normal eye examination in association with refractive error or cataract, were used as controls. A logistic regression analysis that jointly modeled all race groups was used to determine if the relationship between IOP asymmetry and glaucoma differed by race.

 
Results
 

IOP asymmetry was significantly associated with glaucoma status overall and in each race group (p<0.001). The probability of having glaucoma at a particular value of IOP asymmetry differed significantly by race (p = 0.012). These probabilities were noticeably higher for Blacks and Latinos and noticeably lower for Asians. AUC values were similar across race groups and ranged from 0.69 for Asians to 0.83 for Blacks, Europeans and Latinos. The sensitivity and specificity of an optimal cut point of IOP asymmetry in predicting glaucoma status was also calculated for each racial group (Table 1).

 
Conclusions
 

There is a direct relationship between the amount of IOP asymmetry and the probability of having glaucoma. The strength of this relationship varies by race. An IOP difference of 2 mmHg or more between the fellow eyes is a moderately specific indicator for glaucoma in Blacks, Europeans, and Latinos.

  
Keywords: 463 clinical (human) or epidemiologic studies: prevalence/incidence • 464 clinical (human) or epidemiologic studies: risk factor assessment  
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×