Our goal is to understand chronic blepharitis, the role of the meibomian gland in blepharitis and the effect of meibomian gland loss on the dynamics of ocular evaporation. Our hypothesis is that meibomian gland loss, which occurs in some forms of chronic blepharitis, leads to altered meibomian gland function, increased evaporation from the ocular surface, and increased tear osmolarity. By careful analysis of the data obtained on these blepharitis patients, we also hope to achieve a better under- standing of the characteristics of the blepharitis subsets and of the interrelationship between meibomian gland function (gland dropout, volume and viscosity) and the evaporative state (tear evaporation, osmolarity, and tear flow). To achieve these goals we will test our hypothesis by the following specific aims: 1) We will establish the range of normal meibomian gland function on the evaporative state of the eye for 150 patients over a rang in ages. We will measure five quantitative variables: meibomian gland dropout, evaporation rate, tear osmolarity, and tear flow by fluoropho- tometry, and two qualitative variables: excreta volume and viscosity. 2) We will establish the range of meibomian gland function in 150 patients with chronic blepharitis measuring the same variables and using the same age and sex distribution. 3) We will determine the correlation between evaporation rate and gland dropout, tear osmolarity, tear flow and excre- ta volume and viscosity in these 150 chronic blepharitis patients using the data collected above. 4) We will investigate the effect of induced meibomian gland dysfunction resulting from systemic Isotretinoin (accu- tane) on tear evaporation, osmolarity, and tear flow before, during and after treatment in 30 patients by measuring these same variables. 5) We will use our data to characterize better the subsets which comprise ble- pharitis by applying cluster analysis to the large data base collected from these 150 patients with blepharitis.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY010151-03
Application #
2163864
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1992-09-30
Project End
1995-09-29
Budget Start
1994-09-30
Budget End
1995-09-29
Support Year
3
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Iowa
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
041294109
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Mathers, W D; Lane, J A (1998) Meibomian gland lipids, evaporation, and tear film stability. Adv Exp Med Biol 438:349-60
Mathers, W D; Stovall, D; Lane, J A et al. (1998) Menopause and tear function: the influence of prolactin and sex hormones on human tear production. Cornea 17:353-8
Winchester, K; Mathers, W D; Sutphin, J E (1997) Diagnosis of Aspergillus keratitis in vivo with confocal microscopy. Cornea 16:27-31
Mathers, W D; Lane, J A; Zimmerman, M B (1997) Assessment of the tear film with tandem scanning confocal microscopy. Cornea 16:162-8
Mathers, W D; Goldberg, M A; Sutphin, J E et al. (1997) Coexistent Acanthamoeba keratitis and herpetic keratitis. Arch Ophthalmol 115:714-8
Mathers, W D; Daley, T E (1996) Tear flow and evaporation in patients with and without dry eye. Ophthalmology 103:664-9
Mathers, W D; Lane, J A; Sutphin, J E et al. (1996) Model for ocular tear film function. Cornea 15:110-9
Mathers, W D; Lane, J A; Zimmerman, M B (1996) Tear film changes associated with normal aging. Cornea 15:229-34
Goodman, W T; Mathers, W D; Munden, P M et al. (1996) A study of aqueous humor dynamics in keratoconus. Exp Eye Res 62:95-9
Mathers, W D; Daley, T E (1994) In vivo observation of the human tear film by tandem scanning confocal microscopy. Scanning 16:316-9