Objective To assess the change of central corneal thickness (CCT) and corneal endothelium morphology in diabetes mellitus compared with age-matched, healthy control subjects and to test their correlation according to the duration of diabetes. Methods Ultrasound tachymetry and noncontact specular microscopy were performed on 120 patients with diabetes diagnosed by endocrinologists and on 60 control subjects. We compared the values for diabetics and normal persons with ANACOVA to adjust for age. Moreover, we also evaluated the correlation between corneal factors in diabetes and the duration of diabetes using a partial correlation coefficient controlled for age. Results The diabetic subjects had thicker corneas, less cell density and percentage of hexagonal cells,and more irregular cell size of the corneal endothelium than did the controls (P<0.05). Central corneal thickness and the coefficient of variation for cell size significantly increased for diabetes of over 10 years’ duration compared with diabetes of under 10 years’ duration (P<0.05). The endothelial cell density and percentage of hexagonal cells were lower for diabetes of over 10 years’ duration than for diabetes of under 10 years’duration, but not significantly different (P>0.05). Conclusions The central corneal thickness is significantly correlated with the duration of diabetic mellitus after controlling for age.
Key words
diabetes mellitus /
endothelium /
corneal thickness
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
References
[1] Wei Lichen,Chung Tienlin,Horn Feilo,et al.The role of protein tyrosine phosphorylation in the cell-cell interactions,junctional permeability and cell cycle control in post-confluent bovine corneal endothelial cells[J]. Experimental Eye Research, 2007,85(2):259-269.
[2] Rumble J R , Cooper M E , S oulis T, et al. Vascular hypertrophy in experimental diabetes. Rde of advanced glycaton end products [J]. J Clin Invest, 1997,99 (5): 1106-1127.
[3] McCaleb M L , McKean M L , Hohman T C , et al . Intervention with the aldose reductase inhibitor, tolrestat, in renal and retinal lesions of streptozotocin - diabetic rats [J]. Diabetologia,1991,34(10): 695-701.
[4] Aiello L P , Bursell S E , Clermont A , et al . Vascular endothelial growth factor - induced retinal permeability is mediated by protein kinase C in vivo and suppressed by an orally effective beta - is oform - selective inhibitor [J]. Diabetes, 1997,46(9):1473-1480.
[5] 王 惕,韩丽荣,崔贞福,等.高糖对兔角膜内皮细胞的形态学影响[J].中国实用眼科杂志,2001,19(1):14-16.
[6] Kim J, Kim C S, Sohn E,et al. Involvement of advanced glycation end products ,oxidative stress and nuclear factor-kappaB in the development of diabetic keratopathy [J]. Graefes Arch Clin Exp Ophthalmol,2011,249(4):529-536.
[7] Leem H S, Lee K J, Shin K C. Central corneal thickness and corneal endothelial cell changes caused by contact lens use in diabetic patients[J].Yonsei Med J,2011,52(2):322-325.
[8] Mathew P T, David S, Thomas N. Endothelial cell loss and central corneal thickness in patients with and without diabetes after manual small incision cataract surgery [J]. Cornea,2011,30(4):424-428.
(2012-07-02