Original article
Ischemic Diabetic Retinopathy May Protect against Nuclear Sclerotic Cataract

https://doi.org/10.1016/j.ajo.2010.05.013Get rights and content

Purpose

To determine whether diabetes mellitus is protective for nuclear sclerotic cataract at baseline and 6 and 12 months after vitrectomy surgery.

Design

Prospective, interventional cohort study.

Methods

Phakic diabetic and nondiabetic patients undergoing vitrectomy surgery for a variety of retinal conditions underwent Scheimpflug lens photography in the operated and fellow eye at baseline and at 6 and 12 months after vitrectomy surgery.

Results

Of 52 eyes included in the analysis, 23 eyes were from diabetic patients, 14 of which had surgery for ischemic retinopathy. At baseline, eyes with ischemic diabetic retinopathy had less nuclear sclerotic cataract than nonischemic diabetic and nondiabetic eyes. This was true for eyes undergoing vitrectomy surgery (P = .0001) and for fellow eyes (P = .003). Nuclear sclerotic cataract developed after vitrectomy surgery in nonischemic diabetic eyes and nondiabetic eyes at the same rate. Diabetic eyes with ischemic retinopathy showed no significant progression of nuclear opacification, and therefore had significantly less postvitrectomy nuclear cataract at 6 months (P < 1 × 10−6) and at 12 months (P < .001) than nondiabetic or nonischemic diabetic eyes. Normalizing to baseline opacity and adjusting for age and other comorbidities did not alter this result.

Conclusions

Ischemic diabetic retinopathy, not just systemic diabetes mellitus, protected against nuclear sclerotic cataract at baseline and after vitrectomy surgery. These findings are consistent with the hypothesis that increased exposure to oxygen is responsible for nuclear cataract formation.

Section snippets

Methods

In a single academic-based retina practice, patients who were undergoing vitreous surgery for a variety of retinal conditions were asked to participate in the research study. Inclusion criteria were age 51 to 80 years, ability to provide informed consent, better than hand movement vision in the fellow eye, and willingness to be followed up for 1 year. Exclusion criteria were prior cataract surgery, history of traumatic cataract, and prior vitrectomy surgery. Informed consent was obtained by the

Results

Fifty-two patients were enrolled. Three patients were excluded from the analysis because of lens trauma during surgery, poor cooperation with lens photography, or vasculopathy not related to diabetes. For 46 patients, 1 eye was included in the study. For 3 patients, both eyes were included in the study. Therefore, 52 eyes were included in the final analysis. Table 1 shows the retinal diagnoses for the eyes that were included in the study. There were 23 eyes from diabetic patients. Among them,

Discussion

It is well established that vitrectomy surgery causes an acceleration of nuclear sclerotic cataract formation. In fact, within 2 years of vitrectomy surgery, postvitrectomy nuclear sclerosis requiring cataract surgery will develop in 60% to 98% of eyes.14, 15, 16, 17, 18 It has been suggested that the presence of systemic diabetes mellitus may protect against the development of postvitrectomy nuclear cataract.9 The present study suggests that, by itself, systemic diabetes mellitus does not

Nancy Melberg Holekamp, MD, is a Professor of Clinical Ophthalmology and Visual Sciences at the Washington University School of Medicine in St. Louis, Missouri. She is also a partner in the Barnes Retina Institute. Dr. Holekamp is actively involved in clinical research, having been principal investigator or sub-investigator in more than 15 national clinical trials dealing with age-related macular degeneration, retinal vascular occlusion, and diabetic retinopathy. Her efforts in research have

References (21)

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Nancy Melberg Holekamp, MD, is a Professor of Clinical Ophthalmology and Visual Sciences at the Washington University School of Medicine in St. Louis, Missouri. She is also a partner in the Barnes Retina Institute. Dr. Holekamp is actively involved in clinical research, having been principal investigator or sub-investigator in more than 15 national clinical trials dealing with age-related macular degeneration, retinal vascular occlusion, and diabetic retinopathy. Her efforts in research have resulted in more than 55 peer-reviewed publications, more than 15 book chapters, and numerous speaking invitations both nationally and internationally. She is a member of the major subspecialty societies, including the Retina Society and the Macula Society. She acts as a reviewer for all the major ophthalmology journals and as a consultant to two ophthalmic pharmaceutical companies. After 6 years on the American Academy of Ophthalmology Ethics Committee, she has developed an interested in medical ethics.

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