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Journal List > J Korean Ophthalmol Soc > v.48(12) > 1007986

Moon, Song, Koo, Cho, and Yu: Short-term Effects and Side Effects of Tacrolimus for Behçet's Uveitis

Abstract

Purpose

To investigate the clinical effects and side effects of Tacrolimus for ocular Behçet's disease.

Methods

Eight patients (male: 5, age: 35±7.5 (25-48) years) with Behçet's uveitis, refractory posterior uveitis unresponsive to combination treatment with cyclosporine, azathioprine, and oral steroid or significant cyclosporine-related adverse effects were recruited prospectively, and cyclosporine was switched to Tacrolimus. Visual acuity, degree of anterior chamber, and vitreous haze were compared before the conversion and three months after. Oral glucose tolerance, plasma insulin, cholesterol, creatinine, and aspartate (AST)/alanine aminotransferase (ALT) were measured to monitor systemic effects.

Results

Visual acuity did not change significantly after conversion to Tacrolimus. Anterior chamber (seven patients) and vitreous (four patients) inflammation were found before conversion and decreased or disappeared after conversion. Overall plasma levels of glucose, insulin, creatinine, and AST/ALT were similar before and after conversion. However, cholesterol was significantly decreased after conversion (p=0.028). One patient developed diabetes mellitus.

Conclusions

Tacrolimus may be effective for Behçet's uveitis unresponsive to or intolerable of traditional treatments. In addition, periodic monitoring for side effects, such as hyperglycemia and diabetes mellitus, may be necessary.

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jkos-48-1654f1.tif
Figure 1.
Comparison of plasma glucose concentrations (oral glucose tolerance test) before and 3 months after conversion from cyclosporine to Tacrolimus. No significant differences are found at all points.
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jkos-48-1654f2.tif
Figure 2.
Comparison of plasma insulin concentrations during oral glucose tolerance test before and 3 months after conversion from cyclosporine to Tacrolimus. No significant differences are found at all points.
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Table 1.
Patient data
  Sex Age Baseline VA (R/L) Reasons for vonversion from cyclosporine to tacrolimus previous systemic medication
1 F 38 0.04/FC osteopenia, nausea, vomiting PD 10 mg gd
AZA 100 mg bid
CSA 100 mg bid
2 M 27 0.4/0.4 hypertension PD 10 mg gd
AZA 100 mg bid
CSA 100 mg bid
3 F 30 1.2/0.3 refractory uveitis PD 10 mg gd
AZA 100 mg bid
CSA 100 mg bid
4 M 25 0.06/0.02 refractory uveitis PD 10 mg gd
AZA 100 mg bid
CSA 100 mg bid
5 M 39 HM/0.2 burning sensation PD 10 mg gd
AZA 100 mg bid
CSA 50 mg bid
6 F 37 0.3/HM refractory retinal vasculitis AZA 100 mg bid
CSA 100 mg bid
7 M 48 HM/0.1 refractory uveitis PD 15 mg gd
AZA 100 mg bid
CSA 100 mg bid
8 M 38 0.3/0.5 facial swelling PD 30 mg gd
AZA 100 mg bid
CSA 100 mg bid

FC: finger count, HM: hand motion, PD: prednisone, AZA: azathioprine, CSA: cyclosporine.

Table 2.
Results of treatment
    VA Inflammatory activity TDM Tacrolimus adverse effects
pre post anterior chamber Viterous 1 Mo 3 Mo  
pre post pre post  
1 R 0.04 0.04 +3 0 0 0 3.2 4.5 Diabetes mellitus
L FC FC 0 0 0 0
2 R 0.4 0.4 0 0 0 0 5.6 6.8
L 0.4 0.4 0 0 0 0
3 R 1.2 1.2 +1/2 0 +1/2 0 4.5 4.9 Gastric soreness
L 0.3 0.4 +1 0 +2 + 1/2
4 R 0.06 0.04 +2 0 +2 + 1/2 1.2 1.7 Polyuria
L 0.02 0.04 +1/2 0 0 0
5 R HM HM 0 0 0 0 6.1 1.5
L 0.2 0.08 +0.5 0 0 0
6 R 0.3 0.3 0 0 +1 0 7.3 5.5
L HM HM +1/2 0 +2 1
7 R HM FC +1 +1 +1/2 + 1/2 6.2 6.7 Facial flush
L 0.1 0.15 0 + 1/2 +2 + 1/2
8 R 0.3 0.4 +2 +1 0 0 8.1 6.2
L 0.5 0.5 +1 + 1/2 0 0

VA=visual acuity; TDM=therapeutic drug monitoring; R=right eye; L=left eye; FC=finger counting; HM=hand motion.

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