Lutein supplementation in retinitis pigmentosa: PC-based vision assessment in a randomized double-masked placebo-controlled clinical trial [NCT00029289]

Hossein Bahrami, Michele Melia, Gislin Dagnelie, Hossein Bahrami, Michele Melia, Gislin Dagnelie

Abstract

Background: There is no generally accepted medical or surgical treatment to stop the progressive course of retinitis pigmentosa. Previous studies have suggested lutein as a potential treatment with positive effects on macular pigment density. The objective of this study was to examine the effect of lutein supplementation on preservation of visual function in patients with retinitis pigmentosa (RP) METHODS: In a double-masked randomized placebo-controlled phase I/II clinical trial with a cross-over design, 34 adult patients with RP were randomized to two groups. One group, consisted of 16 participants, received lutein supplementation (10 mg/d for 12 wks followed by 30 mg/d) for the first 24 weeks and then placebo for the following 24 weeks, while the other group included 18 participants for whom placebo (24 weeks) was administered prior to lutein. Visual acuity, contrast sensitivity, and central visual field were measured at different illumination levels at baseline and every week using a PC-based test at home.

Results: For visual acuity (VA) at normal illumination level, treatment with lutein reduced logMAR, i.e. improved VA, but this effect was not statistically significant. The changes in normal (100%), low (4%), and very low (0.1%) illumination log CS were not statistically significant (p-values: 0.34, 0.23, and 0.32, respectively). Lutein had a statistically significant effect on visual field (p-value: 0.038) and this effect increased in the model assuming a 6-week delay in effect of lutein. Comparing the development of vision measures against the natural loss expected to occur over the course of 48 weeks, most measures showed reduced decline, and these reductions were significant for normal illumination VA and CS.

Conclusion: These results suggest that lutein supplementation improves visual field and also might improve visual acuity slightly, although these results should be interpreted cautiously. As a combined phase I and II clinical trial, this study demonstrated the efficacy and safety of lutein supplementation.

Trial registration: ClinicalTrials.gov NCT00029289.

Figures

Figure 1
Figure 1
Flow diagram of study participants.
Figure 2
Figure 2
Allocation of lutein supplementation and placebo in two groups during The Trial Note: All participants received multi-vitamin supplement beginning 4 weeks before and continuing throughout the study.
Figure 3
Figure 3
Changes of mean LogMAR and mean log CS at different illumination levels in Washout and Buildup groups. Note: Bars indicate 1.96*standard error
Figure 4
Figure 4
Changes of the visual field (mean log retinal area) at normal illumination level in Washout and Buildup groups. Note: Bars indicate 1.96*standard error

References

    1. Weleber RG, Gregory-Evans K. In: Retinitis pigmentosa and allied disorders. Ryan SJ, editor. Retina. Mosby, St. Louis; 2001. pp. 362–470.
    1. Grant CA, Berson EL. Treatable forms of retinitis pigmentosa associated with systemic neurological disorders. Int Ophthalmol Clin. 2001;41:103–10. doi: 10.1097/00004397-200101000-00010.
    1. Berson EL, Rosner B, Sandberg MA, Hayes KC, Nicholson BW, Weigel-DiFranco C, Willett W. A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa. Arch Ophthalmol. 1993;111:761–772.
    1. Massof RW, Finkelstein D. Supplemental vitamin A retards loss of ERG amplitude in retinitis pidmentosa. Arch Ophthalmol. 1993;111:751–4.
    1. Marmor MF. A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa. Arch Ophthalmol. 1993;11:1460–1.
    1. Clowes DD. A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa. Arch Ophthalmol. 1993;11:1461–2.
    1. Hoffman DR, Locke KG, Wheaton DH, Fish GE, Spencer R, Birch DG. A randomized, placebo-controlled clinical trial of docosahexaenoic acid supplementation for X-linked retinitis pigmentosa. Am J Ophthalmol. 2004;137:704–18. doi: 10.1016/S0002-9394(03)01408-9.
    1. Berson EL, Rosner B, Sandberg MA, Weigel-DiFranco C, Moser A, Brockhurst RJ, Hayes KC, Johnson CA, Anderson EJ, Gaudio AR, Willett WC, Schaefer EJ. Clinical trial of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment. Arch Ophthalmol. 2004;122:1297–305. doi: 10.1001/archopht.122.9.1297.
    1. Semba RD, Dagnelie G. Are lutein and zeaxanthin conditionally essential nutrients for eye health? Med Hypotheses. 2003;61:465–72. doi: 10.1016/S0306-9877(03)00198-1.
    1. Hammond BR, Jr, Johnson EJ, Russell RM, Krinsky NI, Yeum KJ, Edwards RB, Snodderly DM. Dietary modification of human macular pigment density. Invest Ophthalmol Vis Sci. 1997;38:1795–1801.
    1. Johnson EJ, Hammond BR, Yeum KJ, Qin J, Wang XD, Castaneda C, Snodderly DM, Russell RM. Relation among serum and tissue concentrations of lutein and zeaxanthin and macular pigment density. Am J Clin Nutr. 2000;71:1555–1562.
    1. Goldberg J, Flowerdew G, Smith E, Brody JA, Tso MO. Factors associated with age-related macular degeneration. An analysis of data from the first national health and nutrition examination survey. Am J Epidemiol. 1988;128:700–710.
    1. Eye Disease Case-Control Study Group Risk factors for neovascular age-related macular degeneration. Arch Ophthalmol. 1992;110:1701–1708.
    1. Eye Disease Case-Control Study Group Antioxidant status and neovascular age-related macular degeneration. Arch Ophthalmol. 1993;111:104–109.
    1. Landrum JT, Bone RA, Joa H, Kilburn MD, Moore LL, Sprague KE. A one year study of the macular pigment: the effect of 140 days of a lutein supplement. Exp Eye Res. 1997;65:57–62. doi: 10.1006/exer.1997.0309.
    1. Dagnelie G, Zorge IS, McDonald TM. Lutein improves visual function in some retinal degeneration patients – a pilot study via Internet. Optometry. 2000;71:147–64.
    1. Richer S. Part II. ARMD-pilot (case series) environmental intervention data. J Am Optom Assoc. 1999;70:24–36.
    1. Blumberg J, Block G. The Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study in Finland. Nutr Rev. 1994;52:242–245.
    1. Dagnelie G, Melia BM, Sunness JS. Lutein supplementation in RP: Vision measures in the clinic. Invest Ophthalmol Vis Sci. 2003:44. #780 [ARVO E-abstract]
    1. Dagnelie G. Conversion of planimetric visual field data into solid angles and retinal areas. Clin Vis Sci. 1990;5:95–100.
    1. Dagnelie G, Yang L, Bahrami H, et al. Vision tests for the home PC: Test validation and results from a lutein supplementation trial [Abstract] Journal of Vision. 2003;3:57a. doi:10.1167/3.12.57.
    1. Bach M. The Freiburg Visual Acuity test – Automatic measurement of visual acuity. Opt Vis Sci. 1996;73:49–53.
    1. Piantodosi S. Clinical Trials: A Methodologic Perspective. John Wiley & Sons, New York; 1997.
    1. Liang KY, Zeger SL. Longitudinal data analysis using generalized linear models. Biometrika. 1986;73:13–22. doi: 10.2307/2336267.
    1. Massof RW, Dagnelie G, Benzchawel T, Palmer RW, Fikelstein D. First order dynamics of visual field loss in retinitis pigmentosa. Clin Vision Sci. 1990;5:1–26.
    1. Berendschot TT, Goldbohm RA, Klopping WA, van de Kraats J, van Norel J, van Norren D. Influence of lutein supplementation on macular pigment, assessed with two objective techniques. Invest Ophthalmol Vis Sci. 2000;41:3322–6.
    1. Grover S, Fishman GA, Anderson RJ, Alexander KR, Derlacki DJ. Rate of visual field loss in retinitis pigmentosa. Ophthalmology. 1997;104:460–5.
    1. Grover S, Fishman GA, Anderson RJ, Tozatti MS, Heckenlively JR, Weleber RG, Edwards AO, Brown J., Jr Visual acuity impairment in Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older. Ophthalmology. 1999;106:1780–5. doi: 10.1016/S0161-6420(99)90342-1.
    1. Hammond BR, Jr, Wooten BR, Snodderly DM. Individual variations in the spatial profile of human macular pigment. J Opt Soc Am A Opt Image Sci Vis. 1997;14:1187–96.

Source: PubMed

3
S'abonner