Summary
Aufgrund der pathogenetischen Vorstellungen über die Entstehung einer AMD (altersabhängige
Makuladegeneration) wird auf einer genetisch prädisponierenden Grundlage oxidativen
Prozessen in der Netzhaut und metabolischen Limitierungen im retinalen Pigmentepithel
eine wesentliche Rolle zugesprochen. In einer großen prospektiven klinischen Studie
(ARED-Study) wurde nach kombinierter Verabreichung von Vitamin C (550 mg), Vitamin
E (400 IU), β-Carotin (15 mg) sowie Zink (80 mg) und Kupfer (2 mg) ein protektiver
prophylaktischer Effekt auf die Progression der AMD und den Sehverlust bei Personen
mit bilateralen weichen Drusen bzw. einseitiger später AMD im Partnerauge nachgewiesen.
Über einen Zeitraum von fünf Jahren konnte das Risiko der Entstehung einer späten
AMD mit konsekutivem Sehverlust um ca. 25 % gesenkt werden.
Neben diesen Substanzen wird dem makulären Pigment (MP), bestehend aus Lutein und
Zeaxanthin, durch dessen filternden Effekt und die direkte antioxidative Wirkung eine
Schutzfunktion gegen oxidative Prozesse in der zentralen Netzhaut zugesprochen. So
wurden bei AMD-Patienten niedrige Konzentrationen an MP gefunden. Da Lutein und Zeaxanthin
nur über die Nahrung aufgenommen werden und durch eine entsprechende Ernährung oder
Supplementation eine Erhöhung der MP-Konzentration erreicht werden kann, wäre das
MP ein beeinflussbarer Risikofaktor für die Entstehung einer AMD. Dies muss in weiteren
Studien aber noch differenzierter bestätigt werden.
Summary
Next to genetic predisposition, oxidative damage in the retina and limitations of
the metabolism of the retinal pigment epithelium is believed to play a major role
in the pathogenesis of age-related macular degeneration (AMD). In a large prospective
randomized clinical intervention trial (ARED-Study) in patients with either bilateral
large drusen or fellow eyes in patients with unilateral late AMD, a protective effect
was observed by administration of a combination of vitamin C (500 mg), vitamin E (400
IU), β-carotene (15 mg), zinc (80 mg) and copper (2 mg) with regard to the progression
of the development of late AMD and future visual loss. The 5year risk of disease progression
could be decreased by 25 %. In addition to these antioxidative substances, macular
pigment (MP) consisting of lutein and zeaxanthin is suggested to have a potential
preventing role limiting the oxidative damage to the central retina by absorption
of blue light in the inner retina and by direct antioxidative properties in the outer
retina. Patients with early AMD were shown to have more often lower concentrations
of MP and, therefore, insufficient concentration of MP in the central retina may be
an important but modifiable risk factor for AMD. Lutein and zeaxanthin are normally
supplied only by dietary intake. Therefore, increase of its concentration in the retina
by special dietary regimens, but also by supplementation, may be a worthwhile approach.
But, before supplementation can be recommended, replication of these results in further
clinical studies seems necessary.
Schlüsselwörte
AMD - Makuladegeneration - makuläres Pigment - Antioxidantien - Spurenelemente - Risikofaktoren
Key words
Eye - macular degeneration - macular pigment - antioxidants - trace elements - lutein
- zeaxanthin
Literatur
- 1
Age-Related Eye Disease Study Research Group .
A randomized, placebo-controlled, clinical trial of high-dose supplementation with
vitamins C and E, beta-arotene, and zinc for age-related macular degeneration and
vision loss.
Arch Ophthalmol.
2001;
119
1417-1436
- 2
Albanes D, Heinonen OP, Taylor PR. et al. .
Alpha-tocopherol and beta-carotene supplements and lung cancer incidence in the Alpha-Tocopherol
Beta-Carotene Prevention Study: Effects of base-line characteristics and study compliance.
J Natl Cancer Inst.
1996;
88
1560-1570
- 3
Augustin AJ, Dick HB, Winkgen A, Schmidt-Erfurth U.
Ursache und Prävention oxidativer Schäden des Auges.
Ophthalmologe.
2001;
98
776-797
- 4
Beatty S, Boulton M, Henson D, Koh HH, Murray IJ.
Macular pigment and age-related macular degeneration.
Br J Ophthalmol.
1999;
83
867-877
- 5
Beatty S, Koh H-H, Henson D, Boulton ME.
The role of oxidative stress in the pathogenesis of age-related macular degeneration.
Surv. Ophthalmol.
2000;
45
115-134
- 6
Berenschot TT, Goldbohm RA, Klopping WA. et al. .
Influence of lutein supplementation on macular pigmemt, assessed with two objective
methods.
Invest Ophthalmol Vis Sci.
2000;
41
3322-3326
- 7
Bird AC.
Age-related macular disease.
Br J Ophthalmol.
1996;
80
1-2
- 8
Eye Disease Case-Control Study Group .
Antioxidant status and neovascular age-related macular degeneration.
Arch Ophthalmol.
1993;
111
104-109
- 9
Gale CR, Hall NF, Phillips DI, Martyn CN.
Plasma antioxidant vitamins and carotenoids and age-related cataract.
Ophthalmology.
2001;
108
1992-1998
- 10
Hammond BR, Johnson EJ, Russel RM. et al. .
Dietary modification of human macular pigment density.
Invest Ophthalmol Vis Sci.
1997;
38
1795-1801
- 11
Handelman GJ, Nightingale ZD, Lichtenstein AH, Schaefer EJ, Blumberg JB.
Lutein and zeaxanthin concentrations in plasma after dietary supplementation with
egg yolk.
Am J Clin Nutr.
1999;
70
247-251
- 12
Hayes KC.
Pathophysiology of vitamin E defiency in monkeys.
Am J Clin Nutr.
1974;
27
1130-1140
- 13
Holz FG, Pauleikhoff D.
Altersabhängige Makuladegeneration.
Springer-Verlag; Heidelberg, Berlin, New York.
1997;
- 14
Landrum JT, Bone RA, Joa H. et al. .
A one year study of the macular pigment: the effect of 140 days of lutein supplement.
Exp Eye Res.
1997;
65
57-62
- 15
Li ZY, Tso MO, Wang HM, Organisciak DT.
Amelioration of photic injury in rat retina by ascorbic acid: a histopathologic study.
Invest Ophthalmol Vis Sci.
1985;
26
1589-1598
- 16
Omenn GS, Goodman GE, Thornquist MD. et al. .
Effects of a combination of beta-carotene and vitamin A on lung cancer and cardiovascular
disease.
N Engl J Med.
1996;
334
1150-1155
- 17
Organisciak DT, Wang HM, Li ZY, Tso MO.
The protective effect of ascorbate in retinal light damage of rats.
Invest Ophthalmol Vis Sci.
1985;
26
1580-1588
- 18
Schütt F, Davies S, Kopitz J, Holz FG, Boulton ME.
Photodamage to human RPE cells by A2-E, a retinoid component of lipofuscin.
Invest Ophthalmol Vis Sci.
2000;
41
2303-2308
- 19
Sommerburg O, Keunen JEE, Bird AC, van Kuijk FJGM.
Fruits and vegetables that are sources for lutein and zeaxanthin: the macular pigment
in human eyes.
Br J Ophthalmol.
1998;
82
907-910
Prof. Dr. Daniel Pauleikhoff
Augenabteilung des St. Franziskus Hospitals
Hohenzollernring 74
D-48145 Münster
eMail: dapauleikhoff@muenster.de