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http://www.lef.org/LEFCMS/aspx/PrintVersionMagic.aspx?CmsID=115172Emerging Options: Hormone Therapy
Research has shown that the hormone dehydroepiandrosterone, or DHEA, is abnormally low in patients with AMD (Bucolo 2005). DHEA also has been shown to protect the eyes against oxidative damage (Tamer 2007). Because the macula requires hormones to function, an emerging theory hypothesizes that low blood sex hormone levels cause the retinal macula to accumulate cholesterol in an attempt to produce its own hormones (Dzugan 2002). The accumulation of cholesterol in macula may lead to the production of pathologic drusen and subsequent macular degeneration. Inverse association of female hormone with neovascular AMD was observed with current and former use of hormone replacement therapy use among Caucasian and Latino women (Edwards 2010). Restoring optimal hormone balance with bioidentical hormones may be an effective new treatment for both men and women. Clinical studies are in process to test this hypothesis and possible hormonal treatment options.
Melatonin is a hormone and strong antioxidant that scavenges free radicals. Several studies have shown that many areas of the eye have melatonin receptors (Rastmanesh 2011, Lundmark 2006). Clinical study has shown that treatment with 3 mg of melatonin at bedtime in those with AMD prevented further vision loss (Yi 2005). In the study, 100 patients with dry or wet AMD received the nighttime dose. After six months, visual acuity had not diminished and the majority of patients had reduced pathologic macular changes upon examination.
Macular Pigments: Lutein, Zeaxanthin, and Meso-zeaxanthin.
The relation between the density of macular pigment and the onset of AMD is well established. The macular pigment is composed principally of three carotenoids: lutein, zeaxanthin, and meso-zeaxanthin. They represent roughly 36, 18, and 18% of the total carotenoid content of the retina. They are found within the macula and surrounding tissues, including blood vessels and capillaries which nourish the retina (Rapp 2000).
Lutein, zeaxanthin and meso-zeaxanthin ensure proper functioning of the macula by filtering out harmful ultraviolet light and by acting as antioxidants (Beatty 2000, Kaya 2010). During the aging process, there is a decrease in levels of lutein and zeaxanthin; low levels of macular pigments are linked to AMD (Johnson 2010). An autopsy study on donated eyes found that levels of all three carotenoids (lutein, zeaxanthin, and meso-zeaxanthin) were reduced in those with macular degeneration compared to control subjects. The most significant finding, however, was the sharp decrease in meso-zeaxanthin in the macula of macular degeneration subjects (Bone 2000). This postmortem study helped confirm other studies indicating the importance of all three carotenoids in maintaining the structural integrity of the macula (Krinsky 2003). These carotenoids protect the macula and the photoreceptor cells beneath via their antioxidant properties and light-filtering capabilities (Landrum 2001).