June 2015
Volume 56, Issue 7
Free
ARVO Annual Meeting Abstract  |   June 2015
Inverse relationship between blood 25-hydroxyvitamin D and age related macular degeneration.
Author Affiliations & Notes
  • Sung Pyo Park
    Hallym University Medical Center, KangDong Sacred Heart Hospital, Seoul, Korea (the Republic of)
  • Won Tae Yoon
    Hallym University Medical Center, KangDong Sacred Heart Hospital, Seoul, Korea (the Republic of)
  • Kyoung Lae Kim
    Hallym University Medical Center, KangDong Sacred Heart Hospital, Seoul, Korea (the Republic of)
  • Footnotes
    Commercial Relationships Sung Pyo Park, None; Won Tae Yoon, None; Kyoung Lae Kim, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2015, Vol.56, 3764. doi:
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      Sung Pyo Park, Won Tae Yoon, Kyoung Lae Kim; Inverse relationship between blood 25-hydroxyvitamin D and age related macular degeneration.. Invest. Ophthalmol. Vis. Sci. 2015;56(7 ):3764.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: Inflammation had been found to play an underlying role in age related macular degeneration (AMD). Vitamin D, a circulating steroid hormone, has properties that counteract inflammation. We aimed to determine the association between the blood 25-hydroxyvitamin D and age related macular degeneration.

Methods: We selected the 25 patients of each groups. The each groups were composed by patients with wet AMD, dry AMD and without any macular degeneration. The patients were not had any cardiovascular diseases which were included in hypertension and diabetes mellitus. We excluded the patients with vitamin D supplement. We sampled the 25-hydroxyvitamin D from blood of the patients at the same day. Every patients were filled in the questionnaire which was about smoking status, height, weight, exposure time at the sunlight, wear of sunglass during outing.

Results: The blood 25-hydroxyvitamin D was statistically lower in patients with dry and wet AMD (21.96ng/mL, 14.30ng/mL : p < 0.001, p < 0.001) which was compared the patients with no macular degeneration. (28.89ng/mL) The blood 25-hydroxyvitamin D was statistically lower in patients with wet AMD (14.30ng/mL : p < 0.001) which was compared the patients with dry AMD. (21.96ng/mL)

Conclusions: The blood 25-hydroxyvitamin D level was inversely associated with dry and wet AMD which was compared of the patients without any macular degeneration. Further research will be needed to reveal the biological mechanism which was about correlation of the vitamin D and AMD.

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