TY - JOUR
T1 - Risk factors associated with reticular pseudodrusen versus large soft drusen
AU - Boddu, Sucharita
AU - Lee, Michele D.
AU - Marsiglia, Marcela
AU - Marmor, Michael
AU - Freund, K. Bailey
AU - Smith, R. Theodore
N1 - Funding Information:
Michele D. Lee, BA, is a fourth-year medical student at Columbia University College of Physicians and Surgeons and a recipient of a Medical Student Eye Research Fellowship through the Research to Prevent Blindness. She will be an ophthalmology resident at Stanford University Medical Center starting in 2015.
Funding Information:
All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Financial disclosures are as follows: K. Bailey Freund: Genentech, Inc (advisor); Regeneron Pharmaceuticals, Inc (advisor); Heidelberg Engineering (advisor); Optos plc (advisor); R. Theodore Smith: NIH/NEI (grant support); Research to Prevent Blindness (grant support); Foundation Fighting Blindness (grant support); Boehringer-Ingelheim (consultant). The research was supported by National Institutes of Health (NIH)/National Eye Institute (NEI) grant R01 EY015520 (R.T.S.), unrestricted funds from Research to Prevent Blindness (R.T.S.), an individual investigator research award from the Foundation Fighting Blindness (R.T.S.), and The Macula Foundation, Inc (K.B.F.). Contributions of authors: design of the study (R.T.S., K.B.F.); conduct of the study (R.T.S., K.B.F.); collection, management, analysis, and interpretation of the data (S.B., M.D.L., M.Marsiglia, M.Marmor, K.B.F., R.T.S.); and preparation, review, or approval of the manuscript (S.B., M.D.L., M.Marsiglia, M.Marmor, K.B.F., R.T.S.).
PY - 2014/5
Y1 - 2014/5
N2 - Purpose To investigate genetic, environmental, and systemic risk factors in prospectively identified subjects with the age-related macular degeneration (AMD) phenotypes of (1) reticular pseudodrusen without large soft drusen and (2) large soft drusen without reticular pseudodrusen. Design Prospective case-case comparison. Methods In a clinical practice setting, patients with AMD were sequentially screened using clinical examination and scanning laser ophthalmoscopy imaging to prospectively identify subjects (n = 73) with the phenotypes of (1) reticular pseudodrusen without large soft drusen (n = 30) or (2) large soft drusen without reticular pseudodrusen (n = 43). Subjects were genotyped for 2 alleles associated with AMD, age-related maculopathy susceptibility 2 (ARMS2) and complement factor H (CFH). A questionnaire was administered to collect history of smoking, hypertension, diabetes, and hyperlipidemia, as well as personal and family history of AMD. Results The reticular pseudodrusen group was older (median age 87 vs 81 years, P =.04) and had more female subjects (83.3% vs 48.8%, P =.003), later ages of AMD onset (83 vs 70 years, P =.0005), and a greater frequency of hypertension (76.7% vs 55.8%, P =.08). No significant differences were found in the distribution of the ARMS2 risk allele (P =.4) between the reticular pseudodrusen (homozygous = 20.0%; heterozygous = 56.7%) and large soft drusen (homozygous = 19.0%; heterozygous = 42.9%) phenotypes, or in the distribution of the CHF risk allele (P =.7) between the reticular pseudodrusen (homozygous = 26.7%; heterozygous = 56.7%) and large soft drusen (homozygous = 21.4%; heterozygous = 66.7%) phenotypes. Conclusions The reticular pseudodrusen phenotype was associated with increased age, later age of AMD onset, and female sex.
AB - Purpose To investigate genetic, environmental, and systemic risk factors in prospectively identified subjects with the age-related macular degeneration (AMD) phenotypes of (1) reticular pseudodrusen without large soft drusen and (2) large soft drusen without reticular pseudodrusen. Design Prospective case-case comparison. Methods In a clinical practice setting, patients with AMD were sequentially screened using clinical examination and scanning laser ophthalmoscopy imaging to prospectively identify subjects (n = 73) with the phenotypes of (1) reticular pseudodrusen without large soft drusen (n = 30) or (2) large soft drusen without reticular pseudodrusen (n = 43). Subjects were genotyped for 2 alleles associated with AMD, age-related maculopathy susceptibility 2 (ARMS2) and complement factor H (CFH). A questionnaire was administered to collect history of smoking, hypertension, diabetes, and hyperlipidemia, as well as personal and family history of AMD. Results The reticular pseudodrusen group was older (median age 87 vs 81 years, P =.04) and had more female subjects (83.3% vs 48.8%, P =.003), later ages of AMD onset (83 vs 70 years, P =.0005), and a greater frequency of hypertension (76.7% vs 55.8%, P =.08). No significant differences were found in the distribution of the ARMS2 risk allele (P =.4) between the reticular pseudodrusen (homozygous = 20.0%; heterozygous = 56.7%) and large soft drusen (homozygous = 19.0%; heterozygous = 42.9%) phenotypes, or in the distribution of the CHF risk allele (P =.7) between the reticular pseudodrusen (homozygous = 26.7%; heterozygous = 56.7%) and large soft drusen (homozygous = 21.4%; heterozygous = 66.7%) phenotypes. Conclusions The reticular pseudodrusen phenotype was associated with increased age, later age of AMD onset, and female sex.
UR - https://www.scopus.com/pages/publications/84898900798
U2 - 10.1016/j.ajo.2014.01.023
DO - 10.1016/j.ajo.2014.01.023
M3 - Article
C2 - 24491417
AN - SCOPUS:84898900798
SN - 0002-9394
VL - 157
SP - 985-993.e2
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
IS - 5
ER -