TY - JOUR
T1 - Prevalence of vitreomacular adhesion in patients without maculopathy older than 40 years
AU - VAST STUDY GROUP
AU - Rodman, Julie A.
AU - Shechtman, Diana
AU - Sutton, Brad M.
AU - Pizzimenti, Joseph J.
AU - Bittner, Ava K.
AU - Wals, Ken
AU - Tolentino, Mike
AU - Ficco, Charlie
AU - Smik, Kirk
AU - Perez, Marisa
AU - Gerson, Jeffry
AU - Gold, Aaron
AU - Murray, Tim
AU - Jones, William
AU - Crandall, Melanie
AU - Demeritt, Marlon
AU - Jarkas, May
AU - Makhlouf, Rim
AU - Reynolds, Sherrol
AU - Tyler, Julie
AU - Vollmer, Lori
AU - Alex, Larry
AU - Lonsberry, Blair
AU - Haynie, Jay
AU - Sheinbaum, Gary
AU - Levy, Jay
AU - Lara, Wilfredo
AU - Schaeffer, Jack
AU - Schaeffer, Mark
AU - Bloomenstein, Marc
AU - Ferrucci, Steven
AU - Chous, Paul
AU - Semes, Leo
N1 - Publisher Copyright:
© 2018 Lippincott Williams and Wilkins. All rights reserved.
PY - 2018/10
Y1 - 2018/10
N2 - PURPOSE: To determine the prevalence and factors influencing vitreomacular adhesion (VMA) or vitreomacular traction (VMT) in subjects without maculopathy older than age 40 years.METHODS: In a prospective cross-sectional study, 1,950 eyes in 1,090 participants aged 40 to 89 years representing various ethnic groups from 14 centers in the United States underwent a comprehensive eye examination, including spectral domain optical coherence tomography. A team of independent, masked readers classified the presence or absence of VMA/VMT on spectral domain optical coherence tomography based on the International Vitreomacular Traction Study Group rubric.RESULTS: Across all eyes, the prevalence of VMA or VMT was 39% or 1%, respectively. For every 1-year increase in age, there was a statistically significant 7% decreased odds of having VMA or VMT (95% confidence interval [CI]: 0.89-0.96; P < 0.001), whereas African Americans had 55% significantly reduced odds of having VMA or VMT when than whites (95% CI: 0.23-0.90; P = 0.025). Vitreomacular adhesion >1,500 μm was significantly more likely than VMA <1,500 μm in younger adults (95% CI: 0.70-0.86; P < 0.001), hyperopes versus emmetropes (95% CI: 1.49-35.9; P = 0.01), primary eye care versus tertiary practices (95% CI: 0.03-0.92; P = 0.04), and patients without hyperlipidemia (95% CI: 0.04-0.83; P = 0.03).CONCLUSION: Vitreomacular adhesion is highly prevalent among middle-aged adults. Diagnostic screening with spectral domain optical coherence tomography may help to accurately detect VMA or VMT, prompting routine monitoring and timely therapeutic intervention.
AB - PURPOSE: To determine the prevalence and factors influencing vitreomacular adhesion (VMA) or vitreomacular traction (VMT) in subjects without maculopathy older than age 40 years.METHODS: In a prospective cross-sectional study, 1,950 eyes in 1,090 participants aged 40 to 89 years representing various ethnic groups from 14 centers in the United States underwent a comprehensive eye examination, including spectral domain optical coherence tomography. A team of independent, masked readers classified the presence or absence of VMA/VMT on spectral domain optical coherence tomography based on the International Vitreomacular Traction Study Group rubric.RESULTS: Across all eyes, the prevalence of VMA or VMT was 39% or 1%, respectively. For every 1-year increase in age, there was a statistically significant 7% decreased odds of having VMA or VMT (95% confidence interval [CI]: 0.89-0.96; P < 0.001), whereas African Americans had 55% significantly reduced odds of having VMA or VMT when than whites (95% CI: 0.23-0.90; P = 0.025). Vitreomacular adhesion >1,500 μm was significantly more likely than VMA <1,500 μm in younger adults (95% CI: 0.70-0.86; P < 0.001), hyperopes versus emmetropes (95% CI: 1.49-35.9; P = 0.01), primary eye care versus tertiary practices (95% CI: 0.03-0.92; P = 0.04), and patients without hyperlipidemia (95% CI: 0.04-0.83; P = 0.03).CONCLUSION: Vitreomacular adhesion is highly prevalent among middle-aged adults. Diagnostic screening with spectral domain optical coherence tomography may help to accurately detect VMA or VMT, prompting routine monitoring and timely therapeutic intervention.
KW - Optical coherence tomography
KW - Vitreomacular adhesion
KW - Vitreomacular traction
UR - https://www.scopus.com/pages/publications/85063043275
UR - https://www.scopus.com/pages/publications/85063043275#tab=citedBy
U2 - 10.1097/IAE.0000000000001792
DO - 10.1097/IAE.0000000000001792
M3 - Article
C2 - 28806215
AN - SCOPUS:85063043275
SN - 0275-004X
VL - 38
SP - 2056
EP - 2063
JO - Retina
JF - Retina
IS - 10
ER -