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Peripapillary chorioretinal atrophy (PPA) area and\n                      <jats:styled-content style=\"fixed-case\">PPA<\/jats:styled-content>\n                      superficial choroidal image intensity (\n                      <jats:styled-content style=\"fixed-case\">PPA<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      ) were calculated with\n                      <jats:sc>image j<\/jats:sc>\n                      software. Clinical characteristics, laser speckle flowgraphy\u2010measured mean blur rate in the temporal tissue area (temporal\n                      <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>\n                      ), the central thresholds (the averaged standard automated perimetry\u2010measured visual field thresholds in the four paracentral points) and 3D\u2010\n                      <jats:styled-content style=\"fixed-case\">OCT<\/jats:styled-content>\n                      \u2010measured ganglion cell complex thickness in the papillomacular bundle (\n                      <jats:styled-content style=\"fixed-case\">PMB<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">GCCT<\/jats:styled-content>\n                      ) were recorded.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The\n                      <jats:styled-content style=\"fixed-case\">NTG<\/jats:styled-content>\n                      patients had significantly lower intraocular pressure,\n                      <jats:styled-content style=\"fixed-case\">PMB<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">GCCT<\/jats:styled-content>\n                      and central threshold values, and a larger\n                      <jats:styled-content style=\"fixed-case\">PPA<\/jats:styled-content>\n                      area, than the controls. The area under the receiver operating characteristics curve to differentiate\n                      <jats:styled-content style=\"fixed-case\">NTG<\/jats:styled-content>\n                      with parafoveal scotoma (PFS) from controls was 0.76 for temporal\n                      <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>\n                      , 0.85 for\n                      <jats:styled-content style=\"fixed-case\">PPA<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      and 0.87 for\n                      <jats:styled-content style=\"fixed-case\">PMB<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">GCCT<\/jats:styled-content>\n                      . Univariate and multivariate analyses revealed that\n                      <jats:styled-content style=\"fixed-case\">PPA<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      was negatively correlated with age, pulse rate, best\u2010corrected visual acuity, axial length and\n                      <jats:styled-content style=\"fixed-case\">PPA<\/jats:styled-content>\n                      area, and positively correlated with temporal\n                      <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">PMB<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">GCCT<\/jats:styled-content>\n                      and the central thresholds.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Peripapillary chorioretinal atrophy (PPA)\u2010\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      was associated with temporal\n                      <jats:styled-content style=\"fixed-case\">MT<\/jats:styled-content>\n                      , ageing, bradycardia, axial length elongation and changes in central retinal structure and visual function in patients with\n                      <jats:styled-content style=\"fixed-case\">NTG<\/jats:styled-content>\n                      and myopic disc. Thus, microcirculation deep within the\n                      <jats:styled-content style=\"fixed-case\">PPA<\/jats:styled-content>\n                      zone might be a clinically useful biomarker of\n                      <jats:styled-content style=\"fixed-case\">PFS<\/jats:styled-content>\n                      in\n                      <jats:styled-content style=\"fixed-case\">NTG<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/aos.13621","type":"journal-article","created":{"date-parts":[[2017,11,24]],"date-time":"2017-11-24T07:56:42Z","timestamp":1511510202000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":30,"title":["Factors associated with deep circulation in the peripapillary chorioretinal atrophy zone in normal\u2010tension glaucoma with myopic 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