PMID- 35513898 OWN - NLM STAT- MEDLINE DCOM- 20220630 LR - 20230912 IS - 1536-481X (Electronic) IS - 1057-0829 (Print) IS - 1057-0829 (Linking) VI - 31 IP - 7 DP - 2022 Jul 1 TI - Association Between Serum Vitamin D Level and Rates of Structural and Functional Glaucomatous Progression. PG - 614-621 LID - 10.1097/IJG.0000000000002046 [doi] AB - PRCIS: In a retrospective cohort study, serum vitamin D levels were not associated with rates of structural or functional loss in glaucoma patients, suggesting that low vitamin D level is not a risk factor for progression. PURPOSE: To investigate the association between serum vitamin D level and rates of functional and structural glaucomatous loss over time. METHODS: This study included 826 eyes of 536 glaucoma or suspect patients with an average follow-up of 4.8+/-1.9 years. All patients had at least 1 serum vitamin D measurement, and all eyes had at least 2 reliable standard automated perimetry (SAP) tests and 2 spectral-domain optical coherence tomography (SD OCT) tests with a minimum follow-up of 6 months. Multivariable linear mixed-effects models were used to estimate the association of vitamin D level with rates of change in SAP mean deviation (MD) and OCT retinal nerve fiber layer (RNFL) thickness over time while adjusting for potential confounding factors. RESULTS: Patients had an average of 3.4+/-1.7 SAP tests, 4.8+/-1.9 SD OCT tests, and 2.3+/-1.9 vitamin D measurements. The average serum vitamin D level was 33.9+/-13.2 ng/mL. Mean rates of MD and RNFL change were -0.03+/-0.08 dB/y and -0.68+/-0.64 microm/y, respectively. After controlling for confounding factors, there was no statistically significant association between mean vitamin D level and rates of MD (beta=0.038, 95% CI: -0.006, 0.082, P =0.09) or RNFL loss over time (beta=-0.018, 95% CI: -0.092, 0.055, P =0.62). CONCLUSIONS: We did not find a significant association between vitamin D level and rates of visual field or RNFL loss over time in individuals with glaucoma and glaucoma suspect patients. CI - Copyright (c) 2022 Wolters Kluwer Health, Inc. All rights reserved. FAU - Lee, Terry AU - Lee T AD - Vision, Imaging and Performance Laboratory (VIP), Duke Eye Center and Department of Ophthalmology, Duke University. FAU - Jammal, Alessandro A AU - Jammal AA AD - Vision, Imaging and Performance Laboratory (VIP), Duke Eye Center and Department of Ophthalmology, Duke University. FAU - Medeiros, Felipe A AU - Medeiros FA AD - Vision, Imaging and Performance Laboratory (VIP), Duke Eye Center and Department of Ophthalmology, Duke University. AD - Department of Electrical and Computer Engineering, Pratt School of Engineering, Duke University, Durham, NC. LA - eng GR - R01 EY029885/EY/NEI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20220506 PL - United States TA - J Glaucoma JT - Journal of glaucoma JID - 9300903 RN - 1406-16-2 (Vitamin D) SB - IM MH - Disease Progression MH - *Glaucoma/diagnosis MH - Humans MH - Intraocular Pressure MH - *Nerve Fibers MH - Retinal Ganglion Cells MH - Retrospective Studies MH - Tomography, Optical Coherence/methods MH - Visual Field Tests/methods MH - Vitamin D PMC - PMC10287058 MID - NIHMS1803112 COIS- Disclosure: F.A.M.: Aeri Pharmaceuticals (C); Allergan (C, F), Annexon (C); Biogen (C); Carl Zeiss Meditec (C, F), Galimedix (C); Google Inc. (F); Heidelberg Engineering (F), IDx (C); nGoggle Inc. (P), Novartis (F); Stealth Biotherapeutics (C); Reichert (C, F). The remaining authors declare no conflict of interest. EDAT- 2022/05/07 06:00 MHDA- 2022/07/01 06:00 PMCR- 2023/07/01 CRDT- 2022/05/06 00:03 PHST- 2021/09/30 00:00 [received] PHST- 2022/04/28 00:00 [accepted] PHST- 2022/05/07 06:00 [pubmed] PHST- 2022/07/01 06:00 [medline] PHST- 2022/05/06 00:03 [entrez] PHST- 2023/07/01 00:00 [pmc-release] AID - 00061198-202207000-00018 [pii] AID - 10.1097/IJG.0000000000002046 [doi] PST - ppublish SO - J Glaucoma. 2022 Jul 1;31(7):614-621. doi: 10.1097/IJG.0000000000002046. Epub 2022 May 6.