PMID- 36372866 OWN - NLM STAT- MEDLINE DCOM- 20230201 LR - 20230313 IS - 1432-1459 (Electronic) IS - 0340-5354 (Linking) VI - 270 IP - 2 DP - 2023 Feb TI - Optical coherence tomography as a prognostic tool for disability progression in MS: a systematic review. PG - 1178-1186 LID - 10.1007/s00415-022-11474-4 [doi] AB - Since multiple sclerosis (MS) is characterized by an unpredictable disease course, accurate prognosis and personalized treatment constitute an important challenge in clinical practice. We performed a qualitative systematic review to assess the predictive value of retinal layer measurement by spectral-domain optical coherence tomography (SD-OCT) in MS patients. Longitudinal MS cohort studies that determined the risk of clinical deterioration based on peripapillary retinal nerve fiber layer (pRNFL) and/or macular ganglion cell-inner plexiform layer (mGCIPL) atrophy were included. Our search strategy and selection process yielded eight articles in total. Of those, five studies only focused on patients with a relapsing-remitting disease pattern (RRMS). After correction for confounders such as disease duration, we found that (1) cross-sectional measurement of pRNFL thickness 1.5 microm/year; and (4) longitudinal measurement of mGCIPL thinning >/= 1.0 microm/year is associated with an increased risk for disability progression in subsequent years. Longitudinal mGCIPL assessment consistently resulted in the highest risk estimates in our analysis. Within these studies, inclusion and exclusion criteria accounted for the retinal degeneration inherent to (acute) optic neuritis (ON). This small systematic review provides additional evidence that OCT-measured pRNFL and/or mGCIPL atrophy can predict disability progression in RRMS patients. We therefore recommend close clinical follow-up or initiation/change of treatment in RRMS patients with increased risk for clinical deterioration based on retinal layer thresholds, in particular when other poor prognostic signs co-occur. CI - (c) 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany. FAU - Swinnen, Stijn AU - Swinnen S AUID- ORCID: 0000-0003-1028-197X AD - Laboratory for Neuroimmunology, Department of Neurosciences, KU Leuven Brain Institute, Leuven, Belgium. AD - Department of Neurology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. FAU - De Wit, Dries AU - De Wit D AD - Laboratory for Neuroimmunology, Department of Neurosciences, KU Leuven Brain Institute, Leuven, Belgium. AD - Department of Neurology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. FAU - Van Cleemput, Liesbeth AU - Van Cleemput L AD - Department of Ophthalmology, University Hospitals Leuven, Leuven, Belgium. FAU - Cassiman, Catherine AU - Cassiman C AD - Department of Ophthalmology, University Hospitals Leuven, Leuven, Belgium. FAU - Dubois, Benedicte AU - Dubois B AUID- ORCID: 0000-0003-0604-8702 AD - Laboratory for Neuroimmunology, Department of Neurosciences, KU Leuven Brain Institute, Leuven, Belgium. benedicte.dubois@uzleuven.be. AD - Department of Neurology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium. benedicte.dubois@uzleuven.be. LA - eng PT - Journal Article PT - Systematic Review DEP - 20221113 PL - Germany TA - J Neurol JT - Journal of neurology JID - 0423161 SB - IM MH - Humans MH - Prognosis MH - Tomography, Optical Coherence/methods MH - *Clinical Deterioration MH - Cross-Sectional Studies MH - *Multiple Sclerosis/diagnostic imaging/complications MH - *Retinal Degeneration MH - *Macular Degeneration MH - Atrophy/complications OTO - NOTNLM OT - Disease progression OT - Multiple sclerosis (MS) OT - Optical coherence tomography (OCT) OT - Prognosis OT - Retinal layer measurement EDAT- 2022/11/15 06:00 MHDA- 2023/02/02 06:00 CRDT- 2022/11/14 00:03 PHST- 2022/10/05 00:00 [received] PHST- 2022/10/30 00:00 [accepted] PHST- 2022/11/15 06:00 [pubmed] PHST- 2023/02/02 06:00 [medline] PHST- 2022/11/14 00:03 [entrez] AID - 10.1007/s00415-022-11474-4 [pii] AID - 10.1007/s00415-022-11474-4 [doi] PST - ppublish SO - J Neurol. 2023 Feb;270(2):1178-1186. doi: 10.1007/s00415-022-11474-4. Epub 2022 Nov 13.