PMID- 30779438 OWN - NLM STAT- MEDLINE DCOM- 20200115 LR - 20200115 IS - 1098-1101 (Electronic) IS - 0733-2459 (Linking) VI - 34 IP - 4 DP - 2019 Aug TI - Excellent response to therapeutic plasma exchange in myasthenia gravis patients irrespective of antibody status. PG - 416-422 LID - 10.1002/jca.21694 [doi] AB - INTRODUCTION: The primary objective of this study was to assess response to plasma exchange (PLEX) in myasthenia gravis (MG) patients with and without autoantibodies (Ab) to acetylcholine receptor (AChR) or muscle-specific kinase (MuSK). Analysis was also done to determine if correlation existed between sex, early or late onset MG, thymoma, or thymectomy and response to PLEX. MATERIALS AND METHODS: Data was analyzed on 58 consecutive MG patients treated with PLEX. Responses were categorized as complete response, clinical improvement requiring maintenance PLEX, or no/minimal response to PLEX. RESULTS: Eighty-eight percent (51/58) of patients were Ab-positive; 44 had AChR and 7 had MuSK Ab. Complete response was seen in 26 patients (24 Ab+), 24 remain on maintenance PLEX (19 Ab+), and 2 had no/minimal response (both AChR Ab+). Ab status (P = 0.43), AChR Ab (P = 0.10), MuSK Ab (P = 0.45), early onset MG (P = 0.63), thymoma (P = 0.46), and thymectomy (P = 0.16) were not significantly associated with outcome. Patient sex did show significant association with outcome (P = 0.01), with men more likely to have complete response and women more likely to require maintenance. Late onset MG is significantly associated with higher likelihood of complete response (P = 0.03). Antibody titers declined after PLEX in 83% of patients with complete response, in whom pre- and post-PLEX titers were available (n = 6). CONCLUSIONS: In conclusion, our study showed 96% response rate to PLEX in MG; however, only patient gender and late onset MG were significantly associated with treatment response. CI - (c) 2019 Wiley Periodicals, Inc. FAU - Usmani, Amena AU - Usmani A AUID- ORCID: 0000-0002-3170-6482 AD - Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas. FAU - Kwan, Laura AU - Kwan L AD - Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas. FAU - Wahib-Khalil, Dina AU - Wahib-Khalil D AD - Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas. FAU - Trivedi, Jaya AU - Trivedi J AD - Department of Neurology, University of Texas Southwestern Medical Center, Dallas, Texas. FAU - Nations, Sharon AU - Nations S AD - Department of Neurology, University of Texas Southwestern Medical Center, Dallas, Texas. FAU - Sarode, Ravi AU - Sarode R AD - Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas. LA - eng PT - Journal Article DEP - 20190219 PL - United States TA - J Clin Apher JT - Journal of clinical apheresis JID - 8216305 RN - 0 (Autoantibodies) RN - 0 (Receptors, Cholinergic) RN - EC 2.7.10.1 (MUSK protein, human) RN - EC 2.7.10.1 (Receptor Protein-Tyrosine Kinases) SB - IM MH - Adult MH - Age of Onset MH - Autoantibodies/*blood MH - Female MH - Humans MH - Male MH - Middle Aged MH - Myasthenia Gravis/diagnosis/*therapy MH - Plasma Exchange/*standards MH - Prognosis MH - Receptor Protein-Tyrosine Kinases/immunology MH - Receptors, Cholinergic/immunology MH - Sex Factors MH - Thymectomy MH - Thymoma MH - Treatment Outcome OTO - NOTNLM OT - acetylcholine receptor antibody (AChR) OT - muscle specific kinase (MuSK) antibody OT - myasthenia gravis (MG) OT - plasma exchange EDAT- 2019/02/20 06:00 MHDA- 2020/01/16 06:00 CRDT- 2019/02/20 06:00 PHST- 2018/05/01 00:00 [received] PHST- 2018/11/30 00:00 [revised] PHST- 2018/12/03 00:00 [accepted] PHST- 2019/02/20 06:00 [pubmed] PHST- 2020/01/16 06:00 [medline] PHST- 2019/02/20 06:00 [entrez] AID - 10.1002/jca.21694 [doi] PST - ppublish SO - J Clin Apher. 2019 Aug;34(4):416-422. doi: 10.1002/jca.21694. Epub 2019 Feb 19.