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Research ArticleOriginal Article
Open Access

Clinical delineation of myasthenia gravis in the Kingdom of Bahrain

Mohamed F. Binfalah, Hussein H. Alhafnawi, Ahmed A. Jaradat, Eslam Shosha, Ali J. Alhilly, Firas K. Al Nidawi, Mariam M. Alhammadi, Moiz O. Bakhiet and Fatema M. Abdulla
Neurosciences Journal January 2022, 27 (1) 16-23; DOI: https://doi.org/10.17712/nsj.2022.1.20210096
Mohamed F. Binfalah
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
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  • For correspondence: [email protected]
Hussein H. Alhafnawi
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
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Ahmed A. Jaradat
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
PhD
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Eslam Shosha
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
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Ali J. Alhilly
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
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Firas K. Al Nidawi
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
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Mariam M. Alhammadi
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
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Moiz O. Bakhiet
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
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Fatema M. Abdulla
From Department of Neurology (Binfalah), Department of Family and Community Medicine (Jaradat), Clinical Research Coordinator (Alhafnawi), Aljawhara Center (Bakhiet), Department of Molecular Medicine, Arabian Gulf University, Manama, and from the Neurology and Internal Medicine (Alhilly), Bahrain Defense Force Hospital, West Riffa, from Department of Internal Medicine (Al Nidawi, Alhammadi), King Hamad University Hospital, Busaiteen, from Department of Neurosciences (Abdulla), Salmanya Medical Complex, Ministry of Health, Juffair, Kingdom of Bahrain, and from the Department of Medicine (Shosha), Neurology Division, McMaster University, Hamilton, Canada.
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    Table 1

    - Comparison of clinical features between early-onset vs. late-onset MG, all patients.

    VariablesEOMG (n=71, 72.4%)LOMG (n=27, 27.6%)Total (n=98)P-value
     n (%) 
    Gender0.495
     Male29 (29.6)9 (9.2)38 (38.8) 
     Female42 (42.8)18 (18.4)60 (61.2) 
    MG classification at onset0.209
     Pure Ocular39 (39.8)11 (11.2)50 (51.0) 
     Generalized32 (32.7)16 (16.3)48 (49.0) 
    Symptoms at onset
     Ocular60 (61.2)25 (25.5)85 (86.7)0.292
     Fatigability46 (46.9)14 (14.3)60 (61.2)0.240
     Fluctuation34 (34.7)10 (10.2)44 (44.9)0.335
     Bulbar16 (16.3)11 (11.2)27 (27.5)0.072
     Facial weakness13 (13.3)6 (6.1)19 (19.4)0.662
     Respiratory symptoms/failure6 (6.1)2 (2.0)8 (8.1)0.866
     Neck weakness20 (20.4)6 (6.1)26 (25.6)0.551
     Limb weakness21 (21.4)8 (8.2)29 (29.6)0.996
    Antibody status
     AChR38 (38.8)18 (18.4)56 (57.1) 
     MuSK2 (2.0)1 (1.0)3 (3.1)0.447
     SN31 (31.6)8 (8.2)39 (39.8) 
    NCS (RNS) (n = 66)
     Positive34 (51.5)12 (18.2)46 (69.7)0.596
     Negative16 (24.2)4 (6.1)20 (30.3) 
    CT scan of the chest (n = 69)
     Normal33 (47.8)12 (17.4)45 (65.2)0.592
     Abnormal (n=24)19 (27.5)5 (7.2)24 (34.8) 
     Thymic hyperplasia12 (48.0)1 (4.0)13 (54.2) 
     Thymoma5 (20.0)3 (12.0)8 (33.3) 
     Thymic atrophy2 (8.0)1 (4.0)3 (12.5) 
    Thymus pathology (n = 20)
     Thymic hyperplasia8 (40.0)3 (15.0)11 (55.0) 
     Thymoma4 (20.0)2(10.0)6 (30.0)0.740
     Thymolipoma2 (10.0)02 (10.0) 
     Normal thymus1 (5.0)01 (5.0) 
    Treatment outcome(n = 58)
     Remission7 (12.1)07 (12.1) 
     Improvement27 (46.6)15 (25.9)42 (72.4)0.165
     Worsening6 (10.3)3 (5.2)9 (15.5) 
    • AChR – acetylcholine receptor, CT – computed tomography, EOMG – early onset myasthenia gravis (≤ 49 years), LOMG – late onset myasthenia gravis (> 49 years), MG – myasthenia gravis, MuSK – muscle specific tyrosine kinase, NCS – nerve conduction studies, RNS – repetitive nerve stimulation, SN - seronegative

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    Table 2

    - Comparison between AChR-positive and double-seronegative MG (excluding MuSK MG patients†).

    VariablesAChR MG (n =56, 58.9%)SN MG (n =39, 41.1%)Total (n=95)P-value
     n (%) 
    Gendern (%) 
     Male23 (24.2)14 (14.7)37 (38.9)0.611
     Female33 (34.7)25 (26.3)58 (61.1) 
    Onset
     EOMG38 (40.0)31 (32.6)69 (72.6)0.211
     LOMG18 (16.8)8 (10.5)26 (27.3) 
    MG types at onset
     Ocular25 (26.3)25 (26.3)50 (52.6)0.062
     Generalized31 (32.6)14 (14.7)45 (47.4) 
    Symptoms at onset
     Ocular49 (51.6)33 (34.7)82 (86.3)0.687
     Fatigability38 (40.0)20 (21.1)58 (61.1)0.103
     Fluctuation26 (27.4)16 (16.8)42 (44.2)0.602
     Bulbar19 (20)7 (7.4)26 (27.4)0.086
     Facial weakness14 (14.7)4 (4.2)18 (18.9)0.071
     Respiratory symptoms/failure6 (6.3)2 (2.1)8 (8.4)0.335
     Neck weakness18 (18.9)7 (7.4)25 (26.3)0.122
     Limb weakness22 (23.1)5 (5.3)27 (28.4)0.005
    NCS (RNS) (n = 63)
     Positive30 (47.6)14 (22.2)44 (68.2)0.007
     Negative6 (9.5)13 (20.6)19 (31.8) 
    Chest CT (n = 67)
     Normal26 (47.6)18 (22.2)44 (65.7)0.006
     Abnormal21 (31.3)02 (3.0)23 (34.3) 
     Thymic hyperplasia10 (15.2)2 (3)12 (18.2) 
     Thymoma8 (12.1)08 (12.1) 
     Thymic atrophy3 (4.5)03 (4.5) 
    Treatment outcome(n = 55)
     Remission4 (7.3)2 (3.6)6 (10.9) 
     Improvement28 (50.9)12 (21.8)40 (72.7)0.972
     Worsening6 (10.9)3 (5.5)9 (16.4) 
    • AChR - acetylcholine receptor, CT - computed tomography, EOMG - early onset myasthenia gravis (≤49 years), LOMG - late onset myasthenia gravis (> 49 years), MG - myasthenia gravis, MuSK - muscle specific tyrosine kinase, NCS - nerve conduction studies, RNS - repetitive nerve stimulation, SN - seronegative, †3 MuSK patients: 2 females and 1 male, 2 with EOMG and 1 LOMG, all generalized disease, 2 with normal CT chest, and 1 with thymic hyperplasia

    • View popup
    Table 3

    - Treatments used in MG patients throughout the disease course, n = 98

    TreatmentPatients, n (%)
    Pyridostigmine88 (89.8)
    Prednisone63 (64.3)
    Mycophenolate Mofetil15 (15.3)
    Azathioprine27 (27.6)
    IVIG23 (23.5)
    Rituximab2(2)
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Clinical delineation of myasthenia gravis in the Kingdom of Bahrain
Mohamed F. Binfalah, Hussein H. Alhafnawi, Ahmed A. Jaradat, Eslam Shosha, Ali J. Alhilly, Firas K. Al Nidawi, Mariam M. Alhammadi, Moiz O. Bakhiet, Fatema M. Abdulla
Neurosciences Journal Jan 2022, 27 (1) 16-23; DOI: 10.17712/nsj.2022.1.20210096

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Clinical delineation of myasthenia gravis in the Kingdom of Bahrain
Mohamed F. Binfalah, Hussein H. Alhafnawi, Ahmed A. Jaradat, Eslam Shosha, Ali J. Alhilly, Firas K. Al Nidawi, Mariam M. Alhammadi, Moiz O. Bakhiet, Fatema M. Abdulla
Neurosciences Journal Jan 2022, 27 (1) 16-23; DOI: 10.17712/nsj.2022.1.20210096
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