Displaying all 12 publications

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  1. Lim, Kheng-Seang, Goh, Khean-Jin, Tan, Ai-Huey, Low, Soon-Chai, Mustapha Muzaimi
    MyJurnal
    The conjoint 17thAsian and Oceanian Myology Centre (AOMC) and 28thMalaysian Society of Neurosciences (MSN) Annual Scientific Meeting, held in Hotel Istana, Kuala Lumpur, Malaysia from 27 to 29 July 2018, was a great success to gather all neurosciences professionals locally and in the Asian-Oceanian region to share the latest updates in Neurology and specifically Myology. This congress attracted 516 local participants and 167 international delegates from 14 countries
  2. Tan, Ai Huey, Low, Soon Chai, Tan, Chong Tin, Fong, Si Lei, Wong, Jin Shyan
    Neurology Asia, 2017;22(1):25-32.
    MyJurnal
    Melioidosis is an infectious disease caused by an aerobic, non-spore forming gram negative bacillus,
    Burkholderia pseudomallei. It is known to be of high incidence in parts of rural South East Asia,
    and in Northern Australia. Pneumonia is the commonest manifestation. We report here three cases of
    neurological melioidosis from the registry of 169 cases of melioidosis in Bintulu Hospital, Sarawak,
    East Malaysia, with a review of neurological melioidosis in the literature. The annual incidence of
    melioidosis is estimated to be 8 per 100,000 populations in the Bintulu district. Neurological melioidosis
    accounts for 1.8% of our melioidosis cases. A review of 76 cases of neurological melioidosis reported
    in the literature inclusive of our 3 cases shows that localized brain or spinal inflammation or abscess
    is the most common manifestation occurring in 80% of patients. Close to half (53%) have intra axial
    abscess (brain or spinal cord), a quarter (27%) have extra axial lesions only (epidural or subdural
    collection, osteomyelitis or scalp abscess), and another quarter (27%) have both intra and extra axial
    lesions. Thus, B. pseudomallei appears to be unique among the bacterial central nervous system
    infection to be able to affect the brain and its contiguous tissues, crossing the tissue plane particularly
    resulting in osteomyelitis, scalp abscess and vice versa. Two thirds of the neurologicalmelioidosis
    patients have only neurological disease with no evidence of disease elsewhere.
  3. Lim, Michael Chung Keat, Zatul Akmar Ahmad, Low, Soon Chai, Woo, Yin Ling, Norlisah Ramli, Nortina Shahrizaila, et al.
    Neurology Asia, 2018;23(1):97-99.
    MyJurnal
    Non-bacterial thrombotic endocarditis (NBTE) denotes the presence of sterile non-infective vegetation
    on structurally normal, or subtly degenerate cardiac valves and is often associated with advanced
    malignancies. In gynaecological cancer in particular, NBTE has been most commonly associated
    with ovarian cancer.1,2 Here we report a rare but interesting case of NBTE in a patient with locally
    advanced cervical adenocarcinoma.
  4. Tan AH, Low SC, Tan CY, Lim KS, Tan CT, Lim SY
    Parkinsonism Relat Disord, 2016 11;32:137-139.
    PMID: 27688197 DOI: 10.1016/j.parkreldis.2016.09.019
  5. Lim SY, Tan AH, Fox SH, Evans AH, Low SC
    Curr Neurol Neurosci Rep, 2017 01;17(1):3.
    PMID: 28102483 DOI: 10.1007/s11910-017-0717-2
    Parkinson's disease (PD) is a complex motor and non-motor disorder and management is often challenging. In this review, we explore emerging approaches to improve the care of patients, drawing from the literature regarding patient-centred care, patient and caregiver perspectives and priorities, gaps in knowledge among patients and caregivers and the need for accurate information, individual variability in disease manifestations, prognostication of disease course, new developments in health technologies and personalized medicine, specialty care, pharmacological and non-pharmacological management, financial burden, lifestyle and work-related issues, support groups and palliative care.
  6. Tan SY, Tan CY, Yahya MA, Low SC, Shahrizaila N, Goh KJ
    Neurol Sci, 2024 Jan 25.
    PMID: 38270729 DOI: 10.1007/s10072-024-07340-y
    INTRODUCTION: There is an increasing need for a reproducible and sensitive outcome measure in patients with hereditary transthyretin amyloidosis (ATTRv) with polyneuropathy (PN) due to the emergence of disease modifying therapies. In the current study, we aimed to investigate the role of quantitative muscle ultrasound (QMUS) as a disease biomarker in ATTRv-PN.

    METHODS: Twenty genetically confirmed ATTRv amyloidosis patients (nine symptomatic, 11 pre-symptomatic) were enrolled prospectively between January to March 2023. Muscle ultrasound was performed on six muscles at standardized locations. QMUS parameters included muscle thickness (MT) and muscle echo intensity (EI). Twenty-five age- and sex-matched healthy controls were recruited for comparison. Significant QMUS parameters were correlated with clinical outcome measures.

    RESULTS: Muscle volume of first dorsal interosseus (FDI) muscle [measured as cross-sectional area (CSA)] was significantly lower in symptomatic patients compared to healthy controls and pre-symptomatic carriers (98.3 ± 58.0 vs. 184.4 ± 42.5 vs. 198.3 ± 56.8, p 

  7. Tan AH, Toh TH, Low SC, Fong SL, Chong KK, Lee KW, et al.
    J Mov Disord, 2018 Sep;11(3):149-151.
    PMID: 30086616 DOI: 10.14802/jmd.18017
  8. Tan AH, Lim SY, Chong KK, A Manap MAA, Hor JW, Lim JL, et al.
    Neurology, 2021 02 02;96(5):e772-e782.
    PMID: 33046607 DOI: 10.1212/WNL.0000000000010998
    OBJECTIVE: To determine whether probiotics are effective for constipation, a common and often difficult-to-treat problem, in Parkinson disease (PD).

    METHODS: In this double-blind, randomized, placebo-controlled, single-center trial, 280 patients with PD were screened, and 72 eligible patients were block-randomized (1:1) to receive either multistrain probiotics capsules (n = 34) or identical-appearing placebo (n = 38), for 4 weeks. The primary endpoint was the change in the average number of spontaneous bowel movements (SBM) per week during the last 2 weeks of intervention compared with the 2-week preintervention phase, recorded by daily stool diary. Secondary outcome measures included changes in stool consistency, constipation severity score, and quality of life related to constipation. Satisfaction with intervention received was assessed. Change in levels of fecal calprotectin, a marker of intestinal inflammation, was an exploratory outcome.

    RESULTS: SBM increased by 1.0 ± 1.2 per week after treatment with probiotics and decreased by 0.3 ± 1.0 per week in the placebo group (mean difference 1.3, 95% confidence interval 0.8-1.8, p < 0.001). Significant improvements were also seen for secondary outcomes after correction for multiple comparisons, including stool consistency (p = 0.009) and quality of life related to constipation (p = 0.001). In the treatment group, 65.6% reported satisfaction with the intervention vs only 21.6% in the placebo group (p < 0.001). One patient (2.9%) in the treatment group withdrew due to a nonserious adverse event. Fecal calprotectin did not change significantly during the study.

    CONCLUSIONS: Multistrain probiotics treatment was effective for constipation in PD. Further studies are needed to investigate the long-term efficacy and safety of probiotics in PD, as well as their mechanisms of action.

    CLINICALTRIALSGOV IDENTIFIER: NCT03377322.

    CLASSIFICATION OF EVIDENCE: This study provides Class I evidence that, for people with PD, multistrain probiotics significantly increased the average number of SBM per week.

  9. Low SC, Md Sari NA, Tan CY, Ahmad-Annuar A, Wong KT, Law WC, et al.
    Neuromuscul Disord, 2021 07;31(7):642-650.
    PMID: 34059423 DOI: 10.1016/j.nmd.2021.03.008
    We report the clinical and genetic characteristics of hereditary transthyretin amyloidosis in the multi-ethnic Malaysian population. Subjects with genetically confirmed transthyretin amyloidosis seen between 2001 till August 2020 were included. There were 30 patients and 14 asymptomatic carriers, of which 26 (59.1%) were men. The majority (86.7%) were ethnic Chinese while two (6.7%) each were Malay and Sri Lankan Tamil ethnicity respectively. Among patients, mean age of symptom-onset was 55.9 ± 9.8 years with mean duration from symptom-onset to diagnosis of 3.2 ± 2.5 years. Common presenting symptoms were sensory symptoms of upper limbs (43.3%), symmetric sensory symptoms of both lower limbs (16.7%) and autonomic symptoms (16.7%). Nerve conduction studies showed sensorimotor polyneuropathy in 25 (83.3%) patients (22, axonal). Abnormal echocardiograms were seen in 24 (80%) patients, although 15 were asymptomatic. Of six different TTR mutations found, Ala97Ser was the commonest, and found exclusively in 84.6% of Chinese patients. Other mutations among Chinese patients were Val30Met, Ala25Thr and Asp39Val. Our Malay and Tamil patients had Glu54Lys and Gly47Val mutations respectively. In conclusion, TTR Ala97Ser is the commonest mutation among ethnic Chinese Malaysians which presented with late-onset progressive sensorimotor polyneuropathy, autonomic dysfunction and subclinical cardiac involvement.
  10. Adams D, Tournev IL, Taylor MS, Coelho T, Planté-Bordeneuve V, Berk JL, et al.
    Amyloid, 2023 Mar;30(1):1-9.
    PMID: 35875890 DOI: 10.1080/13506129.2022.2091985
    BACKGROUND: The study objective was to assess the effect of vutrisiran, an RNA interference therapeutic that reduces transthyretin (TTR) production, in patients with hereditary transthyretin (ATTRv) amyloidosis with polyneuropathy.

    METHODS: HELIOS-A was a phase 3, global, open-label study comparing the efficacy and safety of vutrisiran with an external placebo group (APOLLO study). Patients were randomized 3:1 to subcutaneous vutrisiran 25 mg every 3 months (Q3M) or intravenous patisiran 0.3 mg/kg every 3 weeks (Q3W) for 18 months.

    RESULTS: HELIOS-A enrolled 164 patients (vutrisiran, n = 122; patisiran reference group, n = 42); external placebo, n = 77. Vutrisiran met the primary endpoint of change from baseline in modified Neuropathy Impairment Score +7 (mNIS+7) at 9 months (p = 3.54 × 10-12), and all secondary efficacy endpoints; significant improvements versus external placebo were observed in Norfolk Quality of Life-Diabetic Neuropathy, 10-meter walk test (both at 9 and 18 months), mNIS+7, modified body-mass index, and Rasch-built Overall Disability Scale (all at 18 months). TTR reduction with vutrisiran Q3M was non-inferior to within-study patisiran Q3W. Most adverse events were mild or moderate in severity, and consistent with ATTRv amyloidosis natural history. There were no drug-related discontinuations or deaths.

    CONCLUSIONS: Vutrisiran significantly improved multiple disease-relevant outcomes for ATTRv amyloidosis versus external placebo, with an acceptable safety profile.

    CLINICALTRIALS.GOV: NCT03759379.

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