Literature DB >> 21039118

Survival and prognostic factors of motor neuron disease in a multi-ethnic Asian population.

Khean-Jin Goh1, Sharen Tian, Nortina Shahrizaila, Chiu-Wan Ng, Chong-Tin Tan.   

Abstract

Our objective was to determine the survival and prognostic factors of motor neuron disease (MND) in a multi-ethnic cohort of Malaysian patients. All patients seen at a university medical centre between January 2000 and December 2009 had their case records reviewed for demographic, clinical and follow-up data. Mortality data, if unavailable from records, were obtained by telephone interview of relatives or from the national mortality registry. Of the 73 patients, 64.4% were Chinese, 19.2% Malays and 16.4% Indians. Male: female ratio was 1.43: 1. Mean age at onset was 51.5 + 11.3 years. Onset was spinal in 75.3% and bulbar in 24.7% of the patients; 94.5% were ALS and 5.5% were progressive muscular atrophy (PMA). Overall median survival was 44.9 + 5.8 months. Ethnic Indians had shorter interval from symptom onset to diagnosis and shorter median survival compared to non-Indians. On Cox proportional hazards analysis, poor prognostic factors were bulbar onset, shorter interval from symptom onset to diagnosis and worse functional score at presentation. In conclusion, age of onset and median survival duration are similar to previous reports in Asians. Clinical features and prognostic factors are similar to other populations. In our cohort, ethnic Indians had more rapid disease course accounting for their shorter survival.

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Year:  2010        PMID: 21039118     DOI: 10.3109/17482968.2010.527986

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler        ISSN: 1471-180X


  5 in total

Review 1.  Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin.

Authors:  Benoît Marin; Giancarlo Logroscino; Farid Boumédiene; Anaïs Labrunie; Philippe Couratier; Marie-Claude Babron; Anne Louise Leutenegger; Pierre Marie Preux; Ettore Beghi
Journal:  Eur J Epidemiol       Date:  2015-10-12       Impact factor: 8.082

2.  Phenotypic differences of amyotrophic lateral sclerosis (ALS) in China and Germany.

Authors:  Angela Rosenbohm; Mingsheng Liu; Gabriele Nagel; Raphael S Peter; Bo Cui; Xiaoguang Li; Jan Kassubek; Dietrich Rothenbacher; Dorothée Lulé; Liying Cui; Albert C Ludolph
Journal:  J Neurol       Date:  2018-02-01       Impact factor: 4.849

3.  The first Malay database toward the ethnic-specific target molecular variation.

Authors:  Hashim Halim-Fikri; Ali Etemad; Ahmad Zubaidi Abdul Latif; Amir Feisal Merican; Atif Amin Baig; Azlina Ahmad Annuar; Endom Ismail; Iman Salahshourifar; Ahmad Tajudin Liza-Sharmini; Marini Ramli; Mohamed Irwan Shah; Muhammad Farid Johan; Nik Norliza Nik Hassan; Noraishah Mydin Abdul-Aziz; Noor Haslina Mohd Noor; Ab Rajab Nur-Shafawati; Rosline Hassan; Rosnah Bahar; Rosnah Binti Zain; Shafini Mohamed Yusoff; Surini Yusoff; Soon Guan Tan; Meow-Keong Thong; Hatin Wan-Isa; Wan Zaidah Abdullah; Zahurin Mohamed; Zarina Abdul Latiff; Bin Alwi Zilfalil
Journal:  BMC Res Notes       Date:  2015-04-30

4.  Prognostic Factors in Amyotrophic Lateral Sclerosis: A Population-Based Study.

Authors:  Mirian Conceicao Moura; Maria Rita Carvalho Garbi Novaes; Emanoel Junio Eduardo; Yuri S S P Zago; Ricardo Del Negro Barroso Freitas; Luiz Augusto Casulari
Journal:  PLoS One       Date:  2015-10-30       Impact factor: 3.240

Review 5.  Dysphagia as a risk factor for mortality in Niemann-Pick disease type C: systematic literature review and evidence from studies with miglustat.

Authors:  Mark Walterfang; Yin-Hsiu Chien; Jackie Imrie; Derren Rushton; Danielle Schubiger; Marc C Patterson
Journal:  Orphanet J Rare Dis       Date:  2012-10-06       Impact factor: 4.123

  5 in total

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