On the decline and etiology of high‐incidence motor system disease in West Papua (southwest New Guinea)

The etiology of a high‐incidence focus of amyotrophic lateral sclerosis and parkinsonism–dementia (ALS/P‐D) in south West Papua (Irian Jaya, Indonesia), first described in the 1960s and 1970s, has been attributed to mineral deficiencies, hyperparathyroidism, and metal neurotoxicity arising from reliance on drinking water obtained from springs and shallow wells. More recent visits (1987 and 1990) to the south West Papua focus of neurodegenerative disease cast doubt on this explanation by revealing changes in disease prevalence in communities with an unchanged water supply. These communities have experienced a dramatic decline in ALS and a reversal in the relative prevalence of ALS and parkinsonism. The extrapyramidal disorder can be distinguished from Parkinson disease by pyramidal features (and dementia) reminiscent of Guam P‐D. Topical use of cycad seed (termed kurru) gametophyte to treat large skin lesions is advanced as a plausible but unproven etiologic factor. Medicinal use of untreated cycad seed (Cycas sp.) has also been linked with ALS foci in Japan (oral use) and Guam (topical use), with the additional consumption on Guam of food items prepared from Cycas sp. seed or animals that consume cycad seed components. © 2005 Movement Disorder Society

[1]  G. Keele Letter: Rubella vaccination. , 1973, Lancet.

[2]  A. Salazar,et al.  Amyotrophic lateral sclerosis and parkinsonian syndromes in high incidence among the Auyu and Jakai people of West New Guinea , 1982, Neurology.

[3]  V. Palmer,et al.  CYCAD USE AND MOTOR NEURONE DISEASE IN IRIAN JAYA , 1987, The Lancet.

[4]  G. Kisby,et al.  Content of the neurotoxins cycasin (methylazoxymethanol β‐D‐glucoside) and BNLAA (β‐N‐methylamino‐L‐alanine) in cycad flour prepared by Guam Chamorros , 1992, Neurology.

[5]  R. Petersen,et al.  Guamanian neurodegenerative disease , 1995, Neurology.

[6]  N. Mantel,et al.  Geographic patterns of parkinsonism-dementia complex on Guam. 1956 through 1985. , 1990, Archives of neurology.

[7]  D. Dastur CYCAD TOXICITY IN MONKEYS: CLINICAL, PATHOLOGICAL, AND BIOCHEMICAL ASPECTS. , 1964, Federation proceedings.

[8]  D. Galasko,et al.  Amyotrophic lateral sclerosis and parkinsonism-dementia complex of Guam: changing incidence rates during the past 60 years. , 2003, American journal of epidemiology.

[9]  Paul Alan Cox,et al.  Cycad neurotoxins, consumption of flying foxes, and ALS-PDC disease in Guam. , 2002, Neurology.

[10]  T. Kihira,et al.  Epidemiology of motor neuron disease in the Kii Peninsula of Japan, 1989–1993: Active or disappearing focus? , 1998, Journal of the Neurological Sciences.

[11]  Paul Alan Cox,et al.  Biomagnification of cycad neurotoxins in flying foxes , 2003, Neurology.

[12]  J. Brody,et al.  Amyotrophic lateral sclerosis and parkinsonism dementia in a migrant population from Guam , 1969, Neurology.

[13]  P. Spencer Guam ALS/Parkinsonism-Dementia: A Long-Latency Neurotoxic Disorder Caused by “Slow Toxin(s)” in Food? , 1987, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[14]  V. Palmer,et al.  CYCAD USE AND MOTOR NEURONE DISEASE IN KII PENINSULA OF JAPAN , 1987, The Lancet.

[15]  G. Kisby,et al.  Content of the neurotoxins cycasin (methylazoxymethanol beta-D-glucoside) and BMAA (beta-N-methylamino-L-alanine) in cycad flour prepared by Guam Chamorros. , 1992, Neurology.

[16]  Sanford P. Markey,et al.  2‐Amino‐3‐(methylamino)‐propanoic acid (BMAA) in cycad flour , 1990, Neurology.

[17]  I. Kopin,et al.  2-Amino-3-(methylamino)-propanoic acid (BMAA) in cycad flour: an unlikely cause of amyotrophic lateral sclerosis and parkinsonism-dementia of Guam , 1991 .

[18]  R. Garruto,et al.  Neurodegenerative disorders of the western pacific: the search for mechanisms of pathogenesis , 1986, Trends in Neurosciences.

[19]  L. Kurland,et al.  Epidemiologic Investigations of Amyotrophic Lateral Sclerosis , 1955, Neurology.

[20]  P. Nunn,et al.  Guam amyotrophic lateral sclerosis-parkinsonism-dementia linked to a plant excitant neurotoxin. , 1987, Science.

[21]  G. Schellenberg,et al.  Clinical features and changing patterns of neurodegenerative disorders on Guam, 1997–2000 , 2002, Neurology.

[22]  L Lavine,et al.  Supranuclear disturbances of ocular motility in Lytico‐Bodig , 1988, Neurology.

[23]  A. Ludolph,et al.  Slow toxins, biologic markers, and long‐latency neurodegenerative disease in the western Pacific region , 1991, Neurology.

[24]  L. Kurland,et al.  Epidemiologic Investigations of Amyotrophic Lateral Sclerosis , 1954, Neurology.

[25]  D. Gajdusek Motor-neuron disease in natives of New Guinea. , 1963, The New England journal of medicine.

[26]  N. Mantel,et al.  Motor neuron disease on Guam: geographic and familial Occurrence, 1956–85 , 1996, Acta neurologica Scandinavica.

[27]  D. Gajdusek Foci of motor neuron disease in high incidence in isolated populations of East Asia and the Western Pacific. , 1982, Advances in neurology.

[28]  D. Gajdusek,et al.  Blood group genetic variations in inhabitants of West New Guinea, with a map of the villages and linguistic groups of South West New Guinea. , 1967, American journal of physical anthropology.

[29]  L. Kurland,et al.  Amyotrophic lateral sclerosis and parkinson's disease complex on Guam linked to an environmental neurotoxin , 1988, Trends in Neurosciences.