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The Occurrence of Multiple Sclerosis in the Hutterites of North America

Published online by Cambridge University Press:  18 September 2015

Walter J. Hader*
Affiliation:
Department of Rehabilitation Medicine, College of Medicine, University of Saskatchewan, Saskatoon
T. Peter Seland
Affiliation:
Calgary General Hospital, Department of Clinical Neurosciences, Calgary
Mary B. Hader
Affiliation:
Department of Rehabilitation Medicine, College of Medicine, University of Saskatchewan, Saskatoon
Colleen J. Harris
Affiliation:
Calgary General Hospital, Department of Clinical Neurosciences, Calgary
Dennis W. Dietrich*
Affiliation:
Columbus Professional Building, Adult and Child Neurology, Great Falls, Montana
*
Department of Rehabilitation Medicine, Saskatoon City Hospital, Saskatoon, Saskatchewan, Canada S7K 0M7
Department of Rehabilitation Medicine, Saskatoon City Hospital, Saskatoon, Saskatchewan, Canada S7K 0M7
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Abstract

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Objective: To report the occurrence, clinical characteristics and genealogical analysis of multiple sclerosis in the Hutterites of North-Western United States and Western Canada. Background: The incidence of multiple sclerosis is reported to be lower or rare in certain ethnic groups and genetic isolates and was previously observed to be absent in the Hutterite population. Methods: After long-term surveillance, six patients were identified and clinical examinations and laboratory investigations including VER and MRI were completed. Results: The six cases included two brothers, two first cousins, male and female, another male and female, all representing two of the three endogamous groups of Hutterites, are linked to two common ancestors through lines of descent dating to 1723. The individual pedigrees were analyzed from extensive genealogical records covering eight generations. Conclusion: The incidence of multiple sclerosis in Hutterites is low in a high risk area of North America. A specific mode of inheritance pattern has not been established and a common founder effect may play a role in the development of multiple sclerosis. The genetic contribution of the Hutterites seems greater than previously recognized.

Type
Original Articles
Copyright
Copyright © Canadian Neurological Sciences Federation 1996

References

1.Kurtzke, JF.Epidemiologic contributions to multiple sclerosis: an overview. Neurology (NY) 1980; 30: 6179.CrossRefGoogle ScholarPubMed
2.Ebers, GC, Bulman, D.The geography of multiple sclerosis reflects genetic susceptibility. Neurology 1986; 36: (Suppl.) 108.Google Scholar
3.Compston, A.Genetic factors in the aetiology of multiple sclerosis. In: McAlpines’ Multiple Sclerosis. Matthew, WB, ed. Churchill Livingstone, 1991: 301319.Google Scholar
4.Ebers, GC, Bulman, D, Sadovnick, AD, et al. A population based study of multiple sclerosis in twins. N Engl J Med 1988; 315: 16381642.CrossRefGoogle Scholar
5.McDonald, WL, Batchelor, JR, Francis, DA.The immunogenetics of multiple sclerosis. Trends Neurosci 1984; 7: 369371.CrossRefGoogle Scholar
6.Lynch, GS, Rose, JW, Petajan, JH, Leppert, M.Discordance of the T-cell receptor alpha-chain gene in familial multiple sclerosis. Neurology 1992; 42: 839844.CrossRefGoogle ScholarPubMed
7.Wynn, DR, Rodriguez, M, O’Fallon, M, Kurland, LT.A reappraisal of the epidemiology of multiple sclerosis in Olmstead County, Minnesota. Neurology 1990; 40: 780786.CrossRefGoogle Scholar
8.Hader, WJ.Prevalence of multiple sclerosis in Saskatoon. Can Med J 1982; 127: 295297.Google ScholarPubMed
9.Siedler, HD, Nicoll, W, Kurland, LT.The prevalence and incidence of multiple sclerosis in Missoula County, Montana. Journal Lancet 1958; 78: 358360.Google ScholarPubMed
10.Svenson, L, Woodhead, S, Piatt, GH.Regional variations in the prevalence rates of multiple sclerosis in the province of Alberta, Canada. Neuroepidemiology 1994; 13: 813.CrossRefGoogle ScholarPubMed
11.Warren, SA, Warren, KG.Prevalence of multiple sclerosis in Barrhead County, Alberta, Canada. Can J Neurol Sci 1992; 19: 7275.CrossRefGoogle ScholarPubMed
12.Lowry, RB, Morgan, K, Holmes, TM, Gilroy, SW.Congenital anomalies in the Hutterite Population: a preliminary survey and hypothesis. Am J Med Gen 1985; 22: 545552.CrossRefGoogle ScholarPubMed
13.McFarlin, DE, Lachmann, PJ.Hopeful genes and immunology. Nature 1989; 341: 693694.CrossRefGoogle ScholarPubMed
14.Hostetler, JA.The Hutterite Society. Baltimore and London. The John Hopkins University Press, 1974.Google Scholar
15.Steinberg, AG, Bleibtreu, HK, Kurchynski, TW, Martin, AO, Kurchynski, EM.In: Genetic studies on an inbred human isolate. Proceedings of the Third International Congress of Human Genetics. James F Crow, ed. 1967: 267289.Google Scholar
16.Hostetler, JA.History and relevance of the Hutterite population for genetic studies. Am J Med Gen 1985; 22: 453462.CrossRefGoogle ScholarPubMed
17.Martin, AO.The founder effect in a human isolate. Am J Phys Anthrop 1970; 32: 351368.CrossRefGoogle Scholar
18.Fowlow, B, Holmes, MT, Morgan, K, Snyder, FF.Screening for methylmalonic aciduria in Alberta. A voluntary program with particular significance for the Hutterite Brethern. Am J Med Gen 1985; 22: 513519.CrossRefGoogle Scholar
19.Poser, CM, Paty, DW, Scheinberg, L, et al. New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Ann Neurol 1983; 13: 222231.CrossRefGoogle ScholarPubMed
20.Carmel, R, Watkins, D, Goodman, SI, Rosenblatt, DS.Hereditary defect of cobalamin metabolism (cb1G mutation) presenting as a neurologic disorder in adulthood. N Engl J Med 1988: 318: 17381741.CrossRefGoogle Scholar
21.Shevell, MI, Carson, W, Gavsie, A, et al. Protein-bound homocysteine levels in familial multiple sclerosis. Clin Invest Med 1991; 14: 528.Google Scholar
22.McKusick, VA.Selected aspects of the population genetics of recessive diseases. In: Medical Genetic Studies of the Amish. Baltimore: The John Hopkins University Press, 1978: 515519.Google Scholar
23.Schurig, V, Orman, VA, Bowen, P.Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites. Am J Med Gen 1981; 9: 4353.CrossRefGoogle ScholarPubMed
24.Pallister, PD, Opitz, JM.Brief clinical report: disequilibrium syndrome in Montana Hutterites. Am J Med Gen 1985; 22: 567569.CrossRefGoogle Scholar
25.Fujiwara, TM, Morgan, K, Schwartz, RH, et al. Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplo-types in the Hutterite Brethern. Am J Hum Genet 1989; 44: 327337.Google Scholar
26.Shokeir, MH, Rozdilsky, B.Muscular dystrophy in Saskatchewan Hutterites. Am J Med Genet 1985; 22: 487493.CrossRefGoogle ScholarPubMed
27.Boldt, ED.The recent development of a unique population: the Hutterites of North America. Prairie Forum 1983; 8: 235241.Google Scholar
28.Cross, HE, McKusick, VA.A survey of neurological disorders in a genetic isolate. Neurology 1967; 17: 743751.CrossRefGoogle Scholar
29.Jaworski, MA, Serverini, A, Mansour, G, et al. Genetic conditions among Canadian Mennonites: evidence for a founder effect among the old colony (Chortitza) Mennonites. Clin Invest Med 1989; 12: 127141.Google ScholarPubMed
30.MacKay, RP, Myrianthopoulos, NC.Multiple sclerosis in twins and their relatives. Final Report. Arch Neurol 1966; 15: 449462.CrossRefGoogle Scholar
31.Nora, JJ, Fraser, FC.Genetic basis of heredity. In: Medical Genetics: Principles and Practice. Lea and Febiger Philadelphia, London, 1989: 7394.Google Scholar
32.Sadovnick, AD, Compston, A.Epidemiology and genetics of multiple sclerosis. Current Opinion. Neurol Neurosurg 1992; 5: 175181.Google Scholar
33.Pratt, RT, Compston, ND, McAlpine, D.The familial incidence of multiple sclerosis and its significance. Brain 1952; 74: 191232.CrossRefGoogle Scholar
34.Sadovnick, AD, Ebers, GC.Genetics of multiple sclerosis. In: Antel, JP, ed. Neurologic Clinics. Philadelphia: W.B. Saunders Co., 1995; 13: 99117.Google Scholar