• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Longitudinal study in an island community for aging effects on neurological findings and genetic factors on vascular dementia

Research Project

Project/Area Number 10670596
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Neurology
Research InstitutionKagoshima University

Principal Investigator

NAKAGAWA Masanori  University Hospital, Faculty of Medicine, Kagoshima University, Assistant Professor, 医学部・附属病院, 講師 (50198040)

Co-Investigator(Kenkyū-buntansha) AKIBA Suminori  Faculty of Medicine, Kagoshima University, Professor, 医学部, 教授 (50145554)
OSAME Mitsuhiro  Faculty of Medicine, Kagoshima University, Professor, 医学部, 教授 (10041435)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥2,900,000 (Direct Cost: ¥2,900,000)
Fiscal Year 1999: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1998: ¥2,000,000 (Direct Cost: ¥2,000,000)
KeywordsAging effects on nervous system / Dementia / Genetic factors / Elders in an island community / Cerebrovascular disorders / MMSE / Polymorphism of ACE gene / Mitochondria DNA 5178 / 脳血管性痴呆 / 神経疾患
Research Abstract

Purpose: To clarify aging effects on neurological findings and genetic factors related to vascular dementia, we analyzed neurological findings in elders living an island community and genetic factors in patients with cerebrovascular disorders (CVD).
Methods and materials: 1) Neurological findings, dementia scale (MMSE) and dietary intake in the elders aged 60 year-old or over living in an island in Kagoshima, Japan were studied every other year. 2) Angiotensin converting enzyme (ACE) gene (II, ID, DD) and mitochondria 5178C/A polymorphism were analyzed in patients with CVD (127 cases) and the elders in an island (294 cases).
Results: 1) The longitudinal study in the elders in an island. The score of MMSE in 590 elders was decreased with aging and the decrease ratio was higher in elders with aging. The incidence of cardiac disorders was significantly high in the elders without decrement of MMSE scale, but the incidence of renal disorders was high in the elders with decrement of the scale. Some dietary intake (tempura etc) showed negative correlation with MMSE score. 2) Genetic polymorphism and CVD. The mitochondrial DNA (mtDNA) polymorphism, 5178C, was significantly dominant in patients with CVD (p<0.01). MtDNA5178C was also dominant in all CVD subtypes without statistical difference between CVD subtypes. The women CVD patients with mt5178C showed higher total cholesterol and triglyceride levels in serum. ACE genotypes and allele frequency were not different between CVD patients and control or between CVD subtypes.
Conclusions: In this study, we showed the longitudinal change of dementia scale and the factors that might be related to the change in elders living in an island. We also demonstrated the genetic factors that might be related to the onset of CVD.

Report

(3 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report
  • Research Products

    (29 results)

All Other

All Publications (29 results)

  • [Publications] Isashiki Y, Nakagawa M, Ohba N, et al.: "Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation"Acta Ophthalmologica Scandinavica. 76. 6-13 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yamagata H, nakagawa M, Johnson K, Miki T.: "Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese population. Journal of"Human Genetics. 43. 246-269 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Hirata K, Nakagawa M, higuchi I, et al.: "Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution"Journal of Human Genetics. 44. 210-214 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Nakagawa M, Suehara M, Saito A, et al.: "A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths"Neurology. 52. 1271-1275 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Takashima H, Nakagawa M, Kanzaki A, et al.: "Germline Mosaicism of MPZ Gene in Dejerine-Sottas Syndrome (HMSN III) Associated with Hereditary Stomatocytosis"Neuromuscular Disorders. 9. 232-238 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Takashima H, Nakagawa M, Suehara M, et al.: "Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1"Neuromuscular Disorders. 9. 368-371 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Nakagawa m, Takashima H, Suehara M, et al.: "hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P): clinical, pathological and genetic features"The Annuals of the New York Academy of Sciences. 883. 449-452 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Ohkubo R, Nakagawa M, Higuchi I, et al.: "familial skeletal myopathy with atrioventricular block"Internal medicine. 38. 856-860 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yamada H, Nakagawa M, Higuchi I, et al.: "Detection of DNA fragmentation of myonuclei in myotonic dystrophy by double staining with anti-emerin antibody and by nick end-labeling"Journal of Neurological Sciences. 173. 97-102 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Shimokata S, yamada Y, Nakagawa m, et al.: "Distribution of geriatric disease-related genotypes in the national institute for longevity sciences, longitudinal study of aging (NILS-LSA)"Journal of Epidemiology. (in press).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Isashiki Y, Nakagawa M, Ohba N, Kamimura K, Sakoda Y, Higuchi I, Izumo S, Osame M: "Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation"Acta Ophthalmologica Scandinavica. 76. 6-13 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yamagata H, Nakagawa M, Johnson K, Miki T.: "Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese population."Journal of Human Genetics. 43. 246-249 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Hirata K, Nakagawa M, Higuchi I, Hashimoto K, Hanada K, Takahashi K, Niiyama T, Izumi K, Sakoda S, Yamada H, Osame M: "Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution"Journal of Human Genetics. 44. 210-214 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Nakagawa M, Suehara M, Saito A, Takashima H, Umehara F, Saito M, Kanzato N, Matsuzaki T, Takenaga S, Sakoda S, Izumo S, Osame M.: "A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths."Neurology. 52. 1271-1275 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Takashima H, Nakagawa M, Kanzaki A, Yawata Y, Horikiri T, Matsuzaki T, Suehara M, Izumo S, Osame M.: "Germline Mosaicism of MPZ Gene in Dejerine-Sottas Syndrome (HMSN III) Associated with Hereditary Stomatocytosis."Neuromuscular Disorders. 9. 232-238 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Takashima H, Nakagawa M, Suehara M, Saito M, Saito A, Kanzato N, Matsuzaki T,Hirata K, Terwilliger JD, Osame M.: "Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1"Neuromuscular Disorders. 9. 368-371 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Nakagawa M, Takashima H, Suehara M, Saito M, Saito A, Kamisato N, Matsuzaki T, Keiko Hirata K, Shuji Izumo S, Joseph D Terwilliger JD, Osame M.: "Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) : clinical, pathological and genetic features."The Annals of the New York Academy of Sciences. 883. 449-452 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Ohkubo R, Nakagawa M, Higuchi I, Utatsu Y, Miyazato H, Atsuchi Y, Osame M.: "Familial skeletal myopathy with atrioventricular block."Internal Medicine. 38. 856-860 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yamada H, Nakagawa M, Higuchi I, Horikiri T, Osame M.: "Detection of DNA fragmentation of myonuclei in myotonic dystrophy by double staining with anti-emerin antibody and by nick end-labeling."Journal of Neurological Sciences. 173. 97-102 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Shimokata S, Yamada Y, Nakagawa M, et al.: "Distribution of geriatric disease-related genotypes in the national institute for longevity sciences, longitudinal study of aging (NlLS-LSA)"Journal of Epidemiology. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] hirata k,nakgawa m et al.: "adult onset limb-girdle type mitochondrial myopathy with a mitocitocondrial dna np8291 A-10-G substitution"journal of genetics. 44. 210-214 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] nakgawa M,suehara m et al: "Anovel mpz gene mutationin dominantly inherited neuropathy with fucallyfolded myelin"Neurology. 52. 1271-1275 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Takashima H,Nakagawa M,et al: "Gernline Mosaicism of MPz Gene in Dejerine-Sottas Syndrome(HMSN III)Associated with Hereditary Stomatocytosis."Neuromuscular Disorders. 9. 232-238 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Tkashima H,Nakagawa M,et al.: "Gene for herediary motor and sensory neuropathy(proximal dominant foem)mapped to to 3q13.1"Neuromuscular Disorders. 9. 368-371 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Nakagawa M,Takashima H,etal: "Hereditary motaor and sensory nuurpathy with proximal dominant involvement(HMSN-P):clinical,pathological and genetic features."The Annals of the New York Academy of Sciences. 883. 449-452 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Shimokata S,Yamada y,Nakagawa M,et al: "Distribution of geriatric disease-related genotypes in the national institute for longevity sciences,longitudial study of aging(NILS-LSA)"journal of Epidemiology. in press.

    • Related Report
      1999 Annual Research Report
  • [Publications] Nakagawa M.Suehara M,et al: "A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths." Neurology. (in press).

    • Related Report
      1998 Annual Research Report
  • [Publications] Takashima H,Nakagawa M,et al.: "Germline Mosaicism of MPZ Gene in Dejerine-Sottas Syndrome(HMSN III)Associated with Hereditary Stomatocytosis." Neuromuscular Disorders. (in press).

    • Related Report
      1998 Annual Research Report
  • [Publications] Nakagawa M,Takashima H,et al.: "Hereditary motor and sencory neuropathy with proximal dominant involvement(HMSN-P):clinical,pathological and genetic features." The Annals of the New York Academy of Sciences. (in press).

    • Related Report
      1998 Annual Research Report

URL: 

Published: 1998-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi