Allelic variation in the VMD2 gene in best disease and age-related macular degeneration

Andrew J. Lotery, Francis L. Munier, Gerald A. Fishman, Richard Weleber, Samuel G. Jacobson, Louisa M. Affatigato, Brian E. Nichols, Daniel F. Schorderet, Val C. Sheffield, Edwin M. Stone

Research output: Contribution to journalArticle

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Abstract

PURPOSE. To assess the allelic variation of the VMD2 gene in patients with Best disease and age-related macular degeneration (AMD). METHODS. Three hundred twenty-one AMD patients, 192 ethnically similar control subjects, 39 unrelated probands with familial Best disease, and 57 unrelated probands with the ophthalmoscopic findings of Best disease but no family history were screened for sequence variations in the VMD2 gene by single-strand conformation polymorphism (SSCP) analysis. Amplimers showing a bandshift were reamplified and sequenced bidirectionally. In addition, the coding regions of the VMD2 gene were completely sequenced in six probands with familial Best disease who showed no SSCP shift. RESULTS. Forty different probable or possible disease-causing mutations were found in one or more Best disease or AMD patients. Twenty-nine of these variations are novel. Of the 39 probands with familial Best disease, mutations were detected in all 39 (33 by SSCP and 6 by DNA sequencing). SSCP screening of the 57 probands with a clinical diagnosis of Best disease but no family history revealed 16 with mutations. Mutations were found in 5 of 321 AMD patients (1.5%), a fraction that was not significantly greater than in control individuals (0/192, 0%). CONCLUSIONS. Patients with the clinical diagnosis of Best disease are significantly more likely to have a mutation in the VMD2 gene if they also have a positive family history. These findings suggest that a small fraction of patients with the clinical diagnosis of AMD may actually have a late-onset variant of Best disease, whereas at the same time, a considerable fraction of isolated patients with the ophthalmoscopic features of Best disease are probably affected with some other macular disease.

Original languageEnglish (US)
Pages (from-to)1291-1296
Number of pages6
JournalInvestigative Ophthalmology and Visual Science
Volume41
Issue number6
StatePublished - 2000

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Vitelliform Macular Dystrophy
Macular Degeneration
Genes
Mutation
DNA Sequence Analysis

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Lotery, A. J., Munier, F. L., Fishman, G. A., Weleber, R., Jacobson, S. G., Affatigato, L. M., ... Stone, E. M. (2000). Allelic variation in the VMD2 gene in best disease and age-related macular degeneration. Investigative Ophthalmology and Visual Science, 41(6), 1291-1296.

Allelic variation in the VMD2 gene in best disease and age-related macular degeneration. / Lotery, Andrew J.; Munier, Francis L.; Fishman, Gerald A.; Weleber, Richard; Jacobson, Samuel G.; Affatigato, Louisa M.; Nichols, Brian E.; Schorderet, Daniel F.; Sheffield, Val C.; Stone, Edwin M.

In: Investigative Ophthalmology and Visual Science, Vol. 41, No. 6, 2000, p. 1291-1296.

Research output: Contribution to journalArticle

Lotery, AJ, Munier, FL, Fishman, GA, Weleber, R, Jacobson, SG, Affatigato, LM, Nichols, BE, Schorderet, DF, Sheffield, VC & Stone, EM 2000, 'Allelic variation in the VMD2 gene in best disease and age-related macular degeneration', Investigative Ophthalmology and Visual Science, vol. 41, no. 6, pp. 1291-1296.
Lotery, Andrew J. ; Munier, Francis L. ; Fishman, Gerald A. ; Weleber, Richard ; Jacobson, Samuel G. ; Affatigato, Louisa M. ; Nichols, Brian E. ; Schorderet, Daniel F. ; Sheffield, Val C. ; Stone, Edwin M. / Allelic variation in the VMD2 gene in best disease and age-related macular degeneration. In: Investigative Ophthalmology and Visual Science. 2000 ; Vol. 41, No. 6. pp. 1291-1296.
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abstract = "PURPOSE. To assess the allelic variation of the VMD2 gene in patients with Best disease and age-related macular degeneration (AMD). METHODS. Three hundred twenty-one AMD patients, 192 ethnically similar control subjects, 39 unrelated probands with familial Best disease, and 57 unrelated probands with the ophthalmoscopic findings of Best disease but no family history were screened for sequence variations in the VMD2 gene by single-strand conformation polymorphism (SSCP) analysis. Amplimers showing a bandshift were reamplified and sequenced bidirectionally. In addition, the coding regions of the VMD2 gene were completely sequenced in six probands with familial Best disease who showed no SSCP shift. RESULTS. Forty different probable or possible disease-causing mutations were found in one or more Best disease or AMD patients. Twenty-nine of these variations are novel. Of the 39 probands with familial Best disease, mutations were detected in all 39 (33 by SSCP and 6 by DNA sequencing). SSCP screening of the 57 probands with a clinical diagnosis of Best disease but no family history revealed 16 with mutations. Mutations were found in 5 of 321 AMD patients (1.5{\%}), a fraction that was not significantly greater than in control individuals (0/192, 0{\%}). CONCLUSIONS. Patients with the clinical diagnosis of Best disease are significantly more likely to have a mutation in the VMD2 gene if they also have a positive family history. These findings suggest that a small fraction of patients with the clinical diagnosis of AMD may actually have a late-onset variant of Best disease, whereas at the same time, a considerable fraction of isolated patients with the ophthalmoscopic features of Best disease are probably affected with some other macular disease.",
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T1 - Allelic variation in the VMD2 gene in best disease and age-related macular degeneration

AU - Lotery, Andrew J.

AU - Munier, Francis L.

AU - Fishman, Gerald A.

AU - Weleber, Richard

AU - Jacobson, Samuel G.

AU - Affatigato, Louisa M.

AU - Nichols, Brian E.

AU - Schorderet, Daniel F.

AU - Sheffield, Val C.

AU - Stone, Edwin M.

PY - 2000

Y1 - 2000

N2 - PURPOSE. To assess the allelic variation of the VMD2 gene in patients with Best disease and age-related macular degeneration (AMD). METHODS. Three hundred twenty-one AMD patients, 192 ethnically similar control subjects, 39 unrelated probands with familial Best disease, and 57 unrelated probands with the ophthalmoscopic findings of Best disease but no family history were screened for sequence variations in the VMD2 gene by single-strand conformation polymorphism (SSCP) analysis. Amplimers showing a bandshift were reamplified and sequenced bidirectionally. In addition, the coding regions of the VMD2 gene were completely sequenced in six probands with familial Best disease who showed no SSCP shift. RESULTS. Forty different probable or possible disease-causing mutations were found in one or more Best disease or AMD patients. Twenty-nine of these variations are novel. Of the 39 probands with familial Best disease, mutations were detected in all 39 (33 by SSCP and 6 by DNA sequencing). SSCP screening of the 57 probands with a clinical diagnosis of Best disease but no family history revealed 16 with mutations. Mutations were found in 5 of 321 AMD patients (1.5%), a fraction that was not significantly greater than in control individuals (0/192, 0%). CONCLUSIONS. Patients with the clinical diagnosis of Best disease are significantly more likely to have a mutation in the VMD2 gene if they also have a positive family history. These findings suggest that a small fraction of patients with the clinical diagnosis of AMD may actually have a late-onset variant of Best disease, whereas at the same time, a considerable fraction of isolated patients with the ophthalmoscopic features of Best disease are probably affected with some other macular disease.

AB - PURPOSE. To assess the allelic variation of the VMD2 gene in patients with Best disease and age-related macular degeneration (AMD). METHODS. Three hundred twenty-one AMD patients, 192 ethnically similar control subjects, 39 unrelated probands with familial Best disease, and 57 unrelated probands with the ophthalmoscopic findings of Best disease but no family history were screened for sequence variations in the VMD2 gene by single-strand conformation polymorphism (SSCP) analysis. Amplimers showing a bandshift were reamplified and sequenced bidirectionally. In addition, the coding regions of the VMD2 gene were completely sequenced in six probands with familial Best disease who showed no SSCP shift. RESULTS. Forty different probable or possible disease-causing mutations were found in one or more Best disease or AMD patients. Twenty-nine of these variations are novel. Of the 39 probands with familial Best disease, mutations were detected in all 39 (33 by SSCP and 6 by DNA sequencing). SSCP screening of the 57 probands with a clinical diagnosis of Best disease but no family history revealed 16 with mutations. Mutations were found in 5 of 321 AMD patients (1.5%), a fraction that was not significantly greater than in control individuals (0/192, 0%). CONCLUSIONS. Patients with the clinical diagnosis of Best disease are significantly more likely to have a mutation in the VMD2 gene if they also have a positive family history. These findings suggest that a small fraction of patients with the clinical diagnosis of AMD may actually have a late-onset variant of Best disease, whereas at the same time, a considerable fraction of isolated patients with the ophthalmoscopic features of Best disease are probably affected with some other macular disease.

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