You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 125 No. 6, June 2007 TABLE OF CONTENTS
  Archives
  •  Online Features
  Ophthalmic Molecular Genetics
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on ISI (1)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Topic Collections
 •Genetics
 •Genetic Disorders
 •Alert me on articles by topic

Myocilin Variants in Indian Patients With Open-angle Glaucoma

Ashima Bhattacharjee, MSc; Moulinath Acharya, MSc; Arijit Mukhopadhyay, PhD; Suddhasil Mookherjee, MSc; Deblina Banerjee, BTech; Arun K. Bandopadhyay, MS; Sanjay K. D. Thakur, MS, DO; Abhijit Sen, MS, DNB; Kunal Ray, PhD

Arch Ophthalmol. 2007;125(6):823-829.

Objective  To identify and evaluate MYOC variant alleles among patients with primary open-angle glaucoma (POAG) and age-matched control subjects in an Indian population.

Methods  Three hundred fifteen patients with POAG and 100 unrelated control subjects from the same ethnic background were enrolled in the study. The coding sequence of MYOC was amplified by polymerase chain reaction using genomic DNA, followed by sequencing of the polymerase chain reaction products. Four single nucleotide polymorphisms were genotyped in different Indian subpopulations comprising 1466 individuals using SEQUENOM's homogeneous MassEXTEND assay.

Results  One novel mutation (Gly399Asp), 6 reported mutations (Gln48His, Thr256Met, Thr353Ile, Gln368Stop, Pro370Leu, and Ala427Thr), and 6 single nucleotide polymorphisms were identified in MYOC. Ala427Thr was identified in a patient with POAG and Parkinson disease. Four single nucleotide polymorphisms genotyped in control subjects were highly heterozygous and displayed a similar pattern of linkage disequilibrium among all linguistic groups.

Conclusions  MYOC mutations account for 2.2% of POAG cases. The Gln368Stop mutation (common among persons of the white race) found in 2 families does not seem to be of white race origin. Identification of a MYOC mutation (Ala427Thr) in a patient with POAG and Parkinson disease is interesting with respect to reported interaction of myocilin with synucleins.

Clinical Relevance  Studying the genetics of POAG is helpful for preclinical identification and for better disease management.


Author Affiliations: Molecular and Human Genetics Division, Indian Institute of Chemical Biology (Mss Bhattacharjee and Banerjee, Messrs Acharya and Mookherjee, and Drs Mukhopadhyay and Ray); Regional Institute of Ophthalmology, Medical College (Drs Bandopadhyay and Thakur); and Dristipradip Clinic, Jodhpur Park (Dr Sen); Kolkata, India.







HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2007 American Medical Association. All Rights Reserved.