Literature DB >> 16510341

Consanguinity and eye diseases with a potential genetic etiology. Data from a prevalence study in Andhra Pradesh, India.

Praveen K Nirmalan1, Sannapaneni Krishnaiah, Rishita Nutheti, Bindiganavale R Shamanna, Gullapalli N Rao, Ravi Thomas.   

Abstract

PURPOSE: To determine the prevalence of consanguinity and its potential associations with eye diseases in Andhra Pradesh state of south India.
METHODS: As part of a demographic interview schedule, prior to clinical examinations, trained investigators collected information regarding consanguinity of the parents from subjects randomly chosen for a population-based cross-sectional epidemiological study. Each subject underwent a detailed ocular examination including visual acuity measurements, anterior segment examinations with slit-lamp biomicroscopy, and posterior segment examinations. Adjusted odds ratios (OR), attributable risks (AR) and population attributable risks (PAR) were estimated.
RESULTS: We obtained details regarding consanguinity of the parents from 10,290 of the 10,293 subjects who were enumerated and examined in the study. Parental consanguinity was reported by 1822 (24.7%) rural subjects and 782 (32.9%) urban subjects. Eighty (0.008%, 95% CI: 0.006, 0.010) of the 9757 subjects had an ocular disease with a potential genetic basis. We found microcornea to be significantly associated with both an uncle-niece relationship (adjusted OR: 7.32, 95% CI: 1.73, 30.97, AR = 86.34%, PAR = 42.11%) and a first-cousin relationship between the parents (adjusted OR 4.51, 95% CI: 1.05, 19.40, AR = 77.83%, PAR = 29.02%). Retinitis pigmentosa was significantly associated with a first-cousin relationship between the parents (adjusted OR: 5.31, 95% CI: 1.00, 28.25, AR = 81.17%, PAR = 33.43%).
CONCLUSIONS: The high prevalence of consanguinity in this population does not appear to translate into a high prevalence of ocular malformations; however, studies with larger sample sizes are required to further explore the strength of these associations.

Entities:  

Mesh:

Year:  2006        PMID: 16510341     DOI: 10.1080/09286580500473795

Source DB:  PubMed          Journal:  Ophthalmic Epidemiol        ISSN: 0928-6586            Impact factor:   1.648


  11 in total

1.  Consanguinity and its association with visual impairment in southern India: the Pavagada Pediatric Eye Disease Study 2.

Authors:  Vasudha Kemmanu; Subramanya K Giliyar; Harsha L Rao; Bhujanga K Shetty; Govindasamy Kumaramanickavel; Catherine A McCarty
Journal:  J Community Genet       Date:  2018-12-01

2.  Analyzing Inbreeding and Estimating Its Related Deficiencies in Northeastern Brazil.

Authors:  Cristian Rodrigues do Nascimento; Dyowani Dos Santos Basílio; Johnnatas Mikael Lopes; Isaac Farias Cansanção
Journal:  J Pediatr Genet       Date:  2021-04-01

3.  Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.

Authors:  Maleeha Maria; Muhammad Ajmal; Maleeha Azam; Nadia Khalida Waheed; Sorath Noorani Siddiqui; Bilal Mustafa; Humaira Ayub; Liaqat Ali; Shakeel Ahmad; Shazia Micheal; Alamdar Hussain; Syed Tahir Abbas Shah; Syeda Hafiza Benish Ali; Waqas Ahmed; Yar Muhammad Khan; Anneke I den Hollander; Lonneke Haer-Wigman; Rob W J Collin; Muhammad Imran Khan; Raheel Qamar; Frans P M Cremers
Journal:  PLoS One       Date:  2015-03-16       Impact factor: 3.240

4.  Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum.

Authors:  Maleeha Maria; Ideke J C Lamers; Miriam Schmidts; Muhammad Ajmal; Sulman Jaffar; Ehsan Ullah; Bilal Mustafa; Shakeel Ahmad; Katia Nazmutdinova; Bethan Hoskins; Erwin van Wijk; Linda Koster-Kamphuis; Muhammad Imran Khan; Phil L Beales; Frans P M Cremers; Ronald Roepman; Maleeha Azam; Heleen H Arts; Raheel Qamar
Journal:  Sci Rep       Date:  2016-10-06       Impact factor: 4.379

5.  Descriptive Study of a Cohort of 488 Patients with Inherited Retinal Dystrophies.

Authors:  Rosa M Coco-Martin; Miguel Diego-Alonso; W Andres Orduz-Montaña; M Rosa Sanabria; Hortensia Sanchez-Tocino
Journal:  Clin Ophthalmol       Date:  2021-03-09

6.  Knowledge of genetic eye diseases and genetic services and attitudes toward genetic testing and gene therapy.

Authors:  Pratyusha Ganne; Manikanta Damagatla; Navya Krishna Naidu
Journal:  Taiwan J Ophthalmol       Date:  2021-11-15

Review 7.  Genetics of Inherited Retinal Diseases in Understudied Populations.

Authors:  Chitra Kannabiran; Deepika Parameswarappa; Subhadra Jalali
Journal:  Front Genet       Date:  2022-02-28       Impact factor: 4.599

Review 8.  Approach to inherited retinal diseases.

Authors:  Dhanashree Ratra; Sengul Ozdek; Munispriyan Raviselvan; Sailaja Elchuri; Tarun Sharma
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

9.  Consanguinity and ocular disorders in India: Electronic medical records driven big data analytics.

Authors:  Divya Rauniyar; Anthony Vipin Das
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

10.  Decoding retinitis pigmentosa.

Authors:  Sundaram Natarajan
Journal:  Indian J Ophthalmol       Date:  2013-03       Impact factor: 1.848

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.