Ocular Biometry in Primary Angle-Closure Glaucoma Associated with Retinitis Pigmentosa. (31st December 2017)
- Record Type:
- Journal Article
- Title:
- Ocular Biometry in Primary Angle-Closure Glaucoma Associated with Retinitis Pigmentosa. (31st December 2017)
- Main Title:
- Ocular Biometry in Primary Angle-Closure Glaucoma Associated with Retinitis Pigmentosa
- Authors:
- Xu, Jiangang
Ouyang, Zhikun
Yang, Yangfan
Cai, Xiaoyu
Wang, Zhonghao
Lin, Mingkai
Zhang, Xiulan
Liu, Xing
Yu, Minbin - Other Names:
- Thomas Biju B. Academic Editor.
- Abstract:
- Abstract : Background . Retinitis pigmentosa (RP) comprises a group of inherited disorders in which patients typically lose night vision in adolescence and then lose peripheral vision in young adulthood before eventually losing central vision later in life. A retrospective case-control study was performed to evaluate differences in ocular biometric parameters in primary angle-closure glaucoma (PACG) patients with and without concomitant RP to determine whether a relationship exists between PACG and RP. Methods . We used ultrasound biomicroscopy (UBM) to measure anterior chamber depth (ACD). A-scan biometry was carried out to measure lens thickness (LT) and axial length (AL). Propensity score matching and mixed linear regression model analysis were conducted. 23 patients with chronic primary angle-closure glaucoma (CPACG) associated with RP, 21 patients with acute primary angle-closure glaucoma (APACG) associated with RP, 270 patients with CPACG, and 269 patients with APACG were recruited for this study. Results . There were no significant differences on ACDs, ALs, and relative lens position (RLP) (P > 0.05 ) between patients with PACG associated with RP and patients with PACG; however, patients with APACG associated with RP had a significantly greater LT than patients with APACG (P < 0.05 ). Conclusion . Patients with PACG associated with RP had the same biometric parameter characteristic as the patients with CPACG and APACG. This may suggest that RP is a coincidentalAbstract : Background . Retinitis pigmentosa (RP) comprises a group of inherited disorders in which patients typically lose night vision in adolescence and then lose peripheral vision in young adulthood before eventually losing central vision later in life. A retrospective case-control study was performed to evaluate differences in ocular biometric parameters in primary angle-closure glaucoma (PACG) patients with and without concomitant RP to determine whether a relationship exists between PACG and RP. Methods . We used ultrasound biomicroscopy (UBM) to measure anterior chamber depth (ACD). A-scan biometry was carried out to measure lens thickness (LT) and axial length (AL). Propensity score matching and mixed linear regression model analysis were conducted. 23 patients with chronic primary angle-closure glaucoma (CPACG) associated with RP, 21 patients with acute primary angle-closure glaucoma (APACG) associated with RP, 270 patients with CPACG, and 269 patients with APACG were recruited for this study. Results . There were no significant differences on ACDs, ALs, and relative lens position (RLP) (P > 0.05 ) between patients with PACG associated with RP and patients with PACG; however, patients with APACG associated with RP had a significantly greater LT than patients with APACG (P < 0.05 ). Conclusion . Patients with PACG associated with RP had the same biometric parameter characteristic as the patients with CPACG and APACG. This may suggest that RP is a coincidental relationship with angle-closure glaucoma. … (more)
- Is Part Of:
- Journal of ophthalmology. Volume 2017(2017)
- Journal:
- Journal of ophthalmology
- Issue:
- Volume 2017(2017)
- Issue Display:
- Volume 2017, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 2017
- Issue:
- 2017
- Issue Sort Value:
- 2017-2017-2017-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-12-31
- Subjects:
- Ophthalmology -- Periodicals
Eye Diseases
Ophthalmology
Ophthalmology
Electronic journals
Periodicals
Periodicals
Fulltext
Internet Resources
Periodicals
617.7 - Journal URLs:
- https://www.hindawi.com/journals/joph/ ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/1195/ ↗
http://bibpurl.oclc.org/web/46495 ↗
http://search.ebscohost.com/direct.asp?db=a9h&jid=%229038%22&scope=site ↗ - DOI:
- 10.1155/2017/9164846 ↗
- Languages:
- English
- ISSNs:
- 2090-004X
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library HMNTS - ELD Digital store
- Ingest File:
- 22805.xml