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Ocular Adnexa and Cornea

Association between Family History and Keratoconus Severity

, , , &
Pages 1414-1418 | Received 17 Aug 2015, Accepted 29 Nov 2015, Published online: 09 May 2016
 

ABSTRACT

Purpose: The high prevalence of positive family history of keratoconus (KC) in KC patients is well-known. However, the results regarding the association between family history of KC and disease severity are controversial. The aim of this study was to evaluate the possible association between family history and severity of KC.

Method: Clinical data of 1496 KC patients were evaluated. All participants were asked if they had had a family member with KC. Topographic and keratometric measurements of KC patients, including central corneal thickness (CCT), thinnest corneal thickness (TCT), mean, flat, and steep keratometry values (K) by the use of Pentacam, best-spectacle corrected visual acuity (BCVA), spherical equivalent (SE), and astigmatism were recorded and compared according to patients with and without a family history of KC, first- or second-degree family members, and the number of family members with KC. Severity of KC was classified according to the Amsler–Krumeich classification.

Results: Family history of KC was present in 292 (19.5%) patients. Of those 292 patients who had a family history of KC, 159 (54.5%) had one family member with KC and 133 (45.5%) had two or more family members with KC. There was not a significant difference between corneal pachymetry and K values of the patients with and without a family history of KC (p > 0.05). However, those with a positive family history of KC had more severe disease, according to the Amsler–Krumeich classification (p < 0.05). KC patients who had more family members with KC had significantly lower TCT and significantly higher steep K and astigmatism (p < 0.05), and had more severe disease, according to the Amsler–Krumeich classification (p < 0.05).

Conclusion: We suggest that patients with more family members with KC should be subject to screening to identify early disease.

Declaration of interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper. No funds, grants, or other support were received. This article has not been presented at a meeting or published or submitted for publication elsewhere. The authors take responsibility for all aspects of the reliability and freedom from bias of the data presented and their discussed interpretation.

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