LHON Project.
The Ottawa Eye Institute, University of Ottawa, Ottawa Canada.
Ophthalmology. 2020 May;127(5):679-688. doi: 10.1016/j.ophtha.2019.11.014. Epub 2019 Nov 25.
To study the demographics of Leber's hereditary optic neuropathy (LHON) using a large international database of people affected by LHON.
Cross-sectional study.
One thousand five hundred seventeen people affected by LHON with a known pathogenic genetic mutation.
Self-reported genetic and demographic data were collected. The data were de-identified and then analyzed.
Leber's hereditary optic neuropathy mutation, gender, age at vision loss onset, and geographical region.
The data showed that both females and males can experience symptom onset at any age. We found a 3:1 male-to-female ratio. Interestingly, at younger than 5 years and older than 45 years, the male-to-female ratio of those becoming affected was approximately 1:1. A dramatic peak in age at onset of vision loss was found among males between 14 and 26 years of age. Disease onset in females occurred across all age groups, without any comparable dramatic peak of onset age. This study found that 10% of individuals become affected with LHON after 50 years of age. According to the literature, we found that the m.11778, m.14484, and m.3460 mutations were the most common LHON point mutations in both males and females, with a similar age at onset distribution.
This was the largest study of LHON demographics to date. It showed that women carrying an LHON mutation are at higher risk of losing vision than is generally expected. Unlike the traditional 5:1 male-to-female ratio commonly reported in the literature, we found a 3:1 male-to-female ratio. Earlier studies may have harbored an ascertainment bias of overemphasizing the confirmation of this being a disease of young men. However, our data suggest that LHON is a disease that affects both females and males of all ages. This should prompt physicians to conduct genetic testing for LHON in all patients who meet the clinical criteria, regardless of whether they fit the demographics traditionally associated with the disease. Counseling about LHON should be offered to all maternal bloodline relatives, females and males of all ages, because they are at risk of sudden-onset legal blindness.
利用大型 Leber 遗传性视神经病变(LHON)患者国际数据库,研究 LHON 的人口统计学特征。
横断面研究。
1517 名携带已知致病性基因突变的 LHON 患者。
收集患者的遗传和人口统计学数据。这些数据经过去识别处理,然后进行分析。
Leber 遗传性视神经病变突变、性别、视力丧失起始年龄和地理区域。
数据显示,男性和女性都可能在任何年龄出现症状。我们发现男女比例为 3:1。有趣的是,在 5 岁以下和 45 岁以上,发病的男女比例约为 1:1。男性在 14 至 26 岁之间,视力丧失起始年龄出现明显高峰。女性在所有年龄段均有发病,无类似的发病年龄高峰。本研究发现,10%的人在 50 岁后出现 LHON。根据文献,我们发现 m.11778、m.14484 和 m.3460 突变是男性和女性中最常见的 LHON 点突变,发病年龄分布相似。
这是迄今为止对 LHON 人口统计学特征的最大研究。结果表明,携带 LHON 突变的女性比一般预期更有可能丧失视力。与文献中通常报道的 5:1 的传统男女比例不同,我们发现男女比例为 3:1。早期研究可能存在确认偏倚,过分强调该病是一种青年男性疾病。然而,我们的数据表明,LHON 是一种影响所有年龄段男女的疾病。这应该促使医生对所有符合临床标准的患者进行 LHON 基因检测,无论他们是否符合传统上与该病相关的人口统计学特征。应向所有母系血缘亲属、所有年龄段的女性和男性提供关于 LHON 的咨询,因为他们有突发失明的法律风险。