Raskind W H, Hsu L, Berninger V W, Thomson J B, Wijsman E M
Department of Medicine, University of Washington, Seattle 98195-7720, USA.
Behav Genet. 2000 Sep;30(5):385-96. doi: 10.1023/a:1002700605187.
There is evidence for genetic contributions to reading disability, but the phenotypic heterogeneity associated with the clinical diagnosis may make identification of the underlying genetic basis difficult. In order to elucidate distinct phenotypic features that may be contributing to the genotypic heterogeneity, we assessed the familial aggregation patterns of Verbal IQ and 24 phenotypic measures associated with dyslexia in 102 nuclear families ascertained through probands in grades 1 through 6 who met the criteria for this disorder. Correlations between relatives were computed for all diagnostic phenotypes, using a generalized estimating equation (GEE) approach. GEE is a recently developed semiparametric method for handling correlated data. The method is robust to model misspecification and flexible in adjusting for the subjects' characteristics and pedigree sizes as well as for the ascertainment process, while estimating the correlations between related subjects. The Nonword Memory (NWM) subtest of a prepublication version of the Comprehensive Test of Phonological Processing (CTOPP) and Phonemic Decoding Efficiency (PDE) subtest of a prepublication version of the Test of Word Reading Efficiency (TOWRE) showed correlation patterns in relatives that are strongly supportive of a genetic basis. The Wechsler Scale Digit Span, the Word Attack subtest of the Woodcock Reading Mastery Test--Revised, and the Spelling subtest of the Wide Range Achievement Test--Third Edition had slightly weaker evidence of a genetic basis. Five additional phenotypes (the Spelling subtest of the Wechsler Individual Achievement Test, the Accuracy, Rate, and Comprehension subtests of the Gray Oral Reading Test--Third Edition, and Rapid Automatized Naming of Letters and Numbers) gave suggestive evidence of such a pattern. The results cross-validate in that evidence for a pattern consistent with a genetic basis was obtained for two measures of phonological short-term memory (CTOPP Nonword Memory and WISCIII or WAIS-R Digit Span), for two measures of phonological decoding (WRMT-R Word Attack and TOWRE Phonemic Decoding Efficiency), and for two measures of spelling from dictation (WRAT-3 Spelling and, to a lesser extent, WIAT Spelling). These measures are thus good candidates for more sophisticated segregation analyses that can formulate models for incorporation into linkage analyses.
有证据表明基因对阅读障碍有影响,但与临床诊断相关的表型异质性可能使确定潜在的基因基础变得困难。为了阐明可能导致基因型异质性的不同表型特征,我们评估了102个核心家庭中言语智商和24个与诵读困难相关的表型指标的家族聚集模式,这些家庭是通过1至6年级符合该疾病标准的先证者确定的。使用广义估计方程(GEE)方法计算所有诊断表型亲属之间的相关性。GEE是一种最近开发的用于处理相关数据的半参数方法。该方法对模型误设具有鲁棒性,并且在估计相关受试者之间的相关性时,在调整受试者特征、家系大小以及确定过程方面具有灵活性。语音加工综合测试(CTOPP)预发表版本的非词记忆(NWM)子测试和单词阅读效率测试(TOWRE)预发表版本的音素解码效率(PDE)子测试在亲属中显示出的相关模式强烈支持基因基础。韦氏智力量表数字广度、伍德库克阅读能力测验修订版的单词攻击子测试以及广泛成就测验第三版的拼写子测试显示基因基础的证据稍弱。另外五个表型(韦氏个别成就测验的拼写子测试、格雷口语阅读测验第三版的准确性、速度和理解子测试以及字母和数字的快速自动命名)给出了这种模式的提示性证据。结果相互验证,因为对于语音短期记忆的两项测量(CTOPP非词记忆和WISCIII或WAIS-R数字广度)、语音解码的两项测量(WRMT-R单词攻击和TOWRE音素解码效率)以及听写拼写的两项测量(WRAT-3拼写以及程度稍低的WIAT拼写),都获得了与基因基础一致的模式证据。因此,这些测量是更复杂的分离分析的良好候选对象,分离分析可以制定模型以纳入连锁分析。