O'Leary C A, Duffy D L, Gething M A, McGuckin C, Rand J S
a Centre for Companion Animal Health , The University of Queensland , St Lucia 4072 QLD Australia.
N Z Vet J. 2013 Nov;61(6):354-8. doi: 10.1080/00480169.2013.817295. Epub 2013 Aug 5.
To investigate, in a pilot study, a possible genetic component to type 2 diabetes mellitus (T2D) in Burmese cats in New Zealand by analysing pedigree data.
Pedigrees were obtained for 305 Burmese cats living in New Zealand; diabetes was diagnosed in 19 of these due to presence of polyuria and polydipsia, persistent concentrations of glucose in plasma >16 mmol/L and glucosuria prior to insulin treatment. Pedigrees were also submitted for 16 cats with no clinical signs of T2D. The remaining 270 cats were unobserved relatives of these individuals. Inbreeding coefficients and heritability were calculated, and a single major locus model segregation analysis was conducted using pedigree analysis software.
Nineteen cats were diagnosed with T2D. Males (n = 14) and females (n = 5) were both affected, suggesting that the gene or genes causing diabetes are autosomal rather than sex-linked. Examination of the pedigree revealed few signs of fully penetrant dominant gene action: diabetes was ostensibly rarely seen in sequential generations and nearly always skipped at least one and often more generations; apparently unaffected offspring of apparently unaffected parents sometimes produced affected progeny. The mean relatedness of the affected animals within the core pedigree (16 diabetic cats) was 0.049, and mean inbreeding 0.033. Based on 100,000 permutations of the trait values, the expected relatedness of a random sample of 16 animals taken from the phenotyped animals would be 0.013 (SD 0.007) (permutation p = 0.0009). The observed inbreeding was also significant (permutation p= 0.02). Heritability was estimated to be 9 (95% CI = 0-57)% assuming all animals with unknown status were unaffected. The best fitting genetic model was a major gene model with dominant expression with the risk allele frequency at 15% with 60% penetrance.
In this pilot study the increased inbreeding in the cases, lack of likely sampling bias, the increased frequency of T2D in Burmese, and small number of breed founders are consistent with the involvement of a major locus in diabetes in Burmese cats with a significant risk allele prevalence. However, low case numbers meant this could not be unambiguously confirmed. A genome-wide association study may be useful for investigating the genetic cause of T2D.
在一项初步研究中,通过分析系谱数据,调查新西兰缅甸猫2型糖尿病(T2D)可能存在的遗传因素。
获取了305只生活在新西兰的缅甸猫的系谱;其中19只因出现多尿、多饮、胰岛素治疗前血浆葡萄糖持续浓度>16 mmol/L和糖尿而被诊断为糖尿病。还提交了16只无T2D临床症状的猫的系谱。其余270只猫是这些个体的未观察到的亲属。计算了近亲繁殖系数和遗传力,并使用系谱分析软件进行了单主基因座模型分离分析。
19只猫被诊断为T2D。雄性(n = 14)和雌性(n = 5)均受影响,这表明导致糖尿病的一个或多个基因是常染色体基因而非性连锁基因。对系谱的检查几乎没有发现完全显性基因作用的迹象:糖尿病在连续几代中表面上很少见,几乎总是至少跳过一代,而且常常跳过更多代;明显未受影响的父母的明显未受影响的后代有时会产生受影响的后代。核心系谱(16只糖尿病猫)中受影响动物的平均亲缘关系为0.049,平均近亲繁殖率为0.033。基于性状值的100,000次排列,从表型动物中随机抽取的16只动物的预期亲缘关系为0.013(标准差0.007)(排列p = 0.0009)。观察到的近亲繁殖也很显著(排列p = 0.02)。假设所有状态未知的动物均未受影响,则遗传力估计为9(95%可信区间 = 0 - 57)%。最佳拟合遗传模型是一个显性表达的主基因模型,风险等位基因频率为15%,外显率为60%。
在这项初步研究中,病例中近亲繁殖增加、缺乏可能的抽样偏差、缅甸猫中T2D频率增加以及品种创始者数量少,这些都与一个主要基因座参与缅甸猫糖尿病且存在显著风险等位基因患病率一致。然而,病例数量少意味着无法明确证实这一点。全基因组关联研究可能有助于调查T2D的遗传原因。