Rice Treva, Cooper Richard S, Wu Xiaodong, Bouchard Claude, Rankinen Tuomo, Rao D C, Jaquish Cashell E, Fabsitz Richard R, Province Michael A
Division of Biostatistics, Washington University School of Medicine, St. Louis, Missouri, USA.
Am J Hypertens. 2006 Mar;19(3):270-4. doi: 10.1016/j.amjhyper.2005.09.006.
In many genetic studies of complex traits, sample sizes are often too small to detect linkages of low-to-moderate effects. However, the combined linkage evidence across several studies can be synthesized using meta-analysis with the aim of providing more definitive support of linkage.
In the current study using the National Heart, Lung, and Blood Institute (NHLBI) GeneLink Project, a meta-analysis based on a modification of Fisher's method of pooling P values was used to investigate linkage for systolic blood pressure (SBP) and diastolic blood pressure (DBP) values across three studies involving African American and Nigerian families (HyperGEN, Health, Risk Factors, Exercise Training and Genetics [HERITAGE], and Genetics of Hypertension in Blacks).
The meta results suggest two regions (2p and 7p) provide enhanced linkage evidence compared with the individual study results. The maximal meta Lod score of 2.9 on 2p14-p13.1 (64-78 cM) represented approximately 1-Lod unit increase over the respective individual study scores. This general region has been implicated previously involving primarily families of white ethnicity and provides confirmatory evidence that this QTL is common across ethnic groups. The second finding at 7p21.3-p15.3 (8-25 cM) provided a meta Lod of 3.5. Although region was implicated primarily in the Nigerian subjects the low-level but consistent support involving the African American families (individual Lod score of 1.0) suggests a novel QTL with respect to BP variation in individuals of black ethnicity.
Follow-up studies involving positional cloning efforts of the combined families showing linkage evidence in these regions (particularly 2p) may be warranted to verify these findings and identify the genes and causative variants.
在许多复杂性状的基因研究中,样本量往往过小,难以检测到低至中等效应的连锁关系。然而,通过荟萃分析可以综合多项研究的连锁证据,以提供更确凿的连锁支持。
在当前使用美国国立心肺血液研究所(NHLBI)基因连锁项目的研究中,基于对费舍尔合并P值方法的改进进行荟萃分析,以研究三项涉及非裔美国人和尼日利亚家庭的研究(HyperGEN、健康、风险因素、运动训练与遗传学[HERITAGE]以及黑人高血压遗传学研究)中收缩压(SBP)和舒张压(DBP)值的连锁关系。
荟萃分析结果表明,与各独立研究结果相比,有两个区域(2p和7p)提供了更强的连锁证据。在2p14 - p13.1(64 - 78 cM)处的最大荟萃对数优势分数为2.9,比各自独立研究分数增加了约1个对数优势单位。此前主要在白人种族家庭中涉及到这个大致区域,这提供了确证性证据,表明该数量性状位点在不同种族中是常见的。在7p21.3 - p15.3(8 - 25 cM)处的第二个发现给出了3.5的荟萃对数优势分数。尽管该区域主要在尼日利亚受试者中被涉及,但非裔美国家庭的低水平但一致的支持(个体对数优势分数为1.0)表明,对于黑人种族个体的血压变异而言,这是一个新的数量性状位点。
对于在这些区域(特别是2p)显示连锁证据的合并家庭进行定位克隆的后续研究可能是必要的,以验证这些发现并确定相关基因和致病变异。