Ischaemic stroke in persons of European descent has a genetic basis, but whether the stroke-susceptibility alleles, the strength of any association, and the extent of their attributable risks are the same in persons of non-European descent remains unanswered. Whether ethnicity itself has a relevant or substantial contribution on those effect estimates is controversial. Comparative analyses between the ethnic groups may allow general conclusions to be drawn about polygenic disorders.
Methods and Findings
We performed a literature-based systematic review of genetic association studies in stroke in persons of non-European descent. Odds ratios (ORs) and 95% confidence intervals (CIs) were determined for each gene–disease association using fixed and random effect models. We further performed a comparative genetic analysis across the different ethnic groups (including persons of European descent derived from our previous meta-analysis) to determine if genetic risks varied by ethnicity. Following a review of 500 manuscripts, eight candidate gene variants were analysed among 32,431 individuals (12,883 cases and 19,548 controls), comprising mainly Chinese, Japanese, and Korean individuals. Of the eight candidate genes studied, three were associated with ischaemic stroke: the angiotensin I converting enzyme (ACE) insertion/deletion (I/D) polymorphism with a mean OR of 1.90 (95% CI 1.23–2.93) in the Chinese and 1.74 (95% CI 0.88–3.42) in the Japanese; the summary OR for the C677T variant of 5,10-methylenetetrahydrofolate reductase (MTHFR) was 1.18 (95% CI 0.90–1.56) in Chinese and 1.34 (95% CI 0.87–2.06) in Koreans; and the pooled OR for the apolipoprotein E (APOE) gene was 2.18 (95% CI 1.52–3.13) in Chinese and 1.51 (95% CI 0.93–2.45) in Japanese. Comparing the commonly investigated stroke genes among the Asian groups against studies in persons of European descent, we found an absence of any substantial qualitative or quantitative interaction for ORs by ethnicity. However, the number of individuals recruited per study in the studies of persons of non-European descent was significantly smaller compared to studies of persons of European descent, despite a similar number of studies conducted per gene.
These data suggest that genetic associations studied to date for ischaemic stroke among persons of non-European descent are similar to those for persons of European descent. Claims of differences in genetic effects among different ethnic populations for complex disorders such as stroke may be overstated. However, due to the limited number of gene variants evaluated, the relatively smaller number of individuals included in the meta-analyses of persons of non-European descent in stroke, and the possibility of publication bias, the existence of allele variants with differential effects by ethnicity cannot be excluded.
Citation: Ariyaratnam R, Casas JP, Whittaker J, Smeeth L, Hingorani AD, et al. (2007) Genetics of Ischaemic Stroke among Persons of Non-European Descent: A Meta-Analysis of Eight Genes Involving ∼ 32,500 Individuals. PLoS Med 4(4): e131. doi:10.1371/journal.pmed.0040131
Academic Editor: Peter Sandercock, Western General Hospital, United Kingdom
Received: October 13, 2006; Accepted: February 13, 2007; Published: April 24, 2007
Copyright: © 2007 Ariyaratnam et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was funded by the Stroke Association (UK). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: CI, confidence interval; OR, odds ratio
A stroke occurs when the blood supply to part of the brain is interrupted, either because a blood vessel supplying the brain becomes blocked or because one ruptures. Strokes are a substantial cause of death and disability worldwide, with most of the burden affecting people living in developed countries. Most strokes fall into a category termed ischemic stroke. This type is caused by blockages in the blood vessels supplying the brain, which can happen when there is a buildup of fatty deposits or clots within the blood vessels. Many of the risk factors for this particular type of stroke are affected by an individual's behavior, including for example smoking, high blood pressure, diabetes, inactivity, and so on. In addition, variations in an individual's genetic makeup might affect his or her chance of having a stroke. Previous research studies have shown that variants in many different genes are likely to be involved in determining the overall risk of having a stroke, each variant contributing in a small way to the risk.
Why Was This Study Done?
The group performing this study had previously carried out a systematic review of existing research, looking specifically at the genetics of ischemic stroke among people of European origin (often called “Caucasians”). However, it was not obvious whether the genetic risk factors for stroke they found would be the same for people from a different ethnic background. Therefore the research group wanted to find out what the genetic risk factors were for stroke among people of non-European origin and to compare these findings with those of their previous systematic review. This research might help to find out whether the genetic risk factors for stroke were different in people from different parts of the world.
What Did the Researchers Do and Find?
As a starting point, these researchers wanted to find all the different studies that had already been carried out examining the effect of genetic risk factors on stroke among people of non-European origin. To do this, searches were carried out of electronic databases using a particular set of terms. All resulting studies that involved genetic research in people of non-European origin and in which strokes were confirmed by brain scanning were then evaluated in more detail. The findings of different studies were combined if at least three studies were available for the same genetic variant. Eventually 60 studies were found that looked at the association between eight specific gene variants and stroke. The only data that could be included in a combined analysis came from Chinese, Japanese, and Korean populations. Three of the eight gene variants were associated with an increased risk of stroke. Those three gene variants were ACE I/D (a variant in the gene coding for angiotensin 1-converting enzyme, which is involved in controlling blood pressure); a variant in MTHFR (which codes for the enzyme methylenetetrahydrofolate reductase, and which converts certain amino acids within cells); and a variant in the gene APOE, which codes for a protein that plays a role in breaking down fats. The researchers then compared their findings from this study with the findings of a previous systematic review they had carried out among people of European origin. Overall, each gene studied seemed to have a similar effect in the different populations, with the exception of APOE, which seemed to be associated with stroke in the Asian studies but not in the studies from people of non-European origin. The researchers also found that generally the Asian studies suggested a slightly greater effect of each gene variant than the studies in people of non-European origin did.
What Do These Findings Mean?
These findings suggest that, with the possible exception of APOE, similar gene variants play a role in determining stroke risk in people of European origin and Asian populations. Although generally the studies examined here suggested a slightly greater effect of these gene variants in Asian populations, this is not necessarily a real finding. This greater effect may just be due to small-study bias. Small-study bias describes the observation that small research studies are more likely to produce a false positive result than are large research studies. Therefore, future studies that examine the genetic basis of stroke should recruit much larger numbers of participants from populations made up of people of non-European origin than has previously been the case.
Please access these Web sites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.0040131.
- Health Encyclopedia entry on stroke from NHS Direct (UK National Health Service patient information)
- Stroke Information page from the National Institute of Neurological Disorders and Stroke (provided by the US National Institutes of Health)
- The Stroke Association, a UK charity funding this study
- Information from the World Health Organization on the distribution and burden of stroke worldwide
- The WHO has a world atlas of heart disease and stroke
The incidence and standardised mortality ratios for stroke are known to vary between different ethnic groups , which might reflect genetic or nongenetic differences. Sporadic ischaemic stroke in persons of European descent has a multifactorial aetiology [2–6], with evidence for a genetic basis [7–9].
However, whether stroke susceptibility alleles, their genetic effect sizes, or attributable risks are qualitatively (similarity of gene variants) or quantitatively (size of effects of such variants) homogenous across groups of differing ancestry  remains controversial .
We performed a systematic review of genetic association studies of sporadic ischaemic stroke in persons of non-European descent and compared the findings to a prior overview we conducted among persons of European descent , which allowed us to address both qualitatively and quantitatively the effect of ethnicity on ischaemic stroke, often regarded as a paradigm of the common multifactorial, polygenic disorders. This is, to our knowledge, the largest genetic meta-analysis conducted in persons of non-European descent for any disease.
Electronic databases (Medline, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed; EMBASE, http://www.embase.com; Google Scholar, http://scholar.google.com; and Yahoo, http://www.yahoo.com) were searched up to and including January 2005 for all genetic-association studies evaluating any candidate gene in stroke in persons of non-European descent. The medical subject headings, terms, and text words used for the search were: cerebrovascular disease, stroke, brain infarction, and cerebrovascular disorder, in combination with polymorphism, genotype, gene, allele, or mutation. The search results were limited to humans and all languages were included. The references of all the computer-identified publications were searched for any additional studies, and the related articles option (a feature available on Medline) was used to search for any further possible related articles. Another search to identify all previous genetic meta-analyses in stroke was also performed.
Studies were selected if they were conducted in persons of non-European descent, had neuroimaging (magnetic resonance imaging or computer tomography) confirmation of an ischaemic stroke diagnosis, and were analysed as a dichotomous trait. Studies were excluded if: (i) patients were under 18 years of age; (ii) they evaluated quantitative or intermediate phenotypes exclusively; or (iii) genotype frequency was not reported, in which case authors were contacted for this information where possible. For duplicate publications the smaller dataset was discarded.
Data were analysed using software for preparing and maintaining Cochrane reviews (Review Manager version 4.2.8, Cochrane Collaboration, http://www.cc-ims.net/RevMan) and Comprehensive Meta Analysis version 2.2.023 (Biostat, http://www.biostat.org).
For each single nucleotide polymorphism where data were available from at least three studies, a meta-analysis was carried out as described previously . The genetic models evaluated are given in Table 1 and were based mostly on those used in the primary studies. For each variant a pooled odds ratio (OR) was calculated using random effects models, along with 95% confidence intervals (CI), to measure the strength of the association. For comparability with our previous report in persons of European descent, we used the same genetic model of inheritance for each gene variant when necessary . Heterogeneity was assessed by the DerSimonian and Laird Q test , and I2 was used as a measure to describe the percentage of variability in point estimates that was due to heterogeneity rather than sampling error . For assessment of small-study bias, we used the funnel plot and the Egger regression asymmetry test .
Summary of Candidate Genes in Ischemic Stroke Evaluated in Persons of Non-European Descent
The effects of ethnicity in gene–stroke associations were evaluated using stratified subgroups according to ethnicity. The I2 test was used to evaluate the presence of heterogeneity of genetic size between groups of differing ancestry. For the group of persons of European descent the OR for each gene variant analysed was obtained from our previous work . Differences between populations of non-European descent and persons of European descent in the allele frequencies from control samples across the different candidate genes were evaluated by means of a Chi2 analysis.
While numerous tools exist to help reviewers assess the quality of randomised trials, assessment of study quality in the synthesis of observational and genetic research is more controversial. Most experts working in the field generally advise avoiding the use of quantitative scoring of study quality in meta-analyses, as such an approach has not been validated and can itself introduce bias. One of the reasons, highly relevant in genetic studies, is the often inadequate reporting that constrains the elaboration of such scores to judge the study quality. In addition, there is little or no empirical evidence to guide reviewers on which aspects of study design have an influence on the results obtained. Study size is, however, a widely used proxy for study quality. We therefore undertook a sensitivity analysis, in which concordance of the overall result for each meta-analyses was conducted with the results after excluding the largest study. The key issue in the assessment of stroke as an outcome is classification as ischaemic or haemorrhagic. To minimize outcome misclassification, we therefore restricted our analyses to those studies in which neuroimaging was used to classify the stroke as ischaemic.
Candidate Genes in Persons of Non-European Descent
A total of 500 manuscripts were identified in our initial search, of which 60 met the inclusion criteria including studies among Chinese, Japanese, Koreans, African Americans, and South Asians. Of these, only studies among the former three Asian groups had sufficient data to allow inclusion into a meta-analysis. We analysed eight candidate genes. Table 1 shows the candidate genes studied by ethnic group.
The Chinese population was by far the most extensively studied across the various candidate genes (Table 2). The second most-studied ethnic group was the Japanese. Overall, the two most extensively studied candidate genes in persons of non-European descent were angiotensin I converting enzyme (ACE) and 5,10-methylenetetrahydrofolate reductase (MTHFR), followed by apolipoprotein E (APOE) and SERPINE1 (plasminogen activator inhibitor-1 [PAI-1]) (Table 2).
Comparative Total Number of Cases, Controls, and Studies by Ethnicity
The insertion/deletion polymorphism of ACE (ACE I/D) was the most investigated polymorphism in all three ethnic groups (a total of 3,572 Chinese individuals, 1,601 Japanese individuals, and 2,750 Korean individuals). The overall OR for the nine studies in the Chinese population was 1.90 (95% CI 1.23–2.93) (Figure 1) [15–23]. There was evidence for heterogeneity (I2 = 75.4; pHET < 0.0001) among studies within this ethnic grouping. For the six Japanese studies [24–29] the OR was 1.74 (95% CI 0.88–3.42) (Figure 1). Heterogeneity of the OR was also observed within this grouping (I2 = 78.6; pHET = 0.0003). We identified four Korean studies [30–33], but they were not included in the meta-analysis because of suspicion of duplicate publication. The overall OR in the Asian group combined (Chinese and Japanese) was 1.82 (95% CI 1.28–2.60). Significant interstudy heterogeneity was observed (I2 = 75.4; pHET < 0.0001). The funnel plot was asymmetric, and the Egger test was significant (p = 0.027).
A total of seven studies (1,859 cases and 2,380 controls) among Chinese populations evaluating the C677T variant in the MTHFR gene were identified [22,34–39]. A summary OR of 1.18 (95% CI 0.90–1.56) was observed for individuals homozygous for the T allele compared with C-allele carriers (i.e., CT + CC) (Figure 2). No significant interstudy heterogeneity was observed (I2 = 18.8; pHET = 0.29), and although the results were dominated by the relatively large study of Li et al. , excluding this study did not substantially alter the results. We identified three Korean studies [40–42] with a total of 478 cases and 541 controls providing an OR of 1.34 (95% CI 0.87–2.06) with no significant interstudy heterogeneity (I2 = 27.8; pHET = 0.25). A pooled analysis of Chinese and Koreans samples provided an overall OR of 1.22 (95% CI 0.98–1.52), and no evidence of heterogeneity was observed (I2 = 17.9; pHET = 0.28). No evidence of asymmetry was observed in the funnel plot, and the Egger test was not significant (p = 0.42).
A total of seven studies in Asians (four in Chinese [418 cases and 476 controls] [43–46] and three in Japanese [495 cases and 1,304 controls] [47–49]) evaluating the APOE ε4 polymorphism against the pooled ε2/ε3 were identified. The summary OR of the Chinese studies was 2.18 (95% CI 1.52–3.13) (Figure 3). No heterogeneity was observed (I2 = 0; pHET = 0.88). The pooled OR of the three Japanese studies [47–49] was 1.51 (95% CI 0.93–2.45). The overall OR in the seven Asian studies was 1.77 (95% CI 1.30–2.39), and although there was no formal statistical evidence of heterogeneity overall (I2 = 32.1; pHET = 0.18) and between groups (Figure 3), studies conducted in the Chinese population tended to obtain a higher OR than that observed in the Japanese population. Despite the small number of studies, evidence of asymmetry in the funnel plot was observed, and the Egger test suggested the presence of small-study bias (p = 0.08).
Although only three studies [50–52] in Chinese populations evaluated the pentanucleotide TTTTA repeat polymorphism of the apoliproprotein A (APOA) gene on ischaemic stroke with a pooled OR of 1.28 (95% CI 1.08–1.51; I2 = 0%; pHET = 0.39), the total number of cases and controls (4,541 and 5,604) was substantially higher than for all other gene variants. It was mainly due to the large case-control study by Sun et al.  in which a significant increase of risk of stroke was reported.
A number of other gene variants were studied in a smaller number of individuals (Table 1). Polymorphisms in the genes SERPINE1 (PAI-1) [53–55], tumour necrosis factor-alpha (TNF) [56–58], angiotensin II type 1 receptor (AT1R) [17,59–61], and angiotensinogen (AGT) [18,49,61,62] were all studied only in Chinese populations. Nominally significant ORs were observed for TNF and SERPINE1 (PAI-1), with the latter result consistent with previous results in persons of European descent 10. However, the number of studies for each genetic polymorphism was considerable smaller than that for other gene variants (Table 1). In addition, we could not discard the existence of some overlap among the studies that evaluated the TNF gene [56,57].
Genetic Effect Sizes in Individuals of Differing Ancestry
For each of the major four major genes studied (ACE, MTHFR, APOE, and SERPINE1 [PAI-1]), the total number of cases studied were significantly greater in the samples of persons of European descent compared with the combined ethnic group (Table 2). In addition, the mean number of individuals per polymorphism studied was greater in the persons of European descent compared to the combined group of persons of non-European descent (Table 3). The only exception to this finding was for the MTHFR gene, for which the mean was boosted by one large study .
Mean Number of Individuals Studied by Gene according to the Ethnic Background
Of the genes studied, four (ACE, MTHFR, APOE, and SERPINE1 [PAI-1]) had also been extensively studied in persons of European descent, which enabled us to compare their effects against our previous meta-analysis in persons of European descent (Table 4) . With the exception of ACE I/D, there were no significant differences of the allele frequencies between persons of European descent and Asians. A quantitative analysis of OR of these genes shows that the effect sizes are broadly similar across the different ethnic groups apart from APOE, which has a null effect in persons of European descent but a significant association with stroke in the Chinese and Japanese groups (Figure 4).
Allele and Genotype Frequencies by Ethnicity
Despite numerous attempts to address the question of genetic liability in sporadic ischaemic stroke in persons of non-European descent using association studies, the number of susceptibility genes and their relative risk remain unclear, mainly hampered by the lack of power of any individual study. The current meta-analysis suggests the existence of gene variants, similar to those evaluated in persons of European descent, associated with ischaemic stroke in persons of non-European descent, mostly represented by studies from populations of Asian background with scarce data from other ethnic groups.
Although some candidate gene variants showed a statistically significant increase in risk of stroke, the robustness of these results remains open to discussion. The observed genetic effect on stroke in the persons of non-European descent, especially in Chinese samples, tended to be higher than the effect observed in persons of European descent, as well as with that observed in other Asian groups such as the Japanese population. These findings, together with the usually small sample size of studies conducted in the persons of non-European descent, suggest publication bias as one possible explanation for the observed larger genetic effects in Chinese samples. In contrast to APOE and ACE genes, the results from the MTHFR C677T gene variant and stroke risk show an absence of heterogeneity among the different groups of persons of non-European descent studied, as well as between these groups and the genetic effect obtained in samples of persons of European descent . The robustness of this association reported in the meta-analysis has received further support by a large study  in the Japanese population, published after our cutoff point for data collection, in which the MTHFR C677T gene variant was associated with a similar increase in risk of stroke to the one we report here.
A descriptive analysis of the most-studied gene variant indicated that with the exception of the MTHFR C677T gene variant, summary ORs in persons of non-European descent tend to be higher than those reported in persons of European descent, the effect mainly accounted for by the results in the Chinese population (Figure 4). While the results in samples of persons of European descent indicated a null effect of the APOE ε4 allele on stroke, the pooled OR from studies of Chinese people was substantially higher, and their CIs did not overlap (Figure 4). A similar although more attenuated difference between persons of European descent and Japanese was observed. Therefore, it is not surprising that when comparing the pooled results separately for the three groups, substantial heterogeneity was observed (I2 = 89.5%). Interestingly, the genetic effect observed in the Chinese population was even higher than that observed in other Asian ethnic groups, such as the Japanese population, although some overlap of their CIs remains (Figure 4). A similar scenario, although less pronounced, was observed for the ACE I/D gene variant, in which studies conducted in the Chinese population showed a higher estimate of the effect than that observed in persons of European descent, which accounted for most of the heterogeneity observed among these ethnic groups (I2 = 58.4%). In contrast, for the MTHR C677T variant, the effect estimate within the groups of non-European descent (Chinese and Koreans), as well as when compared with that in persons of European descent, was homogenous (I2 = 0%; Figure 4).
Although the existence of genuine genetic heterogeneity in the Chinese population to explain their larger genetic effects is possible, the probable causal reasons to explain this finding may not be always directed toward the same direction (higher risk) for the different candidate genes. Equally likely is that, since association studies conducted in persons of non-European descent are smaller compared to persons of European descent, ethnicity may act as a proxy for the presence of small-study bias, whether it represents publication bias, poorer study quality, or greater random error. Study quality itself is difficult to measure, but heterogeneity forms one aspect of this measurement. Whether the positive gene–disease ORs observed here will reduce toward a null effect in very large studies conducted in different ethnic groups remains to be seen. A plausible scenario is that the genetic effect is indeed genuine but lower than it currently appears to be, such as the case of the MTHFR C677T, in which the summary OR in persons of non-European descent coincides with the result of the largest genetic association study.
The larger genetic effect observed in these candidate gene–stroke meta-analyses for Chinese studies, despite the smaller sample sizes, is in agreement with a recent systematic review of 13 gene–disease associations from a wide variety of complex disorders, in which gene effects in samples from Chinese people tended to be larger than those observed in non-Chinese Asian people, and more accentuated with studies conducted in persons of European descent. An interesting difference with that analysis is the case of the MTHFR C677T gene–coronary heart disease association in which the authors, in contrast to our findings, also observed a larger genetic effect in Chinese samples .
We are aware of one previous study that has attempted to address the question of ethnic differences in genetics of a wide variety of complex traits . These investigators examined the genetic effects for 43 validated gene–disease associations across nearly 700 populations of various descents. Large variations in genetic effect sizes by ethnic group arose in only 14% of cases, suggesting the genetic markers for gene–disease associations may vary across populations, but the biological effects, at least for common diseases, is similar across the traditional ethnic boundaries . Apart from the unusually large effect in Chinese samples, our results do provide some support to the notion of common, underlying biological causes across different ethnic groups for common disorders such as ischaemic stroke. As genotype frequencies do seem to differ to some extent by ethnic group (e.g., ACE I/D in persons of European descent versus Chinese individuals), the impact of similar genetic effects may be different in other ethnic populations.
Despite our attempt to evaluate the gene effects in all ethnic groups, we were limited by the fact that the vast majority of data in persons of non-European descent came from Chinese, Japanese, and Korean populations. The nature and extent of the genetic contribution to stroke and other multifactorial disorders in groups of differing ancestry should be considered an important endeavour for risk evaluation and primary prevention measure across all populations. First, evaluation of genetic effects across multiple ethnic backgrounds with substantial difference in cultural behaviour may prove to be the best scenario for the study of gene–environment interactions. Second, the presence of concordance of gene effects on disease risk, as well as on its effect on the direct intermediate phenotype, are strong tools to reliably identify putative functional variants. Third, since the uses of a genetic approach by using gene variants as tools of common intermediate phenotype is expected to provide great advantage in aetiological research, adequately powered genetic studies may help to unravel aetiological factors for the increasing public health disorders in persons of non-European descent such as stroke, which is rapidly becoming a major cause of mortality in Asia with over 1.6 million deaths in China alone in 2002 . Certainly, such an enterprise would require extensive international collaboration among investigators in the field, since gene effects on disease are usually small. The emergence of recently established networks such as HuGENet (Human Genome Epidemiology, http://www.hugenet.org.uk) will prove to play an essential role for an adequate study of gene effects in persons of non-European descent .
As with all meta-analyses based on aggregate data, our results are dependent on published data. Although, as described above, efforts were conducted to limit small-study bias, (the most likely cause of which is publication bias), significant results of the test for small-study bias indicate that this bias has to be carefully considered..In addition, even ethnicity can be a difficult trait to define and sometimes is inconsistently reported in the literature. That the included studies have tended to come from their native countries, should minimize such misclassification. In addition, self-reported ethnic grouping, which is likely to take place in native countries, is known to be very reliable for categorization purposes . Finally, for some genes our results are based on small numbers of publications, which limits the power of our tests for publication bias and heterogeneity.
We conclude that genetic associations so far studied for ischaemic stroke among persons of non-European descent are similar to those found for persons of European descent. However, all the published data on persons of non-European descent are largely derived from Chinese, Japanese, and Korean populations. To date, the evidence does not support ethnicity playing a major part in the genetic aetiology of common ischaemic stroke. However, people from a more diverse range of ethnic groups need to be recruited into genetic studies in much greater numbers than is currently the case.
LS is supported by a Clinician Scientist Fellowship from the Medical Research Council (United Kingdom). ADH is supported by a Senior Fellowship from the British Heart Foundation. PS is supported by a Senior Fellowship from Department of Health (UK).
PS conceived the study. RA, JPC JW, LS, ADH, and PS analysed the data and all authors contributed to writing the paper.
- 1. Sharma P, Korn S (2005) Management strategies for cerebrovascular disease in South Asians. In: Patel KCR, Shah AM, editors. Prevention, treatment and rehabilitation of cardiovascular disease in South Asians. London: The Stationery Office (TSO). pp. 37–50.
- 2. Kiely DK, Wolf PA, Cupples LA, Beiser AS, Myers RH (1993) Familial aggregation of stroke. The Framingham Study. Stroke 24: 1366–1371.
- 3. Rubattu S, Volpe M, Kreutz R, Ganten U, Ganten D, et al. (1996) Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease. Nat Genet 13: 429–434.
- 4. Sharma P (1996) Genes for ischaemic stroke: Strategies for their detection. J Hypertens 14: 277–285.
- 5. Gretarsdottir S, Thorleifsson G, Reynisdottir ST, Manolescu A, Jonsdottir S, et al. (2003) The gene encoding phosphodiesterase 4D confers risk of ischemic stroke. Nat Genet 35: 131–138.
- 6. Liao D, Myers R, Hunt S, Shahar E, Paton C, et al. (1997) Familial history of stroke and stroke risk. The Family Heart Study. Stroke 28: 1908–1912.
- 7. Hrubec Z, Robinette CD (1984) The study of human twins in medical research. N Engl J Med 310: 435–441.
- 8. Brass LM, Isaacsohn JL, Merikangas KR, Robinette CD (1992) A study of twins and stroke. Stroke 23: 221–223.
- 9. Helgadottir A, Manolescu A, Thorleifsson G, Gretarsdottir S, Jonsdottir H, et al. (2004) The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke. Nat Genet 36: 233–239.
- 10. Casas JP, Hingorani AD, Bautista LE, Sharma P (2004) Meta-analysis of genetic studies in ischemic stroke: Thirty-two genes involving approximately 18,000 cases and 58,000 controls. Arch Neurol 61: 1652–1661.
- 11. Ioannidis JP, Ntzani EE, Trikalinos TA (2004) “Racial” differences in genetic effects for complex diseases. Nat Genet 36: 1312–1318.
- 12. DerSimonian R, Laird N (1986) Meta-analysis in clinical trials. Control Clin Trials 7: 177–188.
- 13. Deek JJ, Altman DG, Bradburn MJ (2001) Statistical methods for examining heterogeneity and combining results from several studies in meta-analysis. In: Egger M, Davey SG, Altman DG, editors. Systemic reviews in health care: Meta-analysis in context. Annapolis Junction (Maryland): BMJ Publishing Group.
- 14. Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629–634.
- 15. Zhang X, Xia J, Jin D (2001) The relationship between angiotensin converting enzyme gene polymorphism and risk factors for cerebral infarct. Zhonghua Liu Xing Bing Xue Za Zhi 22: 435–438.
- 16. Zhang X, Wang D, Xu L, Ma Y, Zhang S (2001) Association between renin-angiotensin system gene polymorphism and type 2 diabetics with stroke in China. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 18: 462–466.
- 17. Yuan XD, Hou QX, Wu SL, Pei HZ, Li HF (2003) A cross-sectional study on angiotensin-converting enzyme and angiotensin II type I receptor gene polymorphism and cerebral infarction. Zhonghua Liu Xing Bing Xue Za Zhi 24: 822–826.
- 18. Wei X, Wang G, Jiang C, Li D, Zhao G (2000) Association between hypertensive cerebrovascular stroke and renin-angiotensin system gene polymorphism from Chinese cohort in Shanghai. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 17: 256–258.
- 19. Wang YM, Liu XD, Dong WW, Yang ZC (2004) The relationship between angiotensin-converting enzyme gene polymorphism and heart rate variability in cerebral stroke. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 21: 156–160.
- 20. Thomas GN, Lin JW, Lam WW, Tomlinson B, Yeung V, et al. (2003) Middle cerebral artery stenosis in type II diabetic Chinese patients is associated with conventional risk factors but not with polymorphisms of the renin-angiotensin system genes. Cerebrovasc Dis 16: 217–223.
- 21. Shen D, Ha D (1998) The relationship between angiotensin-converting enzyme gene polymorphism and brain infarction in Chinese hypertensives. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 15: 136–138.
- 22. Li C, Zhang C, Qiu S, Lu X, Zheng Y, et al. (2002) Polymorphisms of ACE-1 and MTHFR genes and genetic susceptibility of ischemic stroke. Zhonghua Yi Xue Za Zhi 82: 1046–1049.
- 23. Xu Y, Wang X, Zhu J (1998) Angiotensin converting enzyme gene polymorphism and cerebrovascular disease. Zhonghua Shen Jing Ge Za Zhi 31: 152–155.
- 24. Ohkubo R, Nakagawa M, Ikeda K, Kodama T, Arimura K, et al. (2002) Cerebrovascular disorders and genetic polymorphisms: Mitochondrial DNA5178C is predominant in cerebrovascular disorders. J Neurol Sci 198: 31–35.
- 25. Notsu Y, Nabika T, Park HY, Masuda J, Kobayashi S (1999) Evaluation of genetic risk factors for silent brain infarction. Stroke 30: 1881–1886.
- 26. Nakata Y, Katsuya T, Takami S, et al. (1998) Methylenetetrahydrofolate reductase gene polymorphism: Relation to blood pressure and cerebrovascular disease. Am J Hypertens 11: 1019–1023.
- 27. Kario K, Kanai N, Saito K, Nago N, Matsuo T, et al. (1996) Ischemic stroke and the gene for angiotensin-converting enzyme in Japanese hypertensives. Circulation 93: 1630–1633.
- 28. Doi Y, Yoshinari M, Yoshizumi H, Ibayashi S, Wakisaka M, et al. (1997) Polymorphism of the angiotensin-converting enzyme (ACE) gene in patients with thrombotic brain infarction. Atherosclerosis 132: 145–150.
- 29. Seino Y, Ikeda U, Maeda Y, Haga Y, Yashima H, et al. (1998) Angiotensin-converting enzyme gene polymorphism and plasminogen activator inhibitor 1 levels in subjects with cerebral infarction. J Thromb Thrombolysis 5: 263–267.
- 30. Um JY, Joo JC, Kim KY, An NH, Lee KM, et al. (2003) Angiotensin converting enzyme gene polymorphism and traditional Sasang classification in Koreans with cerebral infarction. Hereditas 138: 166–171.
- 31. Um JY, Moon KS, Lee KM, Cho KH, Heo Y, et al. (2003) Polymorphism of angiotensin-converting enzyme, angiotensinogen, and apolipoprotein E genes in Korean patients with cerebral infarction. J Mol Neurosci 21: 23–28.
- 32. Um JY, An NH, Kim SH, Lee KM, Kim YS, et al. (2003) Genetic susceptibility to ischemic cerebrovascular disease in Koreans. J Mol Neurosci 20: 31–38.
- 33. Um JY, Kim HJ, Choi TJ, Jin CS, Park ST, et al. (2001) Polymorphism of the angiotensin-converting enzyme gene in patients with cerebral infarction in Koreans. J Mol Neurosci 17: 279–283.
- 34. Zhang G, Dai C (2001) Gene polymorphisms of homocysteine metabolism-related enzymes in Chinese patients with occlusive coronary artery or cerebral vascular diseases. Thromb Res 104: 187–195.
- 35. Li Z, Sun L, Zhang H, Liao Y, Wang D, et al. (2003) Elevated plasma homocysteine was associated with hemorrhagic and ischemic stroke, but methylenetetrahydrofolate reductase gene C677T polymorphism was a risk factor for thrombotic stroke: A Multicenter Case-Control Study in China. Stroke 34: 2085–2090.
- 36. Huang Y, Zhao YY, Li S (2002) Hyperhomocysteine, methylenetetrahydrofolate reductase gene, and other risk factors in ischemic stroke. Zhonghua Yi Xue Za Zhi 82: 119–122.
- 37. Yingdong Z, Zhigang Z, Yang L, Yingdong Z, Zhigang Z, et al. (2002) Association of plasma homocysteine level and N5,N10-methylenetetrahydrofolate reductase gene polymorphism with cerebral infarction. Chin Med Sci J 17: 231–235.
- 38. Zhang C, Shao Y, Hu X (2003) Relationships between the plasma homocysteine levels and the polymorphisms of its metabolic enzymes and the cerebral infarction. Zhonghua Shen Jing Ge Za Zhi 36: 359–362.
- 39. Zheng YZ, Tong J, Do XP, Pu XQ, Zhou BT (2000) Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population. Br J Haematol 109: 870–874.
- 40. Yoo JH, Choi GD, Kang SS (2000) Pathogenicity of thermolabile methylenetetrahydrofolate reductase for vascular dementia. Arterioscler Thromb Vasc Biol 20: 1921–1925.
- 41. Kim NK, Choi BO, Jung WS, Choi YJ, Choi KG (2003) Hyperhomocysteinemia as an independent risk factor for silent brain infarction. Neurology 61: 1595–1599.
- 42. Choi BO, Kim NK, Kim SH, Kang MS, Lee S, et al. (2003) Homozygous C677T mutation in the MTHFR gene as an independent risk factor for multiple small-artery occlusions. Thromb Res 111: 39–44.
- 43. Peng DQ, Zhao SP, Wang JL, Peng DQ, Zhao SP, et al. (1999) Lipoprotein (a) and apolipoprotein E epsilon 4 as independent risk factors for ischemic stroke. J Cardiovasc Risk 6: 1–6.
- 44. Jin ZQ, Fan YS, Ding J, Chen M, Fan W, et al. (2004) Association of apolipoprotein E 4 polymorphism with cerebral infarction in Chinese Han population. Acta Pharmacol Sin 25: 352–356.
- 45. Cao W, Chen F, Teng L, Wang S, Fu S, et al. (1999) The relationship between apolipoprotein E gene polymorphism and coronary heart disease and arteriosclerotic cerebral infarction. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 16: 249–251.
- 46. Yang G, Jinjin G, Jianfei N (1997) The relationship between polymorphisms of Apolipoprotein E gene and atherosclerotic cerebral infarction. Zhonghua Shen Jing Ge Za Zhi 30: 236–239.
- 47. Kokubo Y, Chowdhury AH, Date C, Yokoyama T, Sobue H, et al. (2000) Age-dependent association of apolipoprotein E genotypes with stroke subtypes in a Japanese rural population. Stroke 31: 1299–1306.
- 48. Ji Y, Urakami K, Adachi Y, Maeda M, Isoe K, et al. (1998) Apolipoprotein E polymorphism in patients with Alzheimer's disease, vascular dementia and ischemic cerebrovascular disease. Dement Geriatr Cogn Disord 9: 243–245.
- 49. Nakata Y, Katsuya T, Rakugi H, Takami S, Sato N, et al. (1997) Polymorphism of angiotensin converting enzyme, angiotensinogen, and apolipoprotein E genes in a Japanese population with cerebrovascular disease. Am J Hypertens 10: 1391–1395.
- 50. Hu B, Zhou X, Shao H (2000) Relationship between pentanucleotide repeat polymorphism of apolipoprotein(a) gene and atherosclerosis cerebral infarction in Han nationality. Zhonghua Shen Jing Ge Za Zhi 33: 172–175.
- 51. Liu X, Sun L, Li Z, Gao Y, Hui R (2002) Relation of pentanucleotide repeat polymorphism of apolipoprotein (a) gene to plasma lipoprotein (a) level among Chinese patients with myocardial infarction and cerebral infarction. Zhonghua Yi Xue Za Zhi 82: 1396–1400.
- 52. Sun L, Li Z, Zhang H, Ma A, Liao Y, et al. (2003) Pentanucleotide TTTTA repeat polymorphism of apolipoprotein(a) gene and plasma lipoprotein(a) are associated with ischemic and hemorrhagic stroke in Chinese: A multicenter case-control study in China. Stroke 34: 1617–1622.
- 53. Zhang C, Li J, Li L, et al. (2001) The study of PAI-1 promotor region gene polymorphism in cerebrovascular disease. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 18: 383–387.
- 54. Zhan M, Zhou Y, Han Z, Zhan M, Zhou Y, et al. (2003) Plasminogen activator inhibitor-1 4G/5G gene polymorphism in patients with myocardial or cerebrovascular infarction in Tianjin, China. Chin Med J 116: 1707–1710.
- 55. Liu S, Yang L, Wang X (1998) The study of the plasma PAI-1 activity and it's promotor region gene polymorphism in acute cerebral infarction. Zhonghua Shen Jing Ge Za Zhi 31: 264–266.
- 56. Um JY, An NH, Kim HM, Um JY, An NH, et al. (2003) TNF-alpha and TNF-beta gene polymorphisms in cerebral infarction. J Mol Neurosci 21: 167–171.
- 57. Um JY, Kim HM, Um JY, Kim HM (2004) Tumor necrosis factor alpha gene polymorphism is associated with cerebral infarction. Brain Res Mol Brain Res 122: 99–102.
- 58. Lee BC, Ahn SY, Doo HK, Yim SV, Lee HJ, et al. (2004) Susceptibility for ischemic stroke in Korean population is associated with polymorphisms of the interleukin-1 receptor antagonist and tumor necrosis factor-alpha genes, but not the interleukin-1beta gene. Neuroscience Letters 357: 33–36.
- 59. Zhong Y, Ha D, Zhong Y, Ha D (2002) Influence of angiotensin II type 1 receptor gene polymorphism on patients with essential hypertension complicated by brain infarction. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 19: 201–204.
- 60. Zhang X, Wang D, Xu L, Ma Y, Zhang S (2001) Association between renin-angiotensin system gene polymorphism and type 2 diabetics with stroke in China. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 18: 462–466.
- 61. Thomas GN, Lin JW, Lam WW, et al. (2003) Middle cerebral artery stenosis in type II diabetic Chinese patients is associated with conventional risk factors but not with polymorphisms of the renin-angiotensin system genes. Cerebrovasc Dis 16: 217–223.
- 62. Guan L, Zhang A, Song B, Xiao S, Gao Y, et al. (2000) The relationship between angiotensinogen gene CD235 met–>Thr substitution polymorphism and brain infarction in Chinese. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 17: 336–339.
- 63. Yamada Y, Metoki N, Yoshida H, et al. (2006) Genetic risk for ischemic and hemorrhagic stroke. Arterioscler Thromb Vasc Biol 26: 1920–1925.
- 64. Pan Z, Trikalinos TA, Kavvoura FK, Lau J, Ioannidis JP (2005) Local literature bias in genetic epidemiology: An empirical evaluation of the Chinese literature. PLoS Medicine 2: e334.. doi:10.1371/journal.pmed.0020334.
- 65. Mackay J, Mensah GA (2004) The atlas of heart disease and stroke. WHO.. Available: http://www.who.int/cardiovascular_diseases/resources/atlas/en/. Accessed:.
- 66. Ioannidis JP, Gwinn M, Little J, Higgins JP, Bernstein JL, et al. (2006) A road map for efficient and reliable human genome epidemiology. Nat Genet 38: 3–5.
- 67. Saxena S, Eliahoo J, Majeed A (2002) Socioeconomic and ethnic group differences in self reported health status and use of health services by children and young people in England: Cross sectional study. BMJ 325: 520.