Abstract:Interleukin-1 (IL-1) has been implicated as a key cytokine in Alzheimer's disease (AD) pathogenesis. IL-1 gene polymorphisms, especially IL-1A C((-)889)T polymorphism, have been suggested to be associated with AD risk and onset age. To determine if IL-1 polymorphisms are genetic risk factors for developing AD in Chinese Mainland population, we analyzed IL-1A ((-)889), IL-1B ((-)511) and IL-1RN variable number of tandem repeat (VNTR) polymorphisms in a sample of 145 sporadic AD patients and 181 healthy controls… Show more
“…Our negative finding was consistent with that of other researchers from Chinese populations, including three from Taiwan (Kuo et al 2003;Tsai et al 2003;Wang et al 2007) and one from Mainland (Li et al 2004), However, there was still a recent study report that there was a association between IL-1A C(-889)T polymorphism and AD in Mainland Chinese population (Zhou et al 2006) and in Spanish (Infante et al 2007). The positive result obtained may be due to effect of different genetic background and/or small sample size.…”
Neuroinflammation has been implicated in the etiology of Alzheimer's disease (AD). Many studies have suggested that C(-889) T promoter polymorphism in one of the proinflammatory cytokine interleukin-1 (IL-1) encoding gene IL-1A may be associated with AD pathogenesis. To determine whether the polymorphism contributes to the risk for late-onset AD (LOAD) in Chinese, we carried out our investigation in 344 sporadic LOAD patients and 224 healthy controls. No statistical significant association was obtained between IL-1A C(-889) T polymorphism and LOAD and no statistical difference was found between cases and controls after stratification for apolipoprotein E allele 4 (APOE epsilon4) status. The results reveal that it is not likely that the IL-1A C(-889) T polymorphism is involved in AD pathogenesis in the Chinese population. Further studies of the associations between other IL-1A genetic polymorphisms and AD should be performed in a larger population and biologic functional analysis of IL-1A gene is required to verify the underlying roles of IL-IA in LOAD.
“…Our negative finding was consistent with that of other researchers from Chinese populations, including three from Taiwan (Kuo et al 2003;Tsai et al 2003;Wang et al 2007) and one from Mainland (Li et al 2004), However, there was still a recent study report that there was a association between IL-1A C(-889)T polymorphism and AD in Mainland Chinese population (Zhou et al 2006) and in Spanish (Infante et al 2007). The positive result obtained may be due to effect of different genetic background and/or small sample size.…”
Neuroinflammation has been implicated in the etiology of Alzheimer's disease (AD). Many studies have suggested that C(-889) T promoter polymorphism in one of the proinflammatory cytokine interleukin-1 (IL-1) encoding gene IL-1A may be associated with AD pathogenesis. To determine whether the polymorphism contributes to the risk for late-onset AD (LOAD) in Chinese, we carried out our investigation in 344 sporadic LOAD patients and 224 healthy controls. No statistical significant association was obtained between IL-1A C(-889) T polymorphism and LOAD and no statistical difference was found between cases and controls after stratification for apolipoprotein E allele 4 (APOE epsilon4) status. The results reveal that it is not likely that the IL-1A C(-889) T polymorphism is involved in AD pathogenesis in the Chinese population. Further studies of the associations between other IL-1A genetic polymorphisms and AD should be performed in a larger population and biologic functional analysis of IL-1A gene is required to verify the underlying roles of IL-IA in LOAD.
“…IL-1a ( À 889) C/T polymorphism has been reported to be associated with Alzheimer disease, and the IL-1a ( À 889) T allele polymorphism has been found to increase the risk of developing Alzheimer disease in whites. [10][11][12] However, no association between the IL-1a ( À 889) T allele polymorphism and Alzheimer disease was noted in Chinese 22,23 or Korean 24 populations. The IL-1a ( À 889) T allele is rarer in Asians than in whites.…”
We conclude that C/T polymorphism at position -889 of the IL-1alpha gene promoter region does not increase the risk of developing NTG. However, further studies on NTG are necessary to investigate the genetic basis and factors involved in the development of the neurodegenerative process.
“…The studies of interleukin-1 ␣ -889 C/T polymorphism in the English population suggest a similar distribution of the C/C genotype, but slight distribution differences in both C/T and T/T genotypes when compared with the Turkish population [11] . On the other hand, the results in Japanese [23] and Chinese [20] populations showed significant differences for all of the genotypes when compared with the Turkish, English [11] and Italian [9] populations. However, the allelic distribution of Turkish population is similar to the English [11] and Italian [9] populations, but differs significantly from Japanese [23] and Chinese [20] populations ( table 2 ).…”
Section: Discussionmentioning
confidence: 78%
“…On the other hand, the results in Japanese [23] and Chinese [20] populations showed significant differences for all of the genotypes when compared with the Turkish, English [11] and Italian [9] populations. However, the allelic distribution of Turkish population is similar to the English [11] and Italian [9] populations, but differs significantly from Japanese [23] and Chinese [20] populations ( table 2 ). These differences in the interleukin-1 ␣ genotype distributions might depend on the ethnic background.…”
Section: Discussionmentioning
confidence: 78%
“…This association was observed in patients from Italy [3,9,14] [14,18,21,22,24,25,28] and Asians [16,17,19,20,23,26,27] .…”
Background/Aims: The polymorphism (rs1800587) in the 5′-flanking regulatory region at –889 of the interleukin-1α gene has been shown to be associated with inflammatory diseases and Alzheimer’s disease (AD). The aim of the current study is to determine whether there is an association between the promoter region polymorphism of the interleukin-1α gene and late-onset AD in a cohort of Turkish patients. Methods: One hundred and four subjects with dementia of the Alzheimer type and 103 age-matched controls were genotyped according to the PCR with confronting two-pair primers method. Results: Although the distribution of genotypes did not significantly differ (p = 0.107), the difference between allelic frequency was nearly significant according to a χ2 test (p = 0.05) when the controls and patients were compared. Conclusion: Our results showed that there is no association between the –889 C/T transition on the interleukin-1α gene and late-onset AD in the Turkish population.
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