Department of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Aurora, Colorado, USA.
Obesity (Silver Spring). 2010 Mar;18(3):555-62. doi: 10.1038/oby.2009.303. Epub 2009 Oct 1.
The IKKbeta/NF-kappaB pathway is known to play an important role in inflammatory response and has also recently been implicated in the process of insulin resistance. We hypothesized that one or more variants in the IkappaBalpha gene (NFKBIA) or surrounding untranslated regions would be associated with insulin sensitivity (S(I)) in Hispanic-American families. We tested for association between 25 single-nucleotide polymorphisms (SNPs) in and near NFKBIA and S(I) in 981 individuals in 90 Hispanic-American families from the Insulin Resistance Atherosclerosis (IRAS) Family Study. SNP rs1951276 in the 3' flanking region of NFKBIA was associated with S(I) in the San Antonio (SA) sample after adjusting for age, gender, and admixture (uncorrected P = 1.69 x 10(-5); conservative Bonferroni correction P = 3.38 x 10(-4)). Subjects with at least one A allele for NFKBIA rs1951276 had approximately 29% lower S(I) compared to individuals homozygous for the G allele in the SA sample. Although not statistically significant, the effect was in the same direction in the San Luis Valley (SLV) sample alone (P = 0.348) and was significant in the combined SA and SLV samples (P = 5.37 x 10(-4); presence of A allele associated with approximately 20% lower S(I)). In SA, when adjusted for subcutaneous adipose tissue area (SAT, cm(2)), the association was modestly attenuated (P = 1.25 x 10(-3)), but the association remained highly significant after adjustment for visceral adipose tissue area (VAT, cm(2); P = 4.41 x 10(-6)). These results provide corroborating evidence that the NF-kappaB/IKKbeta pathway may mediate obesity-induced insulin resistance in humans.
IKKbeta/NF-kappaB 途径在炎症反应中起着重要作用,最近也被牵连到胰岛素抵抗的过程中。我们假设 IkappaBalpha 基因(NFKBIA)或周围非翻译区的一个或多个变体将与西班牙裔美国家庭的胰岛素敏感性(S(I))相关。我们在胰岛素抵抗动脉粥样硬化(IRAS)家族研究中,对 90 个西班牙裔美国家庭的 981 名个体中的 25 个 NFKBIA 内和附近的单核苷酸多态性(SNP)与 S(I)之间进行了关联测试。在调整年龄、性别和混合后,NFKBIA 3'侧翼区域的 SNP rs1951276 与圣安东尼奥(SA)样本中的 S(I)相关(未校正的 P = 1.69 x 10(-5);保守的 Bonferroni 校正 P = 3.38 x 10(-4))。NFKBIA rs1951276 的至少一个 A 等位基因的个体与 SA 样本中纯合 GG 个体相比,S(I)大约低 29%。尽管没有统计学意义,但在圣路易斯谷(SLV)样本中,这种影响的方向相同(P = 0.348),在 SA 和 SLV 样本的合并中具有统计学意义(P = 5.37 x 10(-4);A 等位基因的存在与大约 20%的 S(I)降低相关)。在 SA 中,当调整皮下脂肪组织面积(SAT,cm(2))时,相关性略有减弱(P = 1.25 x 10(-3)),但在调整内脏脂肪组织面积(VAT,cm(2))后,相关性仍然高度显著(P = 4.41 x 10(-6))。这些结果提供了佐证证据,表明 NF-kappaB/IKKbeta 途径可能介导肥胖诱导的人类胰岛素抵抗。