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血清 C3 和 C4 作为狼疮性肾损害生物标志物的复杂性。

The complex nature of serum C3 and C4 as biomarkers of lupus renal flare.

机构信息

The Ohio State University, Columbus, OH 43210, USA.

出版信息

Lupus. 2010 Oct;19(11):1272-80. doi: 10.1177/0961203310371154. Epub 2010 Jul 6.

Abstract

To assess the relationship between serum C3 or C4 levels and lupus renal flare, C3 and C4 levels were measured bimonthly in 71 lupus nephritis patients for a mean of 35 months, during which time 70 renal flares were identified. Comparing baseline, pre-flare, and at-flare values indicated that neither C3 nor C4 levels decreased pre-flare, but both decreased on average significantly at flare. However, sensitivity/specificity for C3 (75%/71%) and C4 (48%/71%) were low. To account for other influencing factors, multiple regression was performed that included bimonthly values of C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR), and genotype data on C3 (S/F), CRP (1846G > A), and the complement regulator factor H (Y402H). This analysis revealed that reduced levels of C4, but not C3, were independently associated with the two-month pre-flare period. Conversely, reduced levels of C3, but not C4, were independently associated with the flare visit. Significant pro-flare interactions included low C3 levels with the factor H 402HH-encoding genotype, and low CRP levels with the C3 F allele. Together these data suggest that C4 activation is critical for initiating renal flare while C3 activation is involved in the actual tissue damage, and that these effects are influenced by genetic variability in complement activation and regulation.

摘要

为了评估血清 C3 或 C4 水平与狼疮性肾炎活动的关系,对 71 例狼疮肾炎患者进行了平均 35 个月的双月 C3 和 C4 水平检测,在此期间共发现 70 例狼疮肾炎活动。比较基线、活动前和活动时的值表明,C3 和 C4 水平在活动前均无下降,但在活动时均显著下降。然而,C3(75%/71%)和 C4(48%/71%)的敏感性/特异性均较低。为了考虑其他影响因素,进行了多元回归分析,其中包括 C 反应蛋白(CRP)和红细胞沉降率(ESR)的双月值以及 C3(S/F)、CRP(1846G > A)和补体调节因子 H(Y402H)的基因型数据。该分析表明,C4 水平降低与活动前两个月独立相关,但 C3 水平降低与活动时独立相关。有意义的促活动相互作用包括 C3 水平降低与因子 H 402HH 编码基因型,以及 CRP 水平降低与 C3 F 等位基因。这些数据表明,C4 激活对于启动肾脏活动至关重要,而 C3 激活参与了实际的组织损伤,并且这些影响受到补体激活和调节的遗传变异性的影响。

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