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十种单一脱矿骨基质产品批间的变异性。

Variability across ten production lots of a single demineralized bone matrix product.

机构信息

Spine Research Foundation, Spine Institute, Santa Monica, CA 90404, USA.

出版信息

J Bone Joint Surg Am. 2010 Feb;92(2):427-35. doi: 10.2106/JBJS.H.01400.

Abstract

BACKGROUND

Demineralized bone matrix is an osteoinductive allograft derived from processed bone that is commonly mixed with autogenous bone in fusion procedures to treat diseases of the spine. An increasing number of demineralized bone matrix-based products are commercially available for spinal fusion procedures, but osteoinductive variability has been found not only across different products but also among production lots from the same demineralized bone matrix formulation. The purpose of this study was to assess the lot-to-lot variability across a single demineralized bone matrix-based product in terms of both extracted bone morphogenetic protein (BMP) concentrations (in vitro) and fusion performance in rats (in vivo). The goal was also to determine whether the in vitro measures could sufficiently and accurately predict the in vivo fusion performance of different demineralized bone matrix-based product lots.

METHODS

BMP-2 and BMP-7 were extracted from ten production lots of InterGro DBM Putty and quantified with use of ELISA (enzyme-linked immunosorbent assay). A posterolateral lumbar spinal fusion was performed on forty athymic rats with implantation of a demineralized bone matrix-based product. Fusion success was determined at eight weeks with use of radiographs and manual palpation of the segments. Logistic regression was used to determine the predictive abilities of BMPs.

RESULTS

Significant lot-to-lot variability was found in terms of both BMP concentrations (22 to 110 pg of BMP-2 per milligram of product and 44 to 125 pg of BMP-7 per milligram of product) and in vivo rates of fusion (0% to 75%; p < 0.04 for all). BMP-2 and BMP-7 concentrations correlated positively with each other across lots (r = 0.77, p < 0.0001). Most notably, extracted amounts of BMP-2 and BMP-7 each predicted in a dose-dependent manner the in vivo fusion performance in rats (R(2) = 0.32, p < 0.01 for BMP-2, and R(2) = 0.22, p < 0.009 for BMP-7).

CONCLUSIONS

Assays for demineralized bone matrix-extracted BMP-2 and BMP-7 levels may be feasible and sufficient for predicting spinal fusion performance of individual production lots from the same demineralized bone matrix-based product.

摘要

背景

脱钙骨基质是一种从处理过的骨中提取的具有成骨诱导作用的同种异体移植物,通常与自体骨混合用于融合手术中,以治疗脊柱疾病。越来越多的基于脱钙骨基质的产品可用于脊柱融合手术,但不仅不同产品之间,而且同一脱钙骨基质配方的生产批次之间也存在成骨诱导的可变性。本研究的目的是评估单一基于脱钙骨基质的产品在提取的骨形态发生蛋白(BMP)浓度(体外)和大鼠融合性能(体内)方面的批次间变异性。目标还在于确定体外测量是否可以充分准确地预测不同基于脱钙骨基质的产品批次的体内融合性能。

方法

从十批 InterGro DBM Putty 中提取 BMP-2 和 BMP-7,并使用 ELISA(酶联免疫吸附测定)进行定量。将 40 只无胸腺大鼠进行后路腰椎融合术,植入脱钙骨基质产品。八周后通过 X 线片和节段的手动触诊确定融合成功率。使用逻辑回归确定 BMP 的预测能力。

结果

在 BMP 浓度(产品每毫克 22 至 110pg 的 BMP-2 和产品每毫克 44 至 125pg 的 BMP-7)和体内融合率(0%至 75%;p<0.04 所有)方面均发现显著的批次间变异性。跨批次的 BMP-2 和 BMP-7 浓度呈正相关(r=0.77,p<0.0001)。值得注意的是,BMP-2 和 BMP-7 的提取量都以剂量依赖性方式预测了大鼠体内融合性能(R2=0.32,p<0.01 对于 BMP-2,R2=0.22,p<0.009 对于 BMP-7)。

结论

脱钙骨基质提取的 BMP-2 和 BMP-7 水平的测定可能可行且足以预测同一脱钙骨基质产品的单个生产批次的脊柱融合性能。

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