Intervariability and Intravariability of Bone Morphogenetic Proteins in Commercially Available Demineralized Bone Matrix Products : Spine

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Basic Science

Intervariability and Intravariability of Bone Morphogenetic Proteins in Commercially Available Demineralized Bone Matrix Products

Bae, Hyun W. MD; Zhao, Li MD, PhD; Kanim, Linda E. A. MA; Wong, Pamela BS; Delamarter, Rick B. MD; Dawson, Edgar G. MD*

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Spine 31(12):p 1299-1306, May 20, 2006. | DOI: 10.1097/01.brs.0000218581.92992.b7

Study Design. 

Enzyme-linked immunosorbent assay was used to detect bone morphogenetic proteins (BMPs) 2, 4, and 7 in 9 commercially available (“off the shelf”) demineralized bone matrix (DBM) product formulations using 3 different manufacturer’s production lots of each DBM formulation.

Objectives. 

To evaluate and compare the quantity of BMPs among several different DBM formulations (inter-product variability), as well as examine the variability of these proteins in different production lots within the same DBM formulation (intra-product variability).

Summary of Background Data. 

DBMs are commonly used to augment available bone graft in spinal fusion procedures. Surgeons are presented with an ever-increasing variety of commercially available human DBMs from which to choose. Yet, there is limited information on a specific DBM product’s osteoinductive efficacy, potency, and constancy.

Methods. 

There were protein extracts from each DBM sample separately dialyzed 4 times against distilled water at 4°C for 48 hours. The amount of BMP-2, BMP-4, and BMP-7 was determined using enzyme-linked immunosorbent assay.

Results. 

The concentrations of detected BMP-2 and BMP-7 were low for all DBM formulations, only nanograms of BMP were extracted from each gram of DBM (20.2–120.6 ng BMP-2/ g DBM product; 54.2–226.8 ng BMP-7/ g DBM). The variability of BMP concentrations among different lots of the same DBM formulation, intra-product variability, was higher than the variability of concentrations among different DBM formulations, inter-product variability (coefficient of variation range BMP-2 [16.34% to 76.01%], P < 0.01; BMP-7 [3.71% to 82.08%], P < 0.001). BMP-4 was undetectable.

Conclusions. 

The relative quantities of BMPs in DBMs are low, in the order of 1 × 10−9 g of BMP/g of DBM. There is higher variability in concentration of BMPs among 3 different lots of the same DBM formulation than among different DBM formulations. This variability questions DBM products’ reliability and, possibly, efficacy in providing consistent osteoinduction.

© 2006 Lippincott Williams & Wilkins, Inc.

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