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Autogenous and Allogeneic Bone Grafts in Periodontal Therapy

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tide size of approximately 250 to 800<br />

Particle sizes with<strong>in</strong> this range have been<br />

shown to promote osteogenesis, whereas a<br />

particle size below 125 |xm <strong>in</strong>duces a macrophage<br />

response (Mellonig <strong>and</strong> Levey,<br />

1984).<br />

5. The graft is aga<strong>in</strong> immersed <strong>in</strong> ethanol.<br />

6. The bone may or may not be dim<strong>in</strong>eralized.<br />

7. The allograft is freeze dried. Freeze dry<strong>in</strong>g<br />

permits long-term storage <strong>and</strong> reduces antigenicity<br />

(Turner <strong>and</strong> Mellonig, 1981;<br />

Quattlebaum et al, 1988).<br />

VII. GUIDED TISSUE REGENERATION<br />

AND BONE GRAFTS<br />

Case reports <strong>and</strong> controlled cl<strong>in</strong>ical trials have<br />

<strong>in</strong>dicated that the placement of a physical barrier<br />

between the g<strong>in</strong>gival flap <strong>and</strong> the root surface<br />

enhances the potential for wound heal<strong>in</strong>g (Nyman<br />

et al, 1982; Becker et al, 1987 <strong>and</strong> 1988; Pontoriero<br />

et al, 1988 <strong>and</strong> 1989; Lekovic et al,<br />

1989; Caffesse et al, 1990; Gager <strong>and</strong> Schultz,<br />

1991). This procedure retards apical migration<br />

of epithelium, excludes g<strong>in</strong>gival connective tissue<br />

cells from the wound, <strong>and</strong> favors heal<strong>in</strong>g<br />

from the periodontal ligament cells (Gottlow et<br />

al., 1986). The histologic result is new attachment<br />

(Gottlow et al, 1986; Becker et al, 1987;<br />

Nyman et al, 1987).<br />

A recent study <strong>in</strong>dicates that the periodontal<br />

ligament cells migrate only a short distance <strong>and</strong>,<br />

at the same rate, with <strong>and</strong> without the placement<br />

of a physical barrier (Aukhil <strong>and</strong> Iglhaut, 1988).<br />

Therefore, the critical role of a physical barrier<br />

may be that of space creation to allow migrat<strong>in</strong>g<br />

cells sufficient time to undergo amplify<strong>in</strong>g cell<br />

division <strong>and</strong> populate the root surface (Aukhil et<br />

al., 1990). In addition, cells from the bone may<br />

play a role <strong>in</strong> guided tissue regeneration. Cells<br />

from the endosteal spaces of alveolar bone can<br />

synthesize cementumlike tissue <strong>and</strong> may migrate<br />

from bone <strong>in</strong>to the periodontal ligament (Melcher<br />

etal, 1986).<br />

A number of case reports suggest that the<br />

comb<strong>in</strong>ation of an osseous graft <strong>and</strong> the physical<br />

barrier enhances bone fill <strong>and</strong> promotes more<br />

favorable results (Schallhorn <strong>and</strong> McCla<strong>in</strong>, 1988).<br />

Anderegg et al (1991) compared 15 pairs of<br />

furcation defects <strong>in</strong> 15 patients treated by DFDBA<br />

plus an exp<strong>and</strong>ed polytetrafluoroethylene (Gore-<br />

Tex <strong>Periodontal</strong> Material, W. L. Gore & Associates,<br />

Flagstaff, AZ) physical barrier or by a<br />

physical barrier alone. They found both horizontal<br />

<strong>and</strong> vertical bone fill to be more favorable<br />

with the use of the graft plus barrier. However,<br />

Garrett et al. (1988), us<strong>in</strong>g a graft of DFDBA<br />

<strong>and</strong> dura mater sheets between the replaced surgical<br />

flaps <strong>and</strong> the tooth surfaces, found limited<br />

improvement of the treated defects over pretreatment<br />

levels. Stahl <strong>and</strong> Froum (1991) have most<br />

recently shown cementogenesis on teeth treated<br />

by osseous allograft <strong>and</strong> an exp<strong>and</strong>ed polytetrafluoroethylene<br />

membrane. Osseous remodel<strong>in</strong>g<br />

<strong>and</strong> crestal osteogenesis were seen <strong>in</strong> association<br />

with cementogenesis. New attachment was histologically<br />

present with<strong>in</strong> two of four calculus<br />

notches <strong>in</strong> this sample.<br />

VIII. FUTURE DIRECTIONS<br />

Although bone grafts have been shown to be<br />

efficacious for the treatment of periodontal osseous<br />

lesions, the reconstruction appears to be<br />

limited to a mean bone fill of approximately 3.0<br />

mm irrespective of the type of bone graft material<br />

(Table 1). Because the ultimate goal of periodontal<br />

therapy is to reverse the disease process<br />

<strong>and</strong> completely regenerate the periodontium, additional<br />

stimuli to enhance the regenerative process<br />

clearly are needed. Polypeptide growth factors,<br />

a potent class of natural biologic response<br />

modifiers, may be the answer. Factors such as<br />

osteogen<strong>in</strong> (Bowers <strong>and</strong> Reddi, 1991) or the comb<strong>in</strong>ation<br />

of platelet-derived growth factor (PDGF)<br />

<strong>and</strong> <strong>in</strong>sul<strong>in</strong>like growth factor (IGF) (Lynch et al,<br />

1989) may have potential. Other growth factors<br />

such as transform<strong>in</strong>g growth factor- (3 <strong>and</strong> basic<br />

fibroblast growth factor may also have a place<br />

(Graves <strong>and</strong> Cochran, 1990). However, the use<br />

of growth factors (GFs) to augment periodontal<br />

regeneration also poses many questions, such as<br />

1. What is the proper dose of GFs?<br />

2. What is the best biologic carrier for the GF?<br />

3. When should the GF be released <strong>in</strong>to the<br />

heal<strong>in</strong>g cascade?<br />

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