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Living Cellular Construct for Increasing the Width of Keratinized Gingiva: Results From a Randomized, Within‐Patient, Controlled Trial
dc.contributor.authorMcGuire, Michael K.
dc.contributor.authorScheyer, E. Todd
dc.contributor.authorNevins, Marc L.
dc.contributor.authorNeiva, Rodrigo
dc.contributor.authorCochran, David L.
dc.contributor.authorMellonig, James T.
dc.contributor.authorGiannobile, William V.
dc.contributor.authorBates, Damien
dc.date.accessioned2018-02-05T16:48:10Z
dc.date.available2018-02-05T16:48:10Z
dc.date.issued2011-10
dc.identifier.citationMcGuire, Michael K.; Scheyer, E. Todd; Nevins, Marc L.; Neiva, Rodrigo; Cochran, David L.; Mellonig, James T.; Giannobile, William V.; Bates, Damien (2011). "Living Cellular Construct for Increasing the Width of Keratinized Gingiva: Results From a Randomized, Within‐Patient, Controlled Trial." Journal of Periodontology 82(10): 1414-1423.
dc.identifier.issn0022-3492
dc.identifier.issn1943-3670
dc.identifier.urihttps://hdl.handle.net/2027.42/142206
dc.publisherAmerican Academy of Periodontology
dc.publisherWiley Periodicals, Inc.
dc.subject.otheroral surgery
dc.subject.othermouth mucosa
dc.subject.otherGingival recession
dc.subject.otherwound healing
dc.subject.otherregenerative medicine
dc.subject.otherperiodontal diseases
dc.titleLiving Cellular Construct for Increasing the Width of Keratinized Gingiva: Results From a Randomized, Within‐Patient, Controlled Trial
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelDentistry
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.contributor.affiliationumMichigan Center for Oral Health Research, University of Michigan School of Dentistry, Ann Arbor, MI.
dc.contributor.affiliationotherDepartment of Periodontics, University of Texas Health Science Center, San Antonio, TX.
dc.contributor.affiliationotherOrganogenesis, Canton, MA.
dc.contributor.affiliationotherPrivate practice, Houston, TX.
dc.contributor.affiliationotherPrivate practice, Boston, MA.
dc.contributor.affiliationotherDepartment of Periodontics, College of Dentistry, University of Florida, Gainesville, FL.
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/142206/1/jper1414.pdf
dc.identifier.doi10.1902/jop.2011.100671
dc.identifier.sourceJournal of Periodontology
dc.identifier.citedreferenceLang NP, Löe H. The relationship between the width of keratinized gingiva and gingival health. J Periodontol 1972; 43: 623 – 627.
dc.identifier.citedreferenceWennström J, Lindhe J. Role of attached gingiva for maintenance of periodontal health. Healing following excisional and grafting procedures in dogs. J Clin Periodontol 1983; 10: 206 – 221.
dc.identifier.citedreferenceNevins M. Attached gingiva–mucogingival therapy and restorative dentistry. Int J Periodontics Restorative Dent 1986; 6(4): 9 – 27.
dc.identifier.citedreferenceChung DM, Oh TJ, Shotwell JL, Misch CE, Wang HL. Significance of keratinized mucosa in maintenance of dental implants with different surfaces. J Periodontol 2006; 77: 1410 – 1420.
dc.identifier.citedreferenceFalanga V, Margolis D, Alvarez O, et al. Rapid healing of venous ulcers and lack of clinical rejection with an allogeneic cultured human skin equivalent. Arch Dermatol 1998; 134: 293 – 300.
dc.identifier.citedreferenceVeves A, Falanga V, Armstrong DG, Sabolinski ML; Apligraf Diabetic Foot Ulcer Study. Graftskin, a human skin equivalent, is effective in the management of noninfected neuropathic diabetic foot ulcers: A prospective randomized multicenter clinical trial. Diabetes Care 2001; 24: 290 – 295.
dc.identifier.citedreferenceBrem H, Young J, Tomic‐Canic M, Isaacs C, Ehrlich HP. Clinical efficacy and mechanism of bilayered living human skin equivalent (HSE) in treatment of diabetic foot ulcers. Surg Technol Int 2003; 11: 23 – 31.
dc.identifier.citedreferenceWaymack P, Duff RG, Sabolinski M; The Apligraf Burn Study Group. The effect of a tissue engineered bilayered living skin analog, over meshed split‐thickness autografts on the healing of excised burn wounds. Burns 2000; 26: 609 – 619.
dc.identifier.citedreferenceEaglstein WH, Alvarez OM, Auletta M, et al. Acute excisional wounds treated with a tissue‐engineered skin (Apligraf). Dermatol Surg 1999; 25: 195 – 201.
dc.identifier.citedreferenceMuhart M, McFalls S, Kirsner RS, et al. Behavior of tissue‐engineered skin: A comparison of a living skin equivalent, autograft, and occlusive dressing in human donor sites. Arch Dermatol 1999; 135: 913 – 918.
dc.identifier.citedreferenceGohari S, Gambla C, Healey M, et al. Evaluation of tissue‐engineered skin (human skin substitute) and secondary intention healing in the treatment of full thickness wounds after Mohs micrographic or excisional surgery. Dermatol Surg 2002; 28: 1107 – 1114, discussion 1114.
dc.identifier.citedreferenceDonohue KG, Carson P, Iriondo M, et al. Safety and efficacy of a bilayered skin construct in full‐thickness surgical wounds. J Dermatol 2005; 32: 626 – 631.
dc.identifier.citedreferenceHu S, Kirsner RS, Falanga V, Phillips T, Eaglstein WH. Evaluation of Apligraf persistence and basement membrane restoration in donor site wounds: A pilot study. Wound Repair Regen 2006; 14: 427 – 433.
dc.identifier.citedreferenceMorelli T, Neiva R, Nevins ML, et al. Angiogenic biomarkers and healing of living cellular constructs [published online ahead of print Jan 19, 2011]. J Dent Res doi: 10.1177/0022034510389334.
dc.identifier.citedreferenceGriffiths M, Ojeh N, Livingstone R, Price R, Navsaria H. Survival of Apligraf in acute human wounds. Tissue Eng 2004; 10: 1180 – 1195.
dc.identifier.citedreferenceMcGuire MK, Scheyer ET, Nunn ME, Lavin PT. A pilot study to evaluate a tissue‐engineered bilayered cell therapy as an alternative to tissue from the palate. J Periodontol 2008; 79: 1847 – 1856.
dc.identifier.citedreferenceMilstone LM, Asgari MM, Schwartz PM, Hardin‐Young J. Growth factor expression, healing, and structural characteristics of Graftskin (Apligraf). Wounds 2000; 12 ( Suppl. 5A ): 12A – 19A.
dc.identifier.citedreferenceWilkins LM, Watson SR, Prosky SJ, Meunier SF, Parenteau NL. Development of a bilayered living skin construct for clinical applications. Biotechnol Bioeng 1994; 43: 747 – 756.
dc.identifier.citedreferenceRyan ME. Clinical attachment level change as an outcome measure for therapies that slow the progression of periodontal disease. J Int Acad Periodontol 2005; 7(Suppl. 4): 162 – 171; discussion 172‐174.
dc.identifier.citedreferenceMiller PD Jr. Root coverage using the free soft tissue autograft following citric acid application. III. A successful and predictable procedure in areas of deep‐wide recession. Int J Periodontics Restorative Dent 1985; 5(2): 14 – 37.
dc.identifier.citedreferenceTakei HH, Azzi RR, Han TJ. Periodontal plastic and esthetic surgery. In: Newman MG, Takei HH, Klokkevold PR, Carranza RA, eds. Carranza’s Clinical Periodontology, 10th ed. St. Louis, MO: Saunders/Elsevier; 2006: 1005 – 1029.
dc.identifier.citedreferenceOrsini M, Orsini G, Benlloch D, Aranda JJ, Lázaro P, Sanz M. Esthetic and dimensional evaluation of free connective tissue grafts in prosthetically treated patients: A 1‐year clinical study. J Periodontol 2004; 75: 470 – 477.
dc.identifier.citedreferenceHatipoğlu H, Keçeli HG, Güncü GN, Sengün D, Tözüm TF. Vertical and horizontal dimensional evaluation of free gingival grafts in the anterior mandible: A case report series. Clin Oral Investig 2007; 11: 107 – 113.
dc.identifier.citedreferenceCardaropoli D, Cardaropoli G. Healing of gingival recessions using a collagen membrane with a hemineralized xenograft: A randomized controlled clinical trial. Int J Periodontics Restorative Dent 2009; 29: 59 – 67.
dc.identifier.citedreferenceSantamaria MP, Ambrosano GM, Casati MZ, Nociti FH Jr., Sallum AW, Sallum EA. Connective tissue graft plus resin‐modified glass ionomer restoration for the treatment of gingival recession associated with non‐carious cervical lesion: A randomized‐controlled clinical trial. J Clin Periodontol 2009; 36: 791 – 798.
dc.identifier.citedreferenceSanz M, Lorenzo R, Aranda JJ, Martin C, Orsini M. Clinical evaluation of a new collagen matrix (Mucograft prototype) to enhance the width of keratinized tissue in patients with fixed prosthetic restorations: A randomized prospective clinical trial. J Clin Periodontol 2009; 36: 868 – 876.
dc.identifier.citedreferenceAgudio G, Nieri M, Rotundo R, Franceschi D, Cortellini P, Pini Prato GP. Periodontal conditions of sites treated with gingival‐augmentation surgery compared to untreated contralateral homologous sites: A 10‐ to 27‐year long‐term study. J Periodontol 2009; 80: 1399 – 1405.
dc.identifier.citedreferenceChambrone L, Sukekava F, Araújo MG, Pustiglioni FE, Chambrone LA, Lima LA. Root‐coverage procedures for the treatment of localized recession‐type defects: A Cochrane systematic review. J Periodontol 2010; 81: 452 – 478.
dc.identifier.citedreferenceAriaudo AA, Tyrrell HA. Repositioning and increasing the zone of attached gingiva. J Periodontol 1957; 28: 106 – 110.
dc.identifier.citedreferenceWennström J. Regeneration of gingiva following surgical excision. A clinical study. J Clin Periodontol 1983; 10: 287 – 297.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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