İNSAN AMNİYOTİK SIVISI VE MEMBRANININ BİR TAVŞAN DİZİ KIKIRDAK DEFEKTİ MODELİNDE KONDRAL İYİLEŞME ÜZERİNE ETKİLERİ
Year 2021,
, 663 - 671, 30.12.2021
İsmail Safa Satoğlu
,
Meric Unal
,
İbrahim Çoban
,
Duygu Gürel
,
Alper Gültekin
,
Necmettin Turgut
,
Osman Karaoğlan
Abstract
Amaç
Artiküler kıkırdağın kısıtlı intrensek iyileşmesi ve tamir
kapasitesinin az olması nedeniyle çoğu tedavi
metodları ile normal hyalen kıkırdak rejenerasyonu
sağlanamamakta ve sonuç olarak osteoartroz gelişebilmektedir.
Bu çalışmada insan amniyotik sıvısı ve
membranının tavşanlardaki kondral defektlerdeki etkilerini
incelemek amaçlanmıştır.
Gereç ve Yöntem
32 immatür albino Yeni Zelanda tavşanının 64 dizi bu
çalışmaya dahil edildi. Tam kat kıkırdak defektleri tavşanların
medial kondillerinin yük taşıma yüzeylerinde
cerrahi olarak oluşturuldu. Tavşanlar randomize olarak
dört gruba bölündü: ek tedavi verilmeyenler Grup
1, 0,3 ml insan amniyotik sıvısı (İAS) verilenler Grup
2, sadece insan amniyotik membranı (İAM) verilenler
Grup 3, hem 0,3 ml İAS hem İAM verilenler Grup
4’ü oluşturdu. Kondiller histopatolojik olarak 4. ve 12.
haftalarda modifiye O’Driscoll evreleme skalası ile
değerlendirildi. Sonuçlar Mann-Whitney U ve ANOVA
testleri ile istatistiksel olarak analiz edildi.
Bulgular
Gruplar arasında rejenere dokunun kalitesi açısından
istatistiksel olarak anlamlı fark bulunmadı (p>0.05).
Grupların ortalama sonuçları 12. haftada, 4. hafta sonuçlarından
daha kötü olarak saptandı; buna rağmen
bu farkın, sadece Grup 1 (sham grubu) ve Grup 4 açısından
anlamlı olduğu görüldü (İAS+İAM) (sırasıyla,
p=0,007 ve p=0,014).
Sonuç
Sadece İAS, sadece İAM ve her iki biyomateryalin
kombine edildiği tedavi yöntemlerinin hiçbirinde kıkırdak
defekt iyileşmesi daha iyi ve kaliteli olmadığı
ve birbirlerine de bir üstünlüğü olmadığı görüldü. Bu
çalışmada gösterilmiş olan 4. hafta sonuçlarının 12.
hafta sonuçlarından daha iyi olmasının çalışmada
kullanılan immatür tavşanlardaki intrensek tamir mekanizmasındaki
erken rejenerasyon kapasitesinden
kaynaklandığını düşünmekteyiz.
References
- 1. Steadman JR, Briggs KK, Rodrigo JJ, Kocher MS, Gill TJ, Rodkey
WG. Outcomes of microfracture for traumatic chondral
defects of the knee: Average 11-year follow-up. Arthrosc J Arthrosc
Relat Surg 2003 May;19(5):477–84.
- 2. Brandt KD, Block JA, Michalski JP, Moreland LW, Caldwell JR,
Lavin PT. Efficacy and safety of intraarticular sodium hyaluronate
in knee osteoarthritis. ORTHOVISC Study Group. Clin
Orthop Relat Res. 2001 Apr;(385):130–43.
- 3. Leighton R, Fitzpatrick J, Smith H, Crandall D, Flannery CR,
Conrozier T. Systematic clinical evidence review of NASHA
(Durolane hyaluronic acid) for the treatment of knee osteoarth-
ritis. Open Access Rheumatol Res Rev. 2018 May;10:43–54.
- 4. Dahl LB, Kimpton WG, Cahill RNP, Brown TJ, Fraser RE. The
origin and fate of hyaluronan in amniotic fluid. J Dev Physiol.
1989 Oct;12(4):209–18.
- 5. Longaker MT, Adzick NS, Hall JL, Stair SE, Crombleholme TM,
Duncan BW, Bradley SM, Harrison MR, Stern R. Studies in fetal
wound healing, VII. Fetal wound healing may be modulated
by hyaluronic acid stimulating activity in amniotic fluid. J Pediatr
Surg. 1990 Apr;25(4):430–3.
- 6. Longaker MT, Scott Adzick N. The biology of fetal wound healing:
A review. Plast Reconstr Surg. 1991 Apr;87(4):788–98.
- 7. Gruss JS, Jirsch DW. Human amniotic membrane: A versatile
wound dressing. Can Med Assoc J. 1978 May 20;118(10):1237-
46
- 8. Tabet SK, Conner DM, Guebert DA. The Use of Human Amniotic
Membrane for Cartilage Repair: A Sheep Study. Stem Cell
Discov. 2015;05(04):40–7.
- 9. Willett NJ, Thote T, Lin AS, Moran S, Raji Y, Sridaran S, Stevens
HY, Guldberg RE. Intra-articular injection of micronized
dehydrated human amnion/chorion membrane attenuates osteoarthritis
development. Arthritis Res Ther. 2014;16(1):R47.
- 10. Özgenel GY, Filiz G. Effects of human amniotic fluid on peripheral
nerve scarring and regeneration in rats. J Neurosurg.
2003 Feb;98(2):371–7.
- 11. Özgenel GY, Şamli B, Özcan M. Effects of human amniotic
fluid on peritendinous adhesion formation and tendon healing
after flexor tendon surgery in rabbits. J Hand Surg Am. 2001
Mar;26(2):332–9.
- 12. Özgenel GY, Filiz G. Combined Application of Human Amniotic
Membrane Wrapping and Hyaluronic Acid Injection in Epineurectomized
Rat Sciatic Nerve. J Reconstr Microsurg. 2004
Mar;20(2):153–7.
- 13. Grigolo B, Roseti L, Fiorini M, Fini M, Giavaresi G, Aldini NN,
Giardino R, Facchini A. Transplantation of chondrocytes seeded
on a hyaluronan derivative (Hyaff®-11) into cartilage defects
in rabbits. Biomaterials. 2001 Sep;22(17):2417–24.
- 14. Norris S., Pettifor J., Gray D., Buffenstein R. Calcium metabolism
and bone mass in female rabbits during skeletal maturation:
effects of dietary calcium intake. Bone. 2001 Jul;29(1):62–9.
- 15. Karaçal N, Koşucu P, Çobanoğlu Ü, Kutlu N. Effect of human
amniotic fluid on bone healing. J Surg Res. 2005;
- 16. Wei X, Gao J, Messner K. Maturation-dependent repair of untreated
osteochondral defects in the rabbit knee joint. J Biomed
Mater Res. 1997 Jan;34(1):63–72.
- 17. Solchaga LA, Yoo JU, Lundberg M, Dennis JE, Huibregtse
BA, Goldberg VM, Caplan AI. Hyaluronan-based polymers in
the treatment of osteochondral defects. J Orthop Res. 2000
Sep;18(5):773–80.
- 18. Tuncel M, Halici M, Canoz O, Yildirim Turk C, Oner M, Ozturk F,
Kabak S. Role of insulin like growth factor-I in repair response
in immature cartilage. Knee. 2005 Apr;12(2):113–9.
- 19. O'Driscoll SW, Fitzsimmons JS. The Role of Periosteum in
Cartilage Repair. Clin Orthop Relat Res. 2001 Oct;391(391
SUPPL.):S190–207.
- 20. Elmalı N, Kaygusuz MA, Ozen S, Baysal O, Inan M, Karakaplan
M, Şarlak O. The healing effect of intraarticular hyaluronic
acid injection on osteoarthritic knee: a study on rabbit knees.
Acta Orthop Traumatol Turc. 1999; 33: 211-215
- 21. Adams ME. An analysis of clinical studies of the use of crosslinked
hyaluronan, hylan, in the treatment of osteoarthritis. J
Rheumatol Suppl. 1993 Aug;39:16-8.
- 22. Wobig M, Bach G, Beks P, Dickhut A, Runzheimer J, Schwieger
G, Vetter G, Balazs E. The role of elastoviscosity in the
efficacy of viscosupplementation for osteoarthritis of the knee:
A comparison of Hylan G-F 20 and a lower-molecular-weight
hyaluronan. Clin Ther 1999 Sep;21(9):1549–62.
- 23. Fortier LA, Mohammed HO, Lust G, Nixon AJ. Insulin-like
growth factor-I enhances cell-based repair of articular cartilage.
J Bone Joint Surg Br. 2002 Mar;84(2):276-88.
- 24. Vines J, Aliprantis A, Gomoll A, Farr J. Cryopreserved Amniotic
Suspension for the Treatment of Knee Osteoarthritis. J Knee
Surg. 2015 Dec 18;29(06):443–50.
- 25. Kavakli K, Gurkok S, Caylak H, Genc O, Gamsizkan M, Yucel
O, Karasahin E, Gozubuyuk A, Tasci C. Effects of human
amniotic fluid on costal cartilage regeneration (an experimental
study). Thorac Cardiovasc Surg. 2011 Dec;59(8):484-9.
- 26. You Q, Liu Z, Zhang J, Shen M, Li Y, Jin Y, Liu Y. Human Amniotic
Mesenchymal Stem Cell Sheets Encapsulating Cartilage
Particles Facilitate Repair of Rabbit Osteochondral Defects.
Am J Sports Med. 2020 Mar 15;48(3):599–611.
- 27. Ghanmi S, Trigui M, Baya W, Ellouz Z, Elfeki A, Charfi S, Fricain
JC, Keskes H. The periosteum-like effect of fresh human
amniotic membrane on bone regeneration in a rabbit critical-sized
defect model. Bone. 2018 May;110:392-404.
- 28. Cheng ZJ, So RP, Byung HC, Lee KY, Choong KK, Min BH.
Human amniotic membrane as a delivery matrix for articular
cartilage repair. Tissue Eng. 2007 Apr;13(4):693-702.
- 29. Zhang Z, Zeng L, Yang J, Guo L, Hou Q, Zhu F. Amniotic
membrane-derived stem cells help repair osteochondral defect
in a weight-bearing area in rabbits. Exp Ther Med. 2017
Jul;14(1):187–92.
- 30. Pipino C, Pierdomenico L, Di Tomo P, Di Giuseppe F, Cianci E,
D’Alimonte I, Morabito C, Centurione L, Antonucci I, Mariggiò
MA, Di Pietro R, Ciccarelli R, Marchisio M, Romano M, Angelucci
S, Pandolfi A. Molecular and phenotypic characterization
of human amniotic fluid-derived cells: A morphological and proteomic
approach. Stem Cells Dev. 2015 Jun 15;24(12):1415–
28.
THE EFFECTS OF HUMAN AMNIOTIC FLUID AND MEMBRANE ON CHONDRAL HEALING IN A RABBIT KNEE CARTILAGE DEFECT MODEL
Year 2021,
, 663 - 671, 30.12.2021
İsmail Safa Satoğlu
,
Meric Unal
,
İbrahim Çoban
,
Duygu Gürel
,
Alper Gültekin
,
Necmettin Turgut
,
Osman Karaoğlan
Abstract
Objective
Due to the limited intrinsic healing and repair capacity
of the articular cartilage, most treatment methods
cannot achieve reliable regeneration of normal
hyaline cartilage, resulting in early development
of osteoarthritis. The purpose of this study was to
determine the effects of human amniotic fluid and
membrane on chondral defects.
Material and Methods
Sixty-four knees of 32 immature New Zealand rabbits
were included in the study. Full thickness chondral
defects were created in the weight-bearing surface of
the medial condyles of the rabbits. The rabbits were
divided randomly into four groups: no adjunct treatment
was given in group 1, 0.3 ml human amniotic fluid
(HAF) alone in group 2, human amniotic membrane
(HAM) alone in group 3 and both of 0.3 ml HAF and
HAM in group 4 was administered. The condyles were
histopathologically evaluated at 4th and 12th week
using the modified O’Driscoll Grading Scale.
Results
There were no significant differences in the quality
of the regenerated tissue within and between groups
(p>0.05). The mean results of groups at the 12th week
were worse than results at the 4th week; however,
the difference was statistically significant for only the
sham group (group 1) and the combined therapy
group (group 4) (p=0.007 and p=0.014, respectively).
Conclusion
HAF alone, HAM alone, and combined administration
of both biomaterials neither affected chondral defect
healing nor had any differences between each
other. Nevertheless, we believe that some early
regeneration due to an intrinsic repair mechanism is
possible in immature rabbits as this study showed
better results at 4th week than those at 12th week,
although they are prone to degenerative processes in
long-term follow-up. We suggest that a larger sample
size in an experimental study would probably display
a statistically significant difference when investigating
effects of HAF, HAM, or both.
References
- 1. Steadman JR, Briggs KK, Rodrigo JJ, Kocher MS, Gill TJ, Rodkey
WG. Outcomes of microfracture for traumatic chondral
defects of the knee: Average 11-year follow-up. Arthrosc J Arthrosc
Relat Surg 2003 May;19(5):477–84.
- 2. Brandt KD, Block JA, Michalski JP, Moreland LW, Caldwell JR,
Lavin PT. Efficacy and safety of intraarticular sodium hyaluronate
in knee osteoarthritis. ORTHOVISC Study Group. Clin
Orthop Relat Res. 2001 Apr;(385):130–43.
- 3. Leighton R, Fitzpatrick J, Smith H, Crandall D, Flannery CR,
Conrozier T. Systematic clinical evidence review of NASHA
(Durolane hyaluronic acid) for the treatment of knee osteoarth-
ritis. Open Access Rheumatol Res Rev. 2018 May;10:43–54.
- 4. Dahl LB, Kimpton WG, Cahill RNP, Brown TJ, Fraser RE. The
origin and fate of hyaluronan in amniotic fluid. J Dev Physiol.
1989 Oct;12(4):209–18.
- 5. Longaker MT, Adzick NS, Hall JL, Stair SE, Crombleholme TM,
Duncan BW, Bradley SM, Harrison MR, Stern R. Studies in fetal
wound healing, VII. Fetal wound healing may be modulated
by hyaluronic acid stimulating activity in amniotic fluid. J Pediatr
Surg. 1990 Apr;25(4):430–3.
- 6. Longaker MT, Scott Adzick N. The biology of fetal wound healing:
A review. Plast Reconstr Surg. 1991 Apr;87(4):788–98.
- 7. Gruss JS, Jirsch DW. Human amniotic membrane: A versatile
wound dressing. Can Med Assoc J. 1978 May 20;118(10):1237-
46
- 8. Tabet SK, Conner DM, Guebert DA. The Use of Human Amniotic
Membrane for Cartilage Repair: A Sheep Study. Stem Cell
Discov. 2015;05(04):40–7.
- 9. Willett NJ, Thote T, Lin AS, Moran S, Raji Y, Sridaran S, Stevens
HY, Guldberg RE. Intra-articular injection of micronized
dehydrated human amnion/chorion membrane attenuates osteoarthritis
development. Arthritis Res Ther. 2014;16(1):R47.
- 10. Özgenel GY, Filiz G. Effects of human amniotic fluid on peripheral
nerve scarring and regeneration in rats. J Neurosurg.
2003 Feb;98(2):371–7.
- 11. Özgenel GY, Şamli B, Özcan M. Effects of human amniotic
fluid on peritendinous adhesion formation and tendon healing
after flexor tendon surgery in rabbits. J Hand Surg Am. 2001
Mar;26(2):332–9.
- 12. Özgenel GY, Filiz G. Combined Application of Human Amniotic
Membrane Wrapping and Hyaluronic Acid Injection in Epineurectomized
Rat Sciatic Nerve. J Reconstr Microsurg. 2004
Mar;20(2):153–7.
- 13. Grigolo B, Roseti L, Fiorini M, Fini M, Giavaresi G, Aldini NN,
Giardino R, Facchini A. Transplantation of chondrocytes seeded
on a hyaluronan derivative (Hyaff®-11) into cartilage defects
in rabbits. Biomaterials. 2001 Sep;22(17):2417–24.
- 14. Norris S., Pettifor J., Gray D., Buffenstein R. Calcium metabolism
and bone mass in female rabbits during skeletal maturation:
effects of dietary calcium intake. Bone. 2001 Jul;29(1):62–9.
- 15. Karaçal N, Koşucu P, Çobanoğlu Ü, Kutlu N. Effect of human
amniotic fluid on bone healing. J Surg Res. 2005;
- 16. Wei X, Gao J, Messner K. Maturation-dependent repair of untreated
osteochondral defects in the rabbit knee joint. J Biomed
Mater Res. 1997 Jan;34(1):63–72.
- 17. Solchaga LA, Yoo JU, Lundberg M, Dennis JE, Huibregtse
BA, Goldberg VM, Caplan AI. Hyaluronan-based polymers in
the treatment of osteochondral defects. J Orthop Res. 2000
Sep;18(5):773–80.
- 18. Tuncel M, Halici M, Canoz O, Yildirim Turk C, Oner M, Ozturk F,
Kabak S. Role of insulin like growth factor-I in repair response
in immature cartilage. Knee. 2005 Apr;12(2):113–9.
- 19. O'Driscoll SW, Fitzsimmons JS. The Role of Periosteum in
Cartilage Repair. Clin Orthop Relat Res. 2001 Oct;391(391
SUPPL.):S190–207.
- 20. Elmalı N, Kaygusuz MA, Ozen S, Baysal O, Inan M, Karakaplan
M, Şarlak O. The healing effect of intraarticular hyaluronic
acid injection on osteoarthritic knee: a study on rabbit knees.
Acta Orthop Traumatol Turc. 1999; 33: 211-215
- 21. Adams ME. An analysis of clinical studies of the use of crosslinked
hyaluronan, hylan, in the treatment of osteoarthritis. J
Rheumatol Suppl. 1993 Aug;39:16-8.
- 22. Wobig M, Bach G, Beks P, Dickhut A, Runzheimer J, Schwieger
G, Vetter G, Balazs E. The role of elastoviscosity in the
efficacy of viscosupplementation for osteoarthritis of the knee:
A comparison of Hylan G-F 20 and a lower-molecular-weight
hyaluronan. Clin Ther 1999 Sep;21(9):1549–62.
- 23. Fortier LA, Mohammed HO, Lust G, Nixon AJ. Insulin-like
growth factor-I enhances cell-based repair of articular cartilage.
J Bone Joint Surg Br. 2002 Mar;84(2):276-88.
- 24. Vines J, Aliprantis A, Gomoll A, Farr J. Cryopreserved Amniotic
Suspension for the Treatment of Knee Osteoarthritis. J Knee
Surg. 2015 Dec 18;29(06):443–50.
- 25. Kavakli K, Gurkok S, Caylak H, Genc O, Gamsizkan M, Yucel
O, Karasahin E, Gozubuyuk A, Tasci C. Effects of human
amniotic fluid on costal cartilage regeneration (an experimental
study). Thorac Cardiovasc Surg. 2011 Dec;59(8):484-9.
- 26. You Q, Liu Z, Zhang J, Shen M, Li Y, Jin Y, Liu Y. Human Amniotic
Mesenchymal Stem Cell Sheets Encapsulating Cartilage
Particles Facilitate Repair of Rabbit Osteochondral Defects.
Am J Sports Med. 2020 Mar 15;48(3):599–611.
- 27. Ghanmi S, Trigui M, Baya W, Ellouz Z, Elfeki A, Charfi S, Fricain
JC, Keskes H. The periosteum-like effect of fresh human
amniotic membrane on bone regeneration in a rabbit critical-sized
defect model. Bone. 2018 May;110:392-404.
- 28. Cheng ZJ, So RP, Byung HC, Lee KY, Choong KK, Min BH.
Human amniotic membrane as a delivery matrix for articular
cartilage repair. Tissue Eng. 2007 Apr;13(4):693-702.
- 29. Zhang Z, Zeng L, Yang J, Guo L, Hou Q, Zhu F. Amniotic
membrane-derived stem cells help repair osteochondral defect
in a weight-bearing area in rabbits. Exp Ther Med. 2017
Jul;14(1):187–92.
- 30. Pipino C, Pierdomenico L, Di Tomo P, Di Giuseppe F, Cianci E,
D’Alimonte I, Morabito C, Centurione L, Antonucci I, Mariggiò
MA, Di Pietro R, Ciccarelli R, Marchisio M, Romano M, Angelucci
S, Pandolfi A. Molecular and phenotypic characterization
of human amniotic fluid-derived cells: A morphological and proteomic
approach. Stem Cells Dev. 2015 Jun 15;24(12):1415–
28.