Effect of Different Classes of Gadolinium-based Contrast Agents on Control and Nephrogenic Systemic Fibrosis–derived Fibroblast Proliferation

Published Online:https://doi.org/10.1148/radiol.10091131

We suggest that chelated gadolinium or free gadolinium may be bioactive in stimulating fibroblast proliferation and that a chelated gadolinium-driven mechanism means that all gadolinium-based contrast agents could carry a risk when used in high doses.

Purpose

To determine the ability of different types of gadolinium-based contrast agents (GBCAs) to stimulate fibroblast proliferation in monolayer cell culture.

Materials and Methods

The National Health Service West Glasgow Ethics Committee granted approval for this study. Fibroblasts established from healthy volunteers (control subjects) and from lesional skin of patients with nephrogenic systemic fibrosis were exposed to a range of concentrations of ionic and nonionic linear and macrocyclic contrast agents over 4 days, and the effect on growth was determined. The lowest concentration of contrast agent that stimulated the maximum effect on fibroblast growth was selected for determination of its effect on fibroblast growth over 8 days. The effect of contrast agents on hyaluronan and collagen synthesis was determined with an enzyme-linked immunosorbent assay. Responses were assessed with analysis of variance (general linear model).

Results

The linear gadolinium contrast agents (gadodiamide, gadoversetamide, gadopentetate dimeglumine, and gadobenate dimeglumine) produced a maximum stimulation of fibroblast proliferation at a concentration of 0.1 mmol/L, with cell numbers increasing up to 2.3-fold. The macrocyclic contrast agents (gadoteric acid and gadoteridol) produced a maximum stimulation of fibroblast proliferation at a concentration of 5 mmol/L. The reference gadolinium agents (N-methylglucamine gadolinium ethylenediaminetetraacetic acid and gadolinium trichloride) stimulated fibroblast proliferation at a concentration of 0.01 mmol/L and were toxic at a concentration greater than 1 mmol/L. Growth curves supported the dose-response observations. Hyaluronan synthesis was stimulated by gadoversetamide, gadobenate dimeglumine, gadodiamide, and gadopentetate dimeglumine at a concentration of 0.1 mmol/L and by gadolinium trichloride at a concentration of 0.01 mmol/L, whereas collagen synthesis was unaffected.

Conclusion

This study provides evidence that different classes of gadolinium chelates stimulate human fibroblast proliferation.

© RSNA, 2010

Supplemental material: http://radiology.rsna.org/lookup/suppl/doi:10.1148/radiol.10091131/-/DC1

References

  • 1 Kuo PH , Kanal E , Abu-Alfa AK , Cowper SE . Gadolinium-based MR contrast agents and nephrogenic systemic fibrosis. Radiology 2007;242(3):647–649. LinkGoogle Scholar
  • 2 Deo A , Fogel M , Cowper SE . Nephrogenic systemic fibrosis: a population study examining the relationship of disease development to gadolinium exposure. Clin J Am Soc Nephrol 2007;2(2):264–267. Crossref, MedlineGoogle Scholar
  • 3 Perazella MA . Gadolinium-contrast toxicity in patients with kidney disease: nephrotoxicity and nephrogenic systemic fibrosis. Curr Drug Saf 2008;3(1):67–75. Crossref, MedlineGoogle Scholar
  • 4 Prince MR , Zhang H , Morris M , et al. . Incidence of nephrogenic systemic fibrosis at two large medical centers. Radiology 2008;248(3):807–816. LinkGoogle Scholar
  • 5 Sadowski EA , Bennett LK , Chan MR , et al. . Nephrogenic systemic fibrosis: risk factors and incidence estimation. Radiology 2007;243(1):148–157. LinkGoogle Scholar
  • 6 Cowper SE . Nephrogenic systemic fibrosis: a review and exploration of the role of gadolinium. Adv Dermatol 2007;23:131–154. Crossref, MedlineGoogle Scholar
  • 7 Grobner T . Gadolinium: a specific trigger for the development of nephrogenic fibrosing dermopathy and nephrogenic systemic fibrosis? Nephrol Dial Transplant 2006;21(4):1104–1108. [Published correction appears in Nephrol Dial Transplant 2006;21(6):1745.] Crossref, MedlineGoogle Scholar
  • 8 Marckmann P , Skov L , Rossen K , et al. . Nephrogenic systemic fibrosis: suspected causative role of gadodiamide used for contrast-enhanced magnetic resonance imaging. J Am Soc Nephrol 2006;17(9):2359–2362. Crossref, MedlineGoogle Scholar
  • 9 Collidge TA , Thomson PC , Mark PB , et al. . Gadolinium-enhanced MR imaging and nephrogenic systemic fibrosis: retrospective study of a renal replacement therapy cohort. Radiology 2007;245(1):168–175. LinkGoogle Scholar
  • 10 Abujudeh HH , Kaewlai R , Kagan A , et al. . Nephrogenic systemic fibrosis after gadopentetate dimeglumine exposure: case series of 36 patients. Radiology 2009;253(1):81–89. LinkGoogle Scholar
  • 11 Rydahl C , Thomsen HS , Marckmann P . High prevalence of nephrogenic systemic fibrosis in chronic renal failure patients exposed to gadodiamide, a gadolinium-containing magnetic resonance contrast agent. Invest Radiol 2008;43(2):141–144. Crossref, MedlineGoogle Scholar
  • 12 Idee JM , Port M , Medina C , et al. . Possible involvement of gadolinium chelates in the pathophysiology of nephrogenic systemic fibrosis: a critical review. Toxicology 2008;248(2-3):77–88. Crossref, MedlineGoogle Scholar
  • 13 Reilly RF . Risk for nephrogenic systemic fibrosis with gadoteridol (ProHance) in patients who are on long-term hemodialysis. Clin J Am Soc Nephrol 2008;3(3):747–751. Crossref, MedlineGoogle Scholar
  • 14 Wollanka H , Weidenmaier W , Giersig C . NSF after Gadovist exposure: a case report and hypothesis of NSF development. Nephrol Dial Transplant 2009;24(12):3882–3884. Crossref, MedlineGoogle Scholar
  • 15 Food and Drug Administration . Information for healthcare professionals: gadolinium-based contrast agents for magnetic resonance imaging (marketed as Magnevist, MultiHance, Omniscan, Optimark, ProHance). Food and Drug Administration Web site. http://www.fda.gov/cder/drug/InfoSheets/HCP/gcca_200705HCP.pdf. Published June 2006. Updated May 23, 2007. Accessed June 2009. Google Scholar
  • 16 Cowper SE , Rabach M , Girardi M . Clinical and histological findings in nephrogenic systemic fibrosis. Eur J Radiol 2008;66(2):191–199. Crossref, MedlineGoogle Scholar
  • 17 Jiménez SA , Artlett CM , Sandorfi N , et al. . Dialysis-associated systemic fibrosis (nephrogenic fibrosing dermopathy): study of inflammatory cells and transforming growth factor beta1 expression in affected skin. Arthritis Rheum 2004;50(8):2660–2666. Crossref, MedlineGoogle Scholar
  • 18 Ting WW , Stone MS , Madison KC , Kurtz K . Nephrogenic fibrosing dermopathy with systemic involvement. Arch Dermatol 2003;139(7):903–906. Crossref, MedlineGoogle Scholar
  • 19 Galan A , Cowper SE , Bucala R . Nephrogenic systemic fibrosis (nephrogenic fibrosing dermopathy). Curr Opin Rheumatol 2006;18(6):614–617. Crossref, MedlineGoogle Scholar
  • 20 Lin SP , Brown JJ . MR contrast agents: physical and pharmacologic basics. J Magn Reson Imaging 2007;25(5):884–899. Crossref, MedlineGoogle Scholar
  • 21 Morcos SK . Extracellular gadolinium contrast agents: differences in stability. Eur J Radiol 2008;66(2):175–179. Crossref, MedlineGoogle Scholar
  • 22 High WA , Ayers RA , Cowper SE . Gadolinium is quantifiable within the tissue of patients with nephrogenic systemic fibrosis. J Am Acad Dermatol 2007;56(4):710–712. Crossref, MedlineGoogle Scholar
  • 23 Boyd AS , Zic JA , Abraham JL . Gadolinium deposition in nephrogenic fibrosing dermopathy. J Am Acad Dermatol 2007;56(1):27–30. Crossref, MedlineGoogle Scholar
  • 24 Abraham JL , Thakral C . Tissue distribution and kinetics of gadolinium and nephrogenic systemic fibrosis. Eur J Radiol 2008;66(2):200–207. Crossref, MedlineGoogle Scholar
  • 25 Ortonne N , Lipsker D , Chantrel F , Boehm N , Grosshans E , Cribier B . Presence of CD45RO+ CD34+ cells with collagen synthesis activity in nephrogenic fibrosing dermopathy: a new pathogenic hypothesis. Br J Dermatol 2004;150(5):1050–1052. Crossref, MedlineGoogle Scholar
  • 26 Edward M , Fitzgerald L , Thind C , Leman J , Burden AD . Cutaneous mucinosis associated with dermatomyositis and nephrogenic fibrosing dermopathy: fibroblast hyaluronan synthesis and the effect of patient serum. Br J Dermatol 2007;156(3):473–479. Crossref, MedlineGoogle Scholar
  • 27 Edward M , Quinn JA , Mukherjee S , et al. . Gadodiamide contrast agent ‘activates’ fibroblasts: a possible cause of nephrogenic systemic fibrosis. J Pathol 2008;214(5):584–593. Crossref, MedlineGoogle Scholar
  • 28 Newton BB , Jimenez SA . Mechanism of NSF: new evidence challenging the prevailing theory. J Magn Reson Imaging 2009;30(6):1277–1283. Crossref, MedlineGoogle Scholar
  • 29 Grebe SO , Borrmann M , Altenburg A , Wesselman U , Hein D , Haage P . Chronic inflammation and accelerated atherosclerosis as important cofactors in nephrogenic systemic fibrosis following intravenous gadolinium exposure. Clin Exp Nephrol 2008;12(5):403–406. Crossref, MedlineGoogle Scholar
  • 30 Singh AK , Szczech L , Tang KL , et al. . Correction of anemia with epoetin alfa in chronic kidney disease. N Engl J Med 2006;355(20):2085–2098. Crossref, MedlineGoogle Scholar
  • 31 Albaaj F , Hutchison AJ . Hyperphosphataemia in renal failure: causes, consequences and current management. Drugs 2003;63(6):577–596. Crossref, MedlineGoogle Scholar
  • 32 Joffe P , Thomsen HS , Meusel M . Pharmacokinetics of gadodiamide injection in patients with severe renal insufficiency and patients undergoing hemodialysis or continuous ambulatory peritoneal dialysis. Acad Radiol 1998;5(7):491–502. Crossref, MedlineGoogle Scholar
  • 33 Varani J , DaSilva M , Warner RL , et al. . Effects of gadolinium-based magnetic resonance imaging contrast agents on human skin in organ culture and human skin fibroblasts. Invest Radiol 2009;44(2):74–81. Crossref, MedlineGoogle Scholar
  • 34 Perone PA , Weber SL , DaSilva M , et al. . Collagenolytic activity is suppressed in organ-cultured human skin exposed to a gadolinium-based MRI contrast agent. Invest Radiol 2010;45(1):42–48. Crossref, MedlineGoogle Scholar
  • 35 Marckmann P , Skov L , Rossen K , Heaf JG , Thomsen HS . Case-control study of gadodiamide-related nephrogenic systemic fibrosis. Nephrol Dial Transplant 2007;22(11):3174–3178. Crossref, MedlineGoogle Scholar
  • 36 Frenzel T , Lengsfeld P , Schirmer H , Hütter J , Weinmann HJ . Stability of gadolinium-based magnetic resonance imaging contrast agents in human serum at 37 degrees C. Invest Radiol 2008;43(12):817–828. Crossref, MedlineGoogle Scholar
  • 37 High WA , Ayers RA , Chandler J , Zito G , Cowper SE . Gadolinium is detectable within the tissue of patients with nephrogenic systemic fibrosis. J Am Acad Dermatol 2007;56(1):21–26. Crossref, MedlineGoogle Scholar
  • 38 Wermuth PJ , Del Galdo F , Jiménez SA . Induction of the expression of profibrotic cytokines and growth factors in normal human peripheral blood monocytes by gadolinium contrast agents. Arthritis Rheum 2009;60(5):1508–1518. Crossref, MedlineGoogle Scholar
  • 39 Cabella C , Crich SG , Corpillo D , et al. . Cellular labeling with Gd(III) chelates: only high thermodynamic stabilities prevent the cells acting as ‘sponges’ of Gd3+ ions. Contrast Media Mol Imaging 2006;1(1):23–29. Crossref, MedlineGoogle Scholar
  • 40 Daniels CE , Wilkes MC , Edens M , et al. . Imatinib mesylate inhibits the profibrogenic activity of TGF-β and prevents bleomycin-mediated lung fibrosis. J Clin Invest 2004;114(9):1308–1316. Crossref, MedlineGoogle Scholar
  • 41 Kay J , High WA . Imatinib mesylate treatment of nephrogenic systemic fibrosis. Arthritis Rheum 2008;58(8):2543–2548. Crossref, MedlineGoogle Scholar

Article History

Received July 3, 2009; revision requested August 24; revision received January 29, 2010; accepted March 1; final version accepted March 9.
Published online: Sept 2010
Published in print: Sept 2010