Rofo 2015; 187(1): 29-35
DOI: 10.1055/s-0034-1385211
Abdomen
© Georg Thieme Verlag KG Stuttgart · New York

Multivariable Analysis of Clinical Influence Factors on Liver Enhancement of Gd-EOB-DTPA-Enhanced 3T MRI

Multivariable Analyse klinischer Einflussfaktoren auf die Signalintensität bei Gd-EOB-DTPA 3T-MRT der Leber
N. Verloh
1   Department of Radiology, University Hospital Regensburg
,
M. Haimerl
1   Department of Radiology, University Hospital Regensburg
,
F. Zeman
2   Center for Clinical Trials, University Hospital Regensburg
,
A. Teufel
3   Department of Gastroenterology, University Hospital Regensburg
,
S. Lang
4   Department of Surgery, University Hospital Regensburg
,
C. Stroszczynski
1   Department of Radiology, University Hospital Regensburg
,
C. Fellner
1   Department of Radiology, University Hospital Regensburg
,
P. Wiggermann
1   Department of Radiology, University Hospital Regensburg
› Author Affiliations
Further Information

Publication History

04 April 2014

01 August 2014

Publication Date:
22 December 2014 (online)

Abstract

Purpose: The purpose of this study was to identify clinical factors influencing Gd-EOB-DTPA liver uptake in patients with healthy liver parenchyma.

Materials and Methods: A total of 124 patients underwent contrast-enhanced MRI with a hepatocyte-specific contrast agent at 3 T. T1-weighted volume interpolated breath-hold examination (VIBE) sequences with fat suppression were acquired before and 20 minutes after contrast injection. The relative enhancement (RE) between plain and contrast-enhanced signal intensity was calculated. Simple and multiple linear regression analyses were performed to evaluate clinical factors influencing the relative enhancement. Patients were subdivided into three groups according to their relative liver enhancement (HRE, RE ≥ 100 %; MRE, 100 % > RE > 50 %; NRE, RE ≤ 50 %) and were analyzed according to the relevant risk factors.

Results: Simple regression analyses revealed patient age, transaminases (AST, ALT, GGT), liver, spleen and delta-liver volume (the difference between the volumetrically measured liver volume and the estimated liver volume based on body weight) as significant factors influencing relative enhancement. In the multiple analysis the transaminase AST, spleen and delta liver volume remained significant factors influencing relative enhancement. Delta liver volume showed a significant difference between all analyzed groups.

Conclusion: Liver enhancement in the hepatobiliary phase depends on a variety of factors. Body weight-adapted administration of Gd-EOB-DTPA may lead to inadequate liver enhancement after 20 minutes especially when the actual liver volume differs from the expected volume.

Key Points:

• Differences between actual and expected liver volume can cause inadequate liver enhancement after 20 min.

• A liver volume-adapted dose of Gd-EOB-DTPA may help to improve liver enhancement.

Citation Format:

• Verloh N, Haimerl M, Zeman F et al. Multivariable Analysis of Clinical Influence Factors on Liver Enhancement of Gd-EOB-DTPA-Enhanced 3T MRI. Fortschr Röntgenstr 2015; 187: 29 – 35

Zusammenfassung

Ziel: Analyse klinischer Faktoren, welche die Aufnahme von Gd-EOB-DTPA in einem Patientenkollektiv ohne Leberparenchymschädigungen beeinflussen.

Material und Methoden: 124 Patienten erhielten eine 3T-MRT-Untersuchung mit leberspezifischem Kontrastmittel zur sekundären Leberläsionsabklärung. Anhand T1-gewichteter VIBE-Sequenzen der Leber mit Fettunterdrückung wurde die relative Signaländerung (RE) zwischen nativer und hepatobiliärer Phase (20 min) evaluiert. Einfache und multiple lineare Regressionsanalysen wurden durchgeführt, um klinische Einflussfaktoren auf die Signaländerung zu bestimmen. Im Anschluss wurden die Patienten anhand der berechneten relativen Signalveränderung in drei Gruppen aufgeteilt (HRE, RE ≥ 100 %; MRE, 100 % > RE > 50 %; LRE, RE ≤ 50 %) und bezüglich der relevanten Risikofaktoren untersucht.

Ergebnisse: Die einfache Regressionsanalyse zeigte eine Korrelation zwischen relativer Signalverstärkung und dem Patientenalter, dem Leber- und dem Milzvolumen, dem sog. Deltalebervolumen (errechnete Abweichung zwischen dem gemessenen und dem gewichtsbasiert geschätzten Lebervolumen), sowie den Transaminasen AST, ALT, GGT. In der multiplen Analyse verblieben das Milz- und das Deltalebervolumen, sowie die Transaminase AST als signifikante Einflussfaktoren auf die Signalveränderung. Das Deltalebervolumen zeigte als einziger Parameter einen signifikanten Unterschied zwischen allen gebildeten Subgruppen.

Schlussfolgerungen: Die Kontrastierung der Leber in der hepatobiliären Phase ist von verschiedenen Faktoren abhängig. Wird Gd-EOB-DTPA alleine über das Patientengewicht dosiert, so kann dies zu einer inadäquaten Kontrastierung führen, besonders wenn das Lebervolumen nicht in Korrelation zu dem Körpergewicht steht.

Deutscher Artikel/German Article

 
  • References

  • 1 van Montfoort JE, Stieger B, Meijer DK et al. Hepatic uptake of the magnetic resonance imaging contrast agent gadoxetate by the organic anion transporting polypeptide Oatp1. The Journal of pharmacology and experimental therapeutics 1999; 290: 153-157
  • 2 Pascolo L, Cupelli F, Anelli PL et al. Molecular mechanisms for the hepatic uptake of magnetic resonance imaging contrast agents. Biochem Biophys Res Commun 1999; 257: 746-752
  • 3 Reimer P, Rummeny EJ, Shamsi K et al. Phase II clinical evaluation of Gd-EOB-DTPA: dose, safety aspects, and pulse sequence. Radiology 1996; 199: 177-183
  • 4 Hamm B, Staks T, Muhler A et al. Phase I clinical evaluation of Gd-EOB-DTPA as a hepatobiliary MR contrast agent: safety, pharmacokinetics, and MR imaging. Radiology 1995; 195: 785-792
  • 5 Haimerl M, Wachtler M, Platzek I et al. Added value of Gd-EOB-DTPA-enhanced Hepatobiliary phase MR imaging in evaluation of focal solid hepatic lesions. BMC medical imaging 2013; 13: 41
  • 6 Sun HY, Lee JM, Shin CI et al. Gadoxetic acid-enhanced magnetic resonance imaging for differentiating small hepatocellular carcinomas (< or =2 cm in diameter) from arterial enhancing pseudolesions: special emphasis on hepatobiliary phase imaging. Invest Radiol 2010; 45: 96-103
  • 7 Bieze M, van den Esschert JW, Nio CY et al. Diagnostic accuracy of MRI in differentiating hepatocellular adenoma from focal nodular hyperplasia: prospective study of the additional value of gadoxetate disodium. American journal of roentgenology 2012; 199: 26-34
  • 8 Nishie A, Asayama Y, Ishigami K et al. MR prediction of liver fibrosis using a liver-specific contrast agent: Superparamagnetic iron oxide versus Gd-EOB-DTPA. Journal of magnetic resonance imaging: JMRI 2012; 36: 664-671
  • 9 Verloh N, Haimerl M, Rennert J et al. Impact of liver cirrhosis on liver enhancement at Gd-EOB-DTPA enhanced MRI at 3Tesla. European journal of radiology 2013; 82: 1710-1715
  • 10 Ryeom HK, Kim SH, Kim JY et al. Quantitative evaluation of liver function with MRI Using Gd-EOB-DTPA. Korean journal of radiology: official journal of the Korean Radiological Society 2004; 5: 231-239
  • 11 Tsuda N, Okada M, Murakami T. Potential of gadolinium-ethoxybenzyl-diethylenetriamine pentaacetic acid (Gd-EOB-DTPA) for differential diagnosis of nonalcoholic steatohepatitis and fatty liver in rats using magnetic resonance imaging. Invest Radiol 2007; 42: 242-247
  • 12 Nilsson H, Blomqvist L, Douglas L et al. Assessment of liver function in primary biliary cirrhosis using Gd-EOB-DTPA-enhanced liver MRI. HPB the official journal of the International Hepato Pancreato Biliary Association 2010; 12: 567-576
  • 13 Verloh N, Haimerl M, Zeman F et al. Assessing liver function by liver enhancement during the hepatobiliary phase with Gd-EOB-DTPA-enhanced MRI at 3 Tesla. European radiology 2014; DOI: 10.1007/s00330-014-3108-y.
  • 14 Levey AS, Bosch JP, Lewis JB et al. A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group. Annals of internal medicine 1999; 130: 461-470
  • 15 Vauthey JN, Abdalla EK, Doherty DA et al. Body surface area and body weight predict total liver volume in Western adults. Liver transplantation official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society 2002; 8: 233-240
  • 16 Ichikawa T, Saito K, Yoshioka N et al. Detection and characterization of focal liver lesions: a Japanese phase III, multicenter comparison between gadoxetic acid disodium-enhanced magnetic resonance imaging and contrast-enhanced computed tomography predominantly in patients with hepatocellular carcinoma and chronic liver disease. Invest Radiol 2010; 45: 133-141
  • 17 Semelka RC, Martin DR, Balci C et al. Focal liver lesions: comparison of dual-phase CT and multisequence multiplanar MR imaging including dynamic gadolinium enhancement. Journal of magnetic resonance imaging 2001; 13: 397-401
  • 18 Petersein J, Spinazzi A, Giovagnoni A et al. Focal liver lesions: evaluation of the efficacy of gadobenate dimeglumine in MR imaging – a multicenter phase III clinical study. Radiology 2000; 215: 727-736
  • 19 Hamm B, Thoeni RF, Gould RG et al. Focal liver lesions: characterization with nonenhanced and dynamic contrast material-enhanced MR imaging. Radiology 1994; 190: 417-423
  • 20 Kim YK, Kwak HS, Kim CS et al. Hepatocellular carcinoma in patients with chronic liver disease: comparison of SPIO-enhanced MR imaging and 16-detector row CT. Radiology 2006; 238: 531-541
  • 21 Zizka J, Klzo L, Ferda J et al. Dynamic and delayed contrast enhancement in upper abdominal MRI studies: comparison of gadoxetic acid and gadobutrol. European journal of radiology 2007; 62: 186-191
  • 22 Asayama Y, Tajima T, Nishie A et al. Uptake of Gd-EOB-DTPA by hepatocellular carcinoma: radiologic-pathologic correlation with special reference to bile production. European journal of radiology 2011; 80: e243-e248
  • 23 Kobayashi S, Matsui O, Gabata T et al. Relationship between signal intensity on hepatobiliary phase of gadolinium ethoxybenzyl diethylenetriaminepentaacetic acid (Gd-EOB-DTPA)-enhanced MR imaging and prognosis of borderline lesions of hepatocellular carcinoma. European journal of radiology 2012; 81: 3002-3009
  • 24 Akai H, Matsuda I, Kiryu S et al. Fate of hypointense lesions on Gd-EOB-DTPA-enhanced magnetic resonance imaging. European journal of radiology 2012; 81: 2973-2977
  • 25 Weinmann HJ, Bauer H, Frenzel T et al. Mechanism of hepatic uptake of gadoxetate disodium. Academic radiology 1996; 3 (Suppl. 02) S232-S234
  • 26 Van Beers BE, Pastor CM, Hussain HK. Primovist, Eovist: what to expect?. Journal of hepatology 2012; 57: 421-429
  • 27 Tsuboyama T, Onishi H, Kim T et al. Hepatocellular carcinoma: hepatocyte-selective enhancement at gadoxetic acid-enhanced MR imaging – correlation with expression of sinusoidal and canalicular transporters and bile accumulation. Radiology 2010; 255: 824-833
  • 28 Tamada T, Ito K, Sone T et al. Gd-EOB-DTPA enhanced MR imaging: evaluation of biliary and renal excretion in normal and cirrhotic livers. European journal of radiology 2011; 80: e207-e211
  • 29 Muhler A, Heinzelmann I, Weinmann HJ. Elimination of gadolinium-ethoxybenzyl-DTPA in a rat model of severely impaired liver and kidney excretory function. An experimental study in rats. Invest Radiol 1994; 29: 213-216
  • 30 Tajiri K, Shimizu Y. Liver physiology and liver diseases in the elderly. World journal of gastroenterology: WJG 2013; 19: 8459-8467
  • 31 Tong C, Xu X, Liu C et al. Assessment of liver volume variation to evaluate liver function. Frontiers of medicine 2012; 6: 421-427
  • 32 Zhou XP, Lu T, Wei YG et al. Liver volume variation in patients with virus-induced cirrhosis: findings on MDCT. American journal of roentgenology 2007; 189: W153-W159
  • 33 Liu P, Li P, He W et al. Liver and spleen volume variations in patients with hepatic fibrosis. World journal of gastroenterology 2009; 15: 3298-3302
  • 34 Goshima S, Kanematsu M, Watanabe H et al. Gd-EOB-DTPA-enhanced MR imaging: prediction of hepatic fibrosis stages using liver contrast enhancement index and liver-to-spleen volumetric ratio. Journal of magnetic resonance imaging: JMRI 2012; 36: 1148-1153