Liang Zhu1, Hua-dan Xue1, Zhao-yong Sun1, Marcel Dominik Nickel2, Tianyi Qian3, and Zheng-yu Jin4
1Radiology, Peking Union Medical College Hospital, Beijing, China, 2Siemens Healthcare, Erlangen, Germany, 3Siemens Healthcare, Beijing, China, 4Peking Union Medical College Hospital, B, China
Synopsis
This prospective study aims to evaluate the T1 relaxation
time of autoimmune pancreatitis (AIP) in the native state and after
corticosteroid treatment (CST). Thirty-four patients with AIP and twenty control
subjects received pancreatic MR including T1 mapping. All AIP patients had T1
mapping data before and after CST. It turned out that the inflamed pancreatic
parenchyma had significantly elongated T1 relaxation time, and after 4-12 weeks
of CST, the T1 relaxation time shortened significantly towards normalization, in
keeping with the serum biomarkers of disease activity. Therefore MR T1 mapping is
a noninvasive, quantitative method to monitor AIP treatment effect.
Synopsis
This prospective study aims to evaluate the T1 relaxation
time of autoimmune pancreatitis (AIP) in the native state and after
corticosteroid treatment (CST). Thirty-four patients with AIP and twenty control
subjects received pancreatic MR including T1 mapping. All AIP patients had T1
mapping data before and after CST. It turned out that the inflamed pancreatic
parenchyma had significantly elongated T1 relaxation time, and after 4-12 weeks
of CST, the T1 relaxation time shortened significantly towards normalization, in
keeping with the serum biomarkers of disease activity. Therefore MR T1 mapping is
a noninvasive, quantitative method to monitor AIP treatment effect.Introduction
Autoimmune pancreatitis is a special form of
chronic pancreatitis, which often manifests as tumor-like swelling of the
pancreas, and chronic exocrine and endocrine function loss. AIP usually respond
well to steroid treatment, with clinical symptoms relief and pancreatic
function restoring 1-2. However, the incidence of disease relapse is
high 3. Serum biomarkers and pancreatic morphology on
cross-sectional imaging has limitations in monitoring disease activity and
predicting relapse 4-5. The aim of this study is to evaluate the T1 relaxation
time of autoimmune pancreatitis (AIP) in the native state and its change after
corticosteroid treatment (CST).Methods
The institutional review board approved this
prospective study, and all patients provided written informed consent.
Twenty-two patients with diffuse AIP and 12 patients with focal AIP received
pancreatic MR imaging including T1-VIBE-Dixon, T2-HASTE, T2-Blade, DWI and T1
mapping on a MAGNETOM Skyra 3T MR scanner (Siemens Healthcare, Erlangen,
Germany) using an 18-channel body coil and a 32-channel spine coil, both before
and after steroid treatment. T1 maps were acquired using a prototype T1 Look-Locker
sequence with the following parameters:
FOV= 300 x 270 mm2,
matrix = 128 x 115, number of slices=5, slice thickness = 4mm, TR/TE=3.00/1.31 ms, 16 TIs equally distributed from 104 ms to 2354ms. Seven of those patients received additional MR T1
mapping during disease relapse. Twenty patients without pancreatic diseases who
received T1 mapping of the pancreas served as control. In each patient, T1
relaxation time of pancreatic parenchyma in the head, body and tail was
measured. The association of T1 relaxation time and serum biomarkers IgG4 and
C-reactive protein (CRP) was evaluated.Results
The T1 relaxation time of normal pancreatic
parenchyma was 785.4±49.5 msec. For both diffuse and focal AIP, the T1 relaxation
time was significantly elongated compared to the control (both p<0.001).
After 4-12 weeks of CST, the T1 relaxation time of the pancreas shortened
significantly towards normalization, compared to the baseline value (for
diffuse AIP: from 1104.5±121.8 msec to 893.8±108.4 msec, and for focal AIP: from 1220.7±139.3 msec to 931.7±86.4 msec; both p<0.01). The visually
uninvolved parenchyma in focal AIP had longer T1 relaxation time compared to the
normal pancreas (p<0.01), which also shortened significantly after steroid
treatment (from 918.7±128.9 msec to 831.1±94.3 msec, p<0.01). In seven patients with
clinically evident disease relapse, T1 relaxation time of the pancreas
elongated significantly compared to the remission state (from
927.5±95.9 msec to 1287.7±125.6 msec, p<0.01).Discussion
It is known that the pancreatic signal intensity
(SI) on T1-weighted fat-saturated MR images reflects the pancreatic disease
state with a high sensitivity. Inflamed pancreatic parenchyma or tumor usually
has SI lower than or equal to the liver, with a diagnostic accuracy >80%
6. T1 mapping provides a more accurate
quantitative measure of pancreatic parenchyma, and proved to be useful in
diagnosing mild chronic pancreatitis 7. In this study, we found that T1 relaxation
time significantly differs in the inflamed pancreatic parenchyma of AIP and
normal pancreas, and in the same patient, T1 relaxation time changes
significantly according to the inflammation-remission-relapse state. This
suggests the role of T1 mapping as an effective quantitative imaging tool to
monitor treatment effect of AIP and early detection of disease relapse,
therefore guiding a more adequate treatment. Besides, T1 mapping detects more
extensive parenchyma involvement in focal AIP, compared to visual inspection.
Focal AIP often poses a diagnostic challenge, since differentiation with
pancreatic cancer is often difficult 8-9. Although the morphologic features may have
potential overlap, the background parenchyma inflammation of AIP, which could
be sensitively detected by T1 mapping, may provide additional key information
for disease characterization, thus enhancing the diagnostic confidence and
waiving the necessity of more invasive diagnostic procedures.Conclusion
T1 mapping could accurately depict the
inflammatory state and extent in patients with AIP, and monitor parenchyma
change with treatment. Acknowledgements
No acknowledgement found.References
1. Hirano
K, Tada M, Isayama H, et al. Long-term prognosis of autoimmune pancreatitis
with and without corticosteroid treatment. Gut.
Dec 2007;56(12):1719-1724.
2. Church NI, Pereira SP,
Deheragoda MG, et al. Autoimmune pancreatitis: clinical and radiological
features and objective response to steroid therapy in a UK series. The American journal of gastroenterology. Nov
2007;102(11):2417-2425.
3. Hart PA, Topazian MD,
Witzig TE, et al. Treatment of relapsing autoimmune pancreatitis with
immunomodulators and rituximab: the Mayo Clinic experience. Gut. Nov 2013;62(11):1607-1615.
4. Rehnitz C, Klauss M,
Singer R, et al. Morphologic patterns of autoimmune pancreatitis in CT and MRI.
Pancreatology : official journal of the
International Association of Pancreatology. 2011;11(2):240-251.
5. Manfredi R, Graziani R,
Cicero C, et al. Autoimmune pancreatitis: CT patterns and their changes after
steroid treatment. Radiology. May
2008;247(2):435-443.
6. Winston CB, Mitchell
DG, Outwater EK, Ehrlich SM. Pancreatic signal intensity on T1-weighted fat
saturation MR images: clinical correlation. Journal
of magnetic resonance imaging : JMRI. May-Jun 1995;5(3):267-271.
7. Tirkes T, Lin C, Fogel
EL, Sherman SS, Wang Q, Sandrasegaran K. T1 mapping for diagnosis of mild
chronic pancreatitis. Journal of magnetic
resonance imaging : JMRI. Apr 2017;45(4):1171-1176.
8. Choi SY, Kim SH, Kang
TW, Song KD, Park HJ, Choi YH. Differentiating Mass-Forming Autoimmune
Pancreatitis From Pancreatic Ductal Adenocarcinoma on the Basis of Contrast-Enhanced
MRI and DWI Findings. AJR. American
journal of roentgenology. Feb 2016;206(2):291-300.
9. Kamisawa T, Takuma K,
Anjiki H, et al. Differentiation of autoimmune pancreatitis from pancreatic
cancer by diffusion-weighted MRI. The
American journal of gastroenterology. Aug 2010;105(8):1870-1875.