Skip to main content
Download PDF

Outcome of gastric emptying and gastrointestinal symptoms after liver transplantation for hereditary transthyretin amyloidosis

BMC Gastroenterology volume 15, Article number: 51 (2015) Cite this article

Abstract

Background

Hereditary transthyretin amyloid (ATTR) amyloidosis is a rare but fatal autosomal dominant condition that is present all over the world. A liver transplantation has been shown to halt the progress of the disease in selected patients and is currently considered to be the standard treatment. Gastrointestinal manifestations are common in hereditary ATTR amyloidosis and are important for the patients’ morbidity and mortality. The aim of this study was to evaluate the long-term outcome of gastric emptying, gastrointestinal symptoms and nutritional status after liver transplantation for the disease.

Methods

Swedish patients with hereditary ATTR amyloidosis transplanted between 1990 and 2012 were included. A standardized method for measuring gastric emptying with a Tc99m-labelled meal followed by scintigraphy was utilized. Validated questionnaires were used to assess gastrointestinal symptoms and the modified body mass index (mBMI), in which BMI is multiplied by s-albumin, was used to evaluate nutritional status. Non-parametrical statistical tests were used.

Results

Gastric emptying rates and nutritional statuses were evaluated approximately eight months before and two and five years after liver transplantation, whereas gastrointestinal symptoms were assessed in median nine months before and two and nine years after transplantation. No significant change was found in gastric emptying (median half-time 137 vs. 132 vs. 125 min, p = 0.52) or nutritional status (median mBMI 975 vs. 991 vs. 973, p = 0.75) after transplantation. Gastrointestinal symptom scores, however, had increased significantly over time (median score 7 vs. 10 vs. 13, p < 0.01).

Conclusions

Gastric emptying and nutritional status were maintained after liver transplantation for hereditary ATTR amyloidosis, although gastrointestinal symptom scores had increased over time.

Peer Review reports

Background

Hereditary transthyretin amyloid (ATTR) amyloidosis or familial amyloid polyneuropathy (FAP) is a rare autosomal dominant disease caused by mutated transthyretin (TTR). The disease is present all over the world with endemic areas in Sweden, Portugal, Brazil and Japan [1].

The amyloidogenic TTR mutations decrease the stability of the TTR tetramer, which facilitates separation into misfolded monomers that, in turn, assemble into beta structured fibrils that build up the extracellular amyloid deposits [2]. The amyloid deposits elicit structural and toxic effects on the surrounding tissues [3-5] and peripheral and autonomic neuropathies, cardiomyopathy, cardiac arrhythmias and gastrointestinal (GI) disturbances are common complications of the disease.

GI disturbances play an important role in the morbidity and mortality of patients with hereditary ATTR amyloidosis [6,7], and virtually all Swedish patients develop GI complications during the course of the disease [8]. Initial symptoms are often constipation and/or nausea and vomiting. The constipation is later relieved by bursts of diarrhea that successively become continuous and fecal incontinence and severe malnutrition are common in later stages of the disease [9].

A liver transplantation (LTx) ceases the synthesis of mutated TTR and has, in selected patients, been proven to halt the progression of the disease [10,11]. Some studies have even demonstrated a clinical improvement after LTx [12,13], but most studies report unchanged or increased disease manifestations after the procedure [14-18]. Previous studies from our centre have demonstrated a largely unchanged GI function after transplantation [19,20].

The aim of the present study was to re-evaluate the long-term outcome of gastric emptying, GI symptoms and nutritional status after LTx for hereditary ATTR amyloidosis, based on data from the Swedish patient material collected over more than 20 years.

Methods

Patients

Symptomatic patients with hereditary ATTR amyloidosis who had been examined at Norrlands University Hospital, Umeå, Sweden and had undergone LTx as of January 2012 were included in the study. The liver transplantations had been performed at the transplantation centers at Karolinska University Hospital, Stockholm or Sahlgrenska University Hospital, Gothenburg, Sweden.

All patients had biopsy proven amyloid deposits and TTR mutations determined by DNA sequencing. Patients with an age at onset of less than 50 years were defined as early-onset cases. The data analyzed in the study, except for questionnaire data, were obtained from routine clinical investigations performed for evaluation of the disease both before and after LTx.

Gastric Emptying Scintigraphy (GES)

Gastric emptying was measured according to the method employed in the Swedish multi-center study of gastric emptying [21]. The scintigraphic acquisitions were performed using the STARCAM and Millennium MPR gamma cameras (General Electric, Milwaukee, WI), both with a low energy, general-purpose collimator and a 128 x 128 matrix. The software used for the scintigraphic data calculations was updated in April 2006 and thereby also integrated in the main software connected to the modality. In connection with the software update, the number of data points was reduced as the time interval between the recordings was extended from approximately 10 to 30 min. The scintigraphic acquisition procedure, however, remained unchanged.

Two variables were used to assess gastric emptying rates – total half-time (T50) and retention (%) at 90 min (Figure 1). Since the scintigraphic software had changed during the study period, the T50 values were manually measured for consistency over time [22]. The retention at 90 min was added for verification of the results, and it was electronically calculated from the curves generated by both the old and the new software.

Figure 1
figure 1

Gastric emptying scintigraphy. Graph showing the result of a normal gastric emptying scintigraphy and the variables used in the study. Lag phase from 0 to 30 min, a T50 of 80 min and a retention at 90 min of approximately 38%.

Full size image

Delayed gastric emptying was defined as T50 above 133 minutes (mean + 2 SD) or a gastric retention of more than 76% (mean + 2 SD) at 90 min, according to the reference values obtained by the Swedish multi-center study of 160 healthy individuals [21]. T50 values over 350 min were entered as 350 min.

Questionnaires

Two different questionnaires were used in the study and consent to participate was considered to be provided if the patient had completed and returned the questionnaires by mail.

The first questionnaire (see Additional files 1 and 2) contained seven items on GI symptoms, of which six were combined into two symptom clusters – upper or lower GI symptoms. Nausea, vomiting and loss of appetite were regarded as upper GI symptoms, whereas constipation, diarrhea and fecal incontinence were regarded as lower GI symptoms. The seventh item, loss of weight, was not included in the symptom clusters. A ten-point rating scale (0–10) was used for symptom assessment, giving a maximum possible score of 70, and the symptom scores were clustered into five levels – 0 (no symptoms), 1–3 (mild symptoms), 4–6 (considerable symptoms), 7–9 (severe symptoms) and 10 (unbearable symptoms). This questionnaire was utilized at all three time-points in the current study, and has previously been validated and used in other studies on Swedish patients with hereditary ATTR amyloidosis [15,23].

The second questionnaire contained four questions regarding concomitant diseases, current medication and consent to access the patients’ medical records for reviewing other factors with possible impact on their GI function. The patients’ medication was recorded and poly-pharmacy was defined as five concomitant drugs or more [24,25].

Nutritional status

The patients’ nutritional status was assessed by the modified body mass index (mBMI), in which BMI (kg/m2) was multiplied by serum albumin (g/L) to compensate for edema. Values below 750 were regarded as consistent with underweight and values below 600 were regarded as consistent with severe malnutrition [6,7].

Statistical analysis

Non-parametrical tests were used for all analyses. Differences between groups were analyzed with the chi2 and the Mann–Whitney U Tests. Changes over time were analyzed with Friedman’s Two-Way Analysis of Variance by Ranks, Cochran’s Q test and the Wilcoxon Signed Rank Test. Data shown are medians (min-max). P values below 0.05 were regarded as statistically significant. IBM SPSS Statistics 20 and 22 for Macintosh were used for the analyses.

Ethics

The Regional Ethics Board in Umeå, Sweden approved the study; reference number 2011-365-31 M.

Results

Patients

One hundred and fifteen patients had undergone LTx from November 1990 to September 2011. All patients but three carried the TTR V30M mutation, the other variants being the TTR L55Q, A97S and F33L mutations.

Twenty-one patients had died during the study period, in median 3.0 (0.0-14.6) years after transplantation. The deceased patients had a significantly higher median age at onset (56.5 vs. 45.5 years, p < 0.01) and at LTx (58.7 vs. 49.1 years, p < 0.01) than those who had survived, but no differences were found for gender (61.9 % vs. 58.5 % males, p = 0.78) or median disease duration at LTx (3.3 vs. 3.3 years, p = 0.56). Virtually all of the deceased patients had completed the evaluations before transplantation and nearly half of them had also completed the first follow-up after LTx, whereas only a few had carried out a second follow-up after LTx. All available data from the deceased patients were included in the analyses of GI function.

GES

Ninety-nine patients (86.1%) had completed a GES prior to LTx, 71 patients (61.7%) at the first follow-up after LTx and 31 patients (27.0%) at the second follow-up. The overall outcome of the patients’ gastric emptying after LTx is presented in Figure 2 and no significant variation was found over time. A similar outcome was found for the retention at 90 min (median retention 78.1% vs. 77.8% vs. 78.6%, p = 0.61) and also for the fraction of patients with a delayed gastric emptying (50.0% vs. 46.2% vs. 42.3%, p = 0.79).

Figure 2
figure 2

Outcome of gastric emptying after liver transplantation. Gastric emptying was scintigraphically measured using a Tc99m-labelled meal and the total half-time of the radioactive marker was used for the analyses. No significant change in gastric emptying half-times was found over time (p = 0.52). Only patients who had completed the scintigraphy at all three time-points were included (n = 26). P < 0.05 was regarded as statistically significant.

Full size image

To investigate a possible deterioration while waiting for LTx, data from the pre-LTx evaluation and the initial assessment after LTx were separately analyzed, however, no significant change in gastric emptying was found between the assessments (median T50 119 vs. 129 min, n = 67, p = 0.24).

Questionnaires

The study questionnaires were sent by mail to the 92 patients (80.0%) who were still alive and Swedish residents at the time of the study and, of those, 77 (83.7%) had responded the questionnaires by June 2012. Six patients (7.8%) had completed the questionnaires less than two years after transplantation and their data were excluded from the outcome analyses of GI symptoms. Detailed pre-transplant characteristics of the patients are outlined in Table 1 and, overall, no significant differences were found between the patients who had responded the questionnaires and those who had not. Equivalent results were found after transplantation; however, at the second post-transplant follow-up, the number of patients was too small for adequate comparisons of gastric emptying half-times between the groups.

Table 1 Patient characteristics
Full size table

Seventy (98.6%) of the patients who had filled out valid study questionnaires had completed corresponding questionnaires prior to their LTx and 59 patients (83.1%) had completed equivalent questionnaires approximately two years after transplantation. Hence, 59 patients had responded all three sets of questionnaires, which were completed in median 0.7 (0.1-1.6) years before LTx and 2.0 (1.0-5.9) and 8.7 (2.3-21.3) years after LTx, respectively.

GI symptoms

The outcomes of the GI symptom scores are displayed in Figure 3 and, overall, the symptom scores had increased after transplantation, as had the prevalence of GI complaints (84.2% vs. 91.2% vs. 96.5%, p = 0.03). As for the upper GI symptoms, there was no significant change in weight loss scores over time (median score 0 vs. 0 vs. 0, p = 0.71).

Figure 3
figure 3

Outcome of gastrointestinal symptoms after liver transplantation. The total and lower gastrointestinal (GI) symptom scores had both increased significantly over time (p < 0.01, for both), whereas no significant change was found for upper GI symptom scores (p = 0.09). Nausea, vomiting and loss of appetite were regarded as upper GI symptoms, whereas constipation, diarrhea and fecal incontinence were regarded as lower GI symptoms. Unintentional weight loss was added to the total GI symptom category. All symptoms were evaluated with a 10-point rating scale and, thus, the maximum possible score was 70 for the total GI symptom category (dashed y axis), while only 30 for both the upper and lower GI symptom categories (solid y axis). Only patients who had completed all three sets of questionnaires were included (n = 57). P < 0.05 was regarded as statistically significant.

Full size image

A significant rise in the total GI symptom score was found both between the pre-transplant evaluation and the initial assessment after LTx (median total GI score 6 vs. 9, n = 67, p = 0.03) and between the two post-transplant evaluations (median total GI score 9 vs. 12, n = 57, p = 0.02). Equivalent results were found for lower GI symptoms, whereas no significant change was found, at any time-point, for upper GI symptoms.

Subgroup analyses of the lower GI symptoms showed that the diarrhea scores (median score 0 vs. 2 vs. 3, p < 0.01) and fecal incontinence scores (median score 0 vs. 1 vs. 1, p < 0.01) had increased significantly over time, whereas no significant variation was found for constipation (median score 2 vs. 1 vs. 2, p = 0.17).

Nutritional status

Data on nutritional status were available for 114 patients prior to transplantation, for 79 patients at first follow-up after LTx and for 41 patients at the last follow-up after LTx. The assessments were made in median 0.7 (0.1-1.8) years before LTx and 1.9 (0.9-4.6) and 4.7 (2.0-12.0) years after LTx, respectively, and no significant change in nutritional status was found over time (median mBMI 975 vs. 991 vs. 973, n = 33, p = 0.75). Moreover, no significant alteration was found between the pre-transplant and the initial post-transplant evaluation (median mBMI 971 vs. 941, n = 78, p = 0.38).

Age at onset and gender

Subgroup analyses showed similar outcomes of gastric emptying, GI symptoms and nutritional status after LTx in early- and late-onset cases, as well as in males and females. However, in early-onset cases, no significant change in total GI symptom scores was found after transplantation (Table 2).

Table 2 Outcome of gastrointestinal function in relation to age at onset and gender
Full size table

Furthermore, early-onset cases reported significantly higher total GI symptom scores before LTx (median score 8 vs. 3.5, p < 0.01) and at the first follow-up after LTx (median score 11 vs. 6, p = 0.02) than late-onset cases. Female patients also reported higher total GI symptom scores (median score 7.5 vs. 4.5, p = 0.04) and had a significantly lower nutritional status (median mBMI 923 vs. 1016, p < 0.01) than males prior to transplantation.

Medications

All patients received immunosuppressive therapy, most often tacrolimus (75.3%) and steroids (70.1%). Two patients were treated with insulin due to diabetes mellitus, whereas none received oral anti-diabetic agents. One patient received diflunisal [26] for his amyloidosis, but no patient was treated with tafamidis [27].

Differences in GI symptoms in relation to current medication were analyzed for the 15 (out of totally 32) drugs taken by ten individuals or more. Significant differences were found for four of the drugs (Table 3).

Table 3 Relationship between medication and gastrointestinal symptoms
Full size table

Poly-pharmacy was observed in 45 (58.4%) of the patients who had responded the study questionnaires. No significant difference in total GI symptom scores (median score 11.5 vs. 12, p = 0.39) was found between the patients who had reported poly-pharmacy and those who had not.

Discussion

The current study presents data on the outcome of the GI function after LTx for hereditary ATTR amyloidosis and is based on a large Swedish patient material collected over more than 20 years. Previous studies have, to the best of our knowledge, been based on smaller patient numbers and shorter follow-up times [19,20,28-31]. Most data used in the study were from routine clinical investigations; however, questionnaire data from the latest follow-up after LTx were collected specifically for the study. A questionnaire response rate of more than 80% supports the reliability of these results and, in addition, no significant differences in patient characteristics or GI function were found between patients who had responded the questionnaires and those who had not. A majority of the patients reported at least one GI symptom prior to LTx and virtually all patients (97%) had GI complaints at the last follow-up almost nine years after the procedure. Unexpectedly, since most previous studies have demonstrated a stable GI function [19,20,31], we found a significant increase both in symptom prevalence and symptom scores after transplantation. However, the symptom scores were generally low and only the lower GI symptom scores (i.e. the diarrhea and fecal incontinence scores) exhibited a significant increase over time. Moreover, the patients’ overall GI function seemed to be preserved as their gastric emptying rates, as well as their nutritional statuses, were maintained at follow-up in median five years after LTx. It is difficult to determine whether the increased GI symptoms were caused by a progression of the ATTR amyloidosis since GI complications, especially diarrhea, are common after LTx [32,33] and since GI symptoms are common side effects of several drugs. In attempt to answer this question, we analyzed the impact of the patients’ medication on GI symptom scores and significant differences were found for some of the drugs; however, none of them directly related to the LTx. It should be noted that loperamide was used to treat diarrhea, and its relationship with GI symptom scores should not be interpreted as loperamide being the cause of the intestinal symptoms, but the opposite. Furthermore, patients with more than five concomitant medications did not report higher GI symptom scores than those with less than five drugs, indicating that the patients’ medication is not the main factor behind their gastrointestinal complaints after LTx.

Despite that most patients received tacrolimus and steroids as immunosuppressive therapy, which both are associated with a risk of de-novo diabetes after transplantation [34,35], only two patients received treatment against diabetes at the time of the study. This suggests that diabetes mellitus is rare among patients with hereditary ATTR amyloidosis and also that a diabetic gastroenteropathy is not the cause of their increased GI symptom scores after LTx. Aging also has an effect on the function of the GI tract, especially with regard to the development of constipation and fecal incontinence [36,37]. Thus, the reported increase in fecal incontinence scores might be related to aging of the patients, however, the parallel increase in diarrhea scores is perhaps a more plausible explanation.

Altogether, the slight increase in GI symptom scores after LTx is most likely multi-factorial, but post-operative complications and medications probably contribute. Deterioration of the ATTR amyloidosis, however, appears to be a less likely cause since the objective measures of the GI function (i.e. gastric emptying half-time and nutritional status) were maintained. Additionally, we found no evidence of deterioration in GI function during the approximately eight month waiting time for transplantation. Since phenotypic differences have been observed between patients with early and late disease onset, subgroup analyses addressing this question were carried out. We found that early-onset cases reported significantly higher GI symptom scores before LTx and at the first follow-up after LTx, which is consistent with a more frequently occurring autonomic neuropathy in these patients [38,39]. Similar outcomes of gastric emptying and nutritional status were found for early- and late-onset cases, however, an increase in GI symptom scores was predominantly found in late-onset cases, who generally also have a poorer outcome after LTx [40]. Subgroup analyses were also performed with regard to gender since functional GI disorders generally are more common in females [41,42]. Indeed, female patients reported significantly higher GI symptom scores and a lower nutritional status prior to LTx, but no major gender related differences were found following transplantation.

Limitations

In individuals with gastric retention, extrapolation is usually required to calculate gastric emptying half-times and the result may, in these cases, be less accurate than measurements based on percentages of retention at fixed time points [43]. Since a 2-hour scintigraphic measurement is the standard procedure at our hospital we used both of these methods to evaluate gastric emptying rates in the study.

The symptom scores used are depending on patients’ ability to correctly describe and grade their GI disturbances. To minimize errors, the same validated questionnaire was used throughout the study and patients were asked to state their current symptoms.

Since patients living outside the northern counties in Sweden are not routinely referred to our department for evaluation, attrition is a problem, especially between the first and second post-transplant follow-ups, and may give a selection bias towards patients with a favorable outcome after transplantation. In addition, the small remaining number of patients increases the risk of a type 2 statistical error, i.e. missing deterioration of gastric emptying after LTx.

Conclusions

Gastric emptying rates and nutritional statuses appeared to be maintained in Swedish patients who had undergone LTx for hereditary ATTR amyloidosis, although their GI symptom scores had increased over time. GI symptom scores were higher in early-onset cases and in females; however, no major differences in the outcome of GI function after LTx were found in these subgroups of patients.

Abbreviations

A97S:

Alanine substituted for serine at gene position 97

ATTR:

Transthyretin amyloid

BMI:

Body mass index

DNA:

Deoxyribonucleic acid

F33L:

Phenylalanine substituted for leucine at gene position 33

FAP:

Familial amyloid polyneuropathy

GES:

Gastric emptying scintigraphy

GI:

Gastrointestinal

L55Q:

Leucine substituted for glutamine at gene position 55

LTx:

Liver transplantation

mBMI:

Modified body mass index

SD:

Standard deviation

T50:

Total half-time

TTR:

Transthyretin

V30M:

Valine substituted for methionine at gene position 30

References

  1. Ando Y, Nakamura M, Araki S. Transthyretin-related familial amyloidotic polyneuropathy. Arch Neurol. 2005;62:1057–62.

    Article  PubMed  Google Scholar 

  2. Saraiva MJ. Transthyretin amyloidosis: a tale of weak interactions. FEBS Lett. 2001;498:201–3.

    Article  CAS  PubMed  Google Scholar 

  3. Sousa MM, Saraiva MJ. Neurodegeneration in familial amyloid polyneuropathy: from pathology to molecular signaling. Prog Neurobiol. 2003;71:385–400.

    Article  CAS  PubMed  Google Scholar 

  4. Merlini G, Westermark P. The systemic amyloidoses: clearer understanding of the molecular mechanisms offers hope for more effective therapies. J Intern Med. 2004;255:159–78.

    Article  CAS  PubMed  Google Scholar 

  5. Pepys MB. A molecular correlate of clinicopathology in transthyretin amyloidosis. J Pathol. 2009;217:1–3.

    Article  PubMed  Google Scholar 

  6. Suhr O, Danielsson A, Holmgren G, Steen L. Malnutrition and gastrointestinal dysfunction as prognostic factors for survival in familial amyloidotic polyneuropathy. J Intern Med. 1994;235:479–85.

    Article  CAS  PubMed  Google Scholar 

  7. Suhr O, Danielsson A, Rydh A, Nyhlin N, Hietala SO, Steen L. Impact of gastrointestinal dysfunction on survival after liver transplantation for familial amyloidotic polyneuropathy. Dig Dis Sci. 1996;41:1909–14.

    Article  CAS  PubMed  Google Scholar 

  8. Steen L, Ek B. Familial amyloidosis with polyneuropathy. A long-term follow-up of 21 patients with special reference to gastrointestinal symptoms. Acta Med Scand. 1983;214:387–97.

    Article  CAS  PubMed  Google Scholar 

  9. Suhr OB, Svendsen IH, Andersson R, Danielsson A, Holmgren G, Ranlov PJ. Hereditary transthyretin amyloidosis from a Scandinavian perspective. J Intern Med. 2003;254:225–35.

    Article  CAS  PubMed  Google Scholar 

  10. Holmgren G, Ericzon BG, Groth CG, Steen L, Suhr O, Andersen O, et al. Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis. Lancet. 1993;341:1113–6.

    Article  CAS  PubMed  Google Scholar 

  11. Suhr OB, Ericzon B-G. Selection of hereditary transthyretin amyloid patients for liver transplantation: the Swedish experience. Amyloid. 2012;19 Suppl 1:78–80.

    Article  PubMed  Google Scholar 

  12. Parrilla P, Ramirez P, Andreu LF, Bueno SF, Robles R, Miras M, et al. Long-term results of liver transplantation in familial amyloidotic polyneuropathy type I. Transplantation. 1997;64:646–9.

    Article  CAS  PubMed  Google Scholar 

  13. Pomfret EA, Lewis WD, Jenkins RL, Bergethon P, Dubrey SW, Reisinger J, et al. Effect of orthotopic liver transplantation on the progression of familial amyloidotic polyneuropathy. Transplantation. 1998;65:918–25.

    Article  CAS  PubMed  Google Scholar 

  14. Suhr OB, Wiklund U, Ando Y, Ando E, Olofsson BO. Impact of liver transplantation on autonomic neuropathy in familial amyloidotic polyneuropathy: an evaluation by spectral analysis of heart rate variability. J Intern Med. 1997;242:225–9.

    Article  CAS  PubMed  Google Scholar 

  15. Jonsén E, Suhr OB, Tashima K, Athlin E. Early liver transplantation is essential for familial amyloidotic polyneuropathy patients’ quality of life. Amyloid. 2001;8:52–7.

    Article  PubMed  Google Scholar 

  16. De Carvalho M, Conceição I, Bentes C, Luís MLS. Long-term quantitative evaluation of liver transplantation in familial amyloid polyneuropathy (Portuguese V30M). Amyloid. 2002;9:126–33.

    PubMed  Google Scholar 

  17. Ohya Y, Okamoto S, Tasaki M, Ueda M, Jono H, Obayashi K, et al. Manifestations of transthyretin-related familial amyloidotic polyneuropathy: long-term follow-up of Japanese patients after liver transplantation. Surg Today. 2011;41:1211–8.

    Article  PubMed  Google Scholar 

  18. Okamoto S, Zhao Y, Lindqvist P, Backman C, Ericzon B-G, Wijayatunga P, et al. Development of cardiomyopathy after liver transplantation in Swedish hereditary transthyretin amyloidosis (ATTR) patients. Amyloid. 2011;18:200–5.

    Article  CAS  PubMed  Google Scholar 

  19. Lång K, Wikström L, Danielsson A, Tashima K, Suhr OB. Outcome of gastrointestinal complications after liver transplantation for familial amyloidotic polyneuropathy. Scand J Gastroenterol. 2000;35:985–9.

    Article  PubMed  Google Scholar 

  20. Suhr OB, Anan I, Ahlström KR, Rydh A. Gastric emptying before and after liver transplantation for familial amyloidotic polyneuropathy, Portuguese type (Val30Met). Amyloid. 2003;10:121–6.

    Article  PubMed  Google Scholar 

  21. Grybäck P, Hermansson G, Lyrenäs E, Beckman KW, Jacobsson H, Hellström PM. Nationwide standardisation and evaluation of scintigraphic gastric emptying: reference values and comparisons between subgroups in a multicentre trial. Eur J Nucl Med. 2000;27:647–55.

    Article  PubMed  Google Scholar 

  22. Wixner J, Karling P, Rydh A, Hörnsten R, Wiklund U, Anan I, et al. Gastric emptying in hereditary transthyretin amyloidosis: the impact of autonomic neuropathy. Neurogastroenterol Motil. 2012;24:1111–e568.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Jonsen E, Suhr O, Athlin E, Wikström L. Quality of life after liver transplantation in patients with familial amyloidotic polyneuropathy. Amyloid. 1996;3:124–9.

    Article  Google Scholar 

  24. Gnjidic D, Hilmer SN, Blyth FM, Naganathan V, Waite L, Seibel MJ, et al. Poly-pharmacy cutoff and outcomes: five or more medicines were used to identify community-dwelling older men at risk of different adverse outcomes. J Clin Epidemiol. 2012;65:989–95.

    Article  PubMed  Google Scholar 

  25. Moen J, Antonov K, Larsson CA, Lindblad U, Nilsson JLG, Råstam L, et al. Factors associated with multiple medication use in different age groups. Ann Pharmacother. 2009;43:1978–85.

    Article  PubMed  Google Scholar 

  26. Berk JL, Suhr OB, Obici L, Sekijima Y, Zeldenrust SR, Yamashita T, et al. Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial. JAMA. 2013;310:2658–67.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Coelho T, Maia LF, da Silva AM, Cruz MW, Planté-Bordeneuve V, Suhr OB, et al. Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy. J Neurol. 2013;260:2802–14.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Suhr OB, Holmgren G, Steen L, Wikström L, Norden G, Friman S, et al. Liver transplantation in familial amyloidotic polyneuropathy. Follow-up of the first 20 Swedish patients. Transplantation. 1995;60:933–8.

    Article  CAS  PubMed  Google Scholar 

  29. Tashima K, Ando Y, Terazaki H, Yoshimatsu S, Suhr OB, Obayashi K, et al. Outcome of liver transplantation for transthyretin amyloidosis: follow-up of Japanese familial amyloidotic polyneuropathy patients. J Neurol Sci. 1999;171:19–23.

    Article  CAS  PubMed  Google Scholar 

  30. Adams D, Samuel D, Goulon-Goeau C, Nakazato M, Costa PM, Feray C, et al. The course and prognostic factors of familial amyloid polyneuropathy after liver transplantation. Brain. 2000;123(Pt 7):1495–504.

    Article  PubMed  Google Scholar 

  31. Yamamoto S, Wilczek HE, Nowak G, Larsson M, Oksanen A, Iwata T, et al. Liver transplantation for familial amyloidotic polyneuropathy (FAP): a single-center experience over 16 years. Am J Transplant. 2007;7:2597–604.

    Article  CAS  PubMed  Google Scholar 

  32. Ginsburg PM, Thuluvath PJ. Diarrhea in liver transplant recipients: etiology and management. Liver Transpl. 2005;11:881–90.

    Article  PubMed  Google Scholar 

  33. Herrero JI, Benlloch S, Bernardos A, Bilbao I, Castells L, Castroagudin JF, et al. Gastrointestinal complications in liver transplant recipients: MITOS study. Transplant Proc. 2007;39:2311–3.

    Article  CAS  PubMed  Google Scholar 

  34. Sgourakis G, Radtke A, Fouzas I, Mylona S, Goumas K, Gockel I, et al. Corticosteroid-free immunosuppression in liver transplantation: a meta-analysis and meta-regression of outcomes. Transpl Int. 2009;22:892–905.

    Article  CAS  PubMed  Google Scholar 

  35. Lankarani KB, Eshraghian A, Nikeghbalian S, Janghorban P, Malek-Hosseini SA. New onset diabetes and impaired fasting glucose after liver transplant: risk analysis and the impact of tacrolimus dose. Exp Clin Transplant. 2014;12:46–51.

    Article  PubMed  Google Scholar 

  36. Chang L, Toner BB, Fukudo S, Guthrie E, Locke GR, Norton NJ, et al. Gender, age, society, culture, and the patient’s perspective in the functional gastrointestinal disorders. Gastroenterology. 2006;130:1435–46.

    Article  PubMed  Google Scholar 

  37. Rayner CK, Horowitz M. Physiology of the ageing gut. Curr Opin Clin Nutr Metab Care. 2013;16:33–8.

    Article  PubMed  Google Scholar 

  38. Conceição I, De Carvalho M. Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal. Muscle Nerve. 2007;35:116–8.

    Article  PubMed  Google Scholar 

  39. Koike H, Sobue G. Late-onset familial amyloid polyneuropathy in Japan. Amyloid. 2012;19 Suppl 1:55–7.

    Article  CAS  PubMed  Google Scholar 

  40. Okamoto S, Wixner J, Obayashi K, Ando Y, Ericzon B-G, Friman S, et al. Liver transplantation for familial amyloidotic polyneuropathy: impact on Swedish patients’ survival. Liver Transpl. 2009;15:1229–35.

    Article  PubMed  Google Scholar 

  41. Agréus L, Svärdsudd K, Nyrén O, Tibblin G. The epidemiology of abdominal symptoms: prevalence and demographic characteristics in a Swedish adult population. A report from the Abdominal Symptom Study. Scand J Gastroenterol. 1994;29:102–9.

    Article  PubMed  Google Scholar 

  42. Corazziari E. Definition and epidemiology of functional gastrointestinal disorders. Best Pract Res Clin Gastroenterol. 2004;18:613–31.

    Article  PubMed  Google Scholar 

  43. Abell TL, Camilleri M, Donohoe K, Hasler WL, Lin HC, Maurer AH, et al. Consensus recommendations for gastric emptying scintigraphy: a joint report of the American Neurogastroenterology and Motility Society and the Society of Nuclear Medicine. J Nucl Med Technol. 2008;36:44–54.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

The study was supported by grants from central and clinical ALF grants, a Spearhead grant from Västerbotten’s County, and research support from the patients’ associations FAMY/AMYL in Norrbotten and Västerbotten. The authors are indebted to the patients and their families for participating in this and other studies.

Author information

Authors and Affiliations

  1. Departments of Public Health and Clinical Medicine, Umeå University, S-90187, Umeå, Sweden

    Jonas Wixner, Pontus Karling, Intissar Anan & Ole B Suhr

  2. Radiation Sciences, Umeå University, S-90187, Umeå, Sweden

    Torbjörn Sundström

Authors
  1. Jonas Wixner
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Torbjörn Sundström
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Pontus Karling
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Intissar Anan
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Ole B Suhr
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Jonas Wixner.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

JW contributed to the design of the study, collected questionnaire data, performed the statistical analyses and wrote the manuscript. TS contributed to the design of the study and was responsible for the collection and the analyses of gastric emptying scintigraphy data. IA and PK participated in the planning of the study, in the data analysis and in the revision of the manuscript. OBS conceived of the study and participated in its design and coordination. All authors read and approved the final manuscript.

Additional files

Additional file 1:

Symptom questionnaire in Swedish.

Additional file 2:

Symptom questionnaire in English.

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wixner, J., Sundström, T., Karling, P. et al. Outcome of gastric emptying and gastrointestinal symptoms after liver transplantation for hereditary transthyretin amyloidosis. BMC Gastroenterol 15, 51 (2015). https://doi.org/10.1186/s12876-015-0284-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12876-015-0284-4

Keywords

BMC Gastroenterology

ISSN: 1471-230X

Contact us