Address for Correspondence Jonas Wixner, Department of medicine, Umeå University, 901 87 Umeå, Sweden. Tel: +46 90 785 00 00; fax: +46 90 14 39 86; e-mail: firstname.lastname@example.org
Background Gastrointestinal (GI) complications are common in hereditary transthyretin amyloidosis and an autonomic dysfunction has been considered to explain these symptoms. The aim of this study was to investigate the impact of autonomic neuropathy on gastric emptying in hereditary transthyretin amyloidosis and to relate these findings to nutritional status, GI symptoms, gender, and age at disease onset.
Methods Gastric emptying was evaluated with gastric emptying scintigraphy. Spectral analysis of the heart rate variability and cardiovascular responses after tilt test were used to assess the autonomic function. The nutritional status was evaluated with the modified body mass index (s-albumine × BMI).
Key Results Gastric retention was found in about one-third of the patients. A weak correlation was found between the scintigraphic gastric emptying rate and both the sympathetic (rs = −0.397, P < 0.001) and parasympathetic function (rs = −0.282, P = 0.002). The gastric emptying rate was slower in those with lower or both upper and lower GI symptoms compared with those without symptoms (median T50 123 vs 113 min, P = 0.042 and 192 vs 113 min, P = 0.003, respectively). Multiple logistic regression analysis showed that age of onset (OR 0.10, CI 0.02–0.52) and sympathetic dysfunction (OR 0.23, CI 0.10–0.51), but not gender (OR 0.76, CI 0.31–1.84) and parasympathetic dysfunction (OR 1.81, CI 0.72–4.56), contributed to gastric retention.
Conclusions and Inferences Gastric retention is common in hereditary transthyretin amyloidosis early after onset. Autonomic neuropathy only weakly correlates with gastric retention and therefore additional factors must be involved.
amyloidogenic transthyretin mutation where methionine is substituted for valine at position 30
body mass index
familial amyloidotic polyneuropathy
gastric emptying scintigraphy
high-frequency component of HRV in a supine position, i.e., parasympathetic function
heart rate variability
interstitial cells of Cajal
low-frequency component of HRV in an upright position, i.e., sympathetic function
modified body mass index (s-albumine x BMI)
nitric oxide synthase
systolic blood pressure
half-life for the radioactive marker after the lag phase in GES
total half-life for the radioactive marker in GES
Hereditary transthyretin amyloidosis or familial amyloidotic polyneuropathy (FAP) is a dominantly inherited transthyretin amyloidosis that is caused by mutated transthyretin (TTR). There are approximately 100 known amyloidogenic transthyretin (ATTR) mutations of which ATTR Val30Met (methionine substituted for valine at position 30) is the most common, leading to a neuropathic form of the disease, FAP.1 FAP Val30Met is present all over the world with endemic areas in Portugal, Brazil, Sweden, and Japan. Symptoms are caused by deposition of amyloid fibrils in various body tissues and include, for example, peripheral polyneuropathy, autonomic neuropathy, cardiac arrhythmias, and gastrointestinal (GI) disturbances. Virtually all patients develop GI complications during the course of the disease2 and the initial constipation is later relieved by bursts of diarrhea that successively become permanent. Nausea and vomiting are also reported by many patients.
Without treatment the average survival in Sweden is 9–13 years after onset2,3 and death is caused by severe malnutrition and opportunistic infections in many cases.3,4 As nearly all circulating TTR is produced by the liver, a liver transplantation (Ltx) that ceases the synthesis of mutated TTR has proved to halt the progression of the disease. The GI disturbances of FAP patients lead to malnutrition, which negatively affects the outcome of Ltx,5 and are hence important for morbidity and mortality after the procedure.
The mechanisms behind the GI complications in FAP are poorly understood, but it has been suggested that an autonomic neuropathy is at least partly responsible.4 The aim of the present investigation was to assess the occurrence of gastric retention in FAP patients and relate the findings to autonomic function measured by heart rate variability (HRV) and tilt test. We also wanted to relate the findings to the patients’ nutritional status measured by the modified body mass index (mBMI), GI symptoms, gender, and age at disease onset.
Materials and Methods
One hundred and eighty-eight Swedish FAP patients were available for the study (Table 1). All patients were examined at the Department of Medicine, Umeå University Hospital, Umeå, Sweden, between 1990 and 2009 as part of an investigation of their disease and, for the majority of the patients, also as part of the evaluation for Ltx. The FAP diagnosis was based on clinical findings consistent with FAP, presence of amyloid fibrils in an intestinal, skin, or abdominal fat biopsy, and identification of an amyloidogenic TTR (ATTR) mutation. Practically all patients carried the Val30Met mutation except 6 who carried the Leu55Gln, Phe33Leu, Tyr69His, His88Arg, Gly57Arg, and Val30Leu mutations, respectively. Clinical data were obtained from the first evaluation after onset of the disease. One hundred and forty-one patients (75%) were still alive at the time of the study (December 2009). For each patient all examinations were carried out within a 6 months period of time.
Table 1. Clinical data of the patients
Patients with T50 ≥ 350 min
FAP, familial amyloidotic polyneuropathy; Val30Met, transthyretin mutation where methionine is substituted for valine at position 30; GI, gastrointestinal; T50, total half-life for the radioactive marker in the gastric emptying scintigraphy, values above 350 min are consistent with a severely delayed gastric emptying.
Total number of patients (men/women)
Median age at onset (range)
57 (22–82) years
63 (31–70) years
Median duration of disease (range)
3 (0–16) years
4 (1–12) years
Number of patients with FAP Val30Met
Number of patients with GI symptoms
Both upper and lower
Gastric emptying scintigraphy (GES)
In 162 (86%) of the patients a GES was performed. Twenty-six patients did not undergo GES, nine because it was not available at the time of the examination, and 17 because of technical problems at the scheduled time of examination. The measurement was carried out according to the method employed in the Swedish multicenter study of gastric emptying.6 The scintigraphic acquisitions were performed using a STARCAM gamma camera (General Electric, Milwaukee, WI, USA) with a low energy, general-purpose collimator and a 128 × 128 matrix.
The collected data were then electronically plotted on a graph (Fig. 1) that was printed and manually analyzed by one examiner (JW) who calculated the lag phase, T50, and T1/2 (T50 being the total half-life and T1/2 the half-life after the lag phase). Abnormal gastric emptying was defined as a T50 above 133 min (mean + 2 SD) according to the reference values obtained by the Swedish national multicenter study of 160 healthy individuals aged 17–80 years.6 T50 over 350 min was entered as 350 min.
The patients’ nutritional status was assessed by the mBMI, in which BMI (kg m−2) is multiplied by serum albumin (g L−1) to compensate for edema.3 mBMI could be calculated in 185 (98%) of the patients. Values below 750 were considered consistent with underweight and values below 600 were regarded as consistent with severe malnutrition.3,5
Heart rate variability was recorded in 177 (94%) of the patients. The power spectral analysis was estimated by auto-regressive modeling, consequently using Burg-algorithm with 30 parameters.7 The spectral power in two frequency bands was used in the investigation – the high-frequency component (0.15–0.50 Hz) recorded in a supine position (HFsup) and the low-frequency component (0.04–0.15 Hz) recorded in an upright position (LFtilt) as presented in Fig. 2. The respiration-related high-frequency component of HRV represents an indirect estimate of vagal cardiac control and the low-frequency component, recorded after postural change from a supine to an upright position, is a useful marker of sympathetic activity.8,9 All frequency-domain HRV indices were log transformed (base 10) because of skewed distribution. As the heart rate was expressed in mHz and as spectral power corresponds to the variance, all spectral indices had the unit mHz2, but became dimensionless after log transformation. All patients with pacemaker treatment and frequent non-sinus beats were excluded from the analysis, where patients with non-neurogenic HRV patterns were identified by comparing with power spectra for respiration and by inspection of the pattern in the beat-to-beat fluctuations in R-R intervals.10–14
During the HRV examinations the blood pressure in the right upper arm was measured with cuff and stethoscope after 3 min in the supine resting position and after 3 min in the tilted (70°) upright position. The mean heart rate (HR) was calculated from the 2 min ECG recordings used for the HRV analysis, of which all were adjacent to the measurements of the blood pressure. The changes in systolic blood pressure (SBP) and mean HR after tilting were then calculated. Data on changes in SBP and mean HR were recorded in 167 (89%) and 138 (73%) of the patients, respectively. A decrease in SBP of 20 mm Hg or more was regarded as consistent with orthostatic hypotension.15
Statistical analyses were, if possible, performed by non-parametrical methods. Differences between groups were tested with the Mann–Whitney U test, Kruskal–Wallis test, and the chi-squared test. Correlation was analyzed with Spearman’s rank order test. The relationship between variables was tested with logistic regression. P values below 0.05 were regarded as statistically significant. PASW Statistics 18 for Macintosh was used for the calculations.
The study is part of a larger project that is approved by the Regional ethics board in Umeå, Sweden; reference number 06–084M.
GI symptoms and nutritional status
Data on GI symptoms were available for all patients except one. Fifty-nine percent suffered from GI disturbances, and median mBMI was 961 (range 550–1535). In 181 (98%) of the patients the mBMI was 600 or more, and in 4 (2%) it was below 600.
All patients with severe malnutrition were women and all of them had GI symptoms. Patients with mBMI below 600 had a lower age at onset (47 vs 57 years), a longer duration of disease (10 vs 3 years), and lower LFtilt (1.33 vs 2.08) and HFsup (1.55 vs 1.77) than those with mBMI of 600 or more. However, the number of patients with severe malnutrition was too small for adequate statistical calculations.
Gastric emptying scintigraphy disclosed gastric retention in 63 of 162 patients (39%). Median T50 was 119 (range 48–350) min. In 13 patients the gastric emptying was severely delayed with T50 of 350 min or more.
A small difference in T50 was found between men and women, with the latter showing a slower gastric emptying rate (median T50 116 vs 128 min, P = 0.043). No significant correlation was found between the age of onset and T50 (rs = −0.026, p = 0.744). There was a weak but significant negative correlation between T50 and mBMI (rs = −0.218, P = 0.006).
Gastric emptying and GI symptoms
When comparing the reported GI symptoms with the outcome of GES, we found significant differences in T50 between the groups (Fig. 3). Post hoc analysis showed the strongest significance between patients without symptoms compared to those with both upper and lower GI symptoms (median T50 113 vs 192 min, P = 0.003). A significant difference in T50 between patients without and those with lower GI symptoms (median T50 113 vs 123 min, P = 0.042) was also found. No significant difference was found between patients without and those with upper GI symptoms (median T50 113 vs 119 min, P = 1).
The spectral analysis of HRV could be performed in 134 (76%) of the patients. In 23 (13%) of the patients arrhythmia precluded the analysis of HRV and in 20 (11%) patients data were missing or not applicable (due to pacemakers or data file errors). The median HFsup was 1.77 (range 0.11–3.49) and the median LFtilt was 2.07 (range 0.02–4.17). In comparison, healthy subjects registered in our database of healthy volunteers had a median HFsup of 2.52 (range 1.16–4.24) and a median LFtilt of 2.98 (range 0.00–4.06).
Significant differences in HRV between female and male patients were found for HFsup (median HFsup 1.98 vs 1.67, P = 0.008) and LFtilt (median HFsup 2.28 vs 1.89, P = 0.015), respectively. Negative correlations between the age of onset and HFsup (rs = −0.194, P = 0.025) and LFtilt (rs = −0.395, P < 0.001) were found, where older patients displayed a lower HRV.
No significant correlation was found between HFsup and mBMI (rs = 0.147, P = 0.089), but there was a correlation between LFtilt and mBMI (rs = 0.280, P = 0.001). No significant difference in HFsup (P = 0.822) or LFtilt (P = 0.765) was seen between patients without GI symptoms or those with upper (median HFsup 1.76 vs 1.78, median LFtilt 2.10 vs 1.83), lower (median HFsup 1.76 vs 1.74, median LFtilt 2.10 vs 2.08), or both upper and lower GI symptoms (median HFsup 1.76 vs 1.58, median LFtilt 2.10 vs 1.71).
Autonomic function and gastric emptying
Weak but significant correlations were found between T50 and HFsup (Fig. 4A) and T50 and LFtilt (Fig. 4B). Patients with retention at GES had a greater decrease in SBP after tilting than those without retention (median ΔSBP −10 vs−5 mm Hg, P = 0.038). No difference in the change in HR after tilting was found between patients with or without retention at GES (median ΔHR 7.56 vs 9.06 beats/min, P = 0.535). Retention at GES was significantly more common in patients with orthostatic hypotension than in those with no orthostatic hypotension (χ2 = 6.66, P = 0.010).
Characteristics of patients with severe gastric retention
To further assess the possible mechanisms behind the GI complications, subgroup analyses were performed for patients with T50 of 350 min or more. Patients’ details are outlined in Table 1.
Patients with a severely delayed gastric emptying had significantly lower LFtilt than those with T50 below 350 min (median LFtilt 1.20 vs 2.14, P = 0.010) and they also had lower HFsup, however, this difference was not statistically significant (median HFsup 1.35 vs 1.79, P = 0.063). Orthostatic hypotension was significantly more common in patients with severe gastric retention (χ2 = 5.74, P = 0.017).
A significant difference was also found for mBMI, where those with severely delayed gastric emptying showed lower mBMI than those without (median mBMI 809 vs 961, P = 0.004). No significant difference was found in age of disease onset (median age at onset 63 vs 56 years, P = 0.075) between patients with or without severe gastric retention. The number of patients was too small for valid statistical analyses on differences related to gender and GI symptoms.
Multiple logistic regression analysis on factors behind gastric retention
To identify factors with an impact on gastric retention, HFsup, LFtilt, gender, and age at disease onset were utilized as independent factors in multiple logistic regression analyses. The age at onset and LFtilt were the only factors significantly contributing to gastric retention. Details are outlined in Table 2.
Table 2. Multiple logistic regression analysis
Univariate (crude OR)
Multivariate (adjusted OR)
OR, odds ratio; CI, 95% confidence interval; Log, log transformed because of skewed distribution.
Gastric retention determined with gastric emptying scintigraphy.
Gender (female reference)
1.40 (CI 0.74–2.67)
0.76 (CI 0.31–1.84)
Age at disease onset (log)
0.74 (CI 0.25–2.22)
0.10 (CI 0.02–0.52)*
0.58 (CI 0.32–1.06)
1.81 (CI 0.72–4.56)
0.45 (CI 0.27–0.74)*
0.23 (CI 0.10–0.51)*
To the best of our knowledge, this is the first and largest study on FAP patients exploring the impact of autonomic dysfunction on GI symptoms and gastric emptying. The study showed a high prevalence of delayed gastric emptying and also that delayed gastric emptying is a common feature even early after disease onset. In consistency, unpublished study data from upper GI endoscopies after an overnight fast showed that 29% of the patients had retention of undigested food.
Contrary to our expectations, only a weak correlation between delayed gastric emptying and autonomic neuropathy was found. Surprisingly, sympathetic activity appeared to be strongly, or at least similarly, related to gastric emptying as parasympathetic activity. This was also supported by a higher frequency of gastric retention in patients with orthostatic hypotension and by subgroup analyses for patients with severely delayed gastric emptying.
Parasympathetic dysfunction often precedes sympathetic dysfunction in FAP patients.16 The fact that the sympathetic function was more strongly correlated with gastric retention in our study probably reflects a more advanced disease in patients with sympathetic dysfunction. In the multiple logistic regression analysis, sympathetic dysfunction significantly contributed to gastric retention, whereas the parasympathetic did not, indicating that an intact parasympathetic function is not the only factor important for a preserved gastric emptying rate. A case report from Ohio has also shown that gastroparesis can occur in patients with pure sympathetic dysfunction,17 suggesting that a reduced sympathetic function itself may negatively affect gastric emptying.
As vagotomy (i.e., loss of parasympathetic control) often leads to gastric retention,18 and as there is evidence of amyloid deposits in the autonomic nervous system with a destruction of the vagal nerve in FAP patients,19 an autonomic neuropathy has been suggested to be the underlying factor for GI disturbances of these patients.20 This is also supported by the findings of a destructed celiac ganglion in FAP patients,21 but our findings of delayed gastric emptying in patients with normal sympathetic and parasympathetic activity implies that additional factors must be involved.
Such possible contributing factors may be a depletion of the GI neuroendocrine cells and a destruction of the enteric nervous system.22–25 However, the enteric nervous system seems to be unaffected in FAP Val30Met26,27 and no improvement of the GI function has been shown after Ltx,28,29 although a normalization of the endocrine cell count was noted.30 In diabetes mellitus a down-regulation of ghrelin and its receptor is linked to GI dysfunction,31,32 and it would be of interest to study if this is also the case in FAP patients.
Likewise, a depletion of the interstitial cells of Cajal (ICC), increased oxidative stress, and smooth muscle degeneration and fibrosis play important roles in the gastroenteropathy of diabetes mellitus,33–35 and need to be investigated in FAP as well. Preliminary results from another of our studies in fact showed a marked decrease of gastric ICC in FAP patients compared with controls. Interestingly, an accumulation of advanced glycation end products, which bind to enteric neurons and cause a decreased production of nitric oxide synthase leading to a delayed gastric emptying in diabetics,34 have also been observed in FAP.36 Analysis of urinary secreted NO2−/NO3− levels has implicated a decreased NO synthesis in FAP patients.37
Nausea, vomiting, and early satiety are classic symptoms of gastroparesis. Unexpectedly, none of the patients with a severely delayed gastric emptying reported upper GI symptoms. Furthermore, there was no difference in the outcome of GES when comparing patients without symptoms with those with upper GI symptoms, whereas lower GI symptoms and, especially, a combination of upper and lower GI symptoms seemed to be more related to gastric retention in FAP. A possible explanation may be that those patients have a more pronounced GI dysfunction and it appears to be difficult to predict the presence of gastroparesis from GI symptoms alone.38
Delayed gastric emptying correlated with a low mBMI and patients with severe gastric retention had significantly lower mBMI compared with those with T50 below 350 min. Previous studies have shown that GI dysfunction and a low mBMI are predictors of an increased mortality after Ltx, as is an early onset of GI disturbances.3,5 Thus, the detection of gastric retention is an important part of the evaluation of FAP patients, and GES is therefore part of our routine investigation of patients under evaluation for Ltx.
We noted that the female patients displayed higher HFsup and LFtilt and slower gastric emptying rates than males and that the group of patients with severe malnutrition consisted of women only. However, no gender related differences in survival after Ltx have been observed, except for a decreased survival of late onset males.39 We do not believe that the gender differences observed have any clinical impact.
Expectedly, a weak negative correlation was found between age at onset and HFsup and LFtilt. A decline in the autonomic nervous function is also found in the general population and HRV values are often age adjusted. The values displayed in the present investigation were, however, not age adjusted. A late onset of the disease also significantly contributes to gastric retention, probably reflecting a poorer autonomic function.
In conclusion, hereditary TTR amyloidosis was associated with delayed gastric emptying early after disease onset in Swedish patients. Furthermore, gastric retention is associated with a poorer nutritional status. Only weak correlations were found between the measures of autonomic neuropathy and gastric retention, indicating that other factors must be involved. Surprisingly, no correlation was found between upper GI symptoms and delayed gastric emptying, suggesting that GI symptoms are poor predictors of the actual GI function in these patients.
The HFsup and LFtilt from spectral analysis of HRV were used as markers of parasympathetic and sympathetic autonomic function, respectively, as they are used as estimates of autonomic cardiac control and one may argue that they do not fully correspond to the autonomic gastric control. However, HRV is generally considered to be a good marker for autonomic function in FAP20 and has also been used in studies on autonomic function and GI motility in diabetics.40,41
A scintigraphic measurement of 4 h would improve the accuracy,42 but a 2-h measurement is the standard procedure at our hospital reflecting current clinical practice. The manual measurement of the lag phase, T50, and T1/2 by a single reviewer has an advantage over the automatic version because the settings of the latter method have been changed over the years making it less homogeneous. However, the manual analysis may not be as precise as the automatic.
This study was supported by grants from the Swedish Heart and Lung Foundation, the patients organizations FAMY/AMYL in Västerbotten and Norrbotten, Umeå University, the 6th research framework of EU, The Euramy project, ALF-grants from Umeå University Hospital, and a ‘Spearhead’ grant from Västerbotten’s county.
The authors have no competing interests.
Co-author OBS examined the patients, designed the research study, contributed to the interpretation of the results, and revised the manuscript; JW analyzed the data and wrote the manuscript; UW and RH provided and analyzed the HRV examinations and revised the manuscript; AR provided the GES examinations and revised the manuscript; PK helped with the interpretation of the results, the statistical analysis, and the revision of the manuscript; IA contributed to the interpretation of the results and revised the manuscript.