|
What’Snew? Data from the present study showed that at least one red flag for cardiac amyloidosis was observed in almost 70% of the patients with heart failure with preserved ejection fraction (HFpEF). The mean number of red flags in a patient with HFpEF was 1.3. Extracardiac and cardiac clinical red flags were extremely rare in patients. Approximately, an electrocardiographic red flag was detected in 2 out of 10 patients, and an echocardiographic red flag was observed in 4 out of 10 patients with HFpEF. What is more, HFpEF patients with wild-type transthyretin cardiac amyloidosis had twice as many red flags as HFpEF patients without cardiac amyloidosis. |
INTRODUCTION
Heart failure (HF) with preserved ejection fraction (HFpEF) is a heterogeneous clinical syndrome with multiple underlying causes with increased prevalence in the elderly population and women. Furthermore, it is more associated with comorbidities such as hypertension (HT), diabetes (DM), obesity, and chronic kidney disease (CKD) [1]. Recently, it has been established that cardiac amyloidosis (CA) is an important cause of HFpEF than previously thought [2, 3]. The disease has two main subtypes: transthyretin CA (ATTR-CA) and immunoglobulin light chain CA (AL-CA). ATTR-CA is further subdivided into wild-type (ATTRwt-CA) and mutant (ATTRm-CA) [4]. Gonzalez-Lopez et al. [5] reported that 13.3% of patients with HFpEF with left ventricular hypertrophy (LVH) showed uptake of 99mTc3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy, which suggested cardiac involvement of ATTRwt-CA. However, diagnosis of CA remains a frequent clinical challenge, especially in the early stages, and CA is still under-diagnosed [6]. Red flags have been defined as a set of cardiac and extracardiac signs and symptoms, which are extremely useful for suspecting the disease in CA [4, 7]. In this study, we evaluated the frequency of cardiac and extracardiac manifestations of ATTR-CA in patients with HFpEF and aimed to identify red flags that would further alert clinicians to the diagnosis of CA in real-life.
METHODS
We conducted a prospective, observational, single-center study. The study was approved by our institutional ethics committee. All participants provided written informed consent.
Study population
A total of 100 patients diagnosed with HFpEF who were admitted to the Department of Cardiology of Eskisehir Osmangazi University were screened between October 2020 and July 2021. The diagnosis of HFpEF was based on the European Society of Cardiology guidelines [8]. Patients with severe valvular heart disease, previous myocardial infarction, sarcomeric hypertrophic cardiomyopathy, or myocardial storage diseases were excluded. Finally, 85 patients who underwent cardiac scintigraphy with the clinician’s suspicion of CA were included in the study.
Study design, data collection, and definition
Demographic characteristics, comorbidities, laboratory findings, and medications were collected during admission. CKD was defined as the presence of an estimated glomerular filtration rate (eGFR) of ≤60 ml/min/1.73 m2. N-terminal pro-brain natriuretic peptide (NT-proBNP) and the serum or urine monoclonal proteins results were evaluated. Comprehensive transthoracic echocardiography (ECHO) was performed and electrocardiograms (ECG) were recorded. Extracardiac clinical red flags including polyneuropathy, dysautonomia, history of carpal tunnel syndrome (CTS), biceps tendon rupture or lumbar spinal stenosis, positive family history, macroglossia, and cardiac red flags, including hypotension or intolerance to β-blockers/angiotensin-converting enzyme inhibitors, low-voltage or pseudoinfarct pattern or atrioventricular (AV) conduction anomalies on ECG were investigated. Findings including granular sparkling of the myocardium, increased right ventricular (RV) wall thickness, increased valve thickness, pericardial effusion, and reduced longitudinal strain with the apical sparing pattern were investigated as ECHO red flags. 99mTechnetium-pyrophosphate (99mTc-PYP) cardiac scintigraphy was performed in 85 patients. Transthyretin (TTR) gene sequencing was performed in positive patients to identify the mutant type. Also, these patients were evaluated for AL-CA with serum-free light chains and immunofixation electrophoresis.
Echocardiography and electrocardiography
Comprehensive ECHO was performed by a physician using a commercially available system (EPIQ 7C, X5-1 transducer, Philips Medical Systems, Andover, MA, US). Echocardiographic raw data were stored digitally as digital imaging and communications in medicine (DICOM) and transferred for offline analysis to a workstation with the Philips QLAB software. All dimensions were obtained from 2D imaging according to the recommendations of the guidelines [9, 10]. Global longitudinal strain (GLS) was measured in the three apical views. The relative apical sparing index was defined using the equation: average apical LS/(average basal LS + mid-LS) [11]. A standard 12-lead ECG was recorded.
Cardiac scintigraphy
For the primary analysis, which was based on myocardial tracer uptake, two methods were used: (1) semi-quantitative visual scoring of cardiac retention (0–1–2–3) at 3 hours; and (2) quantitative analysis of heart retention was calculated by drawing a region of interest (ROI) over the heart in the standard manner at 1 hour. The fraction of mean counts in the heart ROI-to-contralateral chest ROI was calculated as the heart to contralateral lung (H/CL) ratio [12, 13]. In the absence of monoclonal protein in the serum and urine, grade 2 to 3 myocardial uptake or a H/CL ratio of ≥1.5 were considered positive for ATTR-CA. Grade 2–3 uptake with a H/CL ratio ≥1.5 or grade 0–1 uptake with a H/CL ratio <1.5 were considered concordant results. Grade 2–3 uptake with a semi-quantitative score of 1 or H/CL ratio 1–1.5 were considered equivocal [12, 13].
Statistical analysis
Continuous variables were presented as means (standard deviation [SD]) and compared using t-tests if they were normally distributed and described using medians (interquartile ranges [IQR]) if they were not; the Mann–Whitney U test was used for comparisons. Poisson regression analysis was used to evaluate the distribution of RF incidences in the ATTR-CA positive/negative groups. We expressed descriptive data as number (%) for categorical variables and compared them via the χ2 test or Fisher exact test. A P <0.05 was considered statistically significant. IBM SPSS Statistics 21.0 software (IBM Corp. Released 2012. IBM SPSS Statistics for Windows, Version 21.0. Armonk, NY, US; IBM Corp.) was used in the analyses.
RESULTS
The mean (SD) age of the study group was 67.9 (9.8) years and 52 (61.2%) were female. Overall, 20 (23.5%) patients were in New York Heart Association (NYHA) class III–IV, and median (IQR) NT-proBNP was 1000 (433.5–2040.5) pg/ml. Other baseline features are summarized in Table 1.
|
Variable |
TTR-CA negative (n = 70) |
TTR-CA positive (n = 15) |
P-value |
|
Age, years, mean (SD) |
66.8 (10.0) |
72.1 (8) |
0.046 |
|
≥65 years, n (%) |
39 (55.7) |
12 (80) |
0.05 |
|
Male sex, n (%) |
27 (38.6) |
6 (40) |
0.56 |
|
BMI, kg/m2, mean (SD) |
30.4 (5.62) |
30.2 (4.0) |
0.90 |
|
Hypertension, n (%) |
55 (78.6) |
12 (80) |
0.60 |
|
Diabetes, n (%) |
31 (44.3) |
3 (20) |
0.07 |
|
Coronary artery disease, n (%) |
22 (31.4) |
6 (40) |
0.36 |
|
Atrial fibrillation, n (%) |
23 (32.9) |
8 (53.3) |
0.11 |
|
Chronic kidney disease, n (%) |
30 (42.9) |
3 (20) |
0.08 |
|
NYHA class I, n (%) |
1 (1.4) |
0 |
0.61 |
|
NYHA class II, n (%) |
51 (72.9) |
13 (86.7) |
|
|
NYHA class III, n (%) |
13 (18.6) |
2 (13.3) |
|
|
NYHA class IV, n (%) |
5 (7.1) |
0 |
|
|
SBP, mm Hg, mean (SD) |
127.8 (17.7) |
123.7 (19.5) |
0.42 |
|
Heart rate, bpm, mean (SD) |
77.5 (18.3) |
79.3 (24.4) |
0.75 |
|
Creatinine, mg/dl, median (IQR) |
0.96 (0.77–1.3) |
0.89 (0.80–1.10) |
0.28 |
|
NT-proBNP, pg/ml, median (IQR) |
966.5 (425.5–2037.7) |
1113.0 (768.0–2385.0) |
0.37 |
|
β-blocker, n (%) |
53 (75.7) |
12 (80) |
0.51 |
|
Calcium channel blockers, n (%) |
18 (25.7) |
5 (33.3) |
0.38 |
|
ACEI/ARB, n (%) |
37 (52.8) |
7 (46.6) |
0.41 |
|
Furosemide, n (%) |
40 (57.1) |
10 (66.7) |
0.35 |
|
MRA, n (%) |
16 (22.9) |
6 (40) |
0.15 |
Echocardiographic and electrocardiographic findings
Mean (SD) left ventricular ejection fraction (LVEF) was 59.7 (4) %, mean LV-GLS was –14.3 (2.5)%. The number of patients with left ventricular wall thickness (LVWT) ≥15 mm, 12–14 mm, and ≤11 mm was 27 (31.8%), 29 (34.1%), and 29 (34.1%), respectively. Reduced LV-GLS with the apical sparing pattern was detected in 9 (10.5%) patients and granular sparkling of myocardium in 2 (2.3%) patients. According to the ECG findings, 2 (2.3%) patients had low/decreased QRS voltage to degree of LVWT, 5 (5.8%) patients had pseudoinfarct pattern, and 3 (3.5%) patients had AV conduction disease. Other ECHO and ECG findings are summarized in Table 2.
|
Variable |
TTR-CA negative (n = 70) |
TTR-CA positive (n = 15) |
P-value |
|
LV ejection fraction, %, mean (SD) |
60.0 (4.14) |
58.6 (3.76) |
0.22 |
|
LV end-diastolic diameter, mm, mean (SD) |
47.6 (3.72) |
48.4 (3.65) |
0.47 |
|
IVSd, mm, median (IQR) |
12.8 (11.0–15.0) |
13.0 (11.0–16.0) |
0.78 |
|
Posterior wall thickness, mm, median (IQR) |
12.0 (10.0–13.0) |
12.0 (11.0–14.0) |
0.40 |
|
IVS thickness ≥12 mm, n (%) |
45 (64.3) |
11 (73.3) |
0.78 |
|
RWT, median (IQR) |
0.48 (0.42-0.53.5) |
0.47 (0.46-0.60) |
0.44 |
|
Right ventricular wall thickness, mm, median (IQR) |
4.0 (3.0-4.5) |
4.0 (3.0-5.0) |
0.97 |
|
LV mass index, g/m2, median (IQR) |
115.5 (100.0–145.5) |
129.0 (104.0–159.0) |
0.52 |
|
LA diameter, mm, mean (SD) |
43.7 (5.85) |
45.9 (5.83) |
0.20 |
|
LA area (cm2), median (IQR) |
19.5 (16.5–24.0) |
21.0(20.0–26.0) |
0.15 |
|
LAVI, ml/m2, median (IQR) |
34.0 (26.0–45.0) |
37 (32.0–49.0) |
0.24 |
|
LAVI >34 ml/m2, n (%) |
34 (48.6) |
10 (66.7) |
0.16 |
|
GLS, %, mean (SD) |
–14.7 (2.37) |
–12.5 (2.78) |
0.003 |
|
Apical/(mid + basal) LS ratio, median (IQR) |
0.90 (0.84–0.95) |
1.08 (0.85–1.49) |
0.006 |
|
Peak TR velocity> 2.8 m/s, n (%) |
28 (40) |
5 (33.3) |
0.43 |
|
sPAP, mm Hg, median (IQR) |
35.0 (27.7–50.0) |
35.0 (32.0–48.0) |
0.78 |
|
E-wave, cm/s, mean (SD) |
81.8 (21.0) |
77.9 (27.2) |
0.53 |
|
E/e’ lat, means (SD) |
11.6 (3.01) |
12.6 (2.98) |
0.22 |
|
E/e’≥15 E/e’ 9–14 |
12 (17.1) 47 (67.1) |
4 (26.7) 10 (66.7) |
0.52 |
|
TAPSE, mm, mean (SD) |
18.1 (2.78) |
16.7 (2.19) |
0.08 |
|
Right ventricular hypertrophy, n (%) |
8 (11.4) |
2 (13.3) |
0.56 |
|
Interatrial septum hypertrophy, n (%) |
2 (2.9) |
1 (6.7) |
0.45 |
|
Low QRS, n (%) |
— |
2 (13.3) |
0.03 |
|
PR interval, ms, median (IQR) |
150.0 (120.0–160.0) |
160.0 (160.0–200.0) |
0.048 |
|
AV block (first degree), n (%) |
2 (2.9) |
1 (6.7) |
0.44 |
|
BBB, n (%) |
17 (24.3) |
2 (13.3) |
0.29 |
|
Pseudo-infarct pattern, n (%) |
2 (2.9) |
3 (20) |
0.04 |
Scintigraphy results
Scintigraphy showed that 15 (17.6%) patients had a grade 2 or 3 cardiac uptake; the H/CL ratio was ≥1.5, and concordance was positive. In the absence of monoclonal protein in the serum and urine, positive bone scintigraphy is considered diagnostic for ATTR-CA. All patients with a positive scan underwent genetic testing of the TTR gene, and no mutations were found.
Frequency of cardiac and extracardiac amyloidosis red flags in patients with HFpEF
At least 1 red flag was observed in 57 (67%) of the 85 patients with HFpEF. The mean number of red flags in a patient with HFpEF was 1.3. Only 4 (4.7%) patients had more than 3 red flags. Extracardiac clinical red flags were observed in only 9 (10.5%) patients. Among all patients, 31 (36.4%) patients had extracardiac laboratory red flags. Cardiac clinical red flags were extremely rare and were observed in only one of the 85 patients. Approximately, an ECG red flag was detected in 1 out of 10 patients and an ECHO red flag in 4 out of 10 patients with HFpEF. The presence of disproportionately elevated NT-proBNP to degree of HF was present in 8 (9.4%) patients. Patients with ATTR-CA had twice as many red flags as those without (2.46 vs. 1.04). However, ATTR-CA diagnosis was more common in patients with 2 or more red flags (Tables 3 and 4).
|
Variables |
Total (n = 85) |
TTR-CA negative (n = 70) |
TTR-CA positive (n = 15) |
P-value |
|
Extracardiac red flags |
||||
|
Extracardiac clinical, n (%) |
8 (9.4) |
5 (7.1) |
3 (20) |
0.14 |
|
Extracardiac laboratory, n (%) |
40 (47.1) |
34 (48.6) |
6 (40) |
0.38 |
|
Cardiac red flags |
||||
|
Clinical, n (%) |
1( 1.2) |
0 |
1 (6.7) |
0.18 |
|
Electrocardiogram, n (%) |
9 (10.5) |
5 (7.1) |
4 (26.7) |
0.048 |
|
Laboratory, n (%) |
8 (9.4) |
3 (4.3) |
5 (33.3) |
0.004 |
|
Echocardiography, n (%) |
32 (37.6) |
22 (31.4) |
10 (66.7) |
0.013 |
|
Total number of RF |
110 |
73 |
37 |
0.013 |
|
Patients with 0–1 RF number, n (%)a |
55 (64.7) |
51 (72.9) |
4 (26.7) |
0.002 |
|
Patients with 2–7 RF number, n (%)a |
30 (35.2) |
19 (27.1) |
11 (73.3) |
0.001 |
|
RF number/patients number ratio |
1.3 |
1.04 |
2.46 |
<0.001 |
|
Variable |
TTR-CA negative (n = 70) |
TTR-CA positive (n = 15) |
P-value |
|
Polyneuropathy, n (%) |
4 (4.3) |
2 (13.3) |
0.21 |
|
Dysautonomia, n (%) |
2 (2.9) |
1 (6.7) |
0.45 |
|
Macroglossia, n (%) |
— |
— |
— |
|
Bilateral carpal tunnel syndrome, n (%) |
— |
— |
— |
|
Ruptured biceps tendon, n (%) |
— |
— |
— |
|
Lumbar spinal stenosis, n (%) |
— |
— |
— |
|
Family history, n (%) |
— |
— |
— |
|
Renal insufficiency (GFR <60 ml/min/1.73 m2), n (%) |
30 (42.8) |
3 (20) |
0.28 |
|
Proteinuria, n (%) |
12 (17.1) |
3 (20) |
0.52 |
|
Hypotension or normotensive if previous hypertensive, n (%) |
— |
1 (6.7) |
0.18 |
|
Pseudoinfarct pattern, n (%) |
2 (2.9) |
3 (20) |
0.04 |
|
Low/decreased QRS voltage to degree of LV thickness, n (%) |
0 |
2 (13.3) |
0.03 |
|
AV conduction disease, n (%) |
2 (2.9) |
1 (6.7) |
0.44 |
|
Disproportionately elevated NT-proBNP, n (%) |
3 (4.3) |
5 (33.3) |
0.004 |
|
Granular sparkling of the myocardium, n (%) |
0 |
2 (13.3) |
0.03 |
|
Increased right ventricular wall thickness, n (%) |
8 (11.4) |
2 (13.3) |
0.56 |
|
Increased valve thickness, n (%) |
14 (20) |
6 (40) |
0.09 |
|
Pericardial effusion, n (%) |
3 (4.3) |
3 (20) |
0.06 |
|
Reduced LS with apical sparing pattern, n (%) |
1 (1.5) |
8 (57.1) |
<0.001 |
DISCUSSION
The results of this prospective study demonstrated that (1) 67% of patients with HFpEF had at least one of the red flags; (2) HFpEF patients with ATTR-CA had twice as many red flags as those without; (3) extracardiac clinical red flags are rarely seen in patients. We concluded that the presence of ECHO red flags and disproportionately elevated NT-proBNP are more common warnings to suspect CA.
ATTRwt-CA has been increasingly recognized as an underdiagnosed cause of HFpEF. It is valuable to recognize clinical findings for the underlying etiology in patients with HFpEF at an early stage. In previous studies, the prevalence of ATTR-CA was reported to be between 13% and 19% in patients with unexplained LVH with HFpEF [5, 14, 15]. Also, in a study conducted on patients with HFpEF without LVH, it was reported that ATTR-CA was detected in 5% of these patients [2]. In our study, 65.9% of patients had LVH, of which approximately one-third was unexplained LVH. Patients with HFpEF were included in our study regardless of age and LVMT. Although it is frequently reported that ATTR-CA is seen in the elderly and men [16], reports show that it also affects wider age ranges and younger and female patients [17]. Our study included a different patient population than the “elderly male” profile usually included in studies about CA. This reflects the HFpEF patient profile that we encounter in daily practice.
Extracardiac and cardiac clinical red flags
Extracardiac and cardiac clinical red flags are less frequent in patients with HFpEF. Orthostatic hypotension (OH) affecting an estimated 40%–60% of patients with ATTRm-CA is a manifestation of autonomic dysfunction [18]. Orthostatic hypotension is diagnosed in 5-11% of middle-aged adults and approximately 20%–30% of people 65 years and older, but the incidence of OH in the HF population is not clear [19, 20]. However, a recent review showed that the incidence of OH in HF varies from 8% to 83% [21]. Also, there is often accompanying neurological involvement such as sensorimotor polyneuropathy in CA, but purely neurological manifestations are rare (4%) [22]. In addition, ATTRwt-CA is known to be associated with CTS, lumbar spinal stenosis, and ruptured biceps tendon [4]. Carpal tunnel syndrome is the most frequent focal peripheral neuropathy in the general population and has been shown to have a prevalence ranging from 0.2% to 4% [23]. In cases of CA, its frequency varies in relation to variables such as amyloid subtypes, duration of the disease, male sex, and age. CTS is present in about 25% of patients and can occur years before diagnosis [24]. Besides, in patients with a history of HT, “spontaneous” resolution of HT over the preceding few months is a valuable history for the diagnosis of CA and has been identified as a cardiac clinical red flag [4, 25]. In the present study, 3% of the patients with HFpEF had autonomic dysfunction findings, and 6% had polyneuropathy. While 2 patients had unilateral CTS, there was no patient with bilateral CTS. The absence of bilateral CTS may be related to the small size of our patient population. “Spontaneous” resolution of HT was observed in only one patient, and this patient was positive on scintigraphy.
Proteinuria and CKD are characterized as extracardiac clinical red flags, these conditions are already common in the HFpEF population. Although the prevalence of proteinuria and CKD varies depending on the age and comorbidities of the patient population included in the studies, it has been reported that 30%–41% of patients with HfpEF have proteinuria [26–28], and 26%–49% have CKD [29]. Similar to previous studies, in our study population, we observed proteinuria in 15 (17.6%) patients (8 with CKD, 7 without CKD) and CKD in 33 (38.8%) patients. Also, there were no patients planned for kidney transplantation. The most common reasons for the increase in the number of red flags were the presence of CKD and/or proteinuria.
ECG, ECHO, and laboratory red flags
Electrocardiographic abnormalities in HF with reduced ejection fraction are widely described and guide medical and device therapy. However, other than a high prevalence of atrial fibrillation, little is known about ECG features associated with HFpEF. ECG variables can help predict the etiology in patients with HFpEF but are very heterogeneous. It has been reported that 10-30% of patients with HFpEF have electrocardiographic LVH. ECG abnormalities reported in patients with HFpEF include atrial fibrillation (prevalence 12%–46%), long PR interval (11%–20%), pathological Q waves (11%–18%), and left bundle branch block (0%–8) [30]. In our study population, 27% of patients had electrocardiographic LVH, 5 (5.8%) had a pseudo-infarct pattern, and 3 (3.5%) had AV conduction disease. In addition, there were two patients with low voltage on ECG in the limb leads inconsistent with LV wall thickness and these patients were ATTR-CA positive. Analysis of easy-to-assess ECG variables in patients with HFpEF can be of substantial help in the diagnostic workup of ATTRwt-CA.
Besides, ECHO is essential for the initial evaluation of patients with suspected and diagnosed of HFpEF. In addition, it has been reported that cardiac magnetic resonance imaging is a valuable tool in determining the etiology in patients with HFpEF [31]. Diastolic dysfunction, LA enlargement, LVH, RV enlargement, and elevated pulmonary artery systolic pressure were common in patients with HFpEF. Apart from these findings, RV hypertrophy, thickening of cardiac valves and interatrial septum, granular appearance of the myocardium, and pericardial effusion are common in patients with CA. In the present study, the most common finding among ECHO red flags was thickening of cardiac valves, but there was no difference between the two groups (P >0.05). Another “classical” ECHO features of CA were the “granular sparkling and reduced LS with apical sparing pattern”, which were significantly higher in the patients with ATTRwt-CA. The results of this study were similar to the results of previous studies for echocardiographic red flags [4].
NT-proBNP is a marker of neurohormonal activation that is useful in the diagnosis and prognosis of HF. Previous studies comparing NT-proBNP levels in different forms of amyloid cardiomyopathy suggested that NT-proBNP values are lower in ATTR-CA than in AL-CA, besides increased ventricular wall thickness [32]. In addition, NT-proBNP levels that are disproportionate to the degree of HF are suggestive of ATTRwt-CA [33]. It has even been reported that some patients with suspected hypertrophic cardiomyopathy, with LVH and normal NT-proBNP levels, may have undiagnosed ATTR-CA [34]. In this study, there was no significant difference in NT-proBNP levels between HFpEF patients with and without CA. However, “the presence of disproportionately elevated NT-proBNP to degree of HF” was significantly higher in patients with ATTRwt-CA.
Study limitations
The presence of persisting elevated troponin could not be evaluated as a cardiac laboratory red flag. Cardiac magnetic resonance imaging findings that were part of the red flag assessment were not evaluated. Another limitation is that endomyocardial biopsies were not performed in this study. Diagnostic tests were performed for storage diseases and hypertrophic cardiomyopathy in clinically suspected patients, but not routinely in all patients.
CONCLUSION
The results of the study showed that patients diagnosed with HFpEF had an average of 1.3 red flags suggestive of CA. Extracardiac and cardiac clinical red flags were extremely rare in patients. Approximately, an electrocardiographic red flag was detected in 2 out of 10 patients and an echocardiographic red flag in 4 out of 10 patients with HFpEF. Furthermore, red flags were twice as common in HFpEF patients with CA than in HFpEF patients without CA.
Article information
Conflict of interest: None declared.
Funding: Pfizer Pfe Ilaçları (Pfizer Turkey) provided only funding under the independent research grants program for this study.
Open access: This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially. For commercial use, please contact the journal office at kardiologiapolska@ptkardio.pl.
