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Transforming growth factor beta 1 levels predict echocardiographic changes at three years after adjuvant radiotherapy for breast cancer

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Abstract

Background

Transforming growth factor beta 1 (TGF-β1) and platelet-derived growth factor (PDGF) are cytokines involved in fibrotic processes causing radiotherapy (RT)-induced cardiovascular changes. We aimed to investigate the associations between TGF-β1 and PDGF and the echocardiographic changes that occur during RT and during three-year follow-up.

Methods

The study included 63 women receiving adjuvant RT for early-stage breast cancer or ductal carcinoma in situ. Serum TGF-β1 (ng/ml) and PDGF (ng/ml) levels were measured by enzyme-linked immunoassay and echocardiographic examination was performed before RT, after RT and at 3 years. Patients were grouped by biomarker behavior by a trajectory analysis.

Results

TGF-β1 decreased from 19.2 (IQR 17.1–22.3) before RT to 18.8 (14.5–22.0) after RT (p = 0.003) and the decrease persisted at 17.2 (13.7–21.2) 3 years after RT (p = 0.101). PDGF decreased from 15.4 (12.6–19.1) before RT to 13.8 (11.7–16.2) after RT, p = 0.001, and persisted at 15.6 (10.4–18.4) at 3 years, p = 0.661. The TGF-β1 level before RT (Spearman’s rho 0.441, p < 0.001) and the three-year change in TGF-β1 (rho = − 0.302, p = 0.018) correlated with global longitudinal strain (GLS) in echocardiography at 3 years.

In trajectory analysis, two TGF-β1 behavior groups were found. Group 1 had significantly higher TGF-β1 levels before RT, 25.6 (22.3–28.6), than group 2, 17.8 (15.9–19.9), p < 0.001. In multivariable analysis, TGF-β1 trajectory group 1 (β = 0.27, p = 0.013), left-sided breast cancer (β = 0.39, p = 0.001) and the use of aromatase inhibitors (β = 0.29, p = 0.011) were significantly associated with a worsening in GLS from before RT to 3 years.

Conclusion

An elevated pretreatment TGF-β1 may predict RT-associated changes in echocardiography.

Background

Adjuvant radiotherapy (RT) of breast cancer is associated with an increased risk of cardiovascular morbidity and mortality [1]. Transforming growth factor beta 1 (TGF-β1) is involved in the process responsible for the long-term fibrotic effects of RT, including cardiovascular changes and morbidity [2]. TGF-β1 is produced by platelets, macrophages, fibroblasts, monocytes, and epithelial and endothelial cells [2]. In a radiation fibrosis model, the production of profibrotic cytokines, such as TGF-β1 and platelet-derived growth factor (PDGF), is thought to be induced by radiation, which in turn activates fibroblasts. It is suggested that cytokines play an initiative role, but may not be necessary to maintain the fibrotic process [2].

TGF-β1 is also released following myocardial injury, exerting profibrotic actions on the myocardium. This process is involved in the pathogenesis of different myocardial diseases [3]. Elevated levels of TGF-β1 are also present in various fibrotic diseases, such as hepatic fibrosis, idiopathic pulmonary fibrosis, myelofibrosis or systemic sclerosis [4]. In addition, variation in circulating TGF-β1 levels is also caused by genetic factors [5]. Mutations in genes determining TGF-β1 levels may be responsible for susceptibility to radiation injury, such as breast fibrosis or increased cardiovascular morbidity [6, 7].

Only a few studies have examined the effect of adjuvant breast cancer RT on the circulating levels of TGF-β1. Two studies have reported that patients who developed fibrosis of the breast as sequelae of external beam RT had higher baseline levels of TGF-β1 than those who did not develop fibrosis [8, 9]. We reported that patients receiving adjuvant RT for breast cancer with echocardiographic changes from before to after RT had higher baseline TGF- β1 levels and their TGF-β1 and PDGF levels decreased during RT [10].

Our aim was to study the behavior of the TGF-β1 and PDGF levels and their association with the echocardiographic changes from before RT to immediately after and 3 years after RT.

Materials and methods

Patients

Altogether, 63 patients with available serum samples, receiving postoperative RT for breast cancer or ductal carcinoma in situ (DCIS) were included in this prospective, observational, single-center study. The included patients had breast-conserving surgery (n = 62) or a mastectomy (n = 1) before RT, but none received chemotherapy. Earlier publication describes the key inclusion and exclusion criteria in detail [11]. The Tampere University hospital ethics committee approved the study (R10160) and informed consent was obtained from all participants.

Radiotherapy

A detailed description of the RT protocol is found in an earlier publication [12]. Briefly, the planning target volume (PTV) received either 50 Gy in 2 Gy fractions or 42.56 Gy in 2.66 Gy fractions. The remaining breast after breast-conserving surgery or the chest wall after mastectomy with margins constituted the PTV. For the one patient with axillary node-positive disease, PTV included the axillary and supraclavicular areas.

Serum biomarker analysis

TGF-β1, PDGF and N-terminal pro-brain natriuretic peptide (proBNP) were analyzed from serum samples drawn at the start of RT, at the end of RT and 3 years after RT. Concentrations of TGF-β1 and PDGF-AB were measured by enzyme-linked immunosorbent assay with reagents from R&D Systems Europe Ltd. (Abingdon, UK). Samples were stored at − 80 °C and all samples were analyzed simultaneously with reagents from the same batch. Samples from before and after RT were also reanalyzed [10]. The detection limit and the interassay coefficient of variation were 7.8 ng/ml and 5.1% for TGF-β1 and 3.9 ng/ml and 3.5% for PDGF-AB, respectively.

Echocardiographic examination

Echocardiographic examination was performed at the same time points as when the serum samples were drawn. A single cardiologist (ST) performed all the examinations by a commercially available ultrasound machine (Philips iE33 ultrasound system; Philips, Bothell, WA, USA) and a 1–5 MHz matrix-array X5–1 transducer, as described previously [13, 14].

Statistical analysis

The median and interquartile range (IQR) were calculated for variables with skewed distributions. The Wilcoxon signed-rank test was used to test for change in a variable between measurements before RT, after RT and at 3 years. The linear relationship between continuous variables was determined using Spearman’s correlation. The Mann-Whitney U-test for continuous variables was used to test for differences in the biomarkers, echocardiographic measurements or radiation doses between two groups. Group based trajectory modeling was used to determine the two trajectory groups [15]. The trajectory groups were created according to the three measurements of TGF-β1 or PDGF in each patient as a continuous outcome measure and the groups represent clusters of individuals with similar trajectories and outcomes over time [16]. Models were fitted by using the flexmix package [17] of the statistical program R, version 3.3.0, from the R Foundation for Statistical Computing [18]. The relative goodness of fit was assessed using Bayesian information criteria (BIC). Fischer’s exact test was used to test for differences in categorical variables in the two trajectory groups. Linear regression was used to test multivariable associations with the change in GLS over 3 years. IBM SPSS Statistics software, version 25 for Windows (Armonk, NY, USA) was used for statistical testing. P-values under 0.05 were considered statistically significant.

Results

TGF-β1, PDGF and proBNP

Including all 63 patients, the median TGF-β1 decreased significantly during RT, p = 0.003 (Table 1). At the three-year follow-up, the median TGF-β1 level remained lower than before RT, p = 0.001. The median PDGF also decreased during RT, p = 0.001. The difference in median PDGF levels between before RT and at 3 years remained significant, p = 0.046. The median proBNP (n = 62) was stable during RT, p = 0.325, but increased by the three-year follow-up, p < 0.001.

Table 1 TGF-β1, PDGF and proBNP levels in the whole study population

The correlations of TGF-β1 and PDGF at corresponding time points and the changes between these time points are shown in Table 2. There were significant correlations between the TGF-β1 and PDGF as well as between the TGF-β1 and proBNP levels (Table 2), but PDGF and proBNP did not correlate together.

Table 2 Correlations between TGF-β1, PDGF and proBNP

TGF-β1, PDGF and baseline characteristics

Age inversely correlated with the TGF-β1 level at 3 years (rho = − 0.310, p = 0.013) and the change in TGF-β1 from before RT to 3 years (rho = − 0.280, p = 0.026). There was no significant correlation between TGF-β1 and body mass index (BMI) or time from surgery to RT. Furthermore, there was no statistically significant difference in the TGF-β1 levels before RT in groups with different comorbidities or the use of medication, e.g. hypertension, hypothyrosis, coronary artery disease (CAD), smoking, diabetes and use of aromatase inhibitors (AI), tamoxifen, angiotensin convertase inhibitors (ACE), acetylsalicylic acid (ASA), or statins.

PDGF at 3 years also inversely correlated with age (rho = − 0.348, p = 0.005), but not with BMI or time from surgery to RT. Statin-users had lower median PDGF levels before RT than did nonusers, 12.0 (10.2–16.5) ng/ml and 16.5 (13.4–20.4) ng/ml, respectively (p = 0.024). Furthermore, tamoxifen-users had lower median PDGF levels after RT than nonusers did, 12.1 (11.6–17.3) ng/ml and 15.6 (12.8–20.1) ng/ml, respectively (p = 0.041). There were no differences in the median PDGF levels according to the other baseline characteristics.

TGF-β1 and PDGF levels and echocardiographic measurements

The TGF-β1 and PDGF levels before RT, after RT, at 3 years, and the changes between these time points correlated with different structural and functional parameters in echocardiography. Echocardiographic measurements are presented in Additional file 1: Table S1. The significant correlations for TGF-β1 and PDGF after RT and at 3 years and echocardiography are presented in Additional file 2: Table S2.

Correlations with structural echocardiographic measurement

The interventricular septum (IVS) (rho 0.256, p = 0.042) and posterior wall (PW) (rho = 0.318, p = 0.011) thicknesses and the left ventricular end systolic diameter (LVESD) (rho 0.300, p = 0.017) after RT correlated with TGF-β1 before RT. Additionally, the IVS (rho 0.428, p < 0.001) and PW (rho = 0.389, p = 0.002) thicknesses at 3 years correlated with the TGF-β1 level before RT.

Furthermore, the change in TGF-β1 during RT inversely correlated with the change in septal calibrated integrated backscatter (scIBS) during RT (rho = ─0.289, p = 0.023). The change in TGF-β1 from before RT to 3 years inversely correlated with the change in IVS from before RT to 3 years (rho = ─0.255, p = 0.044) and the IVS at 3 years (rho = ─0.383, p = 0.002).

The PDGF level before RT correlated with the change in IVS from before RT to 3 years (rho = 0.306, p = 0.015). The PDGF change during RT correlated inversely with the posterior calibrated integrated backscatter (pcIBS) before RT (rho = ─0.341, p = 0.007) and positively with the change in pcIBS during RT (rho = 0.307, p = 0.016) and the change in pcIBS from baseline to 3 years (rho = 0.336, p = 0.009). The PDGF change from before RT to 3 years correlated positively with the change in left ventricular end diastolic diameter (LVEDD) (rho = 0.267, p = 0.035) and negatively with the change in IVS (rho = ─0.385, p = 0.002) from before RT to 3 years.

Correlations with systolic echocardiographic measurements

The global longitudinal strain (GLS) at 3 years correlated positively with the TGF-β1 level before RT (rho 0.441, p < 0.001) and inversely with the TGF-β1 change during RT (rho = ─0.302, p = 0.018). Furthermore, the GLS change from before RT to 3 years inversely correlated with the PDGF level before RT (rho = ─0.288, p = 0.022). Likewise, the PDGF change during RT correlated with the TAPSE change from before RT to 3 years (rho = 0.262, p = 0.045).

Correlations with measurements of filling pressure and diastology in echocardiography

The TGF-β1 level before RT inversely correlated with the mitral early inflow wave velocity (mitral E) (rho ─0.300, p = 0.017) after RT. The PDGF level before RT inversely correlated with the mitral E before RT (rho = ─0.288, p = 0.022), after RT (rho = ─0.416, p = 0.001) and at three years (rho = ─0.270, p = 0.033).

TGF-β1 trajectories

Trajectory analysis was performed to group the patients by behavior of TGF-β1. Group 1 (n = 19) had significantly higher levels of TGF-β1 before RT, after RT and at 3 years than group 2 (n = 44), p < 0.001 for all time points (Table 3). In group 1, there was a tendency for TGF-β1 levels to decrease from before to after RT and to the three-year follow-up, p = 0.066 and p = 0.080 respectively. In group 2, there was a significant decrease in the TGF-β1 level from baseline to after RT, p = 0.023, and to the three-year follow-up, p = 0.006. The groups were similar in baseline characteristics (Table 3), and there were no significant differences in the proBNP levels at the three time points between the groups.

Table 3 TGF-β1 levels and baseline characteristics according to two groups determined by a TGF-β1 trajectory analysis

Echocardiographic parameters by the two trajectory groups are shown in Table 4. Baseline measurements were similar between the two groups. The IVS at 3 years, the PW after RT and the PW at 3 years were significantly different between the groups, p = 0.016, p = 0.039 and p = 0.010, respectively. There was a tendency for a difference in GLS at 3 years, p = 0.081. During RT, there was a significant change for group 1 in IVS (p = 0.036), PW (p = 0.030), TAPSE (p = 0.021) and scIBS (p = 0.030). For group 2 there was a significant change during RT in TAPSE (p = 0.030) and scIBS (p = 0.007). During the three-year follow-up, GLS and scIBS significantly worsened from baseline in group 1, p = 0.013 and p < 0.001, respectively. In group 2, PW decreased and scIBS increased from baseline to 3 years, p = 0.028 and p = 0.002, respectively. Radiation doses to the heart, left ventricle (LV), right ventricle (RV) and the left anterior descending artery (LAD) were similar between the two trajectory groups (Additional file 3: Table S3).

Table 4 Echocardiographic measurements according to TGF-β1 trajectory groups

To further explore the association between TGF-β1 and GLS suggested by correlation and the significant worsening in trajectory group 1, multivariable linear regression analysis was performed. In the model, TGF-β1 trajectory group 1 (β = 0.27, p = 0.013), left-sided breast cancer (β = 0.39, p = 0.001) and the use of AI (β = 0.29, p = 0.011) were significantly associated with a reduction in GLS from before RT to 3 years. Additionally, there was tendency for age to be associated (β = 0.18, p = 0.071) with worsening GLS during the three-year follow-up. These factors explained 33% of the change in GLS.

PDGF trajectories

A trajectory analysis was also performed for PDGF. PDGF levels were significantly higher at all time-points in group 1 (n = 8) than in group 2 (n = 55), p < 0.001 (Additional file 4: Table S4) for all time-points. The groups did not differ in baseline characteristics (Additional file 4: Table S4). The change in PDGF was only significant in group 2 from before to after RT, p = 0.001.

Only scIBS at 3 years was significantly higher in group 1 than group 2, p = 0.044. The elevated PDGF levels in group 1 were not associated with more changes in echocardiographic parameters, but the group 1 was too small for a meaningful comparison (Additional file 5: Table S5). Furthermore, radiation doses to the heart, LV, RV or LAD were similar in the groups (Additional file 4: Table S4).

Discussion

Elevated baseline TGF-β1 associates with echocardiographic changes

The most important finding in our study was the association of elevated TGF-β1 before RT with a decline in LV systolic function, namely, impairment in GLS during the three-year follow-up. This association was apparent in the correlation between TGF-β1 and GLS at 3 years and further with the trajectory analysis in which patients were grouped into two groups according to TGF-β1 behavior. Group 1 had significantly higher baseline TGF-β1 levels than group 2. At baseline, the echocardiographic parameters were similar, but RT induced a thickening of the IVS and PW during RT in group 1, but not in group 2. These changes most likely depict RT-induced inflammatory changes. During the three-year follow-up, group 1 had a significant worsening of GLS and group 2 did not. In multivariable analysis, the trajectory group 1 remained a significant factor in predicting GLS worsening during the 3 years in addition to AI use and left-sided breast cancer, which we have reported in earlier to affect echocardiographic parameters [12, 13]. Left-sided breast cancer associates with higher radiation doses to the heart [19], which probably explains the significance of the side. Radiation dose is a significant factor determining cardiovascular risk of breast cancer patients and dose-volume constraints are in clinical use to decrease this risk [20]. Radiation doses were similar between the groups, as the grouping mostly reflects a difference in baseline TGF-β1. The worsening in GLS is probably the most clinically significant echocardiographic change, as GLS is an excellent early predictor of major adverse cardiac events [21]. Additionally, the correlation between the levels of TGF-β1 and proBNP, an accepted marker of heart failure [22], at all three time-points further supports the association of elevated TGF-β1 levels and cardiovascular changes.

In previous literature, two other studies with adjuvant external beam RT [8] and intracavitary partial breast brachytherapy [9] reported elevated circulating baseline TGF-β1 levels in patients who developed radiation-induced fibrosis of the breast. Studies with genetic mutations also support the idea that baseline TGF-β1 levels may predispose individuals to normal tissue toxicity from RT. Circulating levels of TGF-β1 are, at least partially, controlled genetically [3]. The TGF-β1 C-509 T variant allele (rs1800469) is associated with elevated levels of circulating TGF-β1 [3]. Prospective studies present contradictory evidence of the association between TGF-β1 C-509 T variant allele and radiation-induced fibrosis of the breast [4, 5]. There is some evidence that mutations in TGF-β1 genes are linked to cardiovascular risk. In patients receiving postoperative RT for breast cancer, patients with the TGF-β1 29C > T variant allele, associated with low TGF-β1 levels, had an increased cardiovascular risk with HR 1.79. However, in this study, there was no association between CV mortality and radiation dose [7]. Furthermore, the role of TGF-β1 is not clear in cardiovascular diseases. The evidence on the role of TGF-β1 in atherosclerosis is contradictory, but most studies suggest TGF-β1 inhibits atherosclerosis [23]. In contrast, elevated levels of TGF-β1 are associated with, for example, hypertrophic cardiomyopathy [23].

Changes in TGF-β1 levels

Earlier, we reported that TGF-β1 and PDGF decrease during RT [10], but this study shows that TGF-β1 remains at a lower level at 3 years compared to before RT. The decreases were small but statistically significant. In a suggested model, RT is thought to induce a cytokine release [2], but since we only have measurements for before and after RT, a cytokine release could have taken place earlier during the RT course. One previous study with intraoperative RT (IORT) for breast cancer reported that IORT had no effect on the TGF-β1 levels measured from wound fluid [24]. We found that a decrease in TGF-β1 during RT and the three-year follow-up correlated with worsening LV systolic function e.g. GLS. Additionally, the three-year change was correlated with an increased echodensity of the myocardium, scIBS, and LV measurements. The inverse correlations between the change in TGF-β1 levels and proBNP levels, further suggest that the decrease in TGF-β1 may be associated with an increased cardiovascular risk.

PDGF levels and associations with echocardiographic measurements

We also found associations between elevated baseline PDGF levels and LV systolic function, e.g. worsening GLS, and LV diastolic function, e.g. decreased mitral E. The change in PDGF during RT also predicted impairment in GLS over 3 years. The trajectory analysis did not further support the usability of PDGF in predicting RT-induced echocardiographic changes. Additionally, there were no correlations between PDGF and proBNP. Therefore, despite the strong correlation between the two biomarkers, TGF-β1 seems to be more usable than PDGF in predicting the cardiovascular effects of RT. To our knowledge, no previous studies exist about the PDGF and RT-induced toxicity in humans.

Limitations

Although we now present results with 3 years of follow-up, the follow-up time is still short, considering that the increased risk of cardiovascular effects of RT takes years to manifest. Longer follow-up will show whether the echocardiographic changes lead to clinical cardiovascular morbidity. This may require larger studies than ours. Additionally, the underlying cause of elevation of TGF-β1 is not known nor do we have information on how well other risk factors of cardiovascular diseases, such as elevated blood pressure, diabetes, and hyperlipidemia, are controlled in the patients. These factors could influence the results.

Conclusions

Our finding supports that elevated TGF-β1 before RT is a risk factor for the susceptibility to normal tissue toxicity and is associated with RT-induced changes in echocardiography, namely, impairment in GLS, a measure of LV systolic function. An elevated TGF-β1 level is an independent risk factor for the impairment in GLS in addition to AI use and left-sided breast cancer, which is likely due to higher radiation doses in left-sided breast cancer. Furthermore, a decrease in TGF-β1 during the three-year follow-up also correlated with echocardiographic changes. More studies and longer follow-up are needed to confirm whether elevated TGF-β1 can be used to determine which patients are at an increased risk for radiation-induced heart disease. Further, this information could even be useful when designing future cardioprotective trials.

Availability of data and materials

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

ACE:

Angiotensin converting enzyme inhibitor

AI:

Aromatase inhibitor

ARB:

Angiotensin II receptor blocker

ASA:

Low dose acetylsalicylic acid

BMI:

Body mass index

CAD:

Coronary artery disease

DCIS:

Ductal carcinoma in situ

Ee’:

Pulsed tissue doppler e’ velocity

EF:

Ejection fraction

GLS:

Global longitudinal strain

IQR:

Interquartile range

IVS:

Interventricular septum thickness

LV:

Left ventricle

LVEDD:

Left ventricle end diastolic diameter

LVESD:

Left ventricle end systolic diameter

Md:

Median

Mitral inflow E:

First peak of diastole

pcIBS:

Posterior wall of left ventricle integrated backscatter

PDGF:

Platelet-derived growth factor

proBNP:

N-terminal pro-brain natriuretic peptide

PTV:

Planning target volume

PW:

Posterior wall thickness

rcIBS:

Right ventricle integrated backscatter

RT:

Radiotherapy

RV:

Right ventricle

scIBS:

Septal calibrated integrated backscatter

TAPSE:

Tricuspid annular plane systolic excursion

TGF-β1:

Transforming growth factor beta 1

TR gradient:

Tricuspid regurgitation maximal gradient

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Acknowledgements

Ms. Salla Hietakangas is acknowledged for excellent technical assistance.

Funding

Financial support was provided by the Seppo Nieminen fund (150620 and 150636), the Ida Montin foundation (20180260), the Finnish Society for Oncology, the Finnish cultural foundation (Pirkanmaa regional fund 50181690), the competitive state financing of the expert responsibility area of the Tampere University Hospital and the Paulo Foundation. The funding sources had no involvement in the collection, analysis and interpretation of data, in the writing of the report or in the decision to submit the article for publication.

Author information

HA prepared the draft of the manuscript and all other authors provided critical revisions of the content. HA, TS, ST, MH, VV, PR, EM and PK contributed to the conception or design of the study. MH and EM were responsible for the analysis of the samples. HA and TL performed and interpreted statistical analyses. All authors read and approved the final manuscript.

Correspondence to Hanna Aula.

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Ethics approval and consent to participate

The Tampere University hospital ethics committee approved the study (R10160) and informed consent was obtained from all participants.

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Additional files

Additional file 1:

Table S1. Echocardiographic measurements in the whole study population. (DOCX 33 kb)

Additional file 2:

Table S2. Echocardiographic measurements with significant correlations with TGF-β1 and PDGF after RT and at 3 years. (DOCX 30 kb)

Additional file 3:

Table S3. Radiation doses to the heart according to groups determined by TGF-β1 trajectory analysis. (DOCX 31 kb)

Additional file 4:

Table S4. PDGF levels and baseline characteristics according to groups determined by PDGF trajectory analysis. (DOCX 33 kb)

Additional file 5:

Table S5. Echocardiographic measurements according to PDGF trajectory groups. (DOCX 38 kb)

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Aula, H., Skyttä, T., Tuohinen, S. et al. Transforming growth factor beta 1 levels predict echocardiographic changes at three years after adjuvant radiotherapy for breast cancer. Radiat Oncol 14, 155 (2019) doi:10.1186/s13014-019-1366-1

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Keywords

  • Transforming growth factor beta 1
  • Platelet-derived growth factor
  • Cardiotoxicity
  • Breast cancer
  • Radiotherapy
  • Echocardiography

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