Relationship of polymorphisms in the tissue inhibitor of metalloproteinase (TIMP)-1 and -2 genes with chronic heart failure

Abstract

Dysregulated expression of tissue inhibitors of matrix metalloproteinases (TIMPs) is associated with systolic dysfunction and worsening heart failure (HF). However, no study has assessed the relationship between TIMP polymorphisms and chronic HF. In this study, 300 HF outpatients with reduced left ventricular ejection fraction and 304 healthy blood donors were genotyped for the 372 T > C polymorphism (Phe124Phe; rs4898) in the TIMP-1 gene and the −418 G > C polymorphism (rs8179090) in the TIMP-2 gene to investigate whether these polymorphisms are associated with HF susceptibility and prognosis. The genotype and allele frequencies of the 372 T > C polymorphism in HF patients were not significantly different from those observed among healthy subjects, and the C allele of the −418 G > C polymorphism was very rare in our population (frequency < 1%). After a median follow-up duration of 5.5 years, 121 patients (40.3%) died (67 of them from HF). Survival analysis did not show statistically significant differences in all-cause death and HF-related death between patients with and without the T allele (P > 0.05 for all comparisons). Thus, our findings do not support the hypothesis that the 372 T > C (Phe124Phe) polymorphism in the TIMP-1 gene and the −418 G > C polymorphism in the TIMP-2 gene are associated with HF susceptibility and prognosis in Southern Brazilians.

Introduction

Heart failure (HF) is a chronic and progressive syndrome of insufficient cardiac output resulting from myocardial injury; it remains a leading cause of morbidity and mortality worldwide¹. HF is a multifactorial disease, and the interaction of several genetic variants results in differential HF susceptibility, therapeutic response, and prognosis². During HF development, the left ventricle (LV) undergoes structural and functional changes involving cardiomyocyte death, fibrosis, inflammation, and electrophysiological remodelling^3,4. This process of cardiac remodelling is mediated by the action of matrix metalloproteinases and their inhibitors^5–7, resulting in the deterioration of cardiac function and progressive HF⁸.

Matrix metalloproteinases (MMPs) are a family of proteolytic enzymes that regulate extracellular matrix (ECM) turnover and inflammatory signalling⁵. Activated MMPs are tightly regulated by endogenous tissue inhibitor of metalloproteinases (TIMPs), which also exert their effects on cell proliferation, differentiation, apoptosis, and angiogenesis by MMP-independent mechanisms^9,10. TIMP-1 inhibits proMMP-9, while TIMP-2 preferentially binds to proMMP-2¹⁰. In heart disease, the expression levels of MMPs and TIMPs are unbalanced, which may contribute to collagen disintegration in myocardial tissue and to alterations in cardiomyocyte intracellular signalling⁹. High levels of TIMP-1 in either the plasma or myocardium have been found in patients with hypertension¹¹, myocardial fibrosis, LV hypertrophy, systolic and diastolic dysfunction, atrial fibrillation, acute myocardial infarction (AMI), end-stage idiopathic dilated cardiomyopathy, and progressive HF. Increased levels of TIMP-2 are also associated with systolic dysfunction, AMI, end-stage idiopathic dilated cardiomyopathy⁹, and acute kidney injury stage 2–3 in decompensated HF¹². However, other studies have reported decreased levels of TIMP-2 in patients with coronary artery disease (CAD)¹³ and systolic HF^14,15 and in those who died from or were admitted for HF following mitral valve surgery¹⁶.

Several functional polymorphisms identified in the MMP gene promoters have been found to be associated with clinical outcomes in patients with LV remodelling and failing hearts⁶. In a previous study, we showed that high serum levels of MMP-9 are associated with carotid plaque vulnerability and stroke in patients who underwent endarterectomy¹⁷. In other studies, we also observed a lower rate of HF-related death in HF patients who carried the 2 G allele of the −1607 1 G/2 G polymorphism in the MMP-1 gene¹⁸, the TT genotype of the −790 G > T polymorphism in the MMP-2 gene¹⁹, or the 6 A allele of the −1171 5 A/6 A polymorphism in the MMP-3 gene¹⁸ than patients with other genotypes. Considering our previous findings and the role of MMPs and TIMPs in HF pathogenesis, we decided to expand our study by investigating the association of TIMP gene variants with HF.

TIMP-1 is located on the Xp11.23–11.4 chromosome, while TIMP-2 is located on the 17q23-25 chromosome^9,10. The T allele of the 372 T > C silent mutation at exon 5 of the TIMP-1 gene (Phe124Phe) is associated with spontaneous deep intracerebral haemorrhage in elderly Taiwanese males²⁰, increased serum levels of TIMP-1, and a higher mortality rate at 30 days from intensive care unit admission in Caucasians with severe sepsis²¹. In the context of LV dysfunction, however, the 372 T > C polymorphism was not associated with AMI, CAD²², acute HF²³, or adverse prognosis in patients with ST elevation myocardial infarction²⁴. The C allele of the G > C transversion at nucleotide position −418 of the TIMP-2 gene promoter is thought to down-regulate gene expression by abolishing the Sp1 binding site²⁵. The C allele was associated with increased magnitude of QT and QTc dispersion prolongation in a healthy elderly Chinese cohort²⁶, increased susceptibility to atrial fibrillation in Chinese Han patients with hypertensive heart disease, and reduced plasma levels of TIMP-2²⁷. To the best of our knowledge, no study has investigated the association between TIMP gene polymorphisms and chronic HF. Therefore, we tested the hypothesis that the 372 T > C polymorphism (Phe124Phe; rs4898) in the TIMP-1 gene and the −418 G > C polymorphism (rs8179090) in the TIMP-2 gene are associated with HF susceptibility, all-cause death, and/or HF-related death in Brazilians with reduced LV ejection fraction (LVEF).

Results

Association of the 372 T > C polymorphism with HF susceptibility and clinical profile

The genotype frequencies were in agreement with those predicted by the Hardy-Weinberg equilibrium for the 372 T > C polymorphism in the TIMP-1 gene in both HF patients and healthy blood donors. The genotype and allele frequencies in HF patients were not significantly different from those observed in blood donors (Table 1). The frequencies of the T and C alleles also did not differ between male and female HF patients (P = 0.561) or blood donors (P = 0.907). Regarding the −418 G > C polymorphism in the TIMP-2 gene, only five heterozygous subjects (GC) were found among the 263 HF patients (n = 4) and 260 blood donors (n = 1) genotyped for this polymorphism. The four heterozygous patients were males and the heterozygous blood donor was a female. All the other subjects were homozygotes for the G allele. Thus, this gene variant could not be further analysed.

Table 1.

Comparison of genotype and allele frequencies of the 372 T > C polymorphism between healthy blood donors and heart failure (HF) patients stratified by gender.

	Blood donors (n = 304)	HF patients (n = 300)	P*
Females
Genotype	n = 93	n = 99
TT, n (%)	26 (28.0)	39 (39.4)	0.226
TC, n (%)	47 (50.5)	40 (40.4)
CC, n (%)	20 (21.5)	20 (20.2)
Allele	n = 186	n = 198
T, n (%)	99 (53.2)	118 (59.6)	0.248
C, n (%)	87 (46.8)	80 (40.4)
Males	n = 211	n = 201
T, n (%)	110 (52.1)	113 (56.2)	0.463
C, n (%)	101 (47.9)	88 (43.8)

*P-values were calculated using the Pearson chi-square test with Yates correction where appropriate.

Subjects included in this study were predominantly male (69.4% and 67.0% of blood donors and HF patients, respectively; P = 0.584) and white (78.3% and 71.3% of blood donors and HF patients, respectively; P = 0.061). Blood donors were younger than HF patients (mean age of 48 ± 10 and 60 ± 13, respectively; P < 0.001). The baseline demographic and clinical characteristics of HF patients according to the presence of the 372 T allele in the TIMP-1 gene are shown in Table 2. Patients were in New York Heart Association (NYHA) class I or II and had predominantly ischaemic aetiology and moderate to severe left ventricular dysfunction. Approximately one-third of the patients had comorbidities such as prior AMI and diabetes mellitus.

Table 2.

Comparison of the baseline profile of HF patients with and without the T allele of the 372 T > C polymorphism.

	All patients (n = 300)	CC + C (n = 108)	TT + TC + T (n = 192)	P*
Age (years, mean ± SD)	60 ± 13	59 ± 12	60 ± 13	0.424
White, n (%)	214 (71.3)	73 (67.6)	141 (73.4)	0.346
HF aetiology
Ischaemic, n (%)	109 (36.3)	41 (38.0)	68 (35.4)	0.753
Idiopathic, n (%)	88 (29.3)	30 (27.8)	58 (30.2)	0.755
Hypertensive, n (%)	72 (24.0)	23 (21.3)	49 (25.5)	0.496
NYHA classes I and II, n (%)†	231 (78.3)	85 (79.4)	146 (77.7)	0.834
Prior myocardial infarction, n (%)	97 (32.3)	32 (29.6)	65 (33.9)	0.534
History of smoking, n (%)	139 (46.3)	56 (51.9)	83 (43.2)	0.188
Diabetes mellitus, n (%)	90 (30.0)	32 (29.6)	58 (30.2)	>0.999
Electrocardiogram
QRS duration (ms, mean ± SD)	129 ± 35	127 ± 34	130 ± 35	0.664
Atrial fibrillation, n (%)‡	71 (24.1)	28 (26.2)	43 (23.0)	0.638
Left bundle branch block, n (%)§	84 (28.7)	22 (20.8)	62 (33.2)	0.034
Right bundle branch block, n (%)§	16 (5.5)	8 (7.5)	8 (4.3)	0.360
Echocardiography
LVEF (%, mean ± SD)	31 ± 8	32 ± 8	31 ± 8	0.537
LVEDD (mm, mean ± SD)	6.6 ± 0.9	6.7 ± 0.9	6.6 ± 0.9	0.185
LVESD (mm, mean ± SD)	5.6 ± 1.0	5.7 ± 1.0	5.5 ± 1.0	0.084
Creatinine (µmol/L, mean ± SD)	113 ± 40	114 ± 42	112 ± 39	0.796
Urea (mmol/L, median [25th–75th percentiles])	17 [13−24]	15 [12−22]	18 [14−27]	0.019
Sodium (mEq/L, mean ± SD)	140 ± 3	140 ± 3	140 ± 4	0.270
Haemoglobin (g/dL, mean ± SD)	13.1 ± 1.7	13.3 ± 1.8	13.0 ± 1.6	0.209
HF medications
Beta-blocker, n (%)	266 (88.7)	97 (89.8)	169 (88.0)	0.779
ACE inhibitor, n (%)	263 (87.7)	96 (88.9)	167 (87.0)	0.764

Abbreviations: HF, heart failure; NYHA, New York Heart Association; LVEF, left ventricular ejection fraction; LVEDD, left ventricular end-diastolic diameter; LVESD, left ventricular end-systolic diameter; and ACE, angiotensin-converting enzyme. *P-values were calculated using the Mann-Whitney U test for continuous variables and the Pearson chi-square test for categorical variables, with Yates correction where appropriate. ^†Data available for 107 and 188 patients without and with the T allele, respectively. ^‡Data available for 107 and 187 patients without and with the T allele, respectively. ^§Data available for 106 and 187 patients without and with the T allele, respectively.

In general, carriers of the 372 T allele had a similar clinical profile to that of female homozygotes and male hemizygotes for the C allele. However, subjects with the T allele more often had left bundle branch block and higher blood urea levels than females with the CC genotype or males with the C allele (Table 2). Considering the left bundle branch block as an outcome, we observed that the T allele was more frequent in males with left bundle branch block than in those who did not have this conduction disorder (see Supplementary Table S1). After controlling for skin colour (white/non-white), age, LVEF, haemoglobin level, and jugular venous pressure, the T allele did not remain associated with left bundle branch block in the multiple logistic regression analysis (adjusted odds ratio, 1.91; 95% confidence interval, 0.86−4.28; P = 0.114).

Association of the 372 T > C polymorphism with HF prognosis

Patients were followed-up for a median duration of approximately 5.5 years (ranging from 1 month to 15 years). During this period, 121 patients (40.3%) died (67 of them from HF). The overall mortality rate was not different between males and females (42.8% vs. 35.4%, respectively; P = 0.268). Figure 1 shows the survival curves for all-cause death (A and B) and HF-related death (C and D) in females and males according to the 372 T > C polymorphism in the TIMP-1 gene. Although females who carried the T allele had a worse prognosis than those who were homozygous for the C allele (Fig. 1a), this difference in survival was not significantly different. Among males, survival curves were quite similar between patients hemizygous for the T and C alleles (Fig. 1b and d).

Figure 1.

Survival curves for females (a and b) and males (c and d) for all-cause death and HF-related death, respectively, according to the 372 T > C polymorphism in the TIMP-1 gene.

Discussion

In this study, we evaluated the 372 T > C (Phe124Phe) polymorphism in the TIMP-1 gene and the −418 G > C polymorphism in the TIMP-2 gene in 300 HF patients with reduced LVEF and 304 healthy blood donors from the State of Rio Grande do Sul (Southern Brazil). We did not find an association between the 372 T > C polymorphism in the TIMP-1 gene and HF susceptibility or mortality among HF patients. Moreover, the presence of the C nucleotide at position −418 in the TIMP-2 gene was very rare in our population.

Although several studies have reported that increased expression of TIMP-1 is associated with echocardiographic parameters of LV systolic dysfunction^28–33 and worse prognosis in HF patients^{30,31,33–38}, to the best of our knowledge, no study has investigated the association between gene polymorphisms of TIMPs and chronic HF. In the context of HF, Goldbergova et al.²³ evaluated the relationship of gene polymorphisms and serum levels of TIMP-1 with AMI, LV dysfunction and symptoms of acute HF in patients with ST elevation treated with primary percutaneous coronary intervention in the Czech population (Caucasians). TIMP-1 levels were higher in males with acute HF as well as in males with reduced LVEF (<40%). However, TIMP-1 levels did not differ depending on the 372 T > C polymorphism, and this polymorphism was not independently associated with LV dysfunction post-AMI (acute HF) after adjusting for clinical and laboratory covariates²³. In a more recent report from Goldbergova et al.²⁴ in the same study population, there was no evidence of association between the 372 T > C polymorphism and a composite endpoint, including hospitalisation due to acute decompensated HF and all causes of death, in the cohort followed-up for a median of 32 months.

In our study, genotype and allele frequencies of the 372 T > C polymorphism were not different between HF patients and healthy blood donors. Similarly, most of the clinical, electrocardiographic, echocardiographic, and laboratory parameters did not differ between carriers of the T allele and subjects without the T allele. These findings indicate that the 372 T > C polymorphism is not associated with the occurrence of HF or AMI (clinical event previously suffered by one-third of the patients), which is also in accordance with the results reported by Horne et al.²². The North-American study evaluated the association of different polymorphisms in seven genes encoding MMPs and TIMPs -1, -2, and -3 with AMI in more than 5000 patients (92% Caucasians) who underwent coronary angiography in tertiary hospitals in Utah. No association of the 372 T > C polymorphism with AMI or CAD was detected in that population²².

Regarding HF prognosis, considering that TIMP-1 levels are increased in patients with systolic dysfunction and worse prognosis and the T allele of the 372 T > C polymorphism is associated with increased TIMP-1 levels, the T allele is expected to be associated with HF susceptibility or a higher mortality rate among HF patients. In our study, the survival analysis showed that female carriers of the T allele seemed to have a higher rate of all-cause death than females homozygous for the C allele, mainly between the sixth and the tenth year of follow-up. However, the difference in survival according to the 372 T > C genotype was not statistically significant. Considering that the frequency of the T allele carriers was 63% among patients who were alive at the end of follow-up (males and females), our study had a statistical power of 79.6% to detect an odds ratio = 2.08 related to all-cause death, as reported by Lorente et al.²¹ in patients with severe sepsis.

The T allele of the 372 T > C polymorphism, which is possibly associated with increased levels of TIMP-1 and worse prognosis, showed a frequency of 53% in the general population (blood donors) from Rio Grande do Sul, which is identical to the frequency detected in the 1000 Genomes Project (database available at https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=4898). Moreover, genotype and allele frequencies of the 372 T > C polymorphism did not differ between white and non-white HF patients or blood donors in our study (see Supplementary Table S2). Regarding the −418 G > C polymorphism in the TIMP-2 gene, the rarity of the C allele in our study population (frequency of 0.8% among HF patients and 0.2% among blood donors) is in accordance with the frequency observed in South-eastern Brazilians without Japanese descent and Europeans³⁹, in whom the frequency of the C allele is 0.5% (https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=8179090).

Because it is located on the X chromosome¹⁰, it is expected that the TIMP-1 gene would have the same level of expression in both males and females due to the X chromosome inactivation phenomenon. However, cell culture studies have shown that the TIMP-1 gene is one of the human genes that escape from X inactivation and is expressed in both the active and inactive X chromosomes, although expression from the latter allele is more variable and may be lower than from the former allele⁴⁰. Moreover, inactivation of the TIMP-1 gene is variable (polymorphic), as some females express both alleles, whereas in others, only the allele in the active chromosome is expressed, which can lead to differences in TIMP-1 expression among homozygous and heterozygous females⁴¹.

Protein levels are also influenced by the transcription rate, mRNA stability, and translation^42,43. Even though it is a silent (synonymous) variant, a functional effect of the 372 T > C polymorphism (Phe124Phe) on the activity of TIMP-1 in the myocardium cannot be ruled out. Although the synonymous mutation has no effect on the sequence of the synthesised protein, its presence can lead to changes in expression, conformation, or substrate specificity, thereby impacting the physiological function of the protein. Approximately 40 diseases affecting different organs and systems have been associated with synonymous mutations. Experimental studies and computational predictions show that there are different mechanisms by which a synonymous mutation can affect the synthesis of an active and correctly folded protein. These mechanisms include changes in the splicing pattern (exon skipping), mRNA secondary structure and stability, and the translation rate due to codon usage bias and altered microRNA binding sites⁴². As the functionality of the 372 T > C polymorphism has not yet been tested, it is unknown how this variant would affect the synthesis of TIMP-1. In addition, the 372 T > C polymorphism may be in linkage disequilibrium with other variants in the same gene whose function may be affected in the presence of two or more synonymous mutations^42,44.

Our findings should be interpreted with consideration of some limitations. The retrospective design (case-control) of our study regarding HF susceptibility does not allow us to examine whether the 372 T > C polymorphism in the TIMP-1 gene influences LV remodelling and HF onset or which allele would be involved in these processes. Due to our focus on systolic dysfunction, we did not collect data on diastolic function of left ventricle, which is another limitation of this study. Although our study had sufficient statistical power for the analysis of mortality as an outcome, the reduced sample size did not allow us to analyse potential modifiers that might contribute to HF variability, such as age and cardiomyopathy aetiology. Apart from this, quantification of the serum levels of TIMP-1 would also help to clarify the functionality of the 372 T > C polymorphism or, at least, the link between this gene variant and TIMP-1 expression. This is the major limitation of our study, as the relationship of the 372 T > C polymorphism with TIMP-1 levels is still doubtful and there is no clear evidence showing this link. Despite all limitations, this was the first study to investigate a polymorphism in the TIMP-1 gene in a cohort of patients with chronic HF who underwent long-term follow-up (up to 15 years). In conclusion, the 372 T > C polymorphism (Phe124Phe; rs4898) in the TIMP-1 gene and the −418 G > C polymorphism (rs8179090) in the TIMP-2 gene are associated with neither HF susceptibility nor survival in HF patients with reduced LVEF in a population from South Brazil.

Methods

Study population

A total of 300 adults with HF of any aetiology and a reduced LVEF (≤45%) were included in this study. HF was diagnosed according to the ACCF/AHA guidelines⁴⁵, and all patients were enrolled consecutively between July 2003 and November 2007 in the Heart Failure and Transplant Outpatient Clinic of a tertiary care university hospital (HCPA) in Porto Alegre, Brazil. Patients underwent a comprehensive clinical and laboratory evaluation consisting of a physical examination, assessment of electro- and echocardiographic parameters, and laboratory exams at baseline. Briefly, two-dimensional transthoracic echocardiography with M-mode and Doppler examination was performed using an adult transducer and a commercial ultrasound system (Philips EnVisor, Andover, USA). Echocardiography was performed by experienced staff cardiologists in the non-invasive cardiac unit of HCPA, as part of the routine management of HF patients, following the recommendations of the American Society of Echocardiography for LVEF estimations⁴⁶. Ischaemic aetiology was defined as previously described¹⁸. A questionnaire was used to collect data on medical history, such as the age at HF diagnosis, smoking habits, presence of comorbidities, and use of medication. Patients were followed in the outpatient clinic at our institution, and their vital status was assessed using hospital records, by telephone contact, or using the State Death Certificate Database. The prognostic endpoints of interest were all-cause death and HF-related death, which was defined as sudden unexpected death (within 1 h of symptom onset) or death caused by advanced refractory disease. Survival data were last updated on April 2014.

We also enrolled 304 unrelated blood donors in the same hospital during the same period as the HF patients. Subjects with a history of cardiovascular disease or related symptoms and those with a positive family history of premature sudden death were not included in the study, and no additional laboratory data were collected from them. Skin colour/ethnicity of all subjects was self-reported and categorized as white or non-white (pardo or black). All experiments were performed in accordance with the relevant guidelines and regulations. The study was approved by the hospital ethics committee (Institutional Review Board [IRB] 0000921 – application number 03–237), and all subjects provided written informed consent prior to their participation.

Genotyping

Genomic DNA was isolated from peripheral blood leukocytes using the salting out procedure described by Lahiri & Nurnberger⁴⁷. Genotypes of the 372 T > C polymorphism in the TIMP-1 gene were determined by real-time polymerase chain reaction (PCR) using the probes and primers provided in the Human Custom TaqMan Genotyping Assay (forward: 5′-GGACTCTTGCACATCACTACCT-3′ and reverse: 5′-GCTAAGCTCAGGCTGTTCCA-3′; Life Technologies, Carlsbad, USA). The probe for the C allele was labelled with FAM dye (5′-AGCCACGAAACTG-3′), while the probe for the T allele was labelled with VIC dye (5′-AGCCACAAAACTG-3′). Amplification reactions were performed in optical tubes in a total volume of 10 µL, containing 2 ng of genomic DNA, 1× TaqMan Genotyping Master Mix, and the 1× genotyping assay. Optical tubes were loaded into a real-time PCR thermal cycler (StepOnePlus; Life Technologies) and heated at 95 °C for 10 min followed by 40 cycles of denaturation at 95 °C for 15 s and annealing/extension at 63 °C for 1 min. Fluorescence data from each run were analysed with the StepOne software version 2.3 (Life Technologies).

Genotypes of the −418 G > C polymorphism in the TIMP-2 gene were determined by the PCR and restriction fragment length polymorphism (PCR-RFLP) method using the primers previously described by Yi et al.⁴⁸ in the amplification reactions and the BsoBI restriction enzyme to digest the amplified fragments (New England Biolabs, Ipswich, USA).

Amplification reactions were done in a total volume of 25 μL containing 50 to 100 ng DNA, 0.3 μM each primer, 1× PCR buffer, 1.5 mM MgCl₂, 200 mM each dNTP, and 1 U Taq DNA polymerase (Fermentas Life Sciences, Burlington, USA). After the initial denaturation step for 3 min at 94 °C, the reaction mixture was subjected to 35 cycles of 40 s at 94 °C, 40 s at 63 °C, and 40 s at 72 °C, followed by a final extension step of 3 min at 72 °C. PCR products were subjected to overnight digestion with 5 U BsoBI following the manufacturer’s instructions (New England Biolabs, Ipswich, USA). The 304-bp amplicon with the C allele is cleaved into fragments of 253 and 51 bp, whereas the G allele creates an additional restriction site, thus generating fragments of 230, 51 and 23 bp. The resulting digested fragments were electrophoresed on 8% polyacrylamide gels and then stained with silver nitrate. To improve genotyping accuracy, a DNA sample of each genotype was used in all runs to serve as a positive control, and the investigators who independently identified the genotypes (E.R.P. and R.C.S.) were blinded to the clinical and laboratory data of the patients. However, we did not repeat the genotyping in a randomly chosen subgroup of subjects.

Statistical analyses

Continuous data are expressed as the mean ± standard deviation (SD) or median (25^th–75^th percentiles) and were compared between the groups using the Mann-Whitney U test. The Shapiro-Wilk test was used to verify the normality of quantitative variables. Categorical variables, including the genotype and allele frequencies, are expressed as an absolute frequency (percentage) and were compared between groups with the Pearson chi-square test; the Yates correction was applied for the comparisons involving 2 × 2 contingency tables. Allele frequencies were determined by gene counting, and departures from Hardy-Weinberg equilibrium were also verified using the chi-square test.

The association of the 372 T > C polymorphism in the TIMP-1 gene with all-cause and HF-related death was evaluated by Kaplan-Meier survival analysis. Survival curves were constructed based on the period between the date of the first visit at the outpatient clinic and the last registry of follow-up or death. Survival curves obtained for the different genotypes were compared by the log-rank test. Wherever needed, logistic regression analysis was used to assess the association of the 372 T > C polymorphism with the clinical profile of HF patients. Statistical analyses were performed using SPSS (version 18.0; SPSS Inc., Chicago, USA) and WinPEPI (version 11.43)⁴⁹ statistical software. Two-tailed P-values < 0.05 were considered statistically significant.

Data availability

Relevant raw data are included in the Supplementary Information files (see Supplementary Data). Age, skin colour, and other variables that could identify the study participants were omitted to protect their confidentiality and privacy.

Author Contributions

R.R.C.V.A. and K.G.S. conceived the study design and performed the statistical analyses. R.C.S. performed the genotyping experiments and identified the genotypes. E.R.P. identified the genotypes, updated the database, helped draft the manuscript, edited the manuscript, and prepared Figure 1. L.E.R. and N.C. enrolled the patients and contributed reagents/funding resources. A.B. enrolled the patients, collected the clinical data and updated the patient database. K.G.S. supervised the study, interpreted the data, and wrote the paper. All authors reviewed the manuscript.

Competing Interests

The authors declare no competing interests.