T1 values and extracellular volume fraction in asymptomatic subjects: variations in left ventricular segments and correlation with cardiovascular risk factors

Abstract

To evaluate variations in pre-contrast (preT1) and post-contrast (postT1) myocardial T1 values and extracellular volume fraction (ECV) according to left ventricular (LV) segments and to find correlations between them and cardiovascular risk factors. The 233 asymptomatic subjects (210 men, 23 women; aged 54.1 ± 6.0 years) underwent cardiac magnetic resonance imaging with preT1 and postT1 mapping on a 1.5-T scanner. T1 values and ECVs were evaluated according to LV segments, age, sex, and estimated glomerular filtration rate (eGFR). Based on the presence of hypertension (HTN) and diabetes mellitus (DM), subjects were subdivided into the control, HTN, DM, and HTN and DM (HTN-DM) groups. T1 values and ECV showed significant differences between septal and lateral segments at the mid-ventricular and basal levels (p ≤ 0.003). In subgroup analysis, the HTN-DM group showed a significantly higher ECV (0.260 ± 0.023) than the control (0.240 ± 0.021, p = 0.011) and HTN (0.241 ± 0.024, p = 0.041) groups. Overall postT1 and ECV of the LV had significant correlation with eGFR (r = 0.19, p = 0.038 for postT1; r =  − 0.23, p = 0.011 for ECV). Septal segments show higher preT1 and ECV but lower postT1 than lateral segments at the mid-ventricular and basal levels. ECV is significantly affected by HTN, DM, and eGFR, even in asymptomatic subjects.

Introduction

Myocardial fibrosis (MF) is closely linked to various adverse cardiovascular events¹. Recent research has found that “diffuse” fibrosis is more intimately correlated with poor outcomes, such as mortality or hospitalization, than “focal” fibrosis^2,3. Even though the biopsy is the gold standard for confirming MF, native and post-contrast T1 mapping via the modified look-locker inversion recovery (MOLLI) sequence has become a foundational method for detecting MF and infiltrative processes^4,5. Native T1 value and extracellular volume fraction (ECV) on cardiac magnetic resonance imaging (CMR) correlate well with the histological quantification of MF on a region-of-interest (ROI) basis^4,6–9.

According to meta-analyses, pooled means of T1 values and ECV in normal subjects showed almost the same ECV and heterogeneous T1 values, and hypertension (HTN) yielded native T1 values and ECV similar to normal subjects^10,11. However, they have not been evaluated segmentally, which could serve as reference values to evaluate localized myocardial abnormalities.

Recent reports have described a possible correlation between MF, demonstrated by elevated native T1 or ECV, and cardiovascular risk factors, such as HTN, diabetes mellitus (DM), and chronic renal disease^3,12–16. As pressure overload of the left ventricle (LV) induces accelerated collagen synthesis and breakdown, MF is followed by left ventricular hypertrophy (LVH) in hypertensive heart disease^3,17. One of the hallmarks of diabetic heart disease is diffuse interstitial MF, generated by increased collagen type III in the perimysium and perivascular regions¹⁸. Decreased glomerular filtration causes various organs to produce pro-fibrotic substances, leading to progress MF^15,19. However, few studies have demonstrated alterations of T1 values and ECV in subjects with subclinical manifestations of those cardiovascular risk factors.

Therefore, this study aimed to report the variation in pre-contrast and post-contrast myocardial T1 values (preT1 and postT1, respectively) and ECV according to LV segments and evaluate any correlation between T1 values and cardiovascular risk factors in asymptomatic subjects.

Results

The baseline characteristics and CMR LV measurements of the subjects and subgroups divided by their status of cardiovascular risk factors are shown in Table 1. The age of total subjects ranges from 40 to 80 years. Except for body mass index (BMI), blood pressure, and glycosylated hemoglobin (HbA1c), there was no statistically significant difference between subgroups with respect to each characteristic. The HTN and DM (HTN-DM) and HTN groups showed higher BMI, systolic blood pressure (SBP), diastolic blood pressure (DBP), and the DM and HTN-DM groups demonstrated higher HbA1c than the rest subgroups (p < 0.05).

Table 1.

Baseline characteristics and cardiac magnetic resonance measurements of study population.

Subgroup	Control group (n = 121, 51.9%)	HTN (n = 58, 24.9%)	DM (n = 25, 10.7%)	HTN-DM (n = 29, 12.4%)	p-value	Total (n = 233)
Baseline characteristics
Age (years)	53.2 ± 4.98	55.8 ± 7.56	54.5 ± 5.56	54.5 ± 6.16	0.051	54.1 ± 5.97
Male	108 (87.8%)	53 (93.0%)	22 (91.7%)	27 (93.1%)	0.111	210 (90.1%)
BSA (m2)	1.83 ± 0.13	1.83 ± 0.15	1.79 ± 0.12	1.90 ± 0.17	0.076	1.83 ± 0.14
BMI (kg/m2)	24.3 ± 2.11	25.4 ± 2.53*‡	23.9 ± 2.54	26.7 ± 3.40*‡	< 0.001	24.8 ± 2.59
Heart rate (bpm)	66.0 ± 10.4	69.0 ± 12	68.5 ± 10.4	67.7 ± 11.3	0.330	67.2 ± 11.0
SBP (mmHg)	114 ± 14.3	125 ± 17.3*‡	114.6 ± 13.0	122 ± 17.4*‡	< 0.001	117 ± 16.0
DBP (mmHg)	76.0 ± 9.32	81.9 ± 10.2*‡	73.6 ± 9.41	79.0 ± 8.05‡	< 0.001	77.6 ± 9.76
Hematocrit (%)	44.1 ± 3.19	44.7 ± 2.99	44.9 ± 2.78	44.3 ± 2.73	0.773	44.3 ± 3.04
Hb (g/L)	15.0 ± 1.19	15.2 ± 1.12	15.3 ± 1.22	15.1 ± 1.06	0.656	15.1 ± 1.16
Hb A1c (%)	5.42 ± 0.22	5.30 ± 0.40	6.42 ± 0.53*†	6.21 ± 0.48*†	< 0.001	5.60 ± 0.36
eGFR (mL/min/1.73 m2)	83.5 ± 11.3	81.8 ± 15.6	83.6 ± 14.4	85.0 ± 10.2	0.720	83.3 ± 12.7
Dyslipidemia	70 (57.9%)	37 (63.8%)	11 (44.0%)	19 (65.5%)	0.269	137 (58.8%)
Hypertension	0	58 (100%)	0	29 (100%)		87 (37.3%)
Diabetes	0	0	25 (100%)	29 (100%)		54 (23.2%)
Left ventricular measurements
EF (%)	65.75 ± 4.81	65.70 ± 5.79	65.25 ± 6.52	67.78 ± 6.07	0.378	65.9 ± 5.43
EDVi (mL/m2)	70.01 ± 10.22	67.79 ± 11.00	68.36 ± 8.24	67.68 ± 8.02	0.439	69.0 ± 9.99
ESVi (mL/m2)	24.16 ± 5.74	23.43 ± 6.25	23.90 ± 6.09	22.10 ± 5.85	0.391	23.7 ± 5.92
SVi (mL/m2)	59.21 ± 10.48	62.70 ± 11.78	54.82 ± 11.08	55.17 ± 10.98	0.097	59.1 ± 11.2
CI (L/min/ m2)	3.01 ± 0.44	3.01 ± 0.50	3.06 ± 0.28	3.22 ± 0.46	0.167	3.04 ± 0.45
ED MASSi (g/m2)	61.35 ± 10.89	65.45 ± 11.56	60.61 ± 9.16	63.24 ± 8.94	0.114	62.5 ± 10.8

BMI body mass index; CI cardiac index; DM diabetes mellitus; DBP diastolic blood pressure; ED MASSi indexed end-diastolic myocardial mass; EDVi indexed end-diastolic volume; EF ejection fraction; ESVi indexed end-systolic volume; eGFR estimated glomerular filtration rate; Hb hemoglobin; HTN hypertension; SBP systolic blood pressure; SVi indexed stroke volume.

Continuous values are presented as mean ± standard deviation.

The proportion of a numeric value is described in parenthesis.

* p < 0.05 versus control group.

^† p < 0.05 versus HTN group.

^‡ p < 0.05 versus DM group.

Segmental analysis of T1 values and ECV

The mean T1 values and ECV with standard deviations for all 16 American Heart Association segments are shown in Fig. 1 and Supplementary Table S1. The overall intraclass correlation coefficient (ICC) for each segmental T1 value was 0.82 (p < 0.001). The ICC (0.64–0.80) for T1 value of each apical segment was significantly poorer than that (0.79–0.88) of each basal and mid-ventricular segment (p < 0.001, respectively). PreT1, postT1, and ECV of global LV myocardium were 989 ± 41 ms, 454 ± 38 ms, and 0.245 ± 0.024, respectively.

Figure 1.

Mean segmental pre-contrast T1 value and mean extracellular volume fraction (ECV) of the left ventricle (LV). (A) Total study population. (B) Male. (C) Female. Pre-contrast T1 value and ECV were significantly higher in women than in men in global LV segments (p < 0.05) except apical inferior segment.

PreT1 and ECV revealed significantly higher values in the septal wall than in the lateral wall at the basal and mid-ventricular levels of the LV myocardium (p < 0.05, Table 2). However, postT1 values in the septal wall were significantly lower than those in the lateral wall at the basal and mid-ventricular levels of the LV myocardium (p < 0.05, Table 2).

Table 2.

Comparing T1 values and ECVs between the septal and lateral walls.

	PreT1			PostT1			ECV
	Septal	Lateral	p	Septal	Lateral	p	Septal	Lateral	p
Basal	992 ± 50	980 ± 52	0.001	458 ± 45	471 ± 40	< 0.001	0.240 ± 0.031	0.225 ± 0.026	< 0.001
Middle	998 ± 48	985 ± 61	0.003	454 ± 39	463 ± 40	< 0.001	0.242 ± 0.028	0.236 ± 0.035	< 0.001
Apical	989 ± 84	1011 ± 77	< 0.001	433 ± 50	430 ± 44	0.150	0.270 ± 0.048	0.278 ± 0.047	0.005
Mean	985 ± 48	992 ± 49	0.014	448 ± 41	454 ± 38	< 0.001	0.251 ± 0.029	0.246 ± 0.028	0.001

ECV extracellular volume fraction; PreT1 pre-contrast myocardial T1 value; PostT1 post-contrast myocardial T1 value.

Values are presented as mean ± standard deviation.

Comparisons of T1 values and ECV for age and sex

PreT1, postT1, and ECV of global LV myocardium in male were 984 ± 40 ms, 457 ± 36 ms, and 0.241 ± 0.021, respectively. Those in female were 1029 ± 25 ms, 443 ± 51 ms, and 0.280 ± 0.026, respectively. PreT1 and ECV were significantly higher in women than in men in all LV segments (p < 0.05, Fig. 1, Supplementary Table S1), except for the apical inferior segment (p = 0.053). However, postT1 showed no significant difference between male and female subjects (p ≥ 0.061).

There was no statistically significant difference in T1 values and ECV of the four age groups divided into quantiles (group 1 ≤ 50 years, n = 68; 50 years < group 2 ≤ 53 years, n = 58; 53 years < group 3 ≤ 56 years, n = 51; group 4 > 56 years, n = 56) (994 ± 46, 987 ± 40, 990 ± 45, and 991 ± 33 for preT1, p = 0.77; 451 ± 33, 454 ± 34, 446 ± 43, and 449 ± 43 for postT1, p = 0.95; 0.243 ± 0.029, 0.245 ± 0.027, 0.246 ± 0.021, and 0.245 ± 0.030 for ECV, p = 0.41, respectively) and no significant correlation (p > 0.46 for T1 values and ECV). In total population nor each sex group, there was no significant linear correlation between the age and T1 values or ECV (preT1, p = 0.58; postT1, p = 0.88; ECV, p = 0.45).

Relations between T1 values and cardiovascular risk factors

A dot scatter plot of ECV with error bars indicating two standard deviations from the average reveals that the HTN-DM group showed significantly higher ECV (0.260 ± 0.023) than the control group (0.240 ± 0.021, p = 0.011) and the HTN group (0.241 ± 0.024, p = 0.041) (Fig. 2). There was a tendency for the ECV to increase among the subgroups in the following order: control, HTN, DM, and HTN-DM groups (p = 0.001). BMI nor dyslipidemia did not affect T1 values and ECVs statistically in the entire population and each subgroup (p > 0.05). PostT1 and ECV of the LV in the control group showed significant correlations to estimated glomerular filtration rate (eGFR) (r = 0.19 p = 0.038 for postT1; r =  − 0.23, p = 0.011 for ECV; Fig. 3). PreT1 demonstrated no significant correlation to eGFR (p = 0.100).

Figure 2.

Relation of extracellular volume fraction (ECV) with hypertension (HTN) and diabetes mellitus (DM). HTN-DM group showed significantly higher ECV (0.260 ± 0.023) than control (0.240 ± 0.021, p = 0.011) and HTN groups (0.241 ± 0.024, p = 0.041). Error bars indicate 2 standard deviations (SDs) from average.

Figure 3.

Relation of post-contrast T1 (PostT1) value and extracellular volume fraction (ECV) with glomerular filtration rate (GFR) in the control group. Overall PostT1 and ECV of left ventricle were proportional to GFR (A: r = 0.19, p = 0.038 for PostT1, B: r =  − 0.23, p = 0.011 for ECV).

Discussion

In this study, we presented reference values for native T1 relaxation time and ECV according to LV segments in asymptomatic subjects using a 1.5 T MR system. We found segmental variation in the myocardial tissue composition using CMR T1 mapping in asymptomatic subjects. The HTN-DM group showed a significantly higher ECV than the control and HTN groups. PostT1 and ECV of the LV showed significant correlations to eGFR.

MF is commonly associated with cardiac hypertrophy and failure and is associated with worsening ventricular systolic function, abnormal cardiac remodeling, and increased ventricular stiffness in animal models²⁰. Although endocardial biopsy is the most specific procedure for measuring MF, it is invasive, and its sensitivity is low due to sampling errors²¹. CMR T1 mapping may serve as a noninvasive biopsy and collagen volume fraction (CVF) was associated with preT1 and ECV in an animal model of MF^22,23.

In a pooled summary of 954 healthy subjects from the literature, 3-T showed longer T1 than 1.5-T with MOLLI variant sequences by approximately 100–200 ms. ECV of the healthy subjects was consistent among the studies (25–27%), irrespective of subject factors, sequences, vendors, and contrast types¹¹. In a recent study, normal myocardial T1 reference ranges were reported as follows; at 3-T: 1129–1309 ms and at 1.5-T: 933–1020 ms (males) and 965–1054 ms (females), which tend to be similar to our findings²⁴.

Our finding included segmental variations in T1 values and ECV, especially between septal and lateral segments. Motion during the T1 map acquisition may induce a poor T1 model fit and falsely deviated T1 values and ECV, because T1 maps are generated from a sequential series of images²⁵. Lateral wall is more vulnerable to partial volume effects which may be a potential cause of the lower preT1 and ECV and the higher postT1 in the lateral segments.^26–29. In addition, considering low reproducibility of apical T1 values, it may be reasonable to measure T1 values in basal to middle septal walls²⁸.

Based on the result that preT1 and ECV were substantially higher in the septal wall than in the lateral wall at the basal and mid-ventricular levels of the LV myocardium, the thresholds of T1 and ECV for detecting MF or infiltrative disease at the lateral wall might be different from those at the septal wall. If the pathologic development and progression of myocardial disease are gradual, the very initial involvement of sarcoidosis or myocarditis at the lateral wall might be underestimated based on the reference values of the septal wall^30,31. However, further investigations into this theory should be warranted as the T1 and ECV differences between septal and lateral walls might be subtler than those between normal and overt myocardial disease^32,33.

On the other hand, in terms of LV anatomy or pathophysiology, there is no obvious consensus associated with variation of native T1 or ECV between septal and lateral segments. The cardiac skeleton and septal branches of the coronary artery may be partly accountable for increased T1 and ECV in the basal septum^34,35. The myocardial perfusion difference between the septum and non-septal wall might also contribute to the variations in native T1^36,37.Given that cardiac diseases with MF, such as hypertrophic cardiomyopathy, dilated cardiomyopathy, and pulmonary HTN, show increased native T1 and ECV, and late gadolinium enhancement (LGE), more frequently at the septal wall, it might be possible that the fibrotic remodeling of the LV starts earlier at the septum than the lateral wall^38–40.

Sex hormones may influence myocardial structure and function^41,42. Especially, a previous study demonstrated that estradiol attenuates myocardial hypertrophy⁴³. Similar to prior literature, our observations of higher preT1 and ECV of females than those of males may suggest that sex hormones affect myocardial histology^26,44. However, since the proportion of females in this study is small (9.9%), that result should be extrapolated carefully, considering other studies with balanced sex distribution.

There is inconsistency in association of age with T1 values and ECV in the published studies^{26,27,44–47}. Rauhalamm et al.²⁶ and Liu et al.⁴⁵ demonstrated a linear correlation between age and T1 values and ECV. According to Rosmini et al., native myocardial T1 decreased slightly with age, while ECV did not change with age⁴⁷. In our study, aging was not a significant factor affecting T1 values and ECV, which is consistent with a previous study by Dabir et al.²⁷.

Our results showed that there was no significant difference in ECV between the HTN and control groups. According to previous reports, T1 mapping revealed increased diffuse MF in well-controlled HTN patients, but the increase was small and only occurred with LVH⁴⁸. Our findings are consistent with the literature, since LVH was contained in the exclusion criteria of our study. Patients with HTN LVH had higher ECV and longer native T1 than HTN non-LVH and control subjects^5,48. According to Venkatesh et al., in a study of 1,813 subjects who underwent CMR, HTN-induced remodeling was related to enhanced replacement and diffuse fibrosis⁴⁹. In an animal study, the ECV and native T1 value of the myocardium in 18 hypertensive swine increased over three months, even though no LGE was found at any of the imaging times²³.

According to Levelt et al., there were no significant differences in native myocardial T1 values and ECV between the patients with DM and the control subjects, indicating the absence of fibrosis in a similar context as our study⁵⁰. Furthermore, our study showed HTN-DM group showed significantly high ECV than the control and HTN groups, which provides a clue about a synergetic effect on ventricular fibrosis of DM and HTN. DM appears to enhance fatty acid metabolism, decrease glucose oxidation, and change intracellular signaling, leading to cardiac structure and function alterations, based on prior research^51–53. Ventricular fibrosis is a common structural and histological hallmark of DM, primarily owing to the deposition of collagen and advanced glycation end-products resulting from altered intracellular signaling and metabolic disturbances⁵⁴. In a study of 135 patients with DM, ECV was significantly different from that of control subjects, while native T1 was not significantly different⁵⁵. ECV values correlated with HbA1c levels in DM⁵⁶. The group with HbA1c ≥ 7.0 had a significantly higher ECV value than the control subjects and the lower HbA1c group (HbA1c < 7.0). There was no statistically significant difference in the native T1 value and postT1 value among the three groups⁵⁶. The lack of significance between the control and DM groups in ECV can be explained by Hb A1c below 7.2 in our research population.

In our study, in the control group, eGFR significantly correlated not with preT1 linearly but with postT1 proportionally and ECV inversely. This interesting finding suggests that postT1 may be associated with the degrees of renal clearance of contrast agent. Increased renal clearance of contrast agent could facilitate washout of contrast agent in myocardium and then increase myocardial postT1 values^57,58. According to Edward et al., patients with chronic kidney disease had increased native T1 values and ECV compared with the control and hypertensive subjects⁵⁹.

The limitations of this study include the retrospective cross-sectional study design, the relatively small number of subjects with DM (n = 25), DM and HTN (n = 29), and female subjects (n = 23). Especially, a relatively narrow range of age distribution concentrated in the 50 s resulting from the consecutive data collection could lower the reliability about the insignificant association between age and T1 values or ECV. Low ICCs for measurement of apical segments are ascribed to small ROIs and image inhomogeneity associated with motion.

In conclusion, there were significant differences between the T1 values and ECV of the septal and lateral walls at the mid-ventricular and basal levels in asymptomatic subjects. ECV is significantly affected by cardiovascular risk factors such as HTN, DM, and eGFR even before cardiovascular symptoms develop.

Methods

This retrospective study was approved and the need for informed consent was waived considering the retrospective study nature by the Samsung Medical Center Institutional Review Board. All methods were carried out in accordance with relevant guidelines and regulations. The authors who have no relationships with the industry controlled the inclusion of all data and information in this article.

We evaluated the records of consecutive asymptomatic subjects who underwent CMR for health screening at the Health Promotion Center of our institution between March 2014 and October 2015. We excluded subjects with one or more following criteria; poor imaging quality (n = 36) or cooperation (n = 40), lack of optimal T1 mapping (n = 22), and previous history of myocardial infarction (n = 5), localized T1 abnormality and LGE suspicious for myocardial infarction or cardiomyopathy (n = 12), LVH defined as LV wall thickness > 13 mm at least 1 segment or indexed end-diastolic mass > 91 g/m² in males and > 77 g/m² in females (n = 9)^60,61. A total of 233 subjects were included (Fig. 4).

Figure 4.

Flow chart of study population enrollment. The total study population was divided into four groups according to cardiovascular risk factors. The control group was defined as subjects who did not have hypertension (HTN) and diabetes mellitus (DM). Abbreviations: CMR, cardiac magnetic resonance imaging; MI, myocardial infarction.

CMR protocol

All patients underwent CMR using a 1.5 T MR system (Magnetom Avanto, Siemens Healthineers) with a 32-channel phased-array receiver coil during repeated breath-holds. After localization, cine images of the LV mass were acquired using a steady-state free precession (SSFP) sequence with 8–10 contiguous short-axis slices to cover the entire LV with a slice thickness of 6 mm and a 4-mm gap. Standard delayed gadolinium-enhanced imaging was acquired using the phase-sensitive inversion recovery (PSIR) technique after injecting 0.15 mmol/kg gadobutrol (Gadovist; Bayer Healthcare) in 10–12 continuous short-axis images of 6 mm thickness with a 4-mm slice gap. Inversion delay times were typically 280–360 ms. Three short-axis images were acquired using the MOLLI sequence before and 15 min after administering gadolinium (Fig. 5).

Figure 5.

Short-axis slices of pre-contrast and post-contrast reconstructed T1 maps. The corresponding regions of interest on left ventricular segments and cavity blood (red circles) were drawn on T1 maps in a 54-year-old male in the control group.

Typical imaging parameters for MOLLI were as follows: two non-selective inversion pulses; number of acquisitions after each inversion pulse, 5, 3; number of recoveries before the second inversion pulse, 3; SSFP single-shot readout in mid-diastolic phase; field of view, 350 × 300 mm²; acquisition matrix, 192 × 150; slice thickness, 8 mm; flip angle, 35°; repetition time, 2.43 ms; echo time, 1.01 ms; bandwidth, 1085 Hz/pixel; minimum inversion time, 120 ms; inversion time increment, 80 ms; generalized autocalibrating partially parallel acquisition factor, 2.

T1 mapping post-processing

The T1 maps were generated automatically by the scanner after the acquisition with MOLLI. To correct for residual cardiac and respiratory motion between individual inversion-recovery images, a non-rigid motion correction algorithm⁶² was used, and T1 values were calculated on a pixel-wise basis by performing a PSIR non-linear curve fitting using the three-parameter signal model.

Image analysis

Image acquisition and analysis were done in a manner consistent with the consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging⁴. Global LV mass and functional parameters were analyzed using a dedicated software (Syngo.via; Siemens Healthineers). Image analysis of T1 maps was performed by two experienced cardiac radiologists (CMR experience of 7 years and 12 years, respectively) blinded to the clinical information. ROIs were drawn on 16 LV segments and blood pools manually (Fig. 5). Areas of nonspecific LGE at the right ventricular insertion points were excluded from measurement with ROIs. A circular ROI was placed in the LV cavity, avoiding papillary muscles, to assess the T1 value of blood. All original images were assessed for artifacts due to susceptibility and cardiac or respiratory motion. Each motion-corrected series was evaluated for correct image alignment and each map was evaluated as to whether the original images were transformed to an acceptable map⁶³.

ECV calculation

ECV was calculated using the following equations:

ΔR1 = 1/T1 time post-contrast—1/T1 time pre-contrast,

λ = ΔR1_myocardium/ΔR1_blood,

$$\text{ECV}=\lambda \ast (1-\text{Hct}).$$

Hct refers to the hematocrit measured in venous blood sampled on the same day of the MRI scan acquisition ^4,64,65.

Clinical information

The clinical information of the subjects was obtained from medical records and laboratory findings on the day of CMR acquisition. BMI was calculated as weight (kg) divided by the square of the height (m²). SBP and DBP were measured after the subject had rested for at least 5 min. Blood samples were collected from the antecubital vein after overnight fasting. Total cholesterol, high-density lipoprotein, triglyceride (TG), fasting plasma glucose (FPG), and serum creatinine (Cr) levels were measured using enzymatic or colorimetric methods. The eGFR was calculated using a formula from the Modification of Diet in Renal Disease study: eGFR (mL/min/1.73 m²) = 186.3 × (Cr)—1.154 × (age)—0.203 × (0.742 for women)⁶⁶. Body surface area (BSA) was calculated as follows: 0.20247 × height (m)^0.725 × weight (kg)^0.425 (Dubois formula). HTN was diagnosed when a person’s SBP in the office or clinic was ≥ 140 mmHg and/or their DBP was ≥ 90 mmHg following repeated examinations⁶⁷. DM was diagnosed using the following criteria: occasional plasma glucose value of ≥ 200 mg/dL (≥ 11.1 mmol/L), FPG of ≥ 126 mg/dL (7.0 mmol/L) (fasting time 8–12 h), oral glucose tolerance test 2-h value in venous plasma ≥ 200 mg/dL (≥ 11.1 mmol/L), HbA1c ≥ 6.5% (≥ 48 mmol/mol Hb), and impaired fasting glucose for the fasting glucose range of 100–125 mg/dL (5.6 mmol/L- 6.9 mmol/L) in venous plasma⁶⁸.

T1 values and ECV were compared among age groups and between sexes. According to their status of cardiovascular risk factors, subjects were divided into four subgroups: (1) HTN group, (2) DM group, (3) HTN-DM group, and (4) control group. The control group was defined as subjects who did not have HTN and DM. We evaluated whether there were any differences in T1 values and ECV between the subgroups.

Statistical analysis

All analyses were conducted using SPSS 26 (IBM, Chicago, United states) and Rex (Version 3.0.3, RexSoft Inc., Seoul, Korea). Categorical variables were reported as percentages and continuous variables are presented as means with standard deviations. The differences between continuous variables were analyzed using the independent or paired t-test. Wilcoxon rank sum test and Mann Whitney U-test were used to analyze the differences between non-continuous variables. According to normality of distribution, analysis of variance or Kruskal–Wallis test was applied for multiple group comparison. For the trend analysis, Jonckheere-Terpstra test was adopted. The relationships between T1 values and cardiovascular risk factors were studied using simple correlation analysis with Pearson correlation coefficient (r). Inter-observer agreement was quantified using ICCs for all subjects. The threshold for statistical significance was set at p = 0.05 in the two-tailed tests.

Author contributions

All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by M.Y.K., S.J.C., and Y.H.C. The first draft of the manuscript was written by M.Y.K. and Y.H.C. and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript. Conceptualization: Y.H.C.; Methodology: M.Y.K., Y.H.C.; Formal analysis and investigation: M.Y.K., S.J.C., Y.H.C.; Writing-original draft preparation: M.Y.K., Y.H.C.; Writing-review and editing: M.Y.K., S.J.C., H.J.K., S.M.K., S.-C.L., Y.H.C.; Funding acquisition: Not applicable. Resources: S.J.C., S.-C.L., M.Y.P.; Supervision: Y.H.C., S.-C.L.

Data availability

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

Competing interests

The authors declare no competing interests.

Supplementary Information

The online version contains supplementary material available at 10.1038/s41598-022-16696-0.