Risk factors for increased left ventricular hypertrophy in patients with chronic kidney disease.

BACKGROUND: Although left ventricular hypertrophy (LVH) has been established as a predictor of cardiovascular events in chronic kidney disease (CKD), the relationship between the prevalence of LVH and CKD stage during the predialysis period has not been fully examined.
METHODS: We measured left ventricular mass index (LVMI) in a cross-sectional cohort of participants in the Chronic Kidney Disease Japan Cohort (CKD-JAC) study in order to identify factors that are associated with increased LVMI in patients with stage 3-5 CKD. LVH was defined as LVMI>125 g/m2 in male patients and >110 g/m2 in female patients.
RESULTS: We analyzed baseline characteristics in 1185 participants (male 63.7%, female 36.3%). Diabetes mellitus was the underlying disease in 41.3% of patients, and mean age was 61.8±11.1 years. LVH was detected in 21.7% of patients at baseline. By multivariate logistic analysis, independent risk factors for LVH were past history of cardiovascular disease (odds ratio [OR] 0.574; 95% confidence interval [CI] 0.360-0.916; P=0.020), systolic blood pressure (OR 1.179; 95% CI 1.021-1.360; P=0.025), body mass index (OR 1.135; 95% CI 1.074-1.200; P<0.001), and serum calcium level (OR 0.589; 95% CI 0.396-0.876; P=0.009).
CONCLUSION: Cross-sectional baseline data from the CKD-JAC study shed light on the association between LVH and risk factors in patients with decreased renal function. Further longitudinal analyses of the CKD-JAC cohort are needed to evaluate the prognostic value of LVH in CKD patients.

Introduction

Chronic kidney disease (CKD) is the leading risk factor for cardiovascular disease (CVD), a great threat to health and an economic burden [1]. In Japan, the prevalence of end-stage kidney disease (ESKD) requiring renal replacement therapy has been increasing over the last three decades. There were 38,893 new cases in 2010, bringing the total number of cases in Japan to 304,592 [2]. Since the number of patients requiring dialysis has continued to increase [3], there appear to be an enormous number of latent cases of CKD in the Japanese population. In a recent study, Imai et al. reported the prevalence of CKD by calculating the estimated glomerular filtration rate (eGFR) using an equation that estimates GFR based on data from the Japanese annual health check program in 2005 [4]. They predicted that 13 % of the Japanese adult population (approximately 13.3 million people) would have CKD in 2005. CKD frequently progresses and becomes severe over time, but the factors that are responsible for the progression of CKD need further elucidation [5].

Renal dysfunction and albuminuria in CKD patients have been established as a risk factor for cardiovascular (CV) events independent of conventional CV risk factors [6-8]. Population-based studies in Western and Asian countries have shown that the risk of CVD increases as renal function declines. Because of this finding, the National Kidney Foundation formed a task force to heighten awareness of CVD in CKD, and defined CKD using parameters such as decreased eGFR < 60 ml/min/1.73 m2. A cohort of CKD patients treated by nephrologists is required to accurately analyze renal and CV events. However, few studies have been conducted on the prevalence of left ventricular hypertrophy (LVH) in a predialysis population [9-12].

The aim of the present study was to clarify whether there is a close correlation between the prevalence of LVH and the stage of CKD classified according to eGFR and to identify factors related to LVH among the participants in the Chronic Kidney Disease Japan Cohort (CKD-JAC) [13].

Subjects and methods

Inclusion and exclusion criteria

Baseline characteristics of CKD-JAC are described elsewhere [14]. The following inclusion criteria were used at screening: (1) Japanese or Asian patients living in Japan; (2) age 20–75 years; and (3) a broad spectrum of CKD with eGFR of 10–59 ml/min/1.73 m2. eGFR was calculated using a modified three-variable equation for eGFR in Japanese patients [15]: eGFR = 194 × age−0.287 × sCr−1.094 (×0.739, if female), where sCr = serum creatinine.

All patients were classified on the basis of CKD stage as described in our previous paper [13]. The following patients were excluded from participation: (1) patients with polycystic kidney disease, human immunodeficiency virus (HIV) infection, liver cirrhosis, active cancer, and patients who had received cancer treatment within the past 2 years; (2) transplant recipients and patients who had previously been on long-term dialysis; (3) patients who refused to provide informed consent.

Information on past medical history, including hypertension, acute myocardial infarction, angina pectoris, congestive heart failure, peripheral arterial disease, cerebrovascular disease, and prescription of antihypertensive agents, including angiotensin-converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARBs), calcium channel blockers (CCBs), diuretics, and β-blockers, statins, and antiplatelet agents, was collected from the medical records at each institution.

Blood pressure and echocardiographic measurements

Blood pressure (BP) was measured in outpatient clinics with an automated sphygmomanometer after a 5-min rest. BP in the right arm was measured three times at intervals of 1 min, and the mean values were used for analyses. A mercury sphygmomanometer was used to measure the BP of patients who had frequent premature contractions, atrial fibrillation, or atrial flutter. Pulse pressure was calculated by subtracting diastolic BP from systolic BP. A 2-dimensional guided M-mode echocardiographic study was performed at each institution. Measurements included the diastolic thickness of the interventricular septum (IVST) and left ventricular posterior wall (PWT), and the internal diameter of the left ventricle at the end of diastole (LVDd) and the end of systole (LVDs). The modified Penn cube formula was used to calculate LV mass [16]: ([1.04 × (0.1 × IVST) + (0.1 × PWT)] × 3 − [(0.1 × LVDd) × 3] × 8 + 0.6, and LV mass was adjusted for body surface area (LVMI). LVH was defined as LVMI > 125 g/m2 in men and >110 g/m2 in women [17].

Definitions of hypertension, diabetes and dyslipidemia

Hypertension was defined as systolic BP ≥ 140 mmHg and/or diastolic BP ≥ 90 mmHg or taking an antihypertensive agent. Diabetes mellitus (DM) was defined as HbA1C ≥ 6.5 % or taking an antidiabetic agent. Diabetic patients were identified as those with diabetic nephropathy as the primary cause of CKD. Dyslipidemia was defined as serum triglyceride level >150 mg/dl, or serum high-density lipoprotein (HDL) cholesterol level <40 mg/dl in men and <50 mg/dl in women.

Collection of biological samples and measurements

Whole blood, serum, and urine samples were collected for measurement of serum Cr and cystatin C, HbA1c, intact parathyroid hormone (iPTH), and urinary albumin and Cr levels at a central laboratory. Urinary albumin excretion was expressed as the albumin to Cr ratio (ACR). HbA1c was measured by the JDS method, and the value was converted to the A1C value measured by the NGSP method by adding 0.4 % as determined by the Japanese Diabetes Society. Each clinical center measured serum Cr at each visit. A 24-h urine specimen was collected from each patient once a year to measure the amount of proteinuria.

Statistical analysis

All variables are reported as mean ± SD and frequency. Descriptive statistics of baseline characteristics were calculated by CKD stage, sex, and the presence or absence of LVH. CKD stages were defined according to the patient’s eGFR. Chi-squared test and Student’s t test or one way analysis of variance (ANOVA) were used to detect between-group differences. ACR values had a skewed distribution, and were log-transformed to achieve a normal distribution. Logistic linear regression was used to investigate the relation of LVMI to eGFR, BMI, and log ACR. Univariate logistic regression analyses were performed in an attempt to identify factors related to LVH. Multivariate logistic regression analyses were used to identify independent variables related to LVH. We considered some variables that had a P value <0.10 in univariate logistic regression analyses as independent variables for multivariate logistic regression analyses. The model included the variables as follows: sex, smoking status, complications of DM, dyslipidemia and hypertension, past history of congestive heart failure, systolic and diastolic BPs, pulse pressure, BMI, eGFR, uric acid, ACR, A1C, iPTH, HDL cholesterol, triglyceride, calcium, phosphorus, and prescription of antihypertensive agents. The two-sided 95 % confidence interval (CI) and odds ratio (OR) were calculated by estimation. A two-sided probability level of 5 % was considered significant. All statistical analyses were performed using the SAS software program for Windows (SAS Inc. Japan, Tokyo, Japan).

Results

Baseline demographics and clinical characteristics of participants according to eGFR level

The baseline characteristics of the 2977 participants in the CKD-JAC study have been described previously [13]. Of them, the subjects in this study, i.e., those who were examined by echocardiography (UCG), consisted of 755 Japanese men (63.7 %) and 430 Japanese women (36.3 %), 489 (41.3 %) and 918 (77.5 %) of whom had DM and dyslipidemia, respectively. Most of the subjects had hypertension (1051, 88.7 %) and were being treated with an antihypertensive agent (1095, 92.4 %), most of them (83.1 %) with ACE inhibitors (302, 25.5 %)/ARBs (901, 76.0 %), as shown in Table 1.

Table 1

Baseline characteristics of study population by eGFR

Variable	All patients	eGFR (ml/min/1.73 m2)				P value
		Stage 3a	Stage 3b	Stage 4	Stage 5
		≥45	30 to <45	15 to <30	<15
N	1185	136	383	464	202
Age (years)	61.8 ± 11.1	56.7 ± 12.8	61.4 ± 11.4	62.9 ± 10.4	63.5 ± 9.8	<0.001
Sex [n (%)]						0.888
Male	755 (63.7)	86 (63.2)	246 (64.2)	299 (64.4)	124 (61.4)
Female	430 (36.3)	50 (36.8)	137 (35.8)	165 (35.6)	78 (38.6)
Medical history [n (%)]
Hypertension	1051 (88.7)	113 (83.1)	328 (85.6)	429 (92.5)	181 (89.6)	0.002
Diabetes	489 (41.3)	57 (41.9)	151 (39.4)	191 (41.2)	90 (44.6)	0.691
Dyslipidemia	918 (77.5)	106 (77.9)	292 (76.2)	363 (78.2)	157 (77.7)	0.916
Cardiovascular disease
MI	80 (6.8)	8 (5.9)	23 (6.0)	33 (7.1)	16 (7.9)	0.792
Angina	129 (10.9)	10 (7.4)	42 (11.0)	50 (10.8)	27 (13.4)	0.386
Congestive heart failure	67 (5.7)	4 (2.9)	21 (5.5)	27 (5.8)	15 (7.4)	0.375
ASO	43 (3.6)	3 (2.2)	9 (2.3)	21 (4.5)	10 (5.0)	0.199
Stroke	147 (12.4)	18 (13.2)	46 (12.0)	55 (11.9)	28 (13.9)	0.881
BMI (kg/m2)	23.6 ± 3.8	24.1 ± 3.3	23.7 ± 3.9	23.5 ± 3.8	23.4 ± 3.6	0.594
Blood pressure (mmHg)
Systolic	132.4 ± 18.1	130.8 ± 17.3	129.6 ± 17.5	133.3 ± 18.2	136.9 ± 18.2	<0.001
Diastolic	75.9 ± 11.8	76.0 ± 10.9	75.1 ± 11.6	76.1 ± 11.9	76.7 ± 12.6	0.255
Pulse pressure (mmHg)	56.5 ± 13.9	54.8 ± 14.1	54.5 ± 13.5	57.2 ± 14.0	60.1 ± 13.6	<0.001
Creatinine (mg/dl)	2.18 ± 1.09	1.09 ± 0.17	1.43 ± 0.25	2.31 ± 0.53	4.05 ± 0.87	<0.001
eGFR (mL/min/1.73 m2)	28.61 ± 12.63	50.78 ± 5.26	37.12 ± 4.19	22.39 ± 4.29	11.85 ± 1.91	<0.001
Uric acid (mg/dl)	7.21 ± 1.51	6.48 ± 1.39	7.01 ± 1.32	7.42 ± 1.54	7.59 ± 1.65	<0.001
Urinary protein (g/day)	1.545 ± 2.128	0.818 ± 1.816	1.206 ± 2.057	1.640 ± 2.166	2.342 ± 2.096	<0.001
Urinary albumin (mg/gCr)	1064.4 ± 1512.3	538.7 ± 958.5	834.4 ± 1562.1	1176.4 ± 1446.3	1596.2 ± 1677.2	<0.001
Total chol (mg/dl)	194.3 ± 43.6	200.0 ± 37.1	197.2 ± 47.0	193.4 ± 41.0	187.1 ± 45.9	0.032
Non-HDL chol (mg/dl)	140.7 ± 42.1	141.8 ± 37.0	142.4 ± 44.8	140.7 ± 39.3	136.7 ± 45.9	0.558
LDL chol (mg/dl)	110.6 ± 34.2	115.7 ± 28.4	112.3 ± 37.9	109.5 ± 32.1	106.3 ± 34.5	0.169
HDL chol (mg/dl)	53.9 ± 18.3	58.6 ± 18.9	55.4 ± 18.8	52.8 ± 17.7	50.4 ± 17.0	0.008
Triglyceride (mg/dl)	170.3 ± 115.2	165.3 ± 139.1	165.9 ± 108.7	175.4 ± 121.4	170.4 ± 93.7	0.499
Calcium (mg/dl)	9.01 ± 0.55	9.26 ± 0.43	9.12 ± 0.50	9.01 ± 0.50	8.66 ± 0.66	<0.001
Phosphorus (mg/dl)	3.53 ± 0.69	3.27 ± 0.56	3.29 ± 0.58	3.56 ± 0.62	4.05 ± 0.77	<0.001
iPTH (pg/ml)	105.6 ± 83.7	55.2 ± 23.9	67.1 ± 34.7	106.4 ± 58.9	208.9 ± 122.8	<0.001
CRP (mg/dl)	0.27 ± 0.96	0.15 ± 0.36	0.24 ± 0.52	0.27 ± 0.77	0.39 ± 1.84	0.271
A1C (%)	5.98 ± 0.93	6.05 ± 1.02	6.07 ± 1.03	5.93 ± 0.84	5.86 ± 0.83	0.028
Hemoglobin (g/dl)	12.14 ± 1.84	13.30 ± 1.75	12.98 ± 1.80	11.69 ± 1.55	10.84 ± 1.38	<0.001
Medication [n (%)]
Antihypertensive agent	1095 (92.4)	115 (84.6)	351 (91.6)	437 (94.2)	192 (95.1)	0.001
ARB	901 (76.0)	100 (73.5)	283 (73.9)	362 (78.0)	156 (77.2)	0.509
ACEI	302 (25.5)	25 (18.4)	104 (27.2)	135 (29.1)	38 (18.8)	0.007
CCB	685 (57.8)	63 (46.3)	194 (50.7)	290 (62.5)	138 (68.3)	<0.001
β-Blocker	315 (26.6)	28 (20.6)	81 (21.1)	137 (29.5)	69 (34.2)	0.001
Statin	510 (43.0)	68 (50.0)	163 (42.6)	195 (42.0)	84 (41.6)	0.331
Diuretic	403 (34.0)	24 (17.6)	119 (31.1)	172 (37.1)	88 (43.6)	<0.001
Antiplatelet	424 (35.8)	37 (27.2)	141 (36.8)	166 (35.8)	80 (39.6)	0.136

MI myocardial infarction, ASO arteriosclerosis obliterans, BMI body mass index, chol cholesterol, LDL low-density lipoprotein, HDL high-density lipoprotein, iPTH intact parathyroid hormone, CRP C-reactive protein, ARB angiotensin receptor blocker, ACEI angiotensin-converting enzyme inhibitor, CCB calcium channel blocker

CKD was stage 3a in 136 patients (11.5 %), stage 3b in 383 patients (32.3 %), stage 4 in 464 patients (39.2 %), and stage 5 in 202 patients (17.0 %) (Table 1). The prevalence of CVD comorbidity tended to be inversely proportional to eGFR, but the correlation did not reach statistical significance. The groups with stage 4–5 CKD were older, and had higher systolic BP and pulse pressure, a higher prevalence of hyperuricemia and anemia, and higher grades of proteinuria and albuminuria than the groups with stage 3a and 3b CKD, and serum levels of phosphorus, and iPTH in stage 4 and 5 CKD patients were significantly higher than those in stage 3a and 3b CKD patients. Antihypertensive agents, including ACE inhibitors and CCBs, statins, and antiplatelet agents were frequently administered in the groups of patients with stage 3b and 4 CKD.

Analysis by sex

Since the proportion of male subjects was 63.7 % in the study population, sex may have affected the results of the present study. As shown in Table 2, female subjects were younger (60.8 ± 11.7 vs. 62.4 ± 10.7 years, P = 0.0160), and had a lower prevalence of hypertension (84.9 vs. 90.9 %, P = 0.0018), DM (36.7 vs. 43.8 %, P = 0.0170), and past history of myocardial infarction (1.9 vs. 9.5 %, P < 0.0001) and stroke (8.4 vs. 14.7 %, P = 0.0015) than male subjects. In addition, female subjects had lower BMI (23.2 ± 4.1 vs. 23.9 ± 3.5 kg/m2, P = 0.0016), lower serum levels of Cr (1.84 ± 0.90 vs. 2.38 ± 1.13 mg/dl, P < 0.0001) and uric acid (6.90 ± 1.51 vs. 7.38 ± 1.49 mg/dl, P < 0.0001), and lower hemoglobin concentration (11.53 ± 1.54 vs. 12.49 ± 1.91 g/dl, P < 0.0001) than male subjects. However, there was no significant sex difference in eGFR (28.61 ± 13.00 vs. 28.61 ± 12.43 ml/min/1.73 m2, P = 0.9986). Female subjects had higher serum levels of lipids, including total cholesterol (207.6 ± 45.3 vs. 186.6 ± 40.7 mg/dl, P < 0.0001), non-HDL cholesterol (147.9 ± 44.3 vs. 136.6 ± 40.3 mg/dl, P < 0.0001), low-density lipoprotein (LDL) cholesterol (118.1 ± 35.2 vs. 106.3 ± 32.9 mg/dl, P < 0.000), and HDL cholesterol (60.8 ± 19.3 vs. 50.0 ± 16.4 mg/dl, P < 0.0001), and lower serum triglyceride level (160.5 ± 106.0 vs. 175.8 ± 119.8 mg/dl, P = 0.0358). Lower percentages of female subjects were prescribed antihypertensive agents, including CCBs and β-blockers, statins and antiplatelet agents. As shown in Table 5, menopause was not significantly associated with LVMI (OR 1.269; 95 % CI 0.858–1.877; P = 0.233) by univariate logistic regression analyses.

Table 2

Baseline characteristics of study population by sex

Variable	All patients	Sex		P value
		Female	Male
N	1185	430	755	<0.001
Age (years)	61.8 ± 11.1	60.8 ± 11.7	62.4 ± 10.7	0.016
Medical history [n (%)]
Hypertension	1051 (88.7)	365 (84.9)	686 (90.9)	0.002
Diabetes	489 (41.3)	158 (36.7)	331 (43.8)	0.017
Dyslipidemia	918 (77.5)	323 (75.1)	595 (78.8)	0.144
Cardiovascular disease
MI	80 (6.8)	8 (1.9)	72 (9.5)	<0.001
Angina	129 (10.9)	30 (7.0)	99 (13.1)	0.001
Congestive heart failure	67 (5.7)	19 (4.4)	48 (6.4)	0.165
ASO	43 (3.6)	9 (2.1)	34 (4.5)	0.033
Stroke	147 (12.4)	36 (8.4)	111 (14.7)	0.002
BMI (kg/m2)	23.6 ± 3.8	23.2 ± 4.1	23.9 ± 3.5	0.002
Blood pressure (mmHg)
Systolic	132.4 ± 18.1	131.2 ± 18.7	133.1 ± 17.6	0.081
Diastolic	75.9 ± 11.8	74.8 ± 12.0	76.5 ± 11.7	0.017
Pulse pressure (mmHg)	56.5 ± 13.9	56.4 ± 14.4	56.6 ± 13.7	0.776
Creatinine (mg/dl)	2.18 ± 1.09	1.84 ± 0.90	2.38 ± 1.13	<0.001
eGFR (ml/min/1.73 m2)	28.61 ± 12.63	28.61 ± 13.00	28.61 ± 12.43	0.999
Uric acid (mg/dl)	7.21 ± 1.51	6.90 ± 1.51	7.38 ± 1.49	<0.001
Urinary protein (g/day)	1.55 ± 2.13	1.30 ± 1.91	1.665 ± 2.22	0.081
Urinary albumin (mg/gCr)	1064.4 ± 1512.3	1013.0 ± 1593.8	1093.8 ± 1464.0	0.386
Total chol (mg/dl)	194.3 ± 43.6	207.6 ± 45.3	186.6 ± 40.7	<0.001
Non-HDL chol (mg/dl)	140.7 ± 42.1	147.9 ± 44.3	136.55 ± 40.3	<0.001
LDL chol (mg/dl)	110.6 ± 34.2	118.1 ± 35.2	106.3 ± 32.9	<0.001
HDL chol (mg/dl)	53.9 ± 18.3	60.8 ± 19.3	50.0 ± 16.4	<0.001
Triglyceride (mg/dl)	170.3 ± 115.2	160.5 ± 106.0	175.8 ± 119.8	0.036
Calcium (mg/dl)	9.01 ± 0.55	9.13 ± 0.54	8.95 ± 0.55	<0.001
Phosphorus (mg/dl)	3.53 ± 0.69	3.77 ± 0.62	3.38 ± 0.68	<0.001
iPTH (pg/ml)	105.6 ± 83.7	109.3 ± 88.0	103.4 ± 81.1	0.253
CRP (mg/dl)	0.27 ± 0.96	0.21 ± 0.44	0.30 ± 1.16	0.145
A1C (%)	5.98 ± 0.93	5.98 ± 0.99	5.98 ± 0.89	0.966
Hemoglobin (g/dl)	12.14 ± 1.84	11.53 ± 1.54	12.49 ± 1.91	<0.001
Medication [n (%)]
Antihypertensive agent	1095 (92.4)	383 (89.1)	712 (94.3)	0.001
ARB	901 (76.0)	313 (72.8)	588 (77.9)	0.070
ACEI	302 (25.5)	103 (24.0)	199 (26.4)	0.394
CCB	685 (57.8)	223 (51.9)	462 (61.2)	0.003
β-Blocker	315 (26.6)	97 (22.6)	218 (28.9)	0.002
Statin	510 (43.0)	214 (49.8)	296 (39.2)	<0.001
Diuretic	403 (34.0)	141 (32.8)	262 (34.7)	0.553
Antiplatelet	424 (35.8)	124 (28.8)	300 (39.7)	<0.001

Table 5

Factors associated with LVMI (univariate logistic regression analysis)

Variables	OR	95 % CI	P value
Sex (female)	1.78	1.308–2.416	<0.001
Age (years)	1.00	0.990–1.015	0.690
Smoking	0.69	0.444–1.064	0.092
Menopause	1.269	0.858–1.877	0.233
Complications
Diabetes	1.66	1.254–2.186	<0.001
Dyslipidemia	1.43	1.007–2.040	0.045
Hypertension	3.73	1.487–9.376	0.005
Medical history
Hypertension	0.91	0.648–1.281	0.592
Cardiovascular disease	0.72	0.518–1.013	0.060
MI	0.79	0.395–1.599	0.519
Angina	0.70	0.419–1.170	0.174
Congestive heart failure	0.40	0.142–1.146	0.088
ASO	1.21	0.562–2.609	0.625
Stroke	0.78	0.478–1.257	0.302
Blood pressure (mmHg)
Systolic	1.23	1.134–1.323	<0.001
Diastolic	1.16	1.031–1.306	0.014
Pulse pressure (mmHg)	1.25	1.137–1.380	<0.001
BMI (kg/m2)	1.15	1.110–1.199	<0.001
eGFR (ml/min/1.73 m2)	0.98	0.968–0.991	<0.001
Uric acid (mg/dl)	1.10	1.002–1.202	0.046
Urinary albumin (mg/gCr)	1.55	1.267–1.905	<0.001
A1C (%)	1.17	1.011–1.345	0.035
Hemoglobin (g/dl)	0.98	0.905–1.052	0.520
iPTH (pg/ml)	1.00	1.001–1.005	<0.001
Total chol (mg/dl)	1.00	0.994–1.001	0.163
Non-HDL chol (mg/dl)	1.00	0.997–1.004	0.743
LDL chol (mg/dl)	1.00	0.997–1.006	0.545
HDL chol (mg/dl)	0.98	0.971–0.989	<0.001
Triglyceride (mg/dl)	1.00	1.001–1.003	<0.001
Calcium (mg/dl)	0.56	0.431–0.720	<0.001
Phosphorus (mg/dl)	1.23	1.004–1.515	0.046
Medication
Antihypertensive agent	3.51	1.601–7.685	0.002
Statin	0.82	0.607–1.098	0.179
ESA	1.12	0.726–1.732	0.605
Phosphate binder	1.06	0.476–2.348	0.892
Vitamin D	0.80	0.438–1.444	0.452

OR odds ratio, CI confidence interval, ESA erythropoiesis-stimulating agent

Comparison of study population with and without LVH according to CKD stage and sex

LVMI in each of the four groups of CKD patients according to eGFR is shown in Fig. 1, and tended to increase with the stage of CKD (P = 0.0005 in men, P = 0.0016 in women). The prevalence of LVH was 257 of 1185 (21.7 %) of the study population (Table 3). Men had a higher prevalence of LVH than women (15.9 vs 5.7 %).

Fig. 1

Comparison of left ventricular mass index (LVMI) in the different subgroups of CKD patients according to their degree of renal dysfunction

Table 3

Baseline characteristics of study population by LVH

Variable	All patients	LVH		P value
		LVH (+)	LVH (−)
N	1185	257	928
Age (years)	61.8 ± 11.1	62.1 ± 10.5	61.8 ± 11.2	0.690
Medical history [n (%)]
Hypertension	1051 (88.7)	245 (95.3)	806 (86.9)	<0.001
Diabetes	489 (41.3)	131 (51.0)	358 (38.6)	<0.001
Dyslipidemia	918 (77.5)	211 (82.1)	707 (76.2)	0.045
Cardiovascular disease
MI	80 (6.8)	10 (3.9)	45 (4.9)	0.518
Angina	129 (10.9)	19 (7.4)	95 (10.2)	0.171
Congestive heart failure	67 (5.7)	4 (1.6)	35 (3.8)	0.078
ASO	43 (3.6)	9 (3.5)	27 (2.9)	0.624
Stroke	147 (12.4)	22 (8.6)	100 (10.8)	0.301
BMI (kg/m2)	23.6 ± 3.8	25.2 ± 3.8	23.2 ± 3.6	<0.001
Blood pressure (mmHg)
Systolic	132.4 ± 18.1	137.7 ± 19.3	131.0 ± 17.4	<0.001
Diastolic	75.9 ± 11.8	77.5 ± 12.6	75.4 ± 11.6	0.013
Pulse pressure (mmHg)	56.5 ± 13.9	60.1 ± 15.5	55.5 ± 13.3	<0.001
Creatinine (mg/dl)	2.18 ± 1.09	2.49 ± 1.26	2.09 ± 1.01	<0.001
eGFR (ml/min/1.73 m2)	28.61 ± 12.63	26.1 ± 12.6	29.3 ± 12.6	<0.001
Uric acid (mg/dl)	7.21 ± 1.51	7.38 ± 1.49	7.16 ± 1.51	0.046
Urinary protein (mg/day)	1.55 ± 2.13	1.49 ± 3.30	1.33 ± 1.72	0.557
Urinary albumin (mg/gCr)	1064.4 ± 1512.3	1472.5 ± 1739.6	950.5 ± 1423.8	<0.001
Total chol (mg/dl)	194.3 ± 43.6	190.7 ± 46.6	195.2 ± 42.7	0.163
Non-HDL chol (mg/dl)	140.7 ± 42.1	141.5 ± 43.7	140.4 ± 42.6	0.744
LDL chol (mg/dl)	110.6 ± 34.2	111.8 ± 35.6	110.2 ± 33.8	0.545
HDL chol (mg/dl)	53.9 ± 18.3	49.4 ± 15.4	55.2 ± 18.8	<0.001
Triglyceride (mg/dl)	170.3 ± 115.2	195.2 ± 138.9	163.3 ± 106.8	<0.001
Calcium (mg/dl)	9.01 ± 0.55	8.87 ± 0.67	9.05 ± 0.51	<0.001
Phosphorus (mg/dl)	3.53 ± 0.69	3.61 ± 0.79	3.50 ± 0.66	0.046
iPTH (pg/ml)	105.6 ± 83.7	124.0 ± 100.9	100.2 ± 77.3	<0.001
CRP (mg/dl)	0.27 ± 0.96	0.33 ± 1.00	0.25 ± 0.95	0.245
A1C (%)	5.98 ± 0.93	6.08 ± 1.00	5.95 ± 0.90	0.035
Hemoglobin (g/dl)	12.14 ± 1.84	12.08 ± 2.11	12.16 ± 1.76	0.521
Medication [n (%)]
Antihypertensive agent	1095 (92.4)	250 (97.3)	845 (91.1)	<0.001
ARB	901 (76.0)	203 (79.3)	698 (79.9)	0.252
ACEI	302 (25.5)	70 (27.3)	232 (25.2)	0.491
CCB	685 (57.8)	187 (73.1)	498 (54.1)	<0.001
β-Blocker	315 (26.6)	68 (26.6)	141 (15.3)	<0.001
Statin	510 (43.0)	82 (33.1)	345 (37.7)	0.179
Diuretic	403 (34.0)	110 (43.0)	293 (31.9)	<0.001

The demographic and biochemical parameters of the study population are compared in Table 4. Female subjects with LVH had a higher prevalence of DM (52.9 vs. 33.7 %, P = 0.003), higher BMI (24.5 ± 4.2 vs. 22.9 ± 4.1 kg/m2, P = 0.004), higher systolic BP (135.5 ± 19.6 vs. 130.4 ± 18.5 mmHg, P = 0.043), lower eGFR (24.4 ± 10.7 vs. 29.4 ± 13.3 ml/min/1.73 m2, P = 0.003), and higher ACR (1515.4 ± 1802.7 vs. 916.0 ± 1534.2 mg/gCr, P = 0.005) than female subjects without LVH. In addition, female subjects with LVH had lower serum calcium level (8.94 ± 0.70 vs. 9.16 ± 0.50 mg/dl, P = 0.004), and higher serum levels of phosphorus (3.95 ± 0.72 vs. 3.74 ± 0.60 mg/dl, P = 0.015) and iPTH (132.4 ± 117.0 vs. 104.9 ± 80.8 mg/dl, P = 0.019) than female subjects without LVH. Moreover, higher proportions of female subjects with LVH were being treated with ACE inhibitors (33.8 vs. 22.1 %, P = 0.036), CCBs (75.0 vs. 47.5 %, P < 0.001), β-blockers (25.0 vs. 13.3 %, P = 0.013), and diuretics (51.5 vs. 29.3 %, P = 0.001).

Table 4

Baseline characteristics of study population by sex and LVH

Variable	All patients	Female		P value	Male		P value
		LVH (+)	LVH (−)		LVH (+)	LVH (−)
N	1185	68	362		189	566
Age (years)	61.8 ± 11.1	62.4 ± 11.4	60.5 ± 11.8	0.212	61.9 ± 10.2	62.6 ± 10.8	0.484
Medical history [n (%)]
Hypertension	1051 (88.7)	61 (89.7)	304 (84.0)	0.226	184 (97.4)	502 (88.7)	0.001
Diabetes	489 (41.3)	36 (52.9)	122 (33.7)	0.003	95 (50.3)	236 (41.7)	0.040
Dyslipidemia	918 (77.5)	55 (80.9)	268 (74.0)	0.231	156 (82.5)	439 (77.6)	0.140
Cardiovascular disease
MI	80 (6.8)	2 (2.9)	20 (5.5)	0.375	8 (4.2)	25 (4.4)	0.915
Angina	129 (10.9)	7 (10.3)	29 (8.0)	0.533	12 (6.3)	66 (11.7)	0.038
Congestive heart failure	67 (5.7)	1 (1.5)	12 (3.3)	0.415	3 (1.6)	23 (4.1)	0.106
ASO	43 (3.6)	0 (0)	7 (1.9)	0.248	9 (4.8)	20 (3.5)	0.447
Stroke	147 (12.4)	9 (13.2)	32 (8.8)	0.258	13 (6.9)	68 (12.0)	0.048
BMI (kg/m2)	23.6 ± 3.8	24.5 ± 4.2	22.9 ± 4.1	0.004	25.5 ± 3.6	23.4 ± 3.3	<0.001
Blood pressure (mmHg)
Systolic	132.4 ± 18.1	135.5 ± 19.6	130.4 ± 18.5	0.043	138.4 ± 19.2	131.3 ± 16.8	<0.001
Diastolic	75.9 ± 11.8	75.7 ± 12.8	74.6 ± 11.8	0.509	78.1 ± 12.6	75.9 ± 11.4	0.027
Pulse pressure (mmHg)	56.5 ± 13.9	59.6 ± 16.1	55.8 ± 14.0	0.051	60.3 ± 15.4	55.4 ± 12.9	<0.001
Creatinine (mg/dl)	2.18 ± 1.09	2.11 ± 1.09	1.79 ± 0.86	0.008	2.62 ± 1.29	2.29 ± 1.06	0.001
eGFR (ml/min/1.73 m2)	28.61 ± 12.63	24.4 ± 10.7	29.4 ± 13.3	0.003	26.8 ± 13.1	29.2 ± 12.1	0.017
Uric acid (mg/dl)	7.21 ± 1.51	7.04 ± 1.35	6.88 ± 1.54	0.424	7.50 ± 1.53	7.34 ± 1.47	0.216
Urinary protein (mg/day)	1.55 ± 2.13	2.46 ± 6.35	1.52 ± 2.20	0.213	1.20 ± 1.52	1.23 ± 1.34	0.909
Urinary albumin (mg/gCr)	1064.4 ± 1512.3	1515.4 ± 1802.7	916.0 ± 1534.2	0.005	1456.7 ± 1720.6	972.6 ± 1349.3	0.001
Total chol (mg/dl)	194.3 ± 43.6	203.5 ± 56.9	208.4 ± 42.8	0.428	186.0 ± 41.4	186.7 ± 40.4	0.839
Non-HDL chol (mg/dl)	140.7 ± 42.1	149.8 ± 50.6	147.6 ± 43.1	0.735	138.6 ± 40.8	135.9 ± 40.1	0.464
LDL chol (mg/dl)	110.6 ± 34.2	120.5 ± 41.4	117.7 ± 34.00	0.577	108.7 ± 32.9	105.5 ± 32.8	0.269
HDL chol (mg/dl)	53.9 ± 18.3	57.4 ± 18.1	61.5 ± 19.5	0.138	46.6 ± 13.3	51.2 ± 17.2	0.002
Triglyceride (mg/dl)	170.3 ± 115.2	174.8 ± 102.4	157.9 ± 106.6	0.253	202.4 ± 149.2	166.8 ± 106.9	0.001
Calcium (mg/dl)	9.01 ± 0.55	8.94 ± 0.70	9.16 ± 0.50	0.004	8.85 ± 0.65	8.98 ± 0.50	0.004
Phosphorus (mg/dl)	3.53 ± 0.69	3.95 ± 0.72	3.74 ± 0.60	0.015	3.49 ± 0.78	3.35 ± 0.65	0.021
iPTH (pg/ml)	105.6 ± 83.7	132.4 ± 117.0	104.9 ± 80.8	0.019	120.9 ± 94.5	97.2 ± 75.0	0.001
CRP (mg/dl)	0.27 ± 0.96	0.29 ± 0.50	0.20 ± 0.43	0.123	0.35 ± 1.13	0.28 ± 1.17	0.536
A1C (%)	5.98 ± 0.93	6.11 ± 0.82	5.95 ± 1.02	0.211	6.08 ± 1.07	5.94 ± 0.82	0.083
Hemoglobin (g/dl)	12.14 ± 1.84	11.22 ± 1.98	11.59 ± 1.44	0.074	12.39 ± 2.08	12.52 ± 1.85	0.394
Medication [n (%)]
Antihypertensive agent	1095 (92.4)	66 (97.1)	317 (87.6)	0.021	184 (97.4)	528 (93.3)	0.037
ARB	901 (76.0)	51 (75.0)	262 (72.4)	0.617	152 (80.4)	436 (77.0)	0.412
ACEI	302 (25.5)	23 (33.8)	80 (22.1)	0.036	47 (24.9)	152 (26.9)	0.557
CCB	685 (57.8)	51 (75.0)	172 (47.5)	<0.001	136 (72.0)	326 (57.6)	0.001
β-Blocker	315 (26.6)	17 (25.0)	48 (13.3)	0.013	51 (27.0)	93 (16.4)	0.002
Statin	510 (43.0)	20 (29.4)	125 (34.5)	0.527	62 (32.8)	220 (38.9)	0.169
Diuretic	403 (34.0)	35 (51.5)	106 (29.3)	0.001	75 (39.7)	187 (33.0)	0.110

On the other hand, higher proportions of male subjects with LVH had hypertension (97.4 vs. 88.7 %, P = 0.001) and DM (50.3 vs. 41.7 %, P = 0.04), and lower proportions had a past history of angina (6.3 vs. 11.7 %, P = 0.038) and stroke (6.9 vs. 12.0 %, P = 0.048). The group of male subjects with LVH had higher BMI (25.5 ± 3.6 vs. 23.4 ± 3.3 kg/m2, P < 0.001), higher systolic BP (138.4 ± 19.2 vs. 131.3 ± 16.8 mmHg, P < 0.001), higher pulse pressure (60.3 ± 15.4 vs. 55.4 ± 12.9 mmHg, P < 0.001), lower eGFR (26.8 ± 13.1 vs. 29.2 ± 12.1 ml/min/1.73 m2, P = 0.017), and higher ACR (1456.7 ± 1720.6 vs. 972.6 ± 1349.3 mg/gCr, P = 0.001) than female subjects without LVH. Among the lipid parameters, male subjects with LVH had significantly lower serum HDL cholesterol level (46.6 ± 13.3 vs. 51.2 ± 17.2 mg/dl, P = 0.002) and higher serum triglyceride level (202.4 ± 149.2 vs. 166.8 ± 106.9 mg/dl, P = 0.001) than female subjects without LVH. Parameters of mineral metabolism showed the same trends in female subjects as in male subjects with LVH. Moreover, higher proportions of male than female subjects with LVH were being treated with β-blockers (27.0 vs. 16.4 %, P = 0.002).

Factors related to LVH

Table 5 shows that the factors associated with LVH were female sex (OR 1.78; 95 % CI 1.308–2.416; P < 0.001), DM (OR 1.66; 95 % CI 1.254–2.186; P < 0.001), dyslipidemia (OR 1.43; 95 % CI 1.007–2.040; P = 0.045), and hypertension (OR 3.73; 95 % CI 1.487–9.376; P = 0.005). Significant clinical factors associated with LVH were systolic BP (OR 1.23; 95 % CI 1.134–1.323; P < 0.001), diastolic BP (OR 1.16; 95 % CI 1.031–1.306; P = 0.014), pulse pressure (OR 1.25; 95 % CI 1.137–1.380; P < 0.001), eGFR (OR 0.98; 95 % CI 0.968–0.9991; P = 0.0004; Fig. 2a, b), BMI (OR 1.15; 95 % CI 1.110–1.199; P < 0.0001; Fig. 3a, b), serum uric acid (OR 1.10; 95 % CI 1.002–1.202; P = 0.046), ACR (OR 1.55; 95 % CI 1.267–1.905; P < 0.001), A1C (OR 1.17; 95 % CI 1.011–1.345; P = 0.035), serum levels of iPTH (OR 1.00; 95 % CI 1.001–1.005; P < 0.001), HDL cholesterol (OR 0.98; 95 % CI 0.971–0.989; P < 0.001), triglyceride (OR 1.00; 95 % CI 1.001–1.003; P < 0.001), calcium (OR 0.56; 95 % CI 0.431–0.720; P < 0.001) and phosphorus (OR 1.23; 95 % CI 1.004–1.515; P = 0.046), and prescription of antihypertensive agents (OR 3.51; 95 % CI 1.601–7.685; P = 0.002).

Fig. 2

Relationship between estimated glomerular filtration rate (eGFR) and left ventricular mass index (LVMI) of patients with stage 3–5 CKD. a female; b male

Fig. 3

Relationship between body mass index (BMI) and left ventricular mass index (LVMI) of patients with stage 3–5 CKD. a Female; b male

As shown in Table 6, the variables independently associated with LVH were past history of CVD (OR 0.574; 95 % CI 0.360–0.916; P = 0.020), systolic BP (OR 1.179; 95 % CI 1.021–1.360; P = 0.025), BMI (OR 1.135; 95 % CI 1.074–1.200; P < 0.001), and serum calcium level (OR 0.595; 95 % CI 0.404–0.876; P = 0.009) by multivariate logistic regression analysis.

Table 6

Factors associated with LVMI (multivariate logistic regression analysis)

Variables	OR	95 % CI	P value
Sex (female)	1.484	0.939–2.344	0.091
Age (years)	1.007	0.986–1.028	0.536
Smoking	0.649	0.388–1.087	0.101
Complications
Diabetes	1.394	0.876–2.218	0.162
Dyslipidemia	1.047	0.644–1.705	0.852
Hypertension	0.835	0.538–1.295	0.421
Medical history
Cardiovascular disease	0.574	0.360–0.916	0.020
Blood pressure
Systolic (10 mmHg)	1.179	1.021–1.360	0.025
Diastolic (10 mmHg)	1.011	0.804–1.255	0.923
BMI (kg/m2)	1.135	1.074–1.200	<0.001
eGFR (ml/min/1.73 m2)	0.993	0.974–1.014	0.526
Uric acid (mg/dl)	1.033	0.909–1.174	0.621
Urinary albumin (mg/gCr)	0.920	0.688–1.231	0.574
A1C (%)	0.867	0.681–1.105	0.250
iPTH (pg/ml)	1.000	0.997–1.002	0.816
HDL chol (mg/ml)	0.997	0.984–1.010	0.621
Triglyceride (mg/dl)	1.001	1.000–1.003	0.108
Calcium (mg/dl)	0.595	0.404–0.876	0.009
Phosphorus (mg/dl)	1.210	0.895–1.637	0.216
Medication
Antihypertensive agent	1.636	0.607–4.411	0.330

OR odds ratio, CI confidence interval

As shown in Table 7, the variables independently associated with LVH in diabetic patients were BMI (OR 1.110; 95 % CI 1.023–1.203; P = 0.012), serum triglyceride level (OR 1.002; 95 % CI 1.000–1.005; P = 0.043), and serum calcium level (OR 0.461; 95 % CI 0.273–0.777; P = 0.004) by multivariate logistic regression analysis.

Table 7

Factors associated with LVMI by diabetic CKD patients (multivariate logistic regression analysis)

Variables	OR	95 % CI	P value
Sex (female)	0.900	0.468–1.729	0.718
Age (years)	1.011	0.977–1.046	0.543
Smoking	0.518	0.243–1.106	0.089
Complications
Dyslipidemia	0.750	0.359–1.571	0.446
Hypertension	0.909	0.479–1.725	0.771
Medical history
Congestive heart failure	0.541	0.275–1.065	0.075
Blood pressure
Systolic (10 mmHg)	1.115	0.919–1.353	0.271
Diastolic (10 mmHg)	1.122	0.819–1.538	0.473
BMI (kg/m2)	1.110	1.023–1.203	0.012
eGFR (ml/min/1.73 m2)	1.000	0.972–1.029	0.995
Uric acid (mg/dl)	1.149	0.949–1.392	0.155
Urinary albumin (log mg/gCr)	0.933	0.611–1.424	0.747
A1C (%)	0.826	0.631–1.080	0.162
iPTH (pg/ml)	0.998	0.995–1.002	0.412
HDL chol (mg/dl)	0.983	0.962–1.005	0.139
Triglyceride (mg/dl)	1.002	1.000–1.005	0.043
Calcium (mg/dl)	0.461	0.273–0.777	0.004
Phosphorus (mg/dl)	1.190	0.779–1.817	0.421
Medication
Antihypertensive agent	0.877	0.236–3.263	0.845

OR odds ratio, CI confidence interval

As shown in Table 8, the variables independently associated with LVH in non-diabetic patients were male gender (OR 2.453; 95 % CI 1.241–4.849; P = 0.010), systolic BP (OR 1.355; 95 % CI 1.076–1.707; P = 0.010), and BMI (OR 1.156; 95 % CI 1.063–1.257; P = 0.001) by multivariate logistic regression analysis.

Table 8

Factors associated with LVMI by non-diabetic CKD patients (multivariate logistic regression analysis)

Variables	OR	95 % CI	P value
Sex (female)	2.453	1.241–4.849	0.010
Age (years)	0.998	0.969–1.027	0.884
Smoking	0.725	0.343–1.531	0.399
Complications
Dyslipidemia	1.201	0.599–2.410	0.605
Hypertension	0.813	0.432–1.529	0.520
Medical history
Congestive heart failure	0.544	0.275–1.077	0.081
Blood pressure
Systolic (10 mmHg)	1.355	1.076–1.707	0.010
Diastolic (10 mmHg)	0.793	0.562–1.118	0.186
BMI (kg/m2)	1.156	1.063–1.257	0.001
eGFR (ml/min/1.73 m2)	0.990	0.960–1.020	0.509
Uric acid (mg/dl)	0.901	0.747–1.087	0.278
Urinary albumin (log mg/gCr)	1.034	0.669–1.599	0.880
A1C (%)	1.084	0.498–2.358	0.839
iPTH (pg/ml)	1.001	0.998–1.005	0.569
HDL chol (mg/dl)	1.002	0.985–1.019	0.806
Triglyceride (mg/dl)	1.000	0.997–1.003	0.904
Calcium (mg/dl)	0.845	0.447–1.600	0.606
Phosphorus (mg/dl)	1.197	0.763–1.877	0.434
Medication
Antihypertensive agent	4.213	0.542–32.756	0.169

OR odds ratio, CI confidence interval

Discussion

In the present cross-sectional study, we enrolled 2977 representative Japanese outpatients, most of whom had stage 3–5 CKD. These 2977 outpatients were being treated by nephrologists and were receiving a good standard of care. UCG was performed in 1185 of them. The UCG carried out was not intended to evaluate selected patients with cardiac complications, but was performed consecutively for evaluation of cardiac function in representative participants in the CKD-JAC study, if they provided informed consent. The prevalence of LVH in the present study was much lower than that reported in previous studies in the general population. The participants in the CKD-JAC study may be better treated by nephrologists. Alternatively, cardiologists could treat more severe cases. The majority of the study subjects had hypertension and proteinuria or albuminuria on enrollment, but systolic and diastolic BP were normal (132/76 mmHg). More than 90 % of the subjects were being treated with antihypertensive agents (n = 1095, 92.4 %), including ACE inhibitors (n = 302, 25.5 %) and/or ARBs (n = 901, 76.0 %). The prevalence rates of pre-existing CVD, i.e., congestive heart failure (5.7 %), myocardial infarction (6.8 %), and stroke (12.4 %), were higher than in the general Japanese population [18]. DM was present in 41.3 % of the study subjects, and more than one-third of enrolled subjects had CKD secondary to glomerulonephritis.

The results of the present study provided information on the prevalence of LVH and factors associated with LVH in stage 3–5 CKD patients in the CKD-JAC study. In the CKD-JAC study, LVH was observed in a small population (21.7 %) of the 1185 study subjects, whereas LVMI tended to increase with the progression of CKD. CKD patients have a high prevalence of LVH, ranging from 34 to 74 % in different studies, and its prevalence increases as renal function declines [10, 12, 19, 20]. However, the relatively wide heterogeneity of the prevalence of LVH in different studies can be attributed to several differences in the characteristics of the populations studied, including differences in ethnicity, age, proportion of subjects with different stages of CKD, prevalence of hypertension, method chosen to evaluate GFR, cut-off GFR used to enroll patients, and definition of LVH.

Elevated systolic BP has a continuous, graded, and independent association with risk of coronary heart disease, stroke, and ESKD [21]. LVH might be a beneficial compensatory process in CKD patients, allowing the left ventricle to produce additional force to increase cardiac work and maintain constant wall tension [22]. Even though mean systolic BP was well controlled (132.4 ± 18.1 mmHg), systolic BP was higher in patients with LVH than in patients without LVH in the present study. According to multivariate logistic regression analysis, systolic BP was an independent variable associated with LVH. Recently, it was reported that systolic arterial hypertension and elevated pulse pressure are closely associated with LVH in pre-dialysis patients, suggesting that fluid overload and increased arterial stiffness play important roles in LVH before starting dialysis therapy [12]. Fluid volume management and maintenance of a near euvolemic state are crucial for the amelioration of LVH [23].

After adjusting for several potential confounders, multivariate logistic regression analyses showed that the presence of a previous CVD was significantly associated with LVH. The potential explanations for how the CKD state can accelerate atherosclerosis and cause CVD have been of considerable interest in clinical practice. The 4 basic explanations are: (1) uncontrolled confounding, or the impact of comorbidities that occur in CKD patients, especially older age; (2) therapeutic nihilism, meaning CKD patients receive lesser degrees of cardioprotective therapies; (3) excess treatment toxicities, intolerances, or risks such that therapy cannot be used or offers a less favorable benefit-to-risk ratio; and (4) a unique vascular pathobiology that occurs in the CKD state [24]. By using the large sample size of the Kidney Early Evaluation Program (KEEP), McCullough et al. [25] demonstrated in stratified analysis that the presence of CKD in young adults was clearly related to premature CVD. These findings suggest the biological changes that occur with CKD promote CVD at an accelerated rate that cannot be fully explained by conventional risk factors or older age.

In accordance with the theory of non-hemodynamic LVH-promoting factors in our CKD patients, BMI was found to be a factor that was independently associated with LVH. Obesity is thought to be a risk factor independent of LVH, and heart disorders in obesity include structural adaptation with LVH and functional abnormalities [26]. Kotsis et al. [27] reported that obesity and daytime pulse pressure are predictors of LVH in true normotensive individuals. In hypertensive obese patients, metabolic syndrome (MetS) maintains its role as a risk factor for LVH independently of age and systolic BP and is a useful predictor of target organ damage in clinical practice [28]. However, MetS is no longer an independent risk factor when BMI is taken into account, suggesting that the effects of MetS on LVH are mainly driven by the degree of abdominal adiposity.

Currently, information about sex differences in renal abnormalities and CVD in healthy individuals is limited and conflicting. In the Prevention of Renal and Vascular End-Stage Disease (PREVEND) study, the prevalence of microalbuminuria in men was almost double that observed in women, and for a higher value of age and BMI was greater in men than in women [29]. In addition, the presence of CKD has been found to be associated with an increased risk of cardiovascular events [30] and of cardiovascular death [31] in both women and men having different degrees of cardiovascular risk or already having CVD. A recent study has shown that logistic regression analysis demonstrated that the factors significantly associated with the prevalence of LVH were age and BMI in women and uric acid in men [32]. In the present study, men were significantly associated with LVH in non-diabetic CKD patients. In our cohort, men had higher prevalence of classical cardiovascular risk factors including hypertension, past history of previous CVD, hyperuricemia, and lower HDL cholesterol, suggesting that classical cardiovascular risk factors may be associated with LVH in men with non-diabetic CKD.

Various abnormalities of mineral–bone metabolism are common in CKD patients, and mineral metabolism disorders such as hypocalcemia, hyperphosphatemia, and vitamin D deficiency have been found to be closely associated with CVD in CKD patients [33]. The mean serum calcium and phosphorus levels in the subjects of the present study were within the normal ranges, but differed between the groups with and without LVH. Serum iPTH level was elevated in patients with LVH and differed from that in the group without LVH. Hypocalcemia was associated with LVH by multivariate logistic regression analysis. Although its mechanism is not completely known, hypocalcemia followed by vitamin D deficiency may be associated with the pathogenesis of LVH. The results of the present study suggested that disorders of mineral metabolism may be involved in the etiology of LVH.

In conclusion, the results of this study showed that the prevalence of LVH was low in stage 3–5 CKD patients treated by nephrologists in Japan. The cross-sectional baseline data from the CKD-JAC study shed light on the association between LVH and risk factors in patients with decreased renal function. Differences in the presence of previous CVD, blood pressure control, and metabolic state may lead to different outcomes of CVD in a longitudinal study. Future analysis of the CKD-JAC cohort will clarify whether the incidence of LVH varies with the causative disease during further follow-up.