BioMed Research International

BioMed Research International / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 1541593 | 9 pages | https://doi.org/10.1155/2019/1541593

Insulin Resistance and Cardiovascular Risks in Different Groups of Hemodialysis Patients: A Multicenter Study

Academic Editor: Koichiro Wada
Received27 Dec 2018
Revised20 Feb 2019
Accepted16 May 2019
Published11 Jun 2019

Abstract

Background. To investigate the association between insulin resistance (IR) and cardiovascular disease (CVD) risks among hemodialysis patients. Methods. We conducted a cross-sectional study between 2013 and 2017, on 384 hemodialysis patients from seven hospital-based-dialysis centers. HOMA-IR is classified according to median value. The CVD risks were defined by the K/DOQI Guidelines. Logistic regression analysis was used. Results. Patients’ age was 60.9 ± 11.8, 58.1% men, and 40.3% overweight/obese. The median of HOMA-IR was 5.4, 82.8% high systolic blood pressure, and 85.7% hyperhomocysteinemia. In multivariate analysis, IR was significantly associated with higher odds of low high-density lipoprotein cholesterol, high triglyceride, and impaired fasting glucose in groups of normal weight, overweight/obese, nondiabetes, diabetes, and overall sample. IR linked with elevated high-sensitive C-reactive protein in normal weight patients (odd ratio, OR=2.21, 95% confidence interval, 1.16-4.22, p < .05), with hypoalbuminemia in normal weight patients (OR=8.31, 95% CI, 2.35-29.37, p < .01), in nondiabetes patients (OR=6.59, 95% CI, 1.81-23.95, p < .01), and overall sample (OR=3.07, 1.51-6.23, p < .01). Conclusions. The level of IR and prevalence of CVD risks were high in hemodialysis patients. IR was independently associated with CVD risks.

1. Introduction

The incidence and prevalence of treated end-stage renal disease (ESRD) have been steadily increased over the past decades across countries. In 2014, Taiwan has reported the highest number of treated ESRD with 455 new cases and the prevalence of 3219 patients per million general population (PMP). Taiwan has also experienced the highest number of maintenance hemodialysis in the world with 3093 patients PMP, 90% of them receiving in-center hemodialysis [1].

Cardiovascular disease (CVD) has been reported as the leading cause of death and disability all over the world. In 2013, CVD accounted for about 17 million deaths and 329 million disability adjusted life-years lost [2]. In ESRD patients, the cardiovascular cause of death is 10-20 times higher in the healthy population and accounted for more than half of all death [3].

Insulin resistance (IR) is with high prevalence in the ESRD patients [4]. IR its self is a risk for CVD and strongly associates with other CVD risks (dyslipidemia, hypertension, and inflammation) through several pathophysiologic mechanisms, which is well documented [5]. In ESRD patients undergoing hemodialysis, the cardiovascular risks worsen the arterial stiffness which contributes to the development of cardiovascular events and diseases [6]. IR is the anterior consequence of obesity [7]. In ESRD patients, IR then links to dyslipidemia, impaired fasting glucose, and cardiovascular risks and events [5, 8, 9]. In empirical researches, IR is closely associated with cardiovascular risks such as obesity, hypertension, and dyslipidemia [10], anemia [4], inflammation [11, 12], and echocardiography parameters [12]. In turn, IR significantly predicts cardiovascular diseases and mortality in ESRD patients [1316]. Therefore, assessment of IR is critically important work for nephrologist and nurses to follow up patients and have appropriate interventions.

The ESRD has created a heavy burden for the healthcare system all around the world over the past decade [1]. However, the number of clinicians has not adequately increased to meet the greater demand for renal treatment [17]. The early detection of the IR and its associated factors might contribute to prevent CVD risks and reduce the burden. On the other hand, improving IR might be an important therapeutic target and contribute to better health outcomes in hemodialysis patients [18, 19]. This study was to assess the prevalence and explore the association between IR and CVD risk factors among ESRD patients undergoing hemodialysis.

2. Materials and Methods

2.1. Study Design

A clinical cross-sectional study was conducted between September 2013 and April 2017 in seven dialysis centers in Taiwan. A total of 384 hemodialysis patients were recruited from Taipei Medical University Hospital (55 patients collected from September to December 2013; 42 patients collected from November 2016 to January 2017); Taipei Medical University, Wan Fang Hospital (51 patients collected from April to May 2014); Taipei Medical University, Shuang Ho Hospital (39 patients collected in December 2014); Cathay General Hospital (41 patients collected in March 2016); Taipei Tzu-Chi Hospital (57 patients collected in November 2016); Wei-Gong Memorial Hospital (59 patients collected from February to March 2017); and Lotung Poh-Ai Hospital (50 patients collected in April 2017).

2.2. Hemodialysis Patients and Data Sources

We included patients aged above 20 years, receiving thrice-weekly hemodialysis treatment for at least 3 months and adequate dialysis quality (equilibrated Kt/V ≥ 1.2 g/kg/day). The exclusion criteria were patients who were diagnosed with pregnancy, amputation, hyperthyroidism, hypothyroidism, and malignancy, received tube feeding, exhibited hepatic failure or cancer, were hospitalized within one month prior to the recruitment, or were scheduled for surgery. Volume overload or edema closely linked with other clinical instability [20]. Therefore, patients with evidence of edema were excluded in the current study and in previous studies [2123].

The eligible patients in selected hospitals signed the informed consents before conducting chart reviews and laboratory evaluations. The patients’ medical records were reviewed. The blood samples were collected by licensed nurses, at the start of the first dialysis session of the week, and then analyzed in the hospital laboratory by using commercially available test kits, which was described carefully in previous studies [24, 25].

2.3. Insulin Resistance Index

The blood samples collected by the registered nurse were centrifuged in each hospital laboratory. The serum was separated and kept in the ice-pack, then sent to the laboratory in Taipei Medical University Hospital for serum insulin analysis. Therefore, all samples were analyzed with the same commercial kit. The homeostatic model assessment of insulin resistance index (HOMA-IR) is used to assess IR. The index is calculated using the formula developed by Matthews et al. [26]: Patients were separated into two groups based on the median value as the nonnormal distribution of HOMA-IR; this method was applied in previous studies [14, 27].

2.4. Cardiovascular Risks

The traditional and nontraditional CVD risks were described in the previous study [22] and the current study with the details below. In the present study, more factors were assessed and reported, such as physical activity, medical history (diabetes, hypertension, and cardiovascular disease), and other biochemical parameters (blood urea nitrogen, uric acid, creatinine, and fasting plasma insulin).

2.4.1. Traditional CVD Risk Factors

The traditional risks of cardiovascular diseases include factors which were mentioned in previous studies [28, 29]. (1) Hypertension: systolic blood pressure (SBP) ≥ 130 mmHg and diastolic blood pressure (DBP) ≥ 85 mmHg [30]; (2) impaired fasting glucose (IFG): patients diagnosed with type 2 diabetes mellitus or fasting plasma glucose (FPG) ≥ 100 mg/dL [30]; (3) dyslipidemia including high serum triglyceride (TG) level at TG ≥150 mg/dL, low level of serum high-density lipoprotein cholesterol (HDL-C) at < 40 mg/dL in men and < 50 mg/dL in women, high level of serum low-density lipoprotein cholesterol (LDL-C) at ≥ 100 mg/dL, and high serum total cholesterol at TC ≥ 200 mg/dL [31].

2.4.2. Nontraditional/Novel CVD Risk Factors

Anemia: the targeted hemoglobin (Hb) level should be 11g/dL or greater, as moderately strong recommended by The National Kidney Foundation Kidney Disease Outcomes Quality Initiative (K/DOQI) Work Group [32]. Anemia is classified as Hb < 11 g/dL. Mineral metabolism abnormalities: albumin-corrected calcium = total calcium (mg/dL) + 0.8 x (4.0 – serum albumin in g/dL) [33]. Corrected calcium and phosphate levels at each time were used to calculate calcium-phosphate product (Ca x PO4). The serum calcium (Ca) is classified into low level (Ca < 8.4 mg/dL), normal level (Ca 8.4- 9.5 mg/dL), and high (Ca > 9.5 mg/dL). The serum phosphate (PO4) is also classified into low level (PO4 < 3.5 mg/dL), normal (PO4 3.5- 5.5 mg/dL), and high (PO4 > 5.5 mg/dL). Calcium-phosphate product is classified into normal (Ca x PO4 < 55 mg2 / dL2) and high (Ca x PO4 ≥ 55 mg2 / dL2). In addition, intact parathyroid hormone (iPTH) is classified as normal (iPTH 150-300 pg/mL), and high (iPTH ≥ 300 pg/mL) [34]. Hyperhomocysteinemia is defined as total plasma homocysteine (Hcy) > 14 μmol/L [29]. Inflammation is defined as high sensitive C-reactive protein (hs-CRP) > 0.3 mg/dL as the risk factor for CVD [35]. The poor nutritional status is defined as serum albumin ≤ 3.5 mg/dL as applied in hemodialysis patients from 11 countries in the Dialysis Outcomes and Practice Patterns Study (DOPPS) [36]. Hyperkalemia is identified as serum potassium ≥ 5.0 mEq/L as the risk of cardiovascular mortality in hemodialysis patients [37].

2.5. Statistical Analysis

The descriptive analyses describe the patients’ characteristics, insulin resistance (IR), cardiovascular disease risk factors via the mean, standard deviation, or median, interquartile range, frequency, and percentage. The independent-samples t-test, Chi-square test, and Mann-Whitney U test were used appropriately to test the distribution of patients’ characteristics, CVD risks, and HOMA-IR in different groups of body mass index (BMI) and DM. In order to carefully examine the association between IR and traditional and nontraditional risk factors, the multivariate logistic regressions are used to estimate the odd ratios. Since obesity is the most common cause of IR [7], we analyzed the association in different groups of BMI (normal weight versus overweight/obese). The associations were also analyzed in a group of patients with diabetes and nondiabetes. The analyses were adjusted for age and gender, hemodialysis vintage, Charlson comorbidity index, and body mass index (for overall sample). These adjusted factors might be the confounders as they showed the relationship with IR [3842]. All statistical analyses are performed by the SPSS for Windows v20.0 (IBM Corp., New York, USA). The significant level is set at p value < .05.

2.6. Ethical Approval

The study is approved by the Joint Institutional Review Board of Taipei Medical University (TMU-JIRB No. 201302024), which was for conducting the study in three hospitals of Taipei Medical University (Taipei Medical University Hospital, Wan-Fang Hospital, Shuang Ho Hospital), Wei-Gong Memorial Hospital, and Lotung Poh-Ai Hospital; the ethical committee of Cathay General Hospital (CGH-OP104001); and Taipei Tzu-Chi Hospital (04-M11-090). All patients involved in the study have signed the informed consent statement.

3. Results

Of the total sample, the average age of patients was 60.9 ± 11.8, 58.1% men, and 40.3% overweight or obese. The traditional CVD risk factors included high SBP (82.8%), high DBP (25.5%), high TC (16.7%), high LDL-C (48.4%), low HDL-C (65.9%), high TG (40.6%), and impaired fasting glucose (69.5%). The nontraditional CVD risks included anemia (58.3%), low calcium (8.3%), high calcium (35.2%), low phosphate (7.0%), high phosphate (35.4%), high calcium-phosphate product (25.5%), high intact parathyroid hormone (42.7%), hyperhomocysteinemia (85.7%), elevated hs-CRP (45.6%), and low serum albumin (12.0%; Table 1).


Total sample
(n=384)
BMI < 24.0
(n=229)
BMI ≥ 24.0
(n=155)
p valueNon-DM
(n=230)
DM
(n=154)
p value

Characteristics
 Age, years60.9 ± 11.861.0 ± 12.060.7 ± 11.50.80959.4 ± 11.963.0 ± 11.20.003
 Gender223 (58.1%)127 (55.5%)96 (61.9%)0.207129 (56.1%)94 (61.0%)0.335
 Dialysis vintage, years5.5 ± 4.96.1 ± 5.44.7 ± 4.00.0076.8 ± 5.63.7 ± 2.8<0.001
 CCI score4.7 ± 1.64.6 ± 1.64.8 ± 1.50.2954.1 ± 1.45.5 ± 1.3<0.001
 PA, MET-min/wk4911.6 ± 1871.84874.5 ± 1900.34966.5 ± 1833.70.6374964.7 ± 1929.04832.4 ± 1786.30.498
 BMI, kg/m223.5 ± 3.921.0 ± 1.927.2 ± 3.0<0.00122.6 ± 3.424.9 ± 4.1<0.001
 DM154 (40.1%)66 (28.8%)88 (56.8%)<0.001---
 HTN191 (49.7%)107 (46.7%)84 (54.2%)0.151108 (47.0%)83 (53.9%)0.183
 CVD115 (29.9%)63 (27.5%)52 (33.5%)0.20555 (23.9%)60 (39.0%)0.002
Traditional CVD risks
 SBP ≥ 130 mmHg318 (82.8%)189 (82.5%)129 (83.2%)0.860181 (78.7%)137 (89.0%)0.009
 DBP ≥ 85 mmHg98 (25.5%)60 (26.2%)38 (24.5%)0.71059 (25.7%)39 (25.3%)0.942
 TC ≥ 200 mg/dL64 (16.7%)33 (14.4%)31 (20.0%)0.14938 (16.5%)26 (16.9%)0.926
 LDL-C ≥ 100 mg/dL186 (48.4%)39 (17.0%)32 (20.6%)0.37145 (19.6%)26 (16.9%)0.507
 HDL-C < 40 mg/dL for men, < 50 mg/dL for women253 (65.9%)133 (58.1%)120 (77.4%)<0.001132 (57.4%)121 (78.6%)<0.001
 TG ≥ 150 mg/dL156 (40.6%)68 (29.7%)88 (56.8%)<0.00168 (29.6%)88 (57.1%)<0.001
 IFG (FPG ≥ 100 mg/dL, or DM)267 (69.5%)145 (63.3%)122 (78.7%)0.001113 (49.1%)154 (100.0%)<0.001
Non-traditional CVD risks
 Hemoglobin < 11 g/dL224 (58.3%)137 (59.8%)87 (56.1%)0.471131 (57.0%)93 (60.4%)0.504
 Calcium < 8.4 mg/dL32 (8.3%)17 (7.4%)15 (9.7%)0.01718 (7.8%)14 (9.1%)0.906
 Calcium > 9.5 mg/dL135 (35.2%)69 (30.1%)66 (42.6%)81 (35.2%)54 (35.1%)
 Phosphate < 3.5 mg/dL27 (7.0%)16 (7.0%)11 (7.1%)0.07916 (7.0%)11 (7.1%)0.992
 Phosphate > 5.5 mg/dL136 (35.4%)71 (31.0%)65 (41.9%)82 (35.7%)54 (35.1%)
 Ca x PO4 ≥ 55 mg2/dL298 (25.5%)45 (19.7%)53 (34.2%)0.00158 (25.2%)40 (26.0%)0.868
 i-PTH ≥ 300 pg/mL164 (42.7%)99 (43.2%)65 (41.9%)0.801111 (48.3%)53 (34.4%)0.007
 Hcy > 14 μmol/L329 (85.7%)196 (59.6%)133 (40.4%)0.953195 (59.3%)134 (40.7%)0.541
 hs-CRP > 0.3 mg/L175 (45.6%)59 (25.8%)55 (35.5%)0.04160 (26.1%)54 (35.1%)0.059
 Albumin ≤ 3.5 g/dL46 (12.0%)26 (11.4%)20 (12.9%)0.64619 (8.3%)27 (17.5%)0.006
 Serum K ≥ 5.0 mEq/L135 (35.2%)82 (35.8%)53 (34.2%)0.74588 (38.3%)47 (30.5%)0.119
HOMA-IR5.4 (2.2, 11.0)3.9 (1.7, 9.8)6.9 (3.8, 14.3)<0.0014.1 (1.8, 9.9)6.4 (3.3, 12.5)<0.001
Others
 Pre-BUN, mg/dL72.5 ± 19.972.6 ± 19.672.3 ± 20.50.87073.9 ± 20.770.4 ± 18.60.090
 Post-BUN, mg/dL20.0 ± 10.419.2 ± 12.021.2 ± 7.20.06619.6 ± 7.620.6 ± 13.50.362
 Uric acid, mg/dL7.3 ± 1.37.1 ± 1.27.5 ± 1.40.0027.4 ± 1.27.0 ± 1.30.003
 Creatinine, mg/dL11.1 ± 2.210.7 ± 1.811.7 ± 2.4<0.00111.4 ± 2.010.6 ± 2.20.001
 FPG, mg/dL132.4 ± 58.1127.2 ± 59.8139.9 ± 54.9.036113.0 ± 41.7161.3 ± 66.7<0.001
 FPI, μU/mL17.2 (8.8, 32.0)14.1 (6.8, 27.0)23.0 (12.7, 36.8)<0.00115.5 (7.6, 32.4)19.2 (9.7, 31.6)0.283

Categorical data is shown as n (%). Continuous data is presented as mean ± SD or median (interquartile range). P values calculated using Chi-square test, independent-samples T test, or Mann-Whitney U test.
The diagnosed values were defined by the National Kidney Foundation Kidney Disease Outcomes Quality Initiative Work Group.
BMI, body mass index; DM, diabetes mellitus; HTN, hypertension; CVD, cardiovascular diseases; CCI, Charlson comorbidity index; PA, physical activity; MET, metabolic equivalent minute/ week; SBP, systolic blood pressure; DBP, diastolic blood pressure; TC, total cholesterol; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; TG, triglyceride; IFG, impaired fasting glucose; CaxPO4, calcium phosphate product; iPTH, intact parathyroid hormone; Hcy, homocysteine; hs-CRP, high sensitive C-reactive protein; K, serum potassium; HOMA-IR, homeostatic model assessment of insulin resistance; BUN, blood urea nitrogen; FPG, fasting plasma glucose; FPI: fasting plasma insulin.

In comparison with normal weight patients, those with overweight/obese had a higher prevalence of low HDL-C, high TG, IFG, low serum Ca, elevated CaxPO4, elevated hs-CRP, and elevated HOMA-IR (p < .05). On the other hand, patients with DM had a higher proportion of high SBP, low HDL-C, high TG, IFG, elevated iPTH, low serum albumin, and elevated HOMA-IR, as compared with non-DM patients (p < .05; Table 1).

The results of multivariate regression analyses are shown in Tables 2 and 3. After control for age, gender, hemodialysis vintage, Charlson Comorbidity Index, and physical activity, in normal weight patients, IR was significantly associated with higher odds of low HDL-C (OR, 1.75, 95%CI, 1.01-3.06, p < .05), high TG (OR, 3.41, 95%CI, 1.78-6.53, p < .001), IFG (OR, 8.15, 95%CI, 4.14-16.02, p < .001), elevated hs-CRP (OR, 2.21, 95%CI, 1.16-4.22, p < .05), and lower odd of hypoalbuminemia (OR, 8.31, 95%CI, 2.35-29.37, p < .01), but with lower odds of high SBP (OR, 0.36, 95%CI, 0.17-0.76, p < .01), high PO4 (OR, 0.52, 95%CI, 0.28-0.96, p < .05), and hyperkalemia (OR, 0.39, 95%CI, 0.22-0.70, p < .01). In overweight/obese patients, IR was significantly linked with higher odds of low HDL-C (OR, 4.15, 95%CI, 1.71-10.06, p < .01), high TG (OR, 3.06, 95%CI, 1.53-6.13, p < .01), and IFG (OR, 10.76, 95%CI, 3.36-34.5, p < .001).


High SBPHigh DBPHigh TCHigh LDL-CLow HDL-CHigh TGIFG
OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)

Normal weight
 Model 10.42 (0.20, 0.86)0.90 (0.50, 1.63)0.80 (0.38, 1.68)0.83 (0.49, 1.39)1.68 (0.99, 2.86)2.79 (1.54, 5.06)8.22 (4.35, 15.52)
 Model 20.36 (0.17, 0.76)1.13 (0.60, 2.12)0.81 (0.37, 1.75)0.78 (0.45, 1.36)1.75 (1.01, 3.06)3.41 (1.78, 6.53)8.15 (4.14, 16.02)
Overweight/Obese
 Model 11.68 (0.71, 3.97)1.05 (0.51, 2.19)1.14 (0.52, 2.50)0.84 (0.45, 1.58)3.65 (1.58, 8.45)2.90 (1.50, 5.61)6.06 (2.33, 15.74)
 Model 21.69 (0.66, 4.29) 0.75 (0.33, 1.68)0.99 (0.42, 2.33)0.80 (0.41, 1.55)4.15 (1.71, 10.06)3.06 (1.53, 6.13)10.76 (3.36, 34.5)
Non-diabetes
 Model 10.69 (0.37, 1.31)1.15 (0.63, 2.07)0.78 (0.39, 1.56)0.90 (0.54, 1.51)2.38 (1.39, 4.07)3.40 (1.85, 6.25)10.64 (5.78, 19.58)
 Model 20.61 (0.31, 1.18)1.21 (0.64, 2.30)0.64 (0.31, 1.35)0.76 (0.44, 1.33)2.14 (1.23, 3.75)3.22 (1.69, 6.12)12.54 (6.39, 24.63)
Diabetes
 Model 11.49 (0.54, 4.15)0.93 (0.45, 1.93)1.00 (0.43, 2.32)0.77 (0.41, 1.45)2.40 (1.07, 5.38)3.75 (1.91, 7.37)
 Model 22.11 (0.70, 6.31)0.94 (0.43, 2.05)1.16 (0.44, 3.05)0.78 (0.40, 1.54)3.07 (1.28, 7.33)4.29 (2.05, 8.98)
Overall
 Model 10.80 (0.47, 1.37)1.00 (0.63, 1.58)0.80 (0.47, 1.37)0.72 (0.48, 1.07)2.65 (1.71, 4.11)3.67 (2.39, 5.66)8.14 (4.77, 13.89)
 Model 20.76 (0.43, 1.32)1.11 (0.68, 1.83)0.75 (0.42, 1.32)0.63 (0.41, 0.96)2.53 (1.59, 4.01)3.58 (2.25, 5.69)7.99 (4.50, 14.18)

Significant level at p < 0.05, p < 0.01, and p < 0.001.
Model 1: elevated HOMA-IR and traditional CVD risk factors.
Model 2: adjusted for age, gender, hemodialysis vintage, Charlson comorbidity index, physical activity, and body mass index (for nondiabetes, diabetes, and overall sample).
SBP, systolic blood pressure; DBP, diastolic blood pressure; TC, total cholesterol; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; TG, triglyceride; IFG, impaired fasting glucose.

AnemiaLow CaHigh CaLow PO4High PO4High CaxPO4High iPTHHigh HcyHigh CRPLow AlbHyperkalemia
OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)OR (95%CI)

Normal weight
 Model 11.17 (0.69, 1.99)0.99 (0.36, 2.72)0.68 (0.38, 1.21)1.86 (0.61, 5.62)0.52 (0.29, 0.93)0.47 (0.24, 0.93)0.77 (0.45, 1.30)1.08 (0.52, 2.27)2.19 (1.18, 4.03)9.25 (2.69, 31.79)0.39 (0.22, 0.68)
 Model 20.98 (0.55, 1.72)1.25 (0.42, 3.69)0.72 (0.39, 1.32)1.71 (0.54, 5.40)0.52 (0.28, 0.96)0.51 (0.25, 1.03)0.83 (0.48, 1.44)0.98 (0.45, 2.12)2.21 (1.16, 4.22)8.31 (2.35, 29.37)0.39 (0.22, 0.70)
Overweight/Obese
 Model 10.84 (0.45, 1.59)4.27 (1.24, 14.69)1.86 (0.95, 3.65)3.72 (0.92, 15.08)1.63 (0.84, 3.15)1.26 (0.65, 2.45)1.39 (0.74, 2.65)0.96 (0.39, 2.36)0.80 (0.41, 1.55)0.83 (0.32, 2.13)0.71 (0.36, 1.38)
 Model 20.82 (0.41, 1.62)3.00 (0.80, 11.20)1.94 (0.96, 3.90)3.54 (0.84, 14.96)1.69 (0.82, 3.51)1.23 (0.60, 2.50)1.36 (0.68, 2.71)0.98 (0.38, 2.53)1.04 (0.51, 2.10)0.68 (0.25, 1.82)0.87 (0.42, 1.79)
Non-diabetes
 Model 11.04 (0.62, 1.75)1.55 (0.57, 4.24)0.87 (0.50, 1.52)2.74 (0.84, 8.93)0.65 (0.37, 1.13)0.83 (0.46, 1.51)0.97 (0.58, 1.62)1.07 (0.52, 2.20)1.58 (0.87, 2.86)6.03 (1.71, 21.32)0.32 (0.18, 0.56)
 Model 21.04 (0.60, 1.82)1.44 (0.49, 4.20)0.75 (0.42, 1.36)2.62 (0.78, 8.85)0.51 (0.27, 0.95)0.62 (0.32, 1.22)0.86 (0.50, 1.48)1.01 (0.47, 2.16)1.58 (0.85, 2.95)6.59 (1.81, 23.95)0.31 (0.17, 0.57)
Diabetes
 Model 11.18 (0.62, 2.25)2.38 (0.74, 7.71)1.79 (0.90, 3.55)2.24 (0.61, 8.22)1.73 (0.87, 3.42)1.00 (0.49, 2.06)1.50 (0.77, 2.93)0.63 (0.24, 1.64)1.26 (0.65, 2.44)2.31 (0.96, 5.52)1.06 (0.54, 2.11)
 Model 21.12 (0.56, 2.21)2.11 (0.55, 8.15)1.59 (0.77, 3.28)2.41 (0.62, 9.40)1.70 (0.82, 3.49)0.97 (0.45, 2.06)1.71 (0.82, 3.54)0.74 (0.27, 2.04)1.22 (0.60, 2.48)2.05 (0.80, 5.26)1.18 (0.57, 2.46)
Overall
 Model 11.09 (0.73, 1.64)1.53 (0.72, 3.25)1.03 (0.67, 1.59)2.53 (1.06, 6.02)1.01 (0.66, 1.54)0.95 (0.60, 1.50)0.88 (0.59, 1.32)1.24 (0.70, 2.19)1.42 (0.91, 2.21)3.23 (1.62, 6.45)0.51 (0.33, 0.78)
 Model 21.06 (0.69, 1.63)1.38 (0.61, 3.15)0.95 (0.60, 1.49)2.35 (0.97, 5.71)0.99 (0.62, 1.57)0.89 (0.54, 1.46)0.93 (0.61, 1.43)1.27 (0.70, 2.30)1.30 (0.82, 2.06)3.07 (1.51, 6.23)0.56 (0.36, 0.88)

Significant level at p < 0.05, p < 0.01, p < 0.001.
Model 1: elevated HOMA-IR and traditional CVD risk factors.
Model 2: adjusted for age, gender, hemodialysis vintage, Charlson comorbidity index, physical activity, and body mass index (for nondiabetes, diabetes, and overall sample).
Ca, serum calcium; PO4, serum phosphorus; CaxPO4, calcium phosphorus product; iPTH, intact parathyroid hormone; hs-CRP, high sensitive C-reactive protein; Alb, serum albumin.

After being adjusted for age, gender, hemodialysis vintage, Charlson Comorbidity Index, and physical activity, and body mass index, in non-DM patients, IR was significantly linked with higher odds of low HDL-C (OR, 2.14, 95%CI, 1.23-3.75, p < .01), high TG (OR, 3.22, 95%CI, 1.69-6.12, p < .001), IFG (OR, 12.54, 95%CI, 6.39-24.63, p < .001), and hypoalbuminemia (OR, 6.59, 95%CI, 1.81-23.95, p <.01), but with lower odd of hyperkalemia (OR, 0.31, 95%CI, 0.17-0.57, p < .001). In DM patients, IR was significantly linked with higher odds of low HDL-C (OR, 3.07, 95%CI, 1.28-7.33, p < .05) and high TG (OR, 4.29, 95%CI, 2.05-8.98, p < .001). In overall sample, the elevated level of HOMA-IR was significantly associated with higher odds of low HDL-C (OR, 2.53, 95%CI, 1.59-4.01, p <.001), high TG (OR, 3.58, 95%CI, 2.25-5.69, p < .001), IFG (OR, 7.99, 95%CI, 4.50-14.18, p < .001), and hypoalbuminemia (OR, 3.07, 95%CI, 1.51-6.23, p <.01), but with lower odd of hyperkalemia (OR, 0.56, 95%CI, 0.36-0.88, p < .05; Tables 2 and 3).

4. Discussion

The level of IR is higher in overweight/obese and DM patients than in normal weight and non-DM patients in the current study. Obesity is also reported as the most common cause of IR previously [7].

In regard to traditional CVD risks, IR is significantly associated with a higher prevalence of dyslipidemia such as low HDL-C, high TG in the current study. The finding was also found in both the general population [43] and hemodialysis patients [9]. In the previous study, IR was found to reduce HDL-C in hemodialysis patients [9]. On the other hand, IR was also associated with higher likelihood of having impaired fasting glucose in all groups of patients, independent of age, gender, hemodialysis vintage, Charlson comorbidity index, Physical activity, and body mass index. The IR was well-documented as the immediate factor between obesity and impaired fasting glucose and cardiovascular diseases in the literature [5, 8]. Therefore, early interventions at stages of obesity or IR are extremely important to prevent and mitigate the adverse consequences of CVD risks, such as dietary intake, physical activities, and medication [5].

Regarding the nontraditional risks, the prevalence of elevated hs-CRP was higher in overweight/obese patients than those with normal weight. A previous study has also reported that patients with central obesity had higher hs-CRP level than those without [44]. The level of hs-CRP was not significantly differed among HD patients with and without DM. This was also found in HD patients in Japan that hs-CRP was similar between HD patients with DM, HD patients with metabolic syndrome (MS), and those with neither DM nor MS [9]. In addition, the prevalence of malnutrition in the current study was with 12.0% hypoalbumin; it is much lower than in the previous study conducted in Turkey with 44.1% hypoalbumin [45].

In the current study, there is also no significant association between IR and hs-CRP in patients with DM or non-DM patients or overweight/obese, but it existed in normal weight patients. The association between IR and hs-CRP was found in the overall sample in Turkey [11, 12] and in 598 overweight/obese patients in Spain [44]. On the other hand, the association between IR and hypoalbumin was found in hemodialysis patients with normal weight, and non-DM, and overall sample. This was also shown in a previous study [12]. It is important to take into account the evaluation of IR level, hs-CRP, and serum albumin, in order to prevent and intervene against CVD risks and diseases.

There were some contradictory findings between the current study and the previous one. Firstly, the IR associated with a lower likelihood of having high SBP in the current study which was in contrast with the previous finding [10]. Next, IR was related to a lower likelihood of hyperkalemia in normal weight, non-DM, and overall sample. This happened as the result of kalemia lowering treatment among hemodialysis patients. Finally, in normal weight, and non-DM sample, IR was associated with a lower likelihood of hyperphosphatemia in the current study. Hyperphosphatemia and high level of CaxPO4 combination were found to link with higher all-cause mortality in hemodialysis patients [46].

The study was of a cross-sectional nature; the causal relationship, therefore, cannot be generated. The interpretation of results should be cautious. The data related to supplement intake and medication was not explored. Therefore, the association between IR and some CVD risks was not well explained. Smoking is known as a major traditional cardiovascular risk factor. It is reported that 85.1% of patients were nonsmokers [47]. In the United State, based on data of USRDS, 6.2% of dialysis patients were smokers [48]. Therefore, we did not collect the data on smoking status in the current study. Future longitudinal, case-control, or intervention studies are encouraged to carefully examine the association.

5. Conclusions

The insulin resistance (IR) and CVD risks were common in hemodialysis patients. IR was associated with a higher prevalence of dyslipidemia (low HDL-C, high TG), impaired fasting glucose, elevated hs-CRP, and hypoalbuminemia. Addressing the assessment and treatment of IR and CVD risks in clinical practice could help with improving the hemodialysis outcomes.

Data Availability

Since the dataset contains sensitive and identifying information, any modification or deidentification on the dataset is restricted. The authors confirm that the data is available upon request. Requests may be sent to the corresponding author, Shwu-Huey Yang (sherry@tmu.edu.tw).

Disclosure

The funder had no role in the decision to collect data, data analysis, or reporting of the results. The abstract was presented at the Annual Dialysis Conference 2018, Mar 3-6, 2018, Orlando, Florida.

Conflicts of Interest

The authors had no conflicts of interest relevant to this article to be disclosed.

Authors’ Contributions

Tuyen Van Duong consulted a statistician, analyzed and interpreted the data, and drafted the manuscript. Chun-Kuang Shih, Te-Chih Wong, Hsi-Hsien Chen, Tso-Hsiao Chen, Yung-Ho Hsu, Sheng-Jeng Peng, Ko-Lin Kuo, Hsiang-Chung Liu, and En-Tzu Lin contributed to conception and design, acquisition of data, and discussion. Chien-Tien Su and Shwu-Huey Yang contributed to the overall conception and design and critically reviewed the manuscript. All authors read and approved the final version of the manuscript.

Acknowledgments

The authors thank medical staff and patients from Taipei Medical University Hospital, Wan-Fang Hospital, Shuang Ho Hospital, Cathay General Hospital, and Taipei Tzu-Chi Hospital, Wei-Gong Memorial Hospital, and Lutong Poh-Ai Hospital. The authors also thank Chi-Sin Huang, I-Hsin Tseng, Yi-Wei Feng, and Tai-Yue Chang for helping with data collection. The research was funded by the Ministry of Science and Technology in Taiwan (NSC-102-2320-B-038-026; MOST 105-2320-B-038-033-MY3).

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