The Association between Persistent Hypertriglyceridemia and the Risk of Diabetes Development: The Kangbuk Samsung Health Study

Yu Hyun Kwon; Seul-Ki Kim; Jung Hwan Cho; Hyemi Kwon; Se Eun Park; Hyung-Geun Oh; Cheol-Young Park; Won-Young Lee; Ki-Won Oh; Sung-Woo Park; Eun-Jung Rhee

doi:10.3803/EnM.2018.33.1.55

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Kwon, Kim, Cho, Kwon, Park, Oh, Park, Lee, Oh, Park, and Rhee: The Association between Persistent Hypertriglyceridemia and the Risk of Diabetes Development: The Kangbuk Samsung Health Study

Original Article

Endocrinology and Metabolism 2018; 33(1): 55-61.

Published online: 30 January 2018

DOI: https://doi.org/10.3803/EnM.2018.33.1.55

The Association between Persistent Hypertriglyceridemia and the Risk of Diabetes Development: The Kangbuk Samsung Health Study

Yu Hyun Kwon¹, Seul-Ki Kim¹, Jung Hwan Cho¹, Hyemi Kwon¹, Se Eun Park¹, Hyung-Geun Oh², Cheol-Young Park¹, Won-Young Lee¹, Ki-Won Oh¹, Sung-Woo Park¹, Eun-Jung Rhee¹

¹Division of Endocrinology and Metabolism, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.

²Department of Neurology, Soonchunhyang University Cheonan Hospital, Soonchunhyang University College of Medicine, Cheonan, Korea.

Corresponding author: Eun-Jung Rhee. Division of Endocrinology and Metabolism, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, 29 Saemunan-ro, Jongno-gu, Seoul 03181, Korea. Tel: +82-2-2001-2485, Fax: +82-2-2001-1588, hongsiri@hanmail.net

Received 2 July 2017 Revised 19 August 2017 Accepted 19 September 2017

Korean Endocrine Society

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Hypertriglyceridemia is known to have an association with increased risks of insulin resistance and diabetes. The aim of this study was to investigate the risk of diabetes mellitus, according to changes in the concentrations of triglycerides, over time.

Methods

A total of 15,932 non-diabetic participants (mean age 43.2 years, 68% men) who attended five consecutive annual health check-ups at Kangbuk Samsung Hospital, between January 2010 and December 2014, were recruited. Participants were classified according to their triglyceride concentrations; normal (<150 mg/dL) and abnormal (≥150 mg/dL). According to the triglyceride levels in 2010 and 2012, subjects were divided into four groups: normal-normal, normal-abnormal, abnormal-normal, and abnormal-abnormal. The risk for incident diabetes was assessed in 2014.

Results

Among the total subjects, 67.5% belonged to the normal-normal group, 8.6% to the normal-abnormal group, 9.4% to the abnormal-normal group, and 14.5% to the abnormal-abnormal group. A total of 234 subjects (1.5%) were newly diagnosed with diabetes, between 2010 and 2014. Over 4 years, 1%, 1.5%, 2.1%, and 3.0% of the subjects developed diabetes in the normal-normal, normal-abnormal, abnormal-normal, and abnormal-abnormal groups, respectively. When the risk for incident diabetes was analyzed in the groups, after adjusting the confounding variables, a 1.58-fold increase in the risk of diabetes (95% confidence interval [CI], 1.10 to 2.26) was observed in the participants with persistent hypertriglyceridemia (abnormal-abnormal group). This was attenuated by further adjustments for body mass index (BMI) (hazard ratio, 1.25; 95% CI, 0.86 to 1.80).

Conclusion

In this large study population, persistent hypertriglyceridemia, over a period of 2 years, was significantly associated with the risk of incident diabetes, which was attenuated after adjustment for BMI.

Keywords: Hypertriglyceridemia, Diabetes, Persistent

INTRODUCTION

With the increase in the global prevalence of diabetes mellitus and the associated economic burden, efforts to reduce the risk of diabetes development, through identifying individuals at a risk of incident diabetes as well as the modifiable factors, are continuously underway [1 2].

Hyperinsulinemia and insulin resistance are the most powerful predictors of the development of type 2 diabetes [3 4]. Insulin resistance, determined by the hyperinsulinemic euglycemic clamp, is traditionally presented as the most fundamental element of the metabolic syndrome, of which a variety of factors vary from the literature, and new standards are being proposed [5 6]. In particular, the abnormality of lipid metabolism, in insulin resistance, is characterized by an increase in triglyceride (TG) levels, a decrease in high density lipoprotein cholesterol (HDL-C) levels, and increase in free fatty acid levels. Diabetic dyslipidemia also includes qualitative and kinetic lipid abnormalities, which are more atherogenic in nature, as the cholesteryl ester transfer protein (CETP) increases the production of small dense low density lipoprotein (LDL) particles [7 8 9]. These abnormalities of multiple lipid metabolisms in cases of insulin resistance are very complex and the precise pathophysiological mechanisms are not fully understood. The most important factor behind this has been suggested to be excess weight, in particular visceral obesity and expansion in adipose tissue, so called active endocrine organ that influence energy expenditure and metabolism in our body [10 11].

There are many studies that predict the development of diabetes by using the pathophysiology of lipid metabolism in insulin resistance [12 13 14 15]. In this retrospective longitudinal study, we investigate the association of the risk of diabetes with changes in TG concentrations, over the course of 4 years.

METHODS

Subjects

This is a retrospective, longitudinal study that evaluated the incidence of diabetes, according to the changes in the TG levels of those who participated in medical health check-up programs at the Health Promotion Center of the Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea. The purpose of these medical health check-up program is not only primary prevention or early diagnosis but also secondary prevention, through the identification of risk factors for major public health problems such as cardiovascular disease and cancers. Most of the examinees are employees of various industrial companies across the country and their family members. The employers largely pay for the costs of the medical examinations, and a considerable proportion of the examinees undergo examinations annually or biannually.

Initial data pertaining to a total of 29,956 participants were extracted from the medical checkup programs performed over 5 consecutive years, between January 2010 and December 2014. Among these, 14,024 participants were excluded due to the presence of diabetes in 2010 and 2012 and/or missing data. After the exclusions, 15,932 participants (10,833 men and 5,099 women) were analyzed in this study.

The participants provided written informed consent for the usage of their medical check-up data for the purpose of this research. The design, protocol, and the consent procedure of this study were reviewed and approved by the Institutional Review Board of Kangbuk Samsung Hospital (KBSMC 2014-11-030). This study was conducted in accordance with the Helsinki Declaration of 1975.

Anthropometric and laboratory measurements

The participants' height and weight were measured twice and then averaged. The body mass index (BMI) was calculated by dividing the weight (kg) by the square of the height (m). The waist circumference was measured, with the participants in the standing position, at the middle point between the anterior iliac crest and the lower border of the ribs, by a single examiner. The blood pressure was measured using a standardized sphygmomanometer, after a 5-minute period of rest.

All the participants were examined after an overnight fast. The hexokinase method was used to measure fasting blood glucose (FBG) concentrations (Hitachi Modular D2400, Roche, Tokyo, Japan). Fasting serum insulin concentrations were determined by electrochemiluminescence immunoassay (Hitachi Modular E170, Roche). An enzymatic colorimetric test was used to measure serum total cholesterol (TC) and TG concentrations. The selective inhibition method was used to measure the level of HDL-C, and a homogeneous enzymatic colorimetric test was used to measure the level of LDL-cholesterol (LDL-C). Glycated hemoglobin (HbA1c) levels were measured by immunoturbidimetric assay with a Cobra Integra 800 automatic analyzer (Roche Diagnostics, Basel, Switzerland), with a reference value of 4.4% to 6.4%. The methodology was aligned with the standard set by the Diabetes Control and Complications Trial (DCCT) and National Glycohemoglobin Standardization Program (NGSP) [14]. The intra-assay coefficient of variation (CV) was 2.3% and the inter-assay CV was 2.4%; both were within the acceptable limits defined by the NGSP [16].

Information regarding smoking status, alcohol consumption, and exercise status was collected through standardized, self-administered questionnaires. Participants were subsequently categorized as ‘current smoker’ and ‘non-current smoker.’ The item of alcohol consumption was divided into two categories by the number of times participants drank per week: three times or more per week, and less than three times per week. Physical activity was divided into ‘stable state,’ ‘light activities,’ ‘average activities,’ and ‘vigorous activities,’ according to the questionnaire.

The participants were divided into four groups, based on their TG levels at the baseline (2010) and 2 years later (2012); serum TGs level <150 mg/dL was defined as normal, and serum TGs level ≥150 mg/dL was defined as abnormal.

(1) Normal TG level in 2010 and normal TG level in 2012
(2) Normal TG level in 2010 and abnormal TG level in 2012
(3) Abnormal TG level in 2010 and normal TG level in 2012
(4) Abnormal TG level in 2010 and abnormal TG level in 2012

As the assessment of the incidence of type 2 diabetes in 2014 was the primary end-point of this study, we excluded participants, with underlying diabetes at the baseline, from the study. The presence of diabetes mellitus was determined according to participants' replies to questionnaires and the diagnostic criteria of the American Diabetes Association [17].

Statistical analysis

All data were analyzed using IBM SPSS for Windows version 24.0 (IBM Co., Armonk, NY, USA) and presented as mean±standard deviation and number with percentages. Comparisons of the variables among the four groups, divided by the change in TG levels in 2010 and 2012, were performed by a one-way analysis of variance for continuous variable and the post hoc test using Tukey method was used. Categorical variables were expressed as percentages and compared between groups using the chi-square test. For the multiple comparison analysis, Bonferroni's correction was used to perform post hoc comparisons. Data that did not follow a normal distribution were analyzed after logarithmic transformation. Comparisons of adjusted odds ratios (ORs) for incident diabetes in the four groups, divided by changes in TG levels in 2010 and 2012, were analyzed by multiple logistic regression analysis after adjusting for confounding baseline variables. All the P values were two-tailed, and P<0.05 was considered statistically significant.

RESULTS

Baseline characteristics

The baseline characteristics of the participants in 2010 are presented in Table 1. The mean age of the participants at the baseline was 43.2 years and 68% of the participants were men. The BMI, FBG level, and HbA1c level at the baseline were 23.6±3.0 kg/m², 91.0±8.5 mg/dL, and 5.6%±0.3%, respectively.

Comparison of the baseline characteristics of the participants assigned to groups based on the level of TGs, in 2010 and 2012

Based on the TG levels in 2010 and 2012, 67.5% of participants were assigned to the normal-normal group, 8.6% to the normal-abnormal group, 9.4% to the abnormal-normal group, and 14.5% to the abnormal-abnormal group (Table 2). The participants in the abnormal-abnormal group had higher mean values of BMI, waist circumference, TC levels, TG levels, FBG levels, and fasting insulin levels, compared to the participants in the other groups. On comparing the normal-abnormal group and the abnormal-normal group, except for the HbA1c and LDL-C levels, the mean values of the BMI, waist circumference, blood pressure, FBG, TGs, HDL-C, and fasting insulin in abnormal-normal group pointed to worse impairment. In terms of lifestyle, the percentage of current smokers and those who consumed alcohol three times or more per week was higher in the order of TG values, and in terms of physical activity, an opposite trend was observed.

Incidence rate of and ORs for diabetes in the groups divided by the level of triglycerides, in 2010 and 2012

A total of 234 subjects (1.5%) in the whole group were newly diagnosed with diabetes, in 2014. The incidence rate for diabetes were 1.0%, 1.5%, 2.1%, and 6.7% in the normal-normal, normal-abnormal, abnormal-normal, and abnormal-abnormal groups, respectively (Table 3, Fig. 1).

Table 3 shows the ORs and 95% confidence intervals (CIs) for the risk of diabetes development, according to the measurements of fasting TG levels, checked 2 years apart. The participants with persistent hypertriglyceridemia (abnormal-abnormal group) had a 2.928-fold increase in the OR for diabetes development (OR, 2.928; 95% CI, 2.16 to 3.97) compared to those in the normal-normal group. After adjusting the OR for age, sex, FBG level, TC level, alcohol consumption, smoking status and exercise status, a 1.576-fold increase in the risk for diabetes development (OR, 1.576; 95% CI, 1.10 to 2.26) was still observed in the participants in the abnormal-abnormal group, but the correlation was less statistically significant on further adjusting for BMI (OR, 1.25; 95% CI, 0.86 to 1.80). After adjusting the confounding variables, it was found that there was no statistically significant correlation of the diabetes risk between the normal-abnormal group and the abnormal-normal group.

DISCUSSION

In this study, an increased risk of diabetes development was observed in the persistent hypertriglyceridemia group, which was assessed after a 2-year interval and compared with the reference group, even after adjusting the confounding factors. When we further adjusted the BMI, a reduction in the risk was observed, which might have been due to the positive correlation between BMI and the TG level [18].

A number of factors may contribute to the alterations in the lipid metabolism that are observed in patients with insulin resistance or hyperinsulinemia. Insulin-controlled apolipoprotein production in the liver, the regulation of lipoprotein lipase, the actions of CETP, and the peripheral actions of insulin on adipose tissue and muscles are considered to be the important mechanisms responsible for diabetic dyslipidemia [9 19 20 21].

Conversely, many previously conducted studies have demonstrated dyslipidemia as a facilitating factor in the development of pancreatic β-cell apoptosis, insulin biosynthesis, defective insulin secretion, and altered glucose metabolism. Fatty acid metabolism, including ceramide formation, endoplasmic reticulum stress, oxidative stress, inflammation, insulin signal pathway, and protein kinase B, is known to be associated with the damage of pancreatic β-cells [22 23 24]. In addition, prolonged exposure to fatty acids could seriously impair insulin biosynthesis, possibly associated with the activities of transcription factors such as pancreatic duodenal homeobox 1 and MafA [22 25]. Several studies have been done on the correlation between insulin secretion deficiency and lipid metabolism, and one of these revealed that islet cholesterol accumulation due to the loss of the ABCA1 gene leads to the impairment of the exocytosis of insulin granules [26 27]. Although the reciprocal relationship between diabetes and lipid metabolism is unclear, there is a complex causal relationship between the factors.

Several studies have pointed to hyperlipidemia values as predictors of diabetes. A significant association between the TC to HDL-C ratio and the risk of diabetes development was found in 5,577 non-diabetic Koreans in a 4-year follow-up [13]. In another study, the risk of development of diabetes, according to changes in the TG level at the baseline and 5 years later, was analyzed in 13,953 Caucasian males with a mean age of 32.4 years [14]. The risk of diabetes showed more than a 12-fold increase in the men who moved from the lowest tertile of the TG levels at the baseline to the highest tertile of the TG levels after 5 years. Among men in whom the highest tertile of the TG levels was maintained at both time points, there was only more than a 7-fold increase in the risk of diabetes development. This is in accordance with a recent study in which the risk for diabetes development increased in participants with large variations in TC levels, among 2,827,950 Koreans [15]. The discrepancy in our research, pertaining to the participants with persistent hypertriglyceridemia showing the highest risk of diabetes, was probably due to the difference in the age, sex, race, and follow-up period.

We could not find any correlation between the risk of diabetes in the normal-abnormal group and abnormal-normal group, after adjusting the compounding variables. This suggests that a single measurement at a particular time point may be insufficient to assess the risk of developing diabetes. The probability of developing diabetes significantly increases only if two consecutive measurements of TGs are above 150 mg/dL. Although this was not of statistical significance, the metabolic parameters at the baseline were more impaired and the incidence of diabetes was higher in the abnormal-normal group than in the normal-abnormal group. This suggests that it could take years for diabetes to develop due to hypertriglyceridemia, as the presence of insulin resistance precedes the onset of the disease by 10 to 20 years [28 29].

Although an elevated risk of diabetes can be predicted in participants with high TG levels, based on the current literature as well as the findings of this study, it cannot be assumed that a reduction in the levels of TGs in a fragmentary manner will lower the risk for the development of diabetes. Statins are effective in lowering LDL-C levels as well as very LDL levels [30]. However, they have been found to modestly increase the risk of developing diabetes mellitus [31]. The inhibition of isoprenoid biosynthesis, downregulation of C/EBPα (CCAAT-enhancer-binding protein) production, downregulation of GLUT4/SLC2A4 (glucose transporter type 4/solute carrier family 2 member 4) in adipocytes, and over-production of nitric oxide are the various mechanisms of statin-induced diabetes mellitus that have been proposed so far, but there are no clear ideas [32]. Therefore, when statins are used, in addition to their TG lowering effects, their diabetogenic potential mechanism should also be considered.

Finally, when BMI was further included in the model, statistical significance was attenuated. However, in a study published in 2014, regardless of obesity, the metabolically unhealthy group based on the component of metabolic syndrome had a higher risk of future diabetes development [33]. Persistent hypertriglyceridemia may not be an independent or sole risk factor for diabetes development and it has definitely weaker influence for diabetes development than BMI. However, subjects with persistent hypertriglycetidemia should be monitored for future diabetes development in clinical setting.

Our study has several limitations. Frist, since this study was observational in design, it is likely that some of the factors that have a significant impact on the outcome have not been controlled. Second, the follow-up period was 4 years, which is perhaps not a long enough period. Extending the length of the follow-up period may result in different outcomes. Third, whether the changes in the TG levels were due to lipid lowering therapy or lifestyle changes was not taken into consideration. Finally, we set the cut-off value of the TG level at 150 mg/dL, but we did not study the changes in the associations below 150 mg/dL or above 150 mg/dL of TGs. Despite these limitations, however, this is the first study to compare the change in TG levels over time and the risk of diabetes development, in community-dwelling Koreans.

In conclusion, this is the first large population-based study to investigate the relationship between the risk of diabetes development and changes in TG levels over time, in Korea. In this study, it was observed that there was an increased risk of diabetes development in the participants with persistent hypertriglyceridemia. Therefore, the sequential measurement of TG levels, more than twice, can help predict the risk of diabetes development in the general population. Further studies are required to find a specific framework than can be used in clinical practice.

Figures and Tables

Fig. 1

Incidences of diabetes in 2014, according to triglyceride levels in 2010 and 2012.

Table 1

Baseline Characteristics of the Participants (n=15,932)

Characteristic	Value
Age, yr	43.2±5.6
Male sex	10,833 (68)
Body mass index, kg/m²	23.6±3.0
Waist circumference, cm	81.8±8.3
Systolic blood pressure, mm Hg	114.5±12.3
Diastolic blood pressure, mm Hg	73.6±9.1
Fasting blood glucose, mg/dL	91.0±8.5
Total cholesterol, mg/dL	199.1±33.3
Triglyceride, mg/dL	120.96±75.0
High density lipoprotein cholesterol, mg/dL	54.5±13.4
Low density lipoprotein cholesterol, mg/dL	120.5±30.0
Glycated hemoglobin, %	5.6±0.3
Fasting insulin, µIU/mL	5.3±0.3
Current smoking	3,725 (23.5)
Alcohol consumption over 3 times/wk	3,395 (21.3)
Physical activity (more than average activity)	3,046 (19.1)

Values are expressed as mean±SD or number (%).

Table 2

Comparisons of Metabolic Parameters among Groups Divided by Triglycerides Level, in 2010 and 2012 (n=15,932)

Variable	Normal-normal (n=10,750)	Normal-abnormal (n=1,371)	Abnormal-normal (n=1,504)	Abnormal-abnormal (n=2,307)	Post hoc analysis^a (using Tukey's method)
Age, yr	43.0±5.7	43.4±5.2	44.1±5.6	43.3±5.0	I≠II, II≠III, II≠IV
Male sex	6,226 (57.9)	1,160 (84.6)	1,284 (85.4)	2,163 (93.8)	I≠III, I≠IV, II≠III, II≠IV, III≠IV
BMI, kg/m²	22.8±2.8	24.4±2.6	25.0±2.8	26.0±2.7	All different
Waist circumference, cm	79.6±7.9	84.4±6.9	85.9±7.2	87.5±6.9	All different
SBP, mm Hg	112.9±12.2	115.9±11.7	118.6±12.2	118.4±11.5	I≠II, I≠III, I≠IV, II≠III, II≠IV
DBP, mm Hg	73.3±9.0	74.5±8.5	76.5±8.8	76.7±8.7	I≠II, I≠III, I≠IV, II≠III, II≠IV
FBG, mg/dL	89.9±8.3	91.5±8.5	93.7±8.2	93.9±8.4	I≠II, I≠III, I≠IV, II≠III, II≠IV
TC, mg/dL	192.9±31.2	206.7±31.9	211.1±33.5	216.1±34.8	All different
TG, mg/dL	85.8±27.9	116.3±23.2	192.9±55.3	240.9±96.7	All different
HDL-C, mg/dL	58.4±13.1	50.4±10.	47.4±9.8	43.7±8.9	All different
LDL-C, mg/dL	115.0±28.2	132.9±28.7	130.2±30.3	132.0±31.5	I≠II, I≠III, I≠IV, II≠III
HbA1c, %	5.6±0.2	5.7±0.2	5.7±0.3	5.7±0.3	I≠II, I≠III, I≠IV, II≠III, II≠IV
Fasting insulin, µIU/mL	4.7±2.7	5.3±3.0	6.7±3.2	7.5±3.7	All different
Current smoking	1,834 (17.1)	431 (31.6)	478 (31.9)	982 (42.7)	I≠III, I≠IV, II≠III, II≠IV, III≠IV
Alcohol consumption over 3 times/wk	1,878 (17.5)	364 (26.5)	415 (27.6)	738 (32.0)	I≠III, I≠IV, II≠III, II≠IV, III≠IV
Physical activity (more than average activity)	2,279 (24.1)	222 (17.8)	237 (17.8)	326 (14.9)	I≠IV, II≠IV, III≠IV

Values are expressed as mean±SD or number (%).

BMI, body mass index; SBP, systolic blood pressure; DBP, diastolic blood pressure; FBG, fasting blood glucose; TC, total cholesterol; TG, triglyceride; HDL-C, high density lipoprotein cholesterol; LDL-C, low density lipoprotein cholesterol; HbA1c, glycated hemoglobin.

^aMean values of all groups were significantly different when analyzed by one-way analysis of variance test.

Table 3

Risk of Diabetes Development in 2014, according to Triglyceride Levels in 2010 and 2012

	Diabetes, n (%)	Odds ratio (95% confidence interval)
	Diabetes, n (%)	Model 1	Model 2	Model 3	Model 4	Model 5
Normal-normal	112 (1.0)	1 (reference)	1.000	1.000	1.000	1.000
Normal-abnormal	21 (1.5)	1.477 (0.924–2.363)	1.376 (0.855–2.213)	1.220 (0.753–1.978)	0.956 (0.554–1.651)	0.852 (0.493–1.472)
Abnormal-normal	32 (2.1)	2.065 (1.389–3.070)	1.862 (1.243–2.789)	1.308 (0.863–1.982)	1.239 (0.798–1.925)	1.048 (0.674–1.631)
Abnormal-abnormal	69 (3.0)	2.928 (2.162–3.966)	2.688 (1.953–3.699)	1.790 (1.277–2.508)	1.576 (1.098–2.264)	1.246 (0.861–1.802)

Model 1, unadjusted; Model 2, adjusted for age and sex; Model 3, adjusted for variables in model 2 plus fasting blood glucose and total cholesterol; Model 4, adjusted for variables in model 3 plus alcohol consumption, smoking habits, and exercise; Model 5, adjusted for variables in model 4 plus body mass index.

Notes

^{CONFLICTS OF INTEREST} No potential conflict of interest relevant to this article was reported.

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ORCID iDs: Eun-Jung Rhee
https://orcid.org/0000-0002-6108-7758
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