Korean J Intern Med > Volume 18(3); 2003 > Article
Jung, Sung, Shin, Rhee, Lee, Kim, Kang, Kim, Kim, Lee, Park, and Kim.: Thyroid Dysfunction and Their Relation to Cardiovascular Risk Factors such as Lipid Profile, hsCRP, and Waist Hip Ratio in Korea

Abstract

Background

Thyroid abnormalities affect a considerable portion of the population, and overt hypothyroidism is associated with an elevated risk of cardiovascular disease and adverse changes in blood lipids. Subclinical hypothyroidism is also associated with an increase risk of cardiovascular disease. So, we undertook this study to investigate the prevalence of overt and subclinical thyroid disorders and their associations with cardiovascular risk factors.

Methods:

This study involved 66260 subjects (43588 men, 22672 women; between 20–80 years of age, mean age 41.5±9.6). Serum free thyroxine (FT4), thyroid stimulating hormone (TSH), total cholesterol, low density lipoprotein cholesterol (LDL-C), and high density lipoprotein cholesterol (HDL-C) were measured by RIA using commercial kits. High sensitivity C-reactive protein (hsCRP) levels were determined by nephelometry.

Results:

The prevalences of overt thyrotoxicosis, subclinical thyrotoxicosis, overt hypothyroidism and subclinical hypothyroidism were 5/1000 (334 subjects), 6.4/1000 (426 subjects), 1.6/1000 (108 subjects), and 6.4/1000 (375 subjects). Mean plasma total cholesterol and LDL-C were elevated in overt hypothyroidism than in normal controls (202.1 mg/dL and 121.8 mg/dL versus 197.1 mg/dL and 120.1 mg/dL, respectively) (p<0.05). In subclinical hypothyroidism, mean total cholesterol and LDL-C levels were also elevated (201.9 mg/dL and 123.7 mg/dL)(p=0.015, p=0.047). Waist-to-hip ratio (WHR) was lower in overt thyrotoxicosis and higher in hypothyroidism.

Conclusion:

The prevalence of thyroid dysfunction in Korea is not significantly different from that reported by other countries. It was also age dependent and higher in women, but this elevation in women was lower than expected. Patients with hypothyroidism exhibited higher waist-to-hip ratios, an index of obesity. Patients with subclinical hypothyroidism exhibited elevated atherogenic parameters (Total cholesterol, LDL-C). Therefore screening and treatment for subclinical hypothyroidism may be warranted due to its adverse effects on lipid metabolism.

List of abbreviation

SBP

systolic blood pressure

DBP

diastolic blood pressure

FBS

fasting blood sugar

LDL-C

low density lipoprotein cholesterol

HDL-C

high density lipoprotein cholesterol

hsCRP

high sensitivity C-reactive protein

TSH

thyroid stimulating hormone

INTRODUCTION

Thyroidism is a relatively common disease but its reported incidence varies, being dependent upon the research subject groups and the diagnostic criteria used. The prevalences of overt hyperthyroidism or overt hypothyroidism and subclinical thyrotoxicosis have been reported to be 5%, 5% and 1% respectively17). Subclinical hypothyroidism has been reported to have prevalences from 4–10% in the general population to 7–26% in the geriatric population811). Such thyroid dysfunctions cause changes in the lipoprotein metabolism. It is generally accepted that overt hypothyroidism accelerates the progress of cardiovascular diseases by increasing the total cholesterol and low density lipoprotein cholesterol, LDL-C, levels. Also, hypercholesterolemia caused by hypothyroidism is known to be a reversible phenomenon that can respond to thyroid hormone therapy1215). However, many contradictory results have been reported on the relationship between subclinical hypothyroidism and abnormal plasma lipids. As a result of comparing patients with subclinical hypothyroidism and normal controls, no significant difference was found in plasma lipids, nor did thyroid hormone therapy cause a significant difference in this respect2, 1518). Whereas recent studies have reported that total cholesterol and low-density lipoprotein cholesterol are more elevated in subclinical hypothyroidism than in normal controls1922). These are crucial risk factors and are the basis of thyroid hormone therapy. However, since many studies on the relationship between subclinical hypothyroidism and hyperlipidemia have been performed using selected groups of subjects of 55 years or older, they do not represent the subject group of interest in terms of cardiovascular diseases prevention23). Thus, we examined the prevalence of thyroid dysfunctions in Korea, and used a large number of subjects covering a wide age range. These subjects had visited hospital for medical check-ups.

MATERIALS AND METHODS

1. Subjects

The subjects were 66,260 individuals (43,588 males and 22,672 females) who resided mainly in the Seoul and Kyunggi areas, and had received medical check-ups at the Kangbook Samsung Hospital, College of Medicine in Sunggyungwan University from January of 1999 to December of 2001.

2. Methods

Serum FT4, TSH, total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, hsCRP, neutral fat, and blood pressure were measured.
The circumferences of the subjects’ waists and hips were measured and their ratios calculated. Their mean serum FT4 was 0.7–2.0 ng/dL and their serum TSH 0.25–5.0 uIU/mL. Cholesterol was determined using an automatic analyzer, (ADVIA1650, Bayer). High sensitivity C-reactive protein (hsCRP) was measured using immunonephelometers (Nephelometry; Behring Nephelometer II, Dade Behring Marburg GmbH, Germany) up to a level of 0.175 mg/L. Overt hyperthyroidism was defined to have a serum TSH of 0.25 uIU/mL or lower, and a serum FT4 of 2 ng/dL or higher. Subclinical thyrotoxicosis was defined as a normal density of serum FT4, but a serum TSH of 0.25 uIU/mL or lower. Overt hypothyroidism was defined as a serum TSH of 5.0 uIU/mL or higher with a serum FT4 of 0.7 ng/dL or lower. Subclinical hypothyroidism was defined as a normal density of serum FT4 with serum TSH of 5.0 uIU/mL or higher.

3. Statistical Analysis

SAS version 8.0 and SPSS version 10.0 were used for the statistical analysis, and the sequential variable data are presented as means±standard deviation. Dunnett’s multiple comparison test was used to determine differences between the groups, and multiple multinomial logistic regression analysis was used to adjust for age and gender. A p value of 0.05 or lower was taken to be statistical significance.

RESULTS

1. Clinical traits of the subjects

The 66,260 subjects included 43,588 males and 22, 672 females, a ratio of 1.92:1 and of average age 41.5±9.6. 31,270 were in their 30’s (30–39) which predominated, and subject frequencies by decade followed in the order 40’s, 50’s, 60’s, 20’s (or younger) and 70’s (or older). The average systolic blood pressure of the subjects was 119.86 mmHg, and diastolic blood pressure was 76.73 mmHg, while the fasting blood sugar was 90.75 mg/dL. The average serum FT4, TSH, total cholesterol, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol were 1.31±0.29 ng/dL, 2.08±1.59 uIU/mL, 196.8±36.4 mg/dL, 51.7±12.6 mg/dL, and 120.1±31.2 mg/dL respectively. The hsCRP was 1.22±1.47 mg/L, and the waist-hip ratio was 0.84±0.24 (Table 1).

2. Prevalence of thyroid dysfunction

Overt hyperthyroidism was found in 334 (referred to as patients) (5/1,000) of the 66,260 subjects. Among these, 152 patients (3.5/1,000) were males (out of 43,588 males), and 182 patients (8.0/1,000) were females (out of 22,672 females) and thus, the condition is more prevalent in females (sex ratio was male:female=1:2.5) (Table 2). The prevalence of overt hyperthyroidism showed a tendency to rise with age to plateau in the 50’s (Figure 1). Subclinical thyrotoxicosis was found in 426 patients (6.4/1,000) and 213 of these were males (4.9/1,000 male prevalence), while 213 were females (9.4/1,000 female prevalence), and thus, prevalence of subclinical thyrotoxicosis is more likely to occur in the females (ratio of male:female=1:2) (Table 3). The prevalence of subclinical thyrotoxicosis showed... tendency to increase with age, and this markedly increased in the 70’s and beyond (Figure 1). Overt more likely to occur in females (ratio of male:female=1:6) (Table 4). The prevalence of overt hypothyroidism showed a hypothyroidism was found in 1.6/1,000 of total subjects. Among these, with a prevalence 0.6/1,000 for males, and 3.6/1,000 for females, and thus overt hypothyroidism is tendency to rise with age, and was highest in the 70’s and higher with a prevalence of 8.7/1,000 (Figure 2). Subclinical hypothyroidism was found in 375 patients (5.7/1,000), and 129 were males (male prevalence 3/1,000) while 246 were females (female prevalence 10.9/1,000), and thus the condition is more likely to occur in the females (ratio of male:female in the study population =1:3.6) (Table 5). The prevalence of subclinical hypothyroidism showed a tendency to increase with age, and reached a maximum in the in the 60’s (Figure 2).

3. The relationship between thyroid dysfunction and risk factors for cardiovascular disease

For patients with overt hypothyroidism, the total cholesterol was 202.1±45.9 mg/dL vs. 197.1 36.3 mg/dL, for the group that showed normal thyroid functions, and similarly the low-density lipoprotein cholesterol level was 121.8±37.0 mg/dL vs. 120.1±31.2 mg/dL. Both values were significantly higher than the normal group, but the differences were small (p<0.05). In the patients with subclinical hypothyroidism, the total cholesterol was 201.9±39.9 mg/dL, which was higher than 197.1±36.3 mg/dL of the normal group, and this was statistically significant even when they were matched for age and sex (p=0.015). The low-density lipoprotein cholesterol levels also showed a statistically significant increase in subclinical hypothyroidal patients (123.7±31.5 mg/dL vs. 121.5±31.2 mg/dL (p<0.0001). The normal group showed a significantly higher level of high-density lipoprotein cholesterol compared to the overt hyperthyroidism (p<0.0001). No statistically significant difference was found between the normal group and the group that showed thyroid dysfunction in by hsCRP. The body mass indices did not show any significant difference between the normal group and the thyroid dysfunction group, but the ratio of waist/buttocks was significantly lower in the overt hyperthyroidism group than in the normal group, whereas this was higher result in the overt hypothyroidism group than in the normal group (p=0.043, p=0.049) (Table 6).

DISCUSSION

The determination of the prevalence of thyroidism in a population can produce different results, according to the subject groups or diagnostic criteria chosen. In this study, the average prevalence of overt hyperthyroidism in Korea for all age levels was 5/1,000 (3.5/1,000 in males and 8.0/1,000 in females), and was highest in the 60’s age group. In 1997, in the English Whickham survey2), the prevalence of thyroidism, including past medical history, was higher than that of the present survey with 19 female patients per 1,000 female patients, and 1.6 male patients per 1,000 male patients, and though it also found a higher prevalence in females, no association was found with age. In a Colorado study3), thyrotoxicosis showed a prevalence of 0.1%, which is lower than that found in the present study, and a study in Spain11) also showed a prevalence rate of 0.2%, which again is lower than that found by the present study. We found that the average prevalence of overt hypothyroidism in Korea is 1.6/1,000 (0.6 males and 3.6 females). In terms of age, those in their 70’s showed the highest with 9.4/1,000, and this was higher than that found in the Whickham or Colorado studies, with 1.9% and 0.4%, respectively. In the present study, the average prevalence of subclinical thyrotoxicosis in Korea was found to be 6.4/1,000 (4.9 in males and 9.4 in females), which is much higher than the prevalences of 0.09% in males, and 0.46% in females found in Norway6), but lower than the 2.1% found in Colorado, and much lower than the 7.3% in males and the 5.9% in females found in Germany7). In the present study, the average prevalence of subclinical hypothyrodism was 5.7/1,000 (3 in males and 10.9 in females), and the condition was found to be significantly more likely to occur in females. Age related prevalence showed a tendency to increase, and the 60’s showed the highest prevalence at 11.6/1,000. In Norwegian study6), the prevalence of subclinical hypothyroidism was 0.37% in males, and 0.9% in females, and the prevalence was highest in the 60’s, which agrees with the results or the present study4). In the Whickham survey, the prevalence of subclinical hypothyroidism was three times higher in females than in men.
The Colorado, Danish5) and Spain Spanish surveys have showed higher prevalences of subclinical hypothyroidism respectively (9%, 7.2% and 5.6%). In view of these results, the prevalence of subclinical hypothyroidism in Korea seems lower than in other countries, but significantly higher in females than in man and is increase with age. Compared to the study of Jung et al.38), who studied the prevalence rates in a population that had received medical check-ups, the present study shows a lower prevalence of thyroid dysfunction. The reasons for this difference are probably due to the different age profiles of the subject groups, and the different diagnostic criteria and tests used to diagnose thyroid dysfunction. In other words, the present study showed that the 30’s predominate, and that the average age of this study was 41.5, whereas though the study by Jung et al. did not state the average age the 40’s predominated. In addition, Jung et al. measured the concentrations of T3, T4, and TSH whereas we measured the concentrations of FT4 and TSH to evaluate the thyroid function. In addition, the concentration of TSH for diagnosing thyrotoxicosis was applied differently, with 0.25 uIU/mL in the present study, and 0.30 uIU/mL in the study by Jung et al. However, the fact that the thyroid dysfunction was more commonly observed in women than in men, and that hypothyroidism is more commonly observed as age increases, are common findings. The limitation of the present study is that patients who were receiving treatment for thyroid dysfunction could have been included in the normal group due to the lack of an investigation into the medical and treatment histories of subjects with respect to thyroidism. To counterbalance the effect of such a limitation, our study involved over 60,000 subjects, which allowed cardiovascular risk factors such as, blood pressures, blood sugar, level of obesity, dyslipidemia, lipoprotein (a), and hsCRP to be analyzed. Thyroid hormones and serum lipids are known to be closely14, 24, 25). Moreover, it has been verified that overt hypothyroidism can cause cardiovascular diseases and arteriosclerosis by increasing the total cholesterol and low-density lipoprotein cholesterol. Its mechanism has been attributed to the fact that the concentration of low-density lipoprotein cholesterol receptors falls in fibroblasts, the liver and in other tissues that the diseased thyroid cannot absorb low-density lipoprotein cholesterol as well as the normal thyroid. Thus, this material accumulates in the blood. With thyroid hormone therapy, adverse effects can be controlled and total cholesterol and low-density lipoprotein cholesterol values can be decreased26). However, there is no clear evidence that subclinical hypothyroidism can cause cardiovascular disease, as results are contradictory2023, 26) Recently, several studies have found than an increase in total cholesterol and low-density lipoprotein cholesterol levels are a primary cause of arteriosclerosis and cardiovascular diseases in subclinical hypothyroidism19, 27, 28). Various mechanisms are involved in the relationships between subclinical hypothyroidism arteriosclerosis and cardiovascular diseases. Thyroid auto-immunity is one such mechanism, which is related to cardiovascular diseases. This is an abnormal immunoreactivity, which is related to vascular injuries mediated by immune-complex29, 31).
In a Rotterdam study19), the incidence of arteriosclerosis or hyperlipidemia was found to be higher in subclinical hypothyroidism in the presence of antibodies for thyroid peroxidase. Moreover, the low-density lipoprotein cholesterol level was found to fall by approximately 12% on thyroid hormone therapy19).
When subclinical hypothyroidism patients, who show hyperlipidemia, receive thyroid hormone therapy, it causes the total cholesterol and low-density lipoprotein cholesterol to drop, and can decrease the incidence of cardiovascular diseases. In addition, it has been reported that this occurs more so when thyroid auto-antibodies are present1921, 32). On the other hand, thyroid hormone therapy causes serum lipid response to changes with TSH level17). It has also been reported that when TSH>10 mU/L, total cholesterol and low-density lipoprotein cholesterol decrease, but when TSH<10 mU/L, there is no effec15, 17, 26). In other words, the higher the severity of hypothyroidism, the larger the effects of the thyroid hormone therapy upon hyperlipidemia, when thyroid autoantibodies are benign. There have not been many systematic studies on the relationship between thyroid function and high-density lipoprotein cholesterol, and studies have shown different results, though many have been reported as statistically insignificant. Some studies have reported that the high-density lipoprotein cholesterol level reduces in thyrotoxicosis and increases in hypothyroidism24, 25). Although Carantoni et al.33) reported that the high-density lipoprotein cholesterol level decreases with hypothyroidism and contributes to the risk of cardiovascular diseases. In the present study, the total cholesterol was lower in overt and subclinical thyrotoxicosis (i.e., by 34 mg/dL and 9 mg/dL respectively, p<0.0001), compared to the normal group, while low-density lipoprotein cholesterol was lower (by 20 mg/dL and 6 mg/dL, respectively (p<0.0001). Similarly, in cases of subclinical hypothyroidism, the total cholesterol was higher by 5 mg/dL and 4 mg/dL, respectively, (p<0.05, p=0.015), as was the low-density lipoprotein cholesterol, by 2 mg/dL and 3 mg/dL (p<0.05, p=0.047). As a result of analyzing the TSH and lipid levels in 279 subjects of ≥65 in America, the total cholesterol was reported to have increased by 8% at high TSH versus the normal group, and the low-density lipoprotein cholesterol to have increased by 13%. Thus, though increases in the total cholesterol and low-density lipoprotein cholesterol shown in the present study are statistically significant, their degrees are small. In the present study, total cholesterol and low-density lipoprotein cholesterol did not increased in the men with only overt hypothyroidism. However, in women, the difference in the lipid levels of the subclinical and overt hypothyroidism groups was large. Therefore, screening tests for lipids are considered necessary for women. As a result of comparing hsCRP34), which has been reported as a strong independent prognostic factor for the risk of arteriosclerosis and cardiovascular diseases, with thyroid dysfunction itself, no significant difference was found. This is considered to be due to the relatively smaller number of the subject patients involved and a study is now being planned to complement address this. Thyroid hormones are known to play an important role in controlling the energy metabolism and obesity genes35). Therefore, body mass may change in cases of thyroid dysfunction. According to the study by Mehta et al.36), 14% of obese people with a body mass index of 30–40 kg/m2 showed hypothyroidism, 8% of these were reported to be overt, and 6% had subclinical hypothyroidism. In this study, body mass index (BMI) and waist-hip ratio were measured as indicators of obesity, which is an important risk factor for cardiovascular diseases. However, thyroid function and BMI did not show any significant correlation, but the waist-hip ratio was found to be significantly higher in the hypothyroidism than in the normal group. Thus central obesity, which is a risk factor for cardiovascular diseases, was found to be significantly higher, especially in the hypothyroidism group. In conclusion, the prevalence of thyroid dysfunction in Korean people who are seemingly healthy was found to be lower than in the West, while the findings that its prevalence was higher in the aged and much higher in women concurred with finding published in West. In subclinical hypothyroidism especially, total cholesterol and low-density lipoprotein cholesterol, which are risk factors for cardiovascular diseases, were significantly elevated even after adjusting the age and gender ratio.
Therefore, we recommend that screening tests and treatment for subclinical hypothyroidism should be undertaken, and that further prospective studies should be initiated on determining the actual incidence of cardiovascular diseases in the subclinical hypothyroidal group.

Figure 1.
Differential prevalence of overt and subclinical hyperthyroidism according to age (percent).
kjim-18-3-146-3f1.gif
Figure 2.
Differential prevalence of overt and subclinical hypothyroidism according to age (percent).
kjim-18-3-146-3f2.gif
Table 1.
Basal characteristics of subjects
Total
Mean±SD
MEN
Mean±SD
women
Mean±SD
age (yr) 41.54±9.62 41.33±8.77 41.96±11.07
body mass index (kg/m2) 23.44±2.98 23.90±2.79 22.56±3.12
waist to hip ratio 0.84±0.24 0.87±0.22 0.78±0.20
SBP (mmHg) 119.86±15.31 121.13±14.25 117.40±16.91
DBP (mmHg) 76.73±10.60 78.59±10.03 73.15±10.76
FBS (mg/dL) 90.75±19.92 91.27±20.72 89.75±18.24
Uric acid (mg/dL) 5.22±1.38 5.84±1.18 4.04±0.91
Total cholesterol (mg/dL) 196.89±36.42 198.92±35.50 192.97±37.7
LDL-C (mg/dL) 120.00±31.27 122.97±30.73 117.30±31.680
HDL-C (mg/dL) 51.74±12.61 48.76±11.11 57.47±13.34
Triglyceride (mg/dL) 128.50±92.14 144.29±99.06 98.13±67.40
hsCRP (mg/L) 1.22±1.47 1.26±1.47 1.14±1.48
Lipoprotein-a (mg/dL) 22.81±16.44 22.50±16.70 23.37±15.97
Apolipoprotein-A1 (g/L) 126.57±22.21 124.27±21.67 131.02±22.55
Apolipoprotein-B (g/L) 96.45±2.38 98.99±24.28 91.54±26.70
FreeT4 (ng/dL) 1.31±0.29 1.35±0.27 1.23±0.31
FreeT3 (pg/mL) 3.36±0.66 3.46±0.64 3.18±0.66
TSH (uIU/mL) 2.08±1.59 1.93±1.35 2.38±1.93

SBP, systolic blood pressure; DBP, diastolic blood pressure; FBS, fasting blood sugar; LDL-C, low density lipoprotein cholesterol; HDL-C, high density lipoprotein cholesterol; hsCRP, high sensitivity C-reactive protein; TSH, thyroid stimulating hormone.

Table 2.
Prevalence of overt thyrotoxicosis according sex and age
Age (years) men women total



subjects affected n/1000 subjects affected n/1000 subjects affected n/1000
≤29 769 2 2.6 1806 18 10 2567 20 7.8
30–39 21394 79 3.7 9813 73 7.4 31207 152 4.9
40–49 14949 41 2.7 5506 40 7.3 20455 81 4.0
50–59 4033 41 10.2 3437 32 9.3 7470 49 6.6
60–69 2105 12 5.7 1870 16 8.6 3975 28 7.0
≥70 338 1 3.0 240 3 12.5 578 4 6.9
total 43588 176 4.0 22672 182 8.0 66260 334 5.0
Table 3.
Prevalence of subclinical thyrotoxicosis according to sex and age
Age (years) men women total



subjects affected n/1000 subjects affected n/1000 subjects affected n/1000
≤29 769 2 2.6 1806 12 6.6 2567 14 5.5
30–39 21394 83 3.9 9813 93 9.5 31207 176 5.6
40–49 14949 87 5.8 5506 48 8.7 20455 135 6.6
50–59 4033 87 21.6 3437 39 11.3 7470 66 8.8
60–69 2105 13 6.2 1870 14 7.5 3975 27 6.8
≥70 338 1 3.0 240 7 29.2 578 8 13.8
total 43588 273 6.3 22672 213 9.4 66260 426 6.4
Table 4.
Prevalence of overt hypothyroidism according to sex and age
Age (years) men women total



subjects affected n/1000 subjects affected n/1000 subjects affected n/1000
≤29 769 0 0 1806 4 2.2 2567 4 1.6
30–39 21394 6 0.3 9813 28 2.9 31207 34 1.1
40–49 14949 8 0.5 5506 15 2.7 20455 23 1.1
50–59 4033 8 1.99 3437 43 12.5 7470 31 4.1
60–69 2105 3 1.4 1870 8 4.3 3975 11 2.8
≥70 338 3 8.9 240 2 8.3 578 5 8.7
total 43588 273 0.6 22672 100 4.4 66260 108 1.6
Table 5.
Prevalence of subclinical hypothyroidism according to sex and age
Age (years) men women total



subjects affected n/1000 subjects affected n/1000 subjects affected n/1000
≤29 769 6 7.8 1806 18 10 2567 24 9.3
30–39 21394 6 0.3 9813 115 11.7 31207 153 4.9
40–49 14949 38 2.5 5506 37 6.7 20455 81 4.0
50–59 4033 44 10.9 3437 24 7.0 7470 66 8.8
60–69 2105 14 6.7 1870 32 17.1 3975 46 11.6
≥70 338 4 11.8 240 1 4.2 578 5 8.7
total 43588 68 1.6 22672 227 10.0 66260 375 5.7
Table 6.
Mean levels of lipid profiles, hsCRP, WHR and BMI in thyroid abnormalities
Overt hypothyroidism Subclinical hypothyroidism Normal Subclinical hypothyroidism Overt hypoerthyroidism
Total-C 202.1±45.9* 201.9±39.9* 139.1±36.3 188.6±33.8 163.6±33.5
LDL-C 121.8±37.0* 123.7±31.5* 120.1±31.2 114.4±30.1 100.0±28.4
HDL-C 5.3±14.6 53.5±13.0 51.8±12.6 52.1±12.5 49.2±12.5
BMI 23.4±3.00 22.8±3.10 23.5±3.0 23.4±3.1 22.6±3.0
hsCRP 1.45±1.77 1.72±1.70 1.21±1.47 1.76±1.78 1.06±1.77
WHR 0.85±0.08* 0.84±0.08 0.84±0.07 0.83±0.07 0.82±0.07

Total-C, Total cholesterol(mg/dL); LDL-C, Low density lipoprotein cholesterol(mg/dL); HDL-C, High density lipoprotein cholesterol (mg/dL); BMI, body mass index (kg/m2); hsCRP, high sensitivity C-reactive protein (mg/L); WHR, waist to hip ration. Values are expressed as mean±S.D.

* age, sex adjusted, p<0.05 ; Significant difference from normal group.

age, sex adjusted, p<0.0001; Significant difference from normal group.

Table 7.
Mean values of TSH and Free T4 in thyroid abnormalities
Free T4 TSH


Men Women Total Men Women Total
Overt hyperthyroidism 3.39±1.72 3.30±1.63 3.34±1.67 0.04±0.04 0.04±0.02 0.04±0.03
Subclinical hyperthyroidism 1.43±0.29 1.42±0.26 1.42±0.28 0.11±0.08 0.09±0.07 0.10±0.07
Subclinical hyperthyroidism 1.11±0.26 1.07±0.22 1.09±0.23 13.01±7.38 10.83±4.10 11.58±5.53
Overt hyperthyroidism 0.58±0.11 0.56±0.13 0.56±0.12 23.38±13.30 19.54±12.07 20.50±12.44

Free T4 (ng/dL); TSH (uIU/mL), thyroid stimulating hormone values are expressed as mean±SD.

REFERENCES

1. Wiersinga WM. Subclinical hypothyroidism and hyperthyroidism. Prevalence and clinical relevance. Neth J Med 46:197–2041995.
crossref pmid
2. Tunbridge WM, Evered DC, Hall R, Appleton D, Brewis M, Clark F, Grimley Evans J, Young E, Bird T, Smith PA. The spectrum of thyroid disease in a community: The Whickham survey. Clin Endocrinol 7:481–4931977.
crossref
3. Canaris GJ, Manowitz NR, Mayor G, Ridgway EC. The Colorado thyroid disease prevalence study. Arch Intern Med 160:526–5342000.
crossref pmid
4. Bjoro T, Holmen J, Kruger O, Midthjell K, Hunstad K, Schreiner T, et al. Prevalence of thyroid disease, thyroid dysfunction and thyroid peroxidase antibodies in a large, unselected population. The Health Study of Nord-Trondelag(HUNT). Eur J Endocrinol 143:639–6472000.
crossref pmid
5. Andersen-Ranberg K, Jeune B, Hoier-Madsen M, Hegedus L. Thyroid function, morphology and prevalence of thyroid population-based study of Danish centenarians. J Am Geriatr Soc 47:1238–12431999.
crossref pmid
6. Brochmann H, Bjoro T, Gaarder PI, Hanson F, Frey HM. Prevalence of thyroid dysfunction in elderly subjects. A study in a Norwegian rural community(Naeroy). Acta Endocrinol 117:7–121998.

7. Seck T, Scheidt-Nave C, Ziegler R, Pfeilschifter J. Prevalence of thyroid gland dysfunction in 50- to 80-year old patients. An epidemiologic cross-sectional study in a southwestern community. Med Klin 15(92):642–6461997.
crossref
8. Ayala C, Cozar MV, Rodriguez JR, Silva H, Pereira JL, Garcia-Luna PP. Subclinical thyroid disease in institutionalised healthy geriatric population. Med Clin 117:534–5352001.
crossref
9. Bindels AJ, Westendorp RG, Frolich M, Seidell JC, Blokstra A, Smelt AH. The prevalence of subclinical hypothyroidism at different total plasma cholesterol levels in middle aged men and women: a need for case-finding? Clin Endocrinol 50:217–2201999.
crossref
10. Lindeman RD, Schade DS, LaRue A, Romero LJ, Liaug CL, Baumgartner RN, et al. Subclinical hypothyroidism in a bi-ethnic, urban community. J Am Geriatr Soc 47:703–7091999.
crossref pmid
11. Fardella C, Poggi H, Gloger S, Rojas A, Velasquez CG, Barroileth S, Figueroa R, Alvarez C, Salgado C, Gajardo C, Foradori A, Montero J. High prevalence of subclinical thyroidal disease among indivisuals attended in health control. Rev Med Chil 129:155–1602001.
crossref pmid
12. Bastenie PA, Vanhaelst L, Bonnyns M, Neve P, Staquet M. Preclinical hypothyroidism : a risk factor for coronary heart disease. Lancet 203–2041971.
crossref
13. Gomberg-Maitland M, Frishman WH. Thyroid hormone and cardiovascular disease. Am Heart J 135:187–1962000.
crossref
14. Deschampheleire M, Luyckx FH, Scheen AJ. Thyroid disorders and dyslipidemias. Rev Med Liege 54:746–7501999.
pmid
15. Diekman T, Lansberg PJ, Kastelein JJ, Wiersinga WM. Prevalence and correction of hypothyroidism in a large cohort of patients referred for dyslipidemia. Arch Intern Med 155:1490–14951995.
crossref pmid
16. Miura S, Iitaka M, Suzuki S, Fukasawa N, Kitahama S, Kawakami Y, Sakatsume Y, Yamanaka K, Kawasaki S, Kinoshita S, Katayama S, Shibosawa T, Ishii J. Decrease in serum levels of thyroid hormone in patients with coronary heart disease. Encocr J 43:657–6631996.
crossref
17. Efstathiadou Z, Bitsis S, Milionis HJ, Kukuvitis A, Bairaktari ET, Elisaf MS, Tsatsoulis A. Lipid profile in subclinical hypothyroidism: L-thyroxine substitution beneficial? Eur J Endocrinol 145:705–7102001.
crossref pmid
18. Vierhapper H, Nardi A, Grosser P, Raber W, Gessel A. Low-density lipoprotein cholesterol in subclinical hypothyroidism. Thyroid 10:981–9842000.
crossref pmid
19. Hak AE, Pols HA, Visser TJ, Drexhage HA, Hofman A, Witteman JC. Subclinical hypothyroidism is an independent risk factor for atherosclerosis and myocardial infarction in elderly women: The Rotterdam study. Ann Intern Med 132:270–2782000.
crossref pmid
20. Feld S, Dickey RA. An Association Between Varying Degrees of Hypothyroidism and Hypercholesterolemia in Women: The Thyroid-Cholesterol Connection. Prev Cardiol 4:179–1822000.
crossref
21. Tanis BC, Westendorp GJ, Smelt HM. Effect of thyroid substitution on hypercholesterolemia in patients with subclinical hypothyroidism:a reanalysis of intervention studies. Clin Endocrinol 44:643–6491996.
crossref
22. Pirich C, Mullner M, Sinzinger H. Prevalence and relevance of thyroid dysfunction in 1922 cholesterol screening participants. J Clin Epidemiol 53:623–6292000.
crossref pmid
23. Bauer DC, Ettinger B, Browner WS. Thyroid Function and Serum Lipids in Older Women:A Populationbased Study. Am J Med 104:546–5511998.
crossref pmid
24. Diekman MJ, Anghelescu N, Endert E, Bakker O, Wiersinga WM. Changes in plasma Low-Density Lipoprotein (LDL)-and High-Density Lipoprotein Cholesterol in Hypo-and Hyperthyroid Patients Are Related to Changes in Free Thyroxine, Not to Polymorphisms in LDL Receptor or Cholesterol Ester Transfer Protein Genes. J Clin Endocrinol Metab 85:1857–18622000.
crossref pmid
25. Aviram M, Luboshitzky R, Brook JG. Lipid and lipoprotein pattern in thyroid dysfunction and the effect of therapy. Clin Biochem 15:62–661982.
crossref pmid
26. Kahaly GJ. Cardiovascular and Atherogenic Aspect of Subclinical Hypothyroidism. Thyroid 10:8. 2000.
crossref
27. Kyoung Ah Kim, Chung Jae Hoon, Kim Yeun Sun, Ahn Kyu Jeung, Koh Eun Mi, Min Yong Ki, Lee Myung-Shik, Lee Moon-Kyu, Hun Lee Jong, Won Kim Kwang. Serum Lipoprotein(a) and Lipid Concentration in Patients with Subclinical Hypothyroidism. Journal of Korean Society of Endocrinology 12:11–151997.

28. Michael T, McDermott MT, Ridgway EC. Subclinical hypothyroidism is mild thyroid failure and should be treated. J Clin Endocrinol Metab 86:4585–45902001.
crossref pmid
29. Tiche M, Lupi GA, Gutzwiller F, Grab PJ, Studer H, Burgi H. Borderline low thyroid function and thyroid autoimmunity. Risk factors for coronary heart disease? Br Heart J 46:202–2061981.
crossref pmid pmc
30. Bastenie PA, Vanhaelst L, Golstein J, Smets P. Asymptomatic autoimmune thyroiditis and coronary heart disease. Cross-sectional and prospective studies. Lancet 2:155–1581977.
crossref pmid
31. Mathews JD, Whittingham S, Mackay IR. Autoimmune mechanisms in human vascular disease. Lancet 2:1423–14271974.
crossref pmid
32. Meier C, Staub JJ, Roth CB, Guglielmetti M, Kunz M, Miserez AR, Drewe J, Huber P, Herzog R, Muller B. TSH-controlled L-thyroxine therapy reduces cholesterol levels and clinical symptoms in subclinical hypothyroidism: a double blind, placebo-controlled trial (Basal Thyroid Study). J Clin Endocrinol Metab 86:4860–48662001.
crossref pmid
33. Carantoni M, Vigna GB, Stucci N, Zanca R, Fellin R. Low level of HDL cholesterol in hypothyroid patients with cardiovascular diseases. Minerva Endocrinol 22(91):1997.

34. Ridker PM. High-Sensitivity C-Reactive Protein: Potential Adjunct for Global Risk Assessment in the Primary Prevention of Cardiovascular Disease. Circulation 103:1813–18182001.
crossref pmid
35. Korischoner NP, Alvarez-Dolado M, Kurz SM, Heikenwalder MF, Hacker C, Vogel F. Thyroid hormone regulate the obesity gene tub. EMBO J 2:499–5042001.
crossref pmid pmc
36. Mehta S, Mathur D, Chaturvedi M, Devpura G, Jat VS. Thyroid hormone profile in obese subjects-a clinical study. J Indian Med Assoc 99:260–2722001.
pmid
37. Jae Hoon Chung, Kim Kwang Won, Joon Kim Byoung, Kim Sung Hoon, Sik Lee Myung, Gyu Lee Moon. Prevalence of Thyrotoxicosis and Hypothyroidism in the Subjects for Health Check-Up. Journal of Korean Society of Endocrinology 14:301–3131999.

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