Correlation Between Thyroid Hormones and

You might also like

Download as pdf or txt
Download as pdf or txt
You are on page 1of 6

ZANCO Journal of Pure and Applied Sciences

The official scientific journal of Salahaddin University-Erbil


ZJPAS (2017), (5); 186-191
http://dx.doi.org/10.21271/ZJPAS.29.5.20

Correlation between thyroid hormones and body weight in female hypothyroids in


Erbil city

Ahmed A. Baban1, Salar Adnan Ahmed2, Baderkhan Saeed Ahmed1, Sazgar Anwar Hameed3

1- Surgery Department, College of Medicine - Hawler Medical University – Erbil -Iraq


2- Clinical Biochemistry Department, College of Medicine - Hawler Medical University – Erbil -Iraq
3- Public Health Lab- Jamhuri Teaching Hospital, Erbil- Iraq

ARTICLE INFO ABSTRACT

Article History: Hypothyroidism, also known as underactive thyroid, is a condition


Received: 21/05/2017 where the thyroid gland does not produce enough of thyroid hormone thyroxine.
Accepted: 30/07/2017 Thyroid hormones regulate the way in which the body uses energy - metabolism -
Published: 28/ 12 /2017 and without enough thyroxine, many of the body's functions slow down. Through
Keywords: this study we aimed to define the relationship of fluctuations that might exist
Hypothyroidism between serum thyroid stimulating hormone, triiodothyronine and its prohormone
thyroxine with body weight in hypothyroidism. The present cross-sectional study
Thyroid stimulating_
deals with estimation of serum thyroid stimulating hormone, triiodothyronine,
hormone thyroxine, 25-Hydroxy vitamin D (25-OH vitamin D3) and calcium levels in (100)
T3 patients with hypothyroidism. The mean ± SE concentrations of serum thyroid
T4 stimulating hormone, triiodothyronine, thyroxine, 25-OH vitamin D3 and calcium
Weight gain were 7.1 ± 0.9 µIU/ml, 10.6 ±1.1 nmole/L, 41.1 ±1.4 nmole/L, 29.5 ± 2.3 nmole/L
and 13.4 ± 2.1 mg/dl, respectively. In the existing study we found, a statistical
positive correlation (r = 0.404 ) between thyroid stimulating hormone and body
*Corresponding Author:
weight. While there were a negative correlation between triiodothyronine (r = -
Dr. Salar A. Ahmed 0,41538 ), thyroxine (r = -0,41538 ) and body weight. Our results demonstrates that
weight gain and obesity are two common manifestation of hypothyroidism.
salarzrari@yahoo.com

1. INTRODUCTION central and peripheral nervous systems, muscle


Thyroid gland is a butterfly-shaped strength, menstrual cycles, as well as regulate
endocrine gland located in the base of neck. It body temperature, and cholesterol levels.
secretes thyroid hormones, which regulate gene (Laurberg et al,2012). However, overt thyroid
transcription and body metabolism in starved disease is associated with marked changes in
and fed states throughout the body (Feldt- energy expenditure and body weight, with
Rasmussen, 2007; Zimmermann-Belsing, enhanced protein breakdown and lipolysis (Riis
2003). The released hormones play a key role et al , 2002; Riis et al, 2005; Zulewski et al,
in the basal metabolic rate as well as vital body 1997). Moreover, subclinical hypothyroidism
functions, including: breathing, heart rate, has been associated with a greater risk for both
187 Baban A. et al. /ZJPAS: 2017,29 (5): 186-191

cardiovascular morbidity and mortality in some hypothyroidism by a clinician and pre surgery
but not all prospective population-based studies diagnoses included benign (Graves disease,
as well as overweight and obesity (Al-Adsani et nodular toxic goiter, nodular nontoxic goiter)
al, 1997). and malignant (differentiated thyroid cancer)
Recently, adipose tissue has been conditions.
recognized as a major endocrine organ,
involved in the regulation of thermogenesis, 2.2. Collection of blood samples
food intake, and energy expenditure, e.g., the Blood samples (5ml) were collected via
change between fed and starved state (Laurberg a traumatic antecubital venipuncture into
et al,2012). Studies of weight reduction by vacutainer tubes. The collected blood samples
bariatric surgery or gastric banding. allowed to stand at room temperature until it
(Chikunguwo et al (2007) and Dall'Asta et al has clotted, and the serum was recovered by
(2010) have found postoperative changes in centrifugation at 3000 rpm for 15 minutes for
levels of thyroid stimulating hormone (TSH), removal of any suspended cells. The samples
triiodothyronine (T3), and prohormons were used immediately for estimation of serum
thyroxine (T4) but in different directions. thyroid hormones (TSH, T3 and T4), calcium
Likewise, a decrease in TSH was observed and 25-OH vitamin D3.
following diet-, exercise-, and behavior
therapy-induced weight loss in children and 2.3. Methods
adolescents (Aeberli et al, 2010; Reinehr et al, a) Estimation of serum TSH, T3 and T4
2006; Araujo et al, 2010). The relationship In vitro quantitative determinations of
between body weight and thyroid hormones TSH, T4 and T3 in human serum were
seems conceivable and the exact mechanisms performed using Automated Cobas e 411
are yet unexplained and temporality is debated. Immunoassay Analyzers based on
Therefore, the aim of the present study was to electrochemiluminescent technology that is the
investigate the possible relationship between using of ruthenium complex and the measuring
serum fluctuations of the TSH, T3 and its cell.
prohormone T4 with body weight in
hypothyroidism under thyroxin therapy. b) Estimation of 25-OH vitamin D3
Diazyme's Enzyme-Immunoassay
2. MATERIALS AND METHODS FemtoQuant™ 25-OH vitamin D3 test is based
2.1. Subjects on the principle of α-complementation of the
The present study was carried out from enzyme β-galactosidase and the competition
May 2016 to January 2017 by collaboration between an enzyme donor-25-OH vitamin D3
between Clinical Biochemistry and Surgery conjugate, an anti-vitamin D3 antibody and the
departments in College of Medicine- Hawler 25-OH vitamin D3 content of a serum sample.
Medical University-Iraq-Kurdistan region. Samples with higher 25-OH vitamin D3
Anthropometric data and thyroid function concentrations produce higher β-galactosidase
parameters were retrospectively reviewed for activities and vice versa. A nitrophenyl-ß-
100 hypothyroidism patients with the mean ± galactoside derivative (NPG) is used as the
SE age 33.6 ± 1.3 years, ranging from 21 - 62 enzyme substrate. The reaction's product has
years of age, all examined samples were maximum absorbance at 415 nm. The 25-OH
collected from patients that have been referred vitamin D3 concentration of a sample is
to the hospital, patients were diagnosed with
188 Baban A. et al. /ZJPAS: 2017,29 (5): 186-191

proportional to the measured β-galactosidase Table (1). The mean ± S.E value for serum
activity (Saida et al, 2014). TSH was 7.1 ± 0.9 µIU/ml with a range of
variation 0.005 – 137 µIU/ml and the mean ±
c) Estimation of calcium S.E value of serum T3 & T4 were 10.6 ±1.1 &
Serum calcium was determined by an 41.1 ±1.4 nmole/L with a range of variation
enzymatic colorimetric method using readily 0.806 – 183.5 & 2.38 – 142.5 nmole/L,
made kits Biomerieux Sa. (France) according respectively.
to the Coms method (Corns and Ludman, The mean ± S.E value for serum calcium
1987). was 13.4 ± 2.1 mg/dl and the range of variation
was 2.49 – 50 mg/dl. The mean value of 25-
d) Statistical analysis OH vitamin D3 in sera of patients with
Data were evaluated by SPSS software hypothyroidism was 29.5 ± 2.3 nmole/L and
version 19 (SPSS Inc.,Chicago, IL, USA). The the range of variation was 5.89 – 100 nmole/L.
correlation coefficient (r) was used to assess
the link between TSH, T3, T4 and weight gain,
T-test for independent samples was used to Table 1: Details of biochemical parameters of the
assess the difference between serum samples. studied group.

Values are reported as mean ± SE. P<0.05 was


considered statistically significant (Daniel,
1983). Parameters Mean ± SE Range
Age (years) 33.6 ± 1.3 21 - 62
Weight (kg) 66.1 ± 2.3 0.59 - 98
2.4. Ethical considerations
TSH (µIU/ml) 7.1 ± 0.9 0.005 - 137
The study was approved by the research
T3 nmole/L 10.6 ±1.1 0.806 - 183.5
Ethical Committee of Hawler Medical
T4 nmole/L 41.1 ±1.4 2.38 - 142.5
University/ College of Medicine-Erbil. An
Calcium mg/dl 13.4 ± 2.1 2.49 - 50
informed and written consent was taken from
25-OH vitamin
each participant before samples collection. D3 nmole/L 29.5 ± 2.3 5.89 - 100

3. RESULTS Figures (1, 2 & 3) shows the correlation


3.1. Characteristics of the study coefficient between serum TSH, T3, T4 and
population body weight. According to our data, a
This retrospectives study was carried out statistical positive correlation (r2 = 0.2347 & r
on 100 women with hypothyroidism = 0.484 ) was observed between TSH and body
(Underactive Thyroid hormone). The mean ± weight. While there were a negative correlation
SE age was 33.6 ± 1.3 with a range of between T3 (r2 = 0.1725 & r= -0,415), T4 (r2 =
variation 21 to 62 years while the mean ± SE 0.17 & r = -0,41 ) and body weight.
weight 66.1 ± 2.3 Kg with a range of variation
59 - 98 Kg.

3.2. Results of biochemical parameters


Details of biochemical parameters of
the studied group (hypothyroidism patients) are
given in Table 1. The laboratory parameters of
patients with hypothyroidism are shown in
189 Baban A. et al. /ZJPAS: 2017,29 (5): 186-191

25 4. DISCUSSION
y = 0.2491x - 14.06 To investigate any possible relationship
20 R² = 0.2347
between serum TSH, T3, T4 and body weight
15 in Kurdistan region we assayed a series of
TSH  IU/ml

serum samples of clinically diagnosed patients


10 with hypothyroidism under thyroxin therapy.
5
Obesity is increasingly being identified as a
major epidemic today raising worldwide health
0 concerns (Solanki et al, 2013; Asvold et al,
50 70 90 110 2009), although the increase in the prevalence
-5
Body Weight (kg) of obesity seems to have stopped in some
countries according to recent investigations
Figure 1: Correlation coefficient between Thyroid-
(Svendstrup et al, 2011). The international
stimulating hormone and body weight.
focus on obesity has led to a steep increase in
the number of studies dealing with possible
16
interactions between obesity and other diseases
Triiodothyronine (T3) nmole/L

y = -0.2686x + 26.585
14
R² = 0.1725 as well as the relation between obesity and
12
physiology and pathophysiology of the various
10
organs and tissues of the body (Laurberg et
8
al,2012).
6
Our study clearly showed that any
4
changes in the level of serum TSH, T3, T4
2
appears to be associated with weight loss,
0
55 65 75 85 weight gain and obesity.
Body Weight (Kg)
The current study found a positive
correlation between TSH and body weight
Figure 2: Correlation coefficient between serum while T3 and T4 inversely proportional with
Triiodothyronine (T3) and body weight the body weight. These finding were in
accordance with the other investigators
(Solanki et al, 2013; Gupta et al, 2015;
25 Milionis and Milionis, 2013; Seo et al, 2016;
y = -0.276x + 32.527
Rotondi et al, 2014).
Thyroxine (T4) nmole/L

20 R² = 0.171
Thyroid hormone (TH) regulates
15 metabolic processes essential for normal
growth and development as well as regulating
10
metabolism (Brent, 2012 a).
5 The causal relationship between body
weight and variations in thyroid function could
0 be explained by the process of thermogenesis
57 67 77 87
increase thermogenesis through an increase in
Body Weight (Kg)
cellular activity to produce ATP (Milionis and
Figure 3: Correlation coefficient between serum Milionis, 2013).
thyroxine (T4) and body weight Reduced thyroid hormone levels
(Hypothyroidism) is associated with
190 Baban A. et al. /ZJPAS: 2017,29 (5): 186-191

hypometabolism characterized by reduced Araujo, R.L., Andrade, B.M., Padron, A.S., Gaidhu,
resting energy expenditure, weight gain, M.P., Perry, R.L., et al 2010. High-fat diet increases
thyrotropin and oxygen consumption without altering
increased cholesterol levels, reduced lipolysis,
circulating 3,5,3′-triiodothyronine (T3) and thyroxine
and reduced gluconeogenesis (Brent, 2012 b). in rats: the role of iodothyronine deiodinases, reverse
TH stimulates both lipogenesis and lipolysis, T3 production, and whole-body fat oxidation,
although when TH levels are elevated, the net Endocrinology, 151, 3460–3469.
effect is fat loss (Oppenheimer et al, 1991). TH
Asvold, B.O., Bjoro, T., Vatten, L.J. 2009. Association
influences key metabolic pathways that control
of serum TSH with high body mass differs between
energy balance by regulating energy storage smokers and never-smokers, J Clin Endocrinol
and expenditure. TH regulates metabolism Metab, 94, 5023-7.
primarily through actions in the brain, white
fat, brown fat, skeletal muscle, liver, and Brent, G.A. 2012 a. Hypothyroidism and thyroiditis, In:
Melmed, S.P.(Ed.), Williams Textbook of
pancreas (Mullur et al, 2014).
Endocrinology, Elsevier, Philadelphia.

5. CONCLUSIONS Brent, G.A. 2012 b. Mechanisms of thyroid hormone


a) In our findings it can be concluded that action, J Clin Invest, 122, 3035–3043.
any change in the level of serum TSH,
Chikunguwo, S., Brethauer, S., Nirujogi, V., Pitt, T.,
T3, T4 can be correlated with gain or
Udomsawaengsup, S., et al 2007. Influence of
lose of body weight. obesity and surgical weight loss on thyroid hormone
b) This study revealed that there is a levels, Surg Obes Relat Dis, 3, 631–635.
statistical positive correlation between
TSH and body weight while the Corns, C.and Ludman, C. 1987. Determination of
Calcium, Ann .Clin.Biochemistry, 24, 345-51.
correlation were negative between T3,
T4 and body weight. Dall'Asta, C., Paganelli, M., Morabito, A., Vedani, P.,
c) Further multicentric and large studies Barbieri, M., et al 2010. Weight loss through gastric
are required for a general assumption banding: effects on TSH and thyroid hormones in
of the correlation between obesity and obese subjects with normal thyroid function, Obesity
(Silver Spring), 18(4), 854–857.
variations of normal thyroid function
with more focused approach on the Daniel, W.W. 1983. Biostatistics: A foundation for
mechanistic aspects. analysis in the Health Science, 3rd Edition, John
Wiley and Sons, USA.

Feldt-Rasmussen, U. 2007. Thyroid and leptin, Thyroid,


REFERENCES 17, 413- 419.
Al-Adsani, H., Hoffer, L.J., Silva, J.E. 1997. Resting
energy expenditure is sensitive to small dose changes
Gupta, G., Sharma, P., Kumar, P., Itagappa, M., Sharma,
in patients on chronic thyroid hormone replacement,
R. 2015. A correlation between thyroid stimulating
J Clin Endocrinol Metab, 82, 1118–1125.
hormone and body mass index in women with
subclinical hypothyroidism, Asian J Pharm Clin Res,
Aeberli, I., Jung, A., Murer, S.B., Wildhaber, J.,
8( 4), 206-208.
Wildhaber-Brooks, J., et al 2010. During rapid
weight loss in obese children, reductions in TSH
Laurberg, P., Knudsen, N., Andersen, S., Carle, A.,
predict improvements in insulin sensitivity
Pedersen, I.B., et al 2012. Thyroid Function and
independent of changes in body weight or fat, J Clin
Obesity, European Thyroid Journal, 1, 159–167.
Endocrinol Metab, 95, 5412–5418.
Milionis, A., Milionis, C.H. 2013. Correlation between
Body Mass Index and Thyroid Function in Euthyroid
191 Baban A. et al. /ZJPAS: 2017,29 (5): 186-191

Individuals in Greece, ISRN Biomarkers, Volume in body mass index in Denmark from 1997/1998 to
2013, Article ID 651494, 7 pages 2004/2005, but with geographical diversity, Dan Med
http://dx.doi.org/10.1155/2013/651494. Bul, 58, 1–5.

Mullur, R., Liu, Y.Y., Brent, G.A. 2014. Thyroid Zimmermann-Belsing, T., Brabant, G., Holst, J.J., Feldt-
Hormone Regulation of Metabolism, Physiological Rasmussen, U. 2003. Circulating leptin and thyroid
Reviews, 94(2), 355–382. dysfunction, Eur J Endocrinol, 149, 257–271.

Oppenheimer, J.H., Schwartz, H.L., Lane, J.T., Zulewski, H., Muller, B., Exer, P., Miserez, A.R., Staub,
Thompson, M.P. 1991. Functional relationship of J.J. 1997. Estimation of tissue hypothyroidism by a
thyroid hormone-induced lipogenesis, lipolysis, and new clinical score: evaluation of patients with
thermogenesis in the rat, J Clin Invest, 87, 125–132. various grades of hypothyroidism and controls, J
Clin Endocrinol Metab, 82, 771–776.
Reinehr, T., de, S.G., Andler, W. 2006.
Hyperthyrotropinemia in obese children is reversible
after weight loss and is not related to lipids, J Clin
Endocrinol Metab, 91, 3088–3091.

Riis, A.L., Gravholt, C.H., Djurhuus, C.B., Norrelund,


H., Jorgensen, J.O., et al 2002. Elevated regional
lipolysis in hyperthyroidism, J Clin Endocrinol
Metab, 87, 4747–4753.

Riis, A.L., Jorgensen, J.O., Gjedde, S., Norrelund, H.,


Jurik, A.G., et al 2005. Whole body and forearm
substrate metabolism in hyperthyroidism: evidence of
increased basal muscle protein breakdown, Am J
Physiol Endocrinol Metab, 288(6) E1067–E1073.

Rotondi, M., Croce, L., Pallavicini, C., Manna, L.L.,


Accornero, S.M., et al 2014. Body Weight Changes
in a Large Cohort of Patients Subjected to
Thyroidectomy for a Wide Spectrum of Thyroid
Diseases, Endocr Pract, 20(11), 1151-1158.

Saida, F.B., Chen, X., Tran, K., Dou, C.H., Yuan, C.H.
2014. First 25 hydroxyvitamin D assay for general
chemistry analyzers, Expert Rev. Mol. Diagn, Early
online, 1–11.

Seo, H.J., Chung, J.K., Kang, K.W., Kim, E.E., Cheon,


G.J., et al 2016. High Serum Levels of Thyroid
Stimulating Hormone and Sustained Weight Gain in
Patients with Thyroid Cancer Undergoing
Radioiodine Therapy, Int J Thyroidol, 9(1), 19-28.

Solanki, A., Bansal, S.H., Jindal, S., Saxena, V., Shukla,


U.S. 2013. Relationship of serum thyroid stimulating
hormone with body mass index in healthy adults,
Indian J Endocrinol Metab, 17, S167–S169.

Svendstrup, M., Knudsen, N.K., Jorgensen, T.,


Rasmussen, L.B., Ovesen, L., et al 2011. Stagnation

You might also like