Abstract
Aim: To determine the association between maternal blood lipid profile and thyroid stimulating hormone in second and third trimester of pregnancy.
Methods & Materials: The present study was carried out at MGM Hospital, Navi Mumbai, India. 200 antenatal cases from October, 2012 to October 2014 were enrolled after taking an informed consent. The blood samples for Thyroid stimulating hormone and lipid profile were taken at 16th and 32nd weeks.
Results: The mean TSH level in second trimester was 1.53 mIU/L, with a standard deviation of 1.147 mIU/L. In third trimester, the mean TSH level was increased to 2.60 mIU/L with a standard deviation of 0.836mIU/L. The t-stat value was found to be -10.649 (p < 0.001). In third trimester, TSH was negatively correlated with Cholesterol (r= -0.214, p < 0.01) and VLDL (r= -0.148, p < 0.05).
Conclusion: TSH levels rises according to the gestational age, being higher in third trimester as compared to second trimester. There is a significant negative correlation between TSH levels and cholesterol & VLDL in third trimester of the pregnancy. Hence, TSH levels should be looked for, especially in third trimester, in order to keep the thyroid related problems in check.
Introduction
Thyroid hormones have important functions in embryogenesis and fetal development [1, 2]. It is widely known that thyroid function undergoes many significant changes during pregnancy [3, 4, 5].
The size of the thyroid gland remains however normal during pregnancy. Thus, the presence of goitre should always be investigated. A meta-analysis of various available studies of thyroid gland’s size and function in pregnancy found out that thyroid size, when estimated by inspection and palpation or measured by ultrasonography (USG), increased only in iodine deficiency, and the increase in glandular size remained within the normal range [6].
Controlled hyper-stimulation of the ovaries with exogenous gonadotropins (for in vitro fertilization) resulted in a rise of serum Thyroid Binding Globulin (TBG), Thyroxine (T4), and triiodothyronine (T3) concentrations while there was a fall in serum free T4 concentration, and a small rise in serum TSH concentrations (usually within the normal range) [7].
The serum TBG concentration usually rises twofold in pregnancy because of estrogen which both increases TBG production and sialylation; the latter generally reduces the clearance of TBG [8, 9]. TBG excess leads to an increment in both serum T4 and T3 concentrations, but not the serum free T4 and T3 concentrations.
Thus, total T4 and T3 concentrations generally, rise during the first half of pregnancy, however plateauing at approximately 20 weeks of gestation is seen, and then a new steady state is reached and the overall production rate of thyroid hormones returns to pre-pregnancy rates. Thus, TBG excess leads to an overall increase in both serum total T4 and T3 concentrations.
Also, TSH levels are usually suppressed due to very high levels of Human chorionic gonadotropin (hCG) during the first half of the pregnancy, especially the first trimester. hCG, a glycoprotein hormone which secreted by placenta, shares a common alpha subunit with TSH, hence can act as a weak TSH-receptor agonist [10]. hCG has a mild stimulatory effect on the thyroid gland, and can cause a transient “physiological” elevation of thyroxine (FT4) and free triiodothyronine (FT3) [11]. TSH levels measurement at this time therefore, may not provide a good indicator of thyroid function. Later phases of gestation, it has been suggested, could be more reflective of maternal thyroid status [12].
Thyroid dysfunction without any primary thyroid disease may result in various qualitative or quantitative changes of triglycerides, phospholipids, cholesterol, and other lipoproteins [13]. Dyslipidemia, a consequence of thyroid dysfunction, generally increases the risk for cardiovascular disease [14, 15, 16]. Previous studies have shown that thyroid stimulating hormone (TSH), free thyroxine (FT4) and free triiodothyronine (FT3) are significantly associated with lipid profile in the euthyroid population, regardless of gender [17, 18].
The influence of TSH on lipid profile has been assumed to be mediated indirectly, through its effect on thyroid hormones. However, additional evidence suggests that this association is partially contributed by the direct extra-thyroidal effect of TSH on lipid profile [19, 20]. Normal pregnancy is associated with predicted changes in lipid metabolism and elevation in lipid concentration as gestation progresses [21]. However, these changes are considered to be generally non-atherogenic, and fall sharply to pre-pregnancy levels following delivery [22, 23].
Understanding the physiology of thyroid stimulating hormone in normal pregnancy have highlighted the importance of the consequences of abnormal function on obstetric outcome and fetal well-being. As to how modification in thyroid stimulating hormone modulates changes in lipid profile is yet to be ascertained in an Indian population. The present study is the continuation of the previous study [24] and it aims to determine the association between thyroid stimulating hormone and lipid profile in Indian pregnant women.
The present study is conducted in order to evaluate the association between thyroid stimulating hormone and lipid profile in Indian normotensive pregnant women.
Material, Methods, Ethics, Statistical Analysis, Inclusion and Exclusion Criteria
The present study is a continuation of our previous study and the material, methods, ethics, inclusion and exclusion criteria could be obtained from our previous study [5].
In brief, the present study was conducted at MGM Hospital, Navi Mumbai, India. 200 antenatal cases from October, 2012 to October 2014 were enrolled after taking an informed consent. Out of the 200 subjects, 10 developed GHTN in late third trimester which was detected after 32nd week during follow-up which were also included. The venous blood sample was collected from all the patients for measurement of lipid and thyroid profile in the 16th week and 32nd week of gestation for analysis.
All pregnant women with a singleton pregnancy with a gestational age of 13-28 weeks, irrespective of parity and gravida were included. Pregnant women in whom hypertension (HTN) was detected before 14 weeks and those with diseases or complications like chronic HTN, Obstetric and Foetal Complications (Hydrops foetalis, congenital foetal anomalies), Diabetes, Renal Disorders and Thyroid Disorders were excluded.
Statistical analyses were performed using Statistical Package for Social Sciences (SPSS) version 20. All reported P values are two-tailed, and confidence intervals were calculated at the 95% level. The data was presented using frequencies, percentages, descriptive statistics followed by charts and graphs. Level of significance was set at 5%. All p-values less than 0.05 were treated as significant.
Results
The mean TSH level in second trimester was 1.53 mIU/L, with a standard deviation of 1.147 mIU/L. In third trimester, the mean TSH level was increased to 2.60 mIU/L with a standard deviation of 0.836mIU/L. The t-stat value was found to be -10.649 (p < 0.001) (table 1) and (figure 1).
Trimester | N | Mean | SD | SEM | T | Df | Sig. |
Second Trimester | 200 | 1.53 | 1.147 | 0.081 | -10.649 | 398 | < 0.001** |
Third Trimester | 200 | 2.60 | 0.836 | 0.059 |
The mean Triglycerides, Cholesterol, High density lipoproteins, low density lipoproteins, very low density lipoproteins and TSH are depicted in (table 2).
Trimester | Second Trimester | Third Trimester |
Serum Cholesterol {mg/dl} | 214.595 ± 18.163 | 242.645± 20.437 |
Serum Triglycerides {mg/dl} | 188.68 ± 20.874 | 216.78± 20.096 |
HDL-CHOLESTEROL {mg/dl} | 49.125 ± 6.147 | 43.065± 4.364 |
LDL-CHOLESTEROL {mg/dl} | 92.410 ±18.938 | 137.815± 13.451 |
VLDL-CHOLESTEROL {mg/dl} | 28.215 ± 7.664 | 36.27± 6.714 |
TSH Level {mIU/L} | 1.528 ± 1.147 | 2.597± 0.836 |
During Second trimester, there is significant positive correlation between VLDL and HDL (r=0.158, p < 0.05). However, there was no significance correlation between TSH levels and lipid profile. (table 3).
TSH | Cholesterol | Triglycerides | HDL | LDL | VLDL | |
TSH | ||||||
Cholesterol | -0.017 | |||||
Triglycerides | -0.130 | 0.061 | ||||
HDL | -0.030 | 0.021 | 0.068 | |||
LDL | 0.052 | -0.088 | -0.002 | 0.010 | ||
VLDL | -0.059 | -0.081 | 0.035 | .158* | 0.010 |
TSH was negatively correlated with Cholesterol (r= -0.214, p < 0.01) and VLDL (r= -0.148, p < 0.05). This indicates that the TSH and Cholesterol, VLDL are directly associated. With increase in TSH level, cholesterol levels decreases. However, they are still within normal range (table 4).
TSH | Cholesterol | Triglycerides | HDL | LDL | VLDL | |
TSH | ||||||
Cholesterol | -.214** | |||||
Triglycerides | .089 | .065 | ||||
HDL | -.007 | .080 | .160* | |||
LDL | .096 | .126 | -.049 | -.049 | ||
VLDL | -.148* | -.086 | .118 | .176* | -.042 |
Discussion
In second trimester mean TSH level was 1.53mIU/L with standard deviation of 1.147mIU/L. In third trimester, the mean TSH level was increased to 2.60mIU/L with a standard deviation of 0.836mIU/L. The t-stat value was found to be -10.649 (p < 0.001), which indicates a significant increase in the serum TSH level in third trimester as compared to second trimester.
In our study a correlations between TSH and Lipid Profile parameters in 2nd and 3rd trimester was made and we found during second trimester, there is significant positive correlation between VLDL and HDL (r=0.158, p < 0.05).
In third trimester TSH was correlated with Cholesterol (r= -0.214, p < 0.01) and VLDL (r= -0.148, p < 0.05). This indicates that the TSH and Cholesterol & VLDL are negatively associated. When TSH level increases, cholesterol levels decreases. Also we observed a positive correlation between HDL & Triglyceride (r=0.160, p <0.05) and VLDL & HDL (r=0.176, p < 0.05).
In a study done by Ibrahem et. al., they found that in the second trimester a significant positive correlation coefficient existed between T3 with triglyceride, VLDL and CHO/HDL. There was a negative correlation coefficient between TSH and triglyceride, VLDL and T3. In third trimester, there was a negative correlation coefficient between T4 with triglyceride and VLDL [25].
Biondi and Klein reported increase in means TSH levels overall in pregnancy [15]. While few other studies have exactly opposite [26, 27]. Previous studies have shown that TSH is significantly associated with lipid profile in the euthyroid population, regardless of gender [18]. The influence of TSH on lipid profile has been assumed to be mediated indirectly, through its effect on thyroid hormones. Furthermore, additional evidence indicates that this association is partially contributed by the direct extra-thyroidal effect of TSH on lipid profile [20]. However, non-significant positive association between TC and TSH, TG and TSH observed among pregnant women may support the assumption that TSH directly affects lipid metabolism [19].
Circulatory FT3 levels are inversely influenced by TSH, consequently the negative relationship with TG among pregnant women could also be attributed to low TSH level and the stimulation of lipid metabolism by FT3. Hyperthyroidism is implicated in hepatic endogenous glucose efflux which triggers lipogenesis [28, 29].
TSH level was found to be associated with gestational age in a study. This may be a physiological role of TSH to maintain FT3 level to regulate TG synthesis with respect to gestational age [30].
Conclusion
TSH levels rises according to the gestational age, being higher in third trimester as compared to second trimester. There is a significant negative correlation between TSH levels and cholesterol & VLDL in third trimester of the pregnancy. However, the levels are still within the normal range. Hence, TSH levels should be looked for, especially in third trimester, in order to keep the thyroid related problems in check.
References
-
Mulder
JE.
Thyroid diseases in women. Med Clin N Am.
1998;
82
(1)
:
103-125
.
View Article Google Scholar -
Guillaume
J,
Schussler
GC,
Goldman
J.
Components of the total serum thyroid hormone concentrations during pregnancy: High free thyroxine and blunted thyrotropin (TSH) response to TSH-releasing hormone in the first trimester. J Clin Endocrinol Metab.
1985;
60
(1)
:
678-884
.
View Article Google Scholar -
Burrow
GN,
Fisher
DA,
Larsen
PR.
Maternal and fetal thyroid function. New England Journal of Medicine 1994 Oct.
20;
331
(16)
:
1072-8
.
View Article Google Scholar -
Haddow
JE,
Palomaki
GE,
Allan
WC,
Williams
JR,
Kinght
GJ,
Gagnon
J,
et
al.
Maternal thyroid deficiency during pregnancy and subsequent neuropsychological development of the child. N Engl J Med.
1999;
341
(8)
:
549-555
.
View Article Google Scholar -
Brent
GA.
Maternal thyroid function: Interpretation of thyroid tests in pregnancy. Clin Obstet Gynecol.
1997;
40
(1)
:
3-15
.
View Article Google Scholar -
Fantz
CR,
Dagogo-Jack
S,
Ladenson
JH,
et
al.
Thyroid function during pregnancy. Clin Chem.
1999;
45
(12)
:
2250-8
.
View Article Google Scholar -
Muller
AF,
Verhoeff
A,
Mantel
MJ,
et
al.
Decrease of free thyroxine levels after controlled ovarian hyperstimulation. J Clin Endocrinol Metab.
2000;
85
(2)
:
545-8
.
View Article Google Scholar -
Santin
AP,
Furlanetto
TW.
Role of estrogen in thyroid function and growth regulation. Journal of Thyroid Research.
2011;
2011
(1)
:
7 pages
.
View Article Google Scholar -
Ain
KB,
Mori
Y,
Refetoff
S.
Reduced clearance rate of thyroxine-binding globulin (TBG) with increased sialylation: a mechanism for estrogen-induced elevation of serum TBG concentration. J Clin Endocrinol Metab.
1987;
65
(4)
:
689-96
.
View Article Google Scholar -
Glinoer
D.
The regulation of thyroid function in pregnancy: Pathways of endocrine adaptation from physiology to pathology. Endocr Rev.
1997;
18
(3)
:
404-33
.
View Article Google Scholar -
Lacka
K,
Lakoma
H.
Thyroid gland and pregnancy: Physiology and pathology. Wiad Lek.
2002;
55
(7-8)
:
450-462
.
View Article Google Scholar -
Lazarus
JH.
Thyroid function in pregnancy. Brit Med Bull.
2011;
97
(1)
:
137-148
.
View Article Google Scholar -
Zhu
X,
Cheng
SY.
New insights into regulation of lipid metabolism by thyroid hormone. Current Opinion in Endocrinology, Diabetes and Obesity.
2010;
17
(5)
:
408-413
.
View Article Google Scholar -
Klein
I,
Ojamaa
K.
Thyroid hormone and the cardiovascular system. New Engl J Med.
2001;
344
(7)
:
501-509
.
View Article Google Scholar -
Biondi
B,
Klein
I.
Hypothyroidism as a risk factor for cardiovascular disease. Endocrine.
2004;
24
(1)
:
1-13
.
View Article Google Scholar -
Biondi
B,
Kahaly
GJ.
Cardiovascular involvement in patients with different causes of hyperthyroidism. Nature Reviews Endocrinology.
2010;
6
(8)
:
431-443
.
View Article Google Scholar -
Roos
A,
Bakker
SJL,
Links
TP,
Gans
ROB,
Wolffenbuttel
BHR.
Thyroid function is associated with components of the metabolic syndrome in euthyroid subjects. J Clin Endocrinol Metab.
2007;
92
(2)
:
491-496
.
View Article Google Scholar -
Garduno-Garcia
JJ,
Alvirde-Garcia
U,
Lopez-Carrasco
G,
Padilla-Mendoza
ME,
et
al.
TSH and free thyroxine concentrations are associated with differing metabolic markers in euthyroid subjects. Eur J Endocrinol.
2010;
163
(2)
:
273-278
.
View Article Google Scholar -
Wang
F,
Tan
Y,
Wang
C,
Zhang
X,
Zhao
Y,
Song
X,
et
al.
Thyroid-stimulating Hormone levels within the reference range are associated with serum lipid profiles independent of thyroid hormones. J Clin Endocrinol Metab.
2012;
97
(8)
:
2724-31
.
View Article Google Scholar -
Ruhla
S,
Weickert
MO,
Arafat
AM,
Osterhoff
M,
Isken
F,
Spranger
J,
et
al.
A high normal TSH is associated with the metabolic syndrome. Clin Endocrinol.
2010;
72
(5)
:
696-701
.
View Article Google Scholar -
Hadden
DR,
McLauglin
C.
Normal and abnormal maternal metabolism during pregnancy. Semin Fetal Neonatal Med.
2009;
14
(6)
:
401
.
View Article Google Scholar -
Vrijkotte
TG,
Krukziener
N,
Hutten
BA,
et
al.
Maternal lipid profile during early pregnancy and pregnancy complications and outcomes: The ABCD study. J Clin Endocrinol Metab.
2012;
97
(11)
:
3917-3925
.
View Article Google Scholar -
Belo
L,
Caslake
M,
Gaffney
D,
et
al.
Changes in LDL size and HDL concentration in normal and preeclamptic pregnancies. Atherosclerosis.
2001;
162
(2)
:
425-32
.
View Article Google Scholar -
Pusukuru
R,
Shenoi
AS,
Kyada
PK,
Ghodke
B,
Mehta
V,
Bhuta
K,
Bhatia
A.
Evaluation of lipid profile in second and third trimester of pregnancy. Journal of clinical and diagnostic research.
2016;
10
(3)
:
QC12-QC16
.
View Article Google Scholar -
Suhad
abdulaziz Ibrahem,
Ahmed
SA.
Study of association between lipid profile and thyroid hormones in Pregnancy. Journal of Al-Nahrain University.
2013;
16
(4)
:
37-45
.
View Article Google Scholar -
McElduff
A.
Measurement of free thyroxine (T4) levels in pregnancy. Obstet Gynecol.
1999;
39
:
158-161
.
View Article Google Scholar -
Pasupathi
PP,
Mathiyalagan
Deepa P,
Rani
KB,
Vidhya
S,
Satish
KSP.
Evaluation of serum lipids and thyroid hormone changes in non-pregnant, pregnant, and preeclampsia women. Thyroid Science.
2009;
4
(10)
:
CLS1-6
.
View Article Google Scholar -
Beylot
M.
Regulation of in vivo ketogenesis: Role of free fatty acids and control by epinephrine, thyroid hormones, insulin and glucagon. Diabetes and Metabolism.
1996;
22
(5)
:
299-304
.
View Article Google Scholar -
Yamashita
H,
Takenoshita
M,
Sakurai
M,
Bruick
RK,
Henzel
WJ,
Shillinglaw
W,
Arnot
D,
Uyeda
K.
A glucose-responsive transcription factor that regulates carbohydrate metabolism in the liver. Cell Biology.
2001;
98
(16)
:
9116-21
.
View Article Google Scholar -
ayite
Aryee N.
Association of thyroid-stimulating hormone and thyroid hormones, T3 and T4 with lipid profile in Ghanaian normotensive pregnant women. Journal of Biomedical and Pharmaceutical Research.
2015;
4
(1)
:
79-84
.
View Article Google Scholar
Comments & Peer Review
Article Details
How to Cite
Copyrights & License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Publication history
Accepted: 28-04-2017
Published: 28-06-2017
Search Panel
Pubmed
JMRI Journal
Google Scholar
Pubmed
JMRI Journal
Google Scholar
Pubmed
JMRI Journal
Search for this article in:
Google Scholar
Researchgate
CNKI Scholar