Year 23 / No 36 / 2021 /
DOI: https://doi.org/10.36995/j.recyt.2021.36.009
Prevalence of thyroid
dysfunction and its relationship with the lipid profile in patients in hospital
from Encarnación
Prevalencia de disfunción tiroidea y su relación
con perfil lípidico de pacientes del Hospital de Encarnación
Edith N., Genéz Yeza1,*;
1- Regional Hospital of Encarnación. Paraguay.
2- Ministry of Public
Health, Province of Misiones. Tucumán 2174, Posadas, Misiones.
3- Faculty of Exact,
Chemical and Natural Sciences. National University of
Misiones. Félix de Azara 1552, Posadas, Misiones.
*E-mail: mati4edith@gmail.com
Received:
18/02/2021; Approved 20/05/2021
Thyroid dysfunctions are a cause of morbidity and disability worldwide.
Little information has been found on the prevalence of thyroid dysfunctions in
Paraguay, so this study provides data on their presentation. The objective was
to determine the prevalence of thyroid dysfunction and its relationship with
the lipid profile in adult outpatients attending the laboratory of the Regional
Hospital of Encarnación, during January-November 2016.
A descriptive cross-sectional study was performed,
based on the review of 250 medical records, 84 % of whom were women; the median
age was 39 (35-47) years in men and 36 (32-43) years in women. Thirty percent
were hypothyroid and 3 % hyperthyroid; the most frequent thyroid dysfunction
was subclinical hypothyroidism with 19 %. Highly significant differences were
found for total cholesterol, LDL, VLDL and thyrotrophin between hypothyroid vs
euthyroid, with the former having more atherogenic profiles. Logistic
regression was used to assess the contribution of dyslipidaemia, finding a
significant association with hypothyroidism (OR=3.24(1.81-5.81), p<0.001).
Thirty-three percent of this population sample, 1 in 3 individuals, had thyroid
dysfunction. These could be managed appropriately and further complications
could be avoided.
Keywords: Thyroid
dysfunction; Lipid profile; Hypothyroidism; Hypothyroidism; Hyperthyroidism;
Euthyroidism; Subclinical hypothyroidism; Thyrotrophin; Dyslipidaemia.
Las
disfunciones tiroideas son causas de morbilidad y discapacidad a nivel mundial.
Se ha encontrado
escasa información sobre la prevalencia de estas en Paraguay, por lo que este
trabajo aporta datos sobre su forma de presentación. El objetivo fue
determinar la prevalencia de disfunciones tiroideas y su relación con el perfil
lipídico en pacientes adultos ambulatorios que concurrieron al laboratorio del
Hospital Regional de Encarnación, durante enero-noviembre del 2016.
Se realizó
un estudio descriptivo-transversal, basado en la revisión de 250 historias
clínicas, de las cuales 84 % eran mujeres; la mediana de edad fue 39 (35-47)
años en los hombres y 36 (32-43) años las mujeres. El 30% eran hipotiroideos y
3% hipertiroideos; la disfunción tiroidea de mayor frecuencia fue el
hipotiroidismo subclínico, con un 19%. Se halló diferencia altamente
significativa para colesterol total, LDL, VLDL y tirotrofina entre los
hipotiroideos vs eutiroideos, donde los primeros presentaban perfiles más
aterogénicos. Se utilizó regresión logística para evaluar la contribución de la
dislipemia, encontrándose asociación significativa con el hipotiroidismo
(OR=3,24(1,81-5,81), p<0,001). El 33% de esta muestra poblacional, 1 de cada
3 individuos, presentaron una disfunción tiroidea. Con los cuales se podría
tener un manejo adecuado de estas y evitar posteriores complicaciones.
Palabras
clave: Disfunciones
tiroideas; Perfil lipídico; Hipotiroideos; Hipertiroideos; Eutiroideos; Hipotiroidismo
subclínico; Tirotrofina; Dislipemia.
The
follicular cells of the gland produce two main thyroid hormones (HT):
Tetrayodothyronine (thyroxine, T4) and Triiodothyronine (T3), while the
parafollicular or C cells secrete the polypeptide calcitonin, an important hormone
for calcium metabolism as it inhibits bone resorption (1).
The growth and function of the thyroid gland are controlled by the
hypothalamic-pituitary-thyroid axis. Hypothalamic
thyrotropin-releasing hormone (TRH) stimulates thyrotrope cells in the anterior
pituitary to produce serum thyrotropin (TSH) which, in turn, promotes thyroid
gland growth and secretion of T3 and T4 hormones by the thyroid gland, both of
which in turn inhibit, by negative feedback, TRH and TSH synthesis and thus
maintain a stable blood level of T4 and T3 (2-4). T4 and T3 act on cells in
almost all body tissues by combining with nuclear receptors and altering gene
expression. Among their actions, HTs promote normal development of brain and
somatic tissue in the foetus, newborn and during childhood; they regulate heart
rate, myocardial contraction and relaxation, affect gastrointestinal motility,
renal water clearance, regulate energy expenditure, heat generation, weight and
lipid metabolism (1,4)
Thyroid
dysfunction (TD) is one of the most prevalent pathologies in all periods of
life and, as the action of thyroid hormones is pleiotropic, thyroid dysfunction
can have multi-organ repercussions (5). Thyroid
function is assessed by laboratory tests for the detection of TD or monitoring
of pre-existing disorders. The most
common conditions of thyroid morpho-function can be classified according to
altered function: hypothyroidism (thyroid hypofunction) and hyperthyroidism
(thyroid hyperfunction); or according to alterations in size: goitre and
thyroid nodule (6) function is determined by testing TSH, T4 and T3, although
there is much controversy, most professional societies suggest to use TSH to determine
thyroid dysfunction in outpatients, provided that the assay used has a
functional sensitivity equal to or less than 0.02 mIU/L (6-8)
Subclinical
TD is defined as a functional disorder of the thyroid gland, asymptomatic and
only detectable by hormonal laboratory tests, especially in middle-aged and
older individuals, manifested by altered TSH concentrations and normal serum
concentrations of free T3 and T4 (9-12). Hyperthyroidism (hyperT) is a clinical
condition characterized by excessive serum T4 and T3, or both, with suppression
of TSH (13). Once diagnosed, the cause must be investigated to establish
treatment and prognosis. Probable causes
include Grave's disease, toxic multinodular goitre, toxic adenoma, postpartum
thyroiditis, subacute thyroiditis, pharmacological, often in patients taking
synthetic levothyroxine as part of treatment for hypothyroidism, amiodarone,
lithium, interferon α,
interleukin-2 or a history of potassium iodide use or exposure to iodinated
radiological contrast agents increase the likelihood of drug- or iodine-induced
hyperthyroidism (13).
Subclinical
hyperthyroidism (HiperSC) is the asymptomatic or symptomless phase of any
disease presenting with hyperT (13). Hypothyroidism (hypoT) is a clinical
syndrome resulting from HT deficiency, which leads to a generalized slowing of
metabolic processes. Most cases originate from a thyroid gland pathology and
are defined as primary hypothyroidism, in other rarer cases it may develop due
to lack of TSH stimulation (secondary hypothyroidism) or TRH (tertiary
hypothyroidism) (14). When initiated in adulthood, hypoT causes a generalized
decrease in metabolism, with slowed heart rate, decreased oxygen consumption
and glycosaminoglycan deposits in intercellular spaces, particularly in skin
and muscle, leading in extreme cases to the clinical syndrome of myxedema (15).
In hypoT, TSH is elevated and the finding of antithyroid antibodies such as
antithyroglobulin (ATG) and anti-thyroid peroxidase (ATPO) point to an
autoimmune cause (16). The diagnosis of
subclinical hypothyroidism (HipoSC) is defined by elevated TSH concentrations
with normal T4L and is classified as mild TSH between 4.5-10.0 mIU/L and severe
TSH greater than 10 mIU/L (14).10.0 mIU/L and severe TSH greater than 10 mIU/L
(14). The most frequent causes of subclinical hypothyroidism may be: - spontaneous:
chronic autoimmune thyroiditis (Hashimoto's) whose prevalence increases with
age; - iatrogenic: undertreatment of hypothyroidism after treatment of
hyperthyroidism especially with radioactive iodine or surgery; - drugs:
amiodarone, lithium and other iodine-containing medications (14-16).
It is well known that TDs are associated with alterations in the lipid
profile; this is due to several factors; firstly, HTs are involved in lipid
metabolism, stimulating by enzymatic action and β-adrenergic stimulation the degradation of
lipids in adipose tissue, thus favouring the β-oxidation of lipids at the level of
muscle and liver. HT also facilitates
the excretion of cholesterol, its conversion to bile acids and accelerates the
turnover of low-density lipoproteins (LDL), perhaps by stimulating the synthesis
of their receptors or their degradation. That is, these hormones influence all
aspects of lipid metabolism, including synthesis, mobilisation and degradation,
since, in thyroid disease, dyslipidaemia and metabolic abnormalities coexist in
combination with HT-induced haemodynamic alterations, which explains the high
risk of cardiovascular disease (17).
A
large number of epidemiological studies show increased risk of cardiovascular
mortality in both clinical and subclinical hypothyroidism (18,19), but not all
studies demonstrate this (20,21). Consistently
elevated levels of total cholesterol (Chol), LDL cholesterol (LDL Chol) and
triglycerides (TG) have been reported in patients with clinical hypothyroidism
(22). In general, these changes tend to reverse with correction of
hypothyroidism. On the other hand, the influence of hypoSC on serum lipid levels is less evident
and some studies have also shown elevated LDL-chol levels (23). It is accepted
that the determining event in the elevation of LDL-chol is a decrease in
intracellular protein synthesis leading to a lower expression of the LDL
receptor (24). Treatment of
hypothyroidism with levothyroxine reverses this process and lowers serum
LDL-chol levels (25). Therefore, this study aims to determine the prevalence of
thyroid dysfunction and its relationship with the lipid profile in adult
patients and outpatients attending the Regional Hospital of Encarnación during
the period January-November 2016.
Materials
y Methods
A descriptive cross-sectional study was carried out, based on a review
of medical records.
A
non-probabilistic sample was made up of 250 medical records of outpatients of
both sexes, aged between 20 and 80 years, who attended the laboratory service
of the Regional Hospital of Encarnación, during the period January-November
2016, with a doctor's order for a health check-up.
Inclusion criteria: Medical records with
complete patient data, as well as TSH, T4L, glycaemia and lipid profile
determinations were selected.
Exclusion criteria: Those receiving
medication that could affect thyroid function, with a personal history of
thyroid dysfunction, goitre or thyroid surgery, with autoimmune diseases, those
with an infectious, renal or oncological disease, pregnant and diabetic
patients, as well as those on antihypertensive treatment were excluded.
1.3.
Laboratory determinations
The following determinations were performed: TSH, T4L, which were
processed using chemiluminescence methods, with Access DxI 800 equipment
(BeckmanCoulter). The ACCESS assay (3rd
IS) is a paramagnetic particle chemiluminescence immunoassay for the quantitative
determination of serum human thyroid stimulating hormone levels, offering 3rd
generation TSH results of functional sensitivity (0.01-0.02 µIU/mL [mIU/L] with
an interassay %CV ≤ 20%) for the measurement of TSH (26). Lipid profile and
glycaemia were also determined using serum as a sample, samples were processed
on automated Beckman Coulter DxC 800 equipment. Cholesterol concentration was
measured by a fixed-time end-point method (27,28). Triglyceride
determination also used a fixed-time endpoint method (29,30). The
HDL-cholesterol and LDL-cholesterol test was determined using a homogeneous
two-reagent system. The VLDL-cholesterol was obtained by calculating:
VLDL-cholesterol = total cholesterol - (HDL-cholesterol + LDL-cholesterol). The
glucose concentration was determined by a kinetic method using the Beckman
Coulter oxygen electrode. A precise volume of sample is injected into a cuvette
containing glucose oxidase solution. The peak rate of oxygen consumption is
directly proportional to the glucose concentration in the sample.
1.4. Definition of variables
Age: this was obtained from the date of birth, data
from the patient's personal file, and was recorded in years. For the analysis,
the variable was treated as a continuous quantitative variable.
Sex: This was used dichotomously: Female, Male.
Euthyroidism: TSH between 0.4 - 4.20 IUU/ml; FT4
between 0.93 - 1.70 ng/dl.
Clinical hypothyroidism: TSH greater than 4.20 IUU/ml;
FT4 less than 0.93 ng/dl.
Subclinical hypothyroidism: TSH greater than 4.20
IUU/ml; TFT4 between 0.93 - 1.70 ng/dl.
Clinical hyperthyroidism: TSH less than 0.27 IUU/ml;
FT4 greater than 1.70 ng/dl.
Subclinical hyperthyroidism: TSH less than 0.27 IUU/ml
and FT4 between 0.93 - 1.70 ng/dl (26).
Hypertriglyceridaemia: Triglycerides (Tg) ≥ 150 mg/dl.
Hypercholesterolaemia: Cholesterol (Chol) ≥ 200 mg/dl.
HDL: HDL cholesterol < 40 mg/dl in men and < 50
mg/dl in women (ATP III) (31).
LDL: Optimal < 100 mg/dl. Near optimal 100 - 129
mg/dl. Borderline 130 - 159 mg/dl. High ≥ 160 mg/dl
Dyslipidaemia: Total cholesterol (Chol) ≥ 200 mg/dl
and triglycerides (TG) ≥ 150 mg/dl, and
Chol LDL≥ 130mg/dl. This variable was categorised as a
dichotomous variable (YES, NO).
Normal blood glucose: <100mg/dl and impaired
fasting blood glucose (IFG) values ≥100 mg/dl and < 126 mg/dl, according to
the American Diabetes Association (ADA) (32).
1.5. Statistical analysis
Qualitative variables were described using percentages
and 95% confidence intervals. For quantitative variables, their distributions
were determined with the Kolmogorov-Smirnov normality test and, as appropriate,
described by mean and standard deviation or median and 25th and 75th
percentiles.
The Student's test was used to compare quantitative
variables with a normal distribution. For non-normally distributed variables,
the non-parametric Mann Whitney U test was used. Logistic regression was used
to assess the contribution of dyslipidaemia to the occurrence or non-occurrence
of thyroid dysfunction.
We worked with a confidence level of 95 %
and with a significance of p<0.05.
The statistical programme Statgraphics Centurión XV
was used for data analysis and Excel 2010 was used for the elaboration of
tables and graphs.
1.6. Ethical challenges
All
patients, whose data were selected, gave their informed consent and the confidentiality
of the results has been respected. The work has been endorsed by the hospital
where this work was carried out and its bioethics committee.
Results
Of the 250
medical records studied, 211 were women (84%) and 39 men (16%). The median age
in men was 39 [35-47] years, while in women it was 36 [32-43] years. Table 1
shows the biochemical characteristics of the individuals studied, for the total
sample and their distribution according to gender.
Table 1. Biochemical characteristics of the study sample (n=250).
Variables |
Total (n=250) |
Femenino (n= 211) |
Masculino (n=39) |
p- value |
Glucose
(mg/dl) b |
85(77-96) |
85(77–95) |
88(77-96) |
0,199 |
Total
cholesterol (mg/dl) a |
208 ± 49 |
209 ± 47 |
202 ± 57 |
0,416 |
HDL
cholesterol (mg/dl) b |
40(37-45) |
41(38-45) |
38(33-44) |
0,002** |
LDL
cholesterol (mg/dl) a |
135± 44 |
136 ± 44 |
128 ± 46 |
0,412 |
VLDL
cholesterol (mg/dl) b |
28(23-39) |
27(23-37) |
30(21-47) |
0,529 |
Triglycerides
(mg/dl) b |
139(111-187) |
138(111-186) |
146(106-220) |
0,650 |
TSH
(uIU/ml) b |
2,52(1,34-4,71) |
2,59(1,35-4,95) |
1,89(1,31-3,46) |
0,185 |
T4L(ng/dl)
b |
1,12(0,76 - 1,45) |
1,09(0,74-1,43) |
1,21 (0,87-2,01) |
0,183 |
References: a Results expressed as
mean ± standard deviation; b Results expressed as median and 25th and 75th
percentiles; TSH: thyrotropin; T4L: free thyroxine. ** Mann Whitney U test.
All
patients had normal baseline blood glucose levels with no significant
difference according to sex (p= 0.199); no patients with OAG were found. There was a significant difference between
men and women for HDL cholesterol. When
analysing the thyroid profile, it was observed that 33% [95%CI 27-39%] of the
individuals had thyroid dysfunction, the most prevalent being hypothyroidism,
in 30% [95%CI 24-36%], with subclinical presentation being the most frequent,
while hyperthyroidism was observed in 3% [95%CI 1-5%] of the samples studied;
figure 1 shows the data on the prevalence of thyroid dysfunction.
Figure 1. Prevalence of thyroid
dysfunction in the samples studied (n=250).
Figure
2 shows the distribution of thyroid dysfunctions according to sex; 34% [95%CI
27-40%] of women and 26% [95%CI 14-43%] of men had some type of thyroid dysfunction.
Figure 2. Prevalence of thyroid
dysfunction by sex (n=250).
To determine the behavior of the thyroid states, a
comparison was made of the biochemical parameters of hypothyroid and
hyperthyroid patients in relation to euthyroid patients, finding in
hypothyroidism a difference between means for total cholesterol, LDL
cholesterol and a difference between medians for VLDL cholesterol and TSH as
shown in table 2.
Table 2. Comparison of biochemical parameters of hypothyroid
and euthyroid patients (n=250).
Variables |
Hypothyroidism n=75 |
Euthyroidism n= 169 |
p-value |
Glucose
(mg/dl) b |
84(76-100) |
87(77-95) |
0,074 |
Total
cholesterol (mg/dl) a |
229 ± 38 |
201 ± 7 |
< 0,001* |
HDL
cholesterol (mg/dl) |
40(36-45) |
41(38-46) |
0,221 |
LDL
cholesterol (mg/dl) a |
154 ± 35 |
128 ± 45 |
< 0,001* |
VLDL
cholesterol (mg/dl) b |
32(25-39) |
27(21-38) |
0,025** |
Triglycerides
(mg/dl) b |
156(122-193) |
136(106-187) |
0,248 |
TSH
(uIU/ml) b |
6,35(4,95-7,78) |
1,81(1,23-2,58) |
< 0,001** |
T4L(ng/dl)
b |
0,97(0,71-1,79) |
1,16(0,78-1,43) |
0,141 |
References: a Results expressed as mean ± standard
deviation; b Results expressed as median and 25th and 75th percentiles. * Student
t-test, ** Mann Whitney U-test.
For hyperthyroidism, a difference between mediums
was found for total cholesterol, with average serum levels being significantly
lower among patients with hyperthyroidism compared to the group without thyroid
dysfunction, and differences were also found for median triglycerides and TSH
as shown in table 3.
Table 3. Comparison of biochemical parameters of
hyperthyroid and euthyroid patients (n=250).
Variables |
Hypothyroidism n=75 |
Euthyroidism n= 169 |
p-value |
Glucose
(mg/dl) b |
83(77-96) |
87(77-95) |
0,971 |
Total
cholesterol (mg/dl) a |
151± 50 |
201 ± 7 |
0,016* |
HDL
cholesterol (mg/dl) |
37(30-46) |
41(38-46) |
0,288 |
LDL
cholesterol (mg/dl) a |
79(59-105) |
122(95-158) |
0,046** |
VLDL
cholesterol (mg/dl) b |
20(16-25) |
27(21-38) |
0,055 |
Triglycerides
(mg/dl) b |
99(81-126) |
136(106-187) |
0,041** |
TSH
(uIU/ml) b |
0,11(0,04-0,15) |
1,81(1,23-2,58) |
<0,001** |
T4L(ng/dl)
b |
1,91(1,21-2,05) |
1,16 (0,78-1,43) |
0,073 |
References: a Results
expressed as mean ± standard deviation; b Results expressed as median and 25th
and 75th percentiles * Student's t-test, ** Mann Whitney U-test.
Dyslipidaemia was found in 34% of the
population sample, 56% (n=48) corresponded to patients with thyroid disorders Logistic regression was used to assess
the contribution of dyslipidaemia to the occurrence or not of thyroid
dysfunction; for hypothyroidism OR= 3.24 (1.81-5.81) and p<0.001; for
hyperthyroidism OR= 0.26 (0.03-2.35) and p= 0.205, finding that dyslipidaemia
is associated with hypothyroidism.
Discussion
In recent years, the diagnosis of thyroid
dysfunction has become more reliable and safer due to the development of more
sensitive methods for the determination of thyroid hormones, in particular T3,
T4 and TSH. This has contributed to the recognition of
subclinical forms of the disease, allowing diagnosis to be reached more
frequently and more efficiently (33). However, little information has been
found on the prevalence of these disorders in Paraguay, which is why this study
is so important, as it provides data on the behaviour of these diseases in the
population.
Different
approaches to screening for thyroid dysfunction have been proposed, with the
American Thyroid Association recommending thyroid function measurements in all
persons over 35 years of age and then every five years if normal, while the
American College of Physicians recommends screening in persons over 50 years of
age with one or more general symptoms that could be caused by thyroid disease
(8,34,35).
In
the present study, individuals of both sexes participated, with a higher
frequency of women (84%); with regard to biochemical characteristics, all had
fasting blood glucose levels within the reference values, with no significant
difference according to sex (p=0.199); a significant difference by sex was only
observed when HDL cholesterol was assessed (p=0.002). TSH
and T4L values were higher than those obtained in other studies such as those
of Builes et al. in Bogotá (35) and those found by Kolbe in a study on Thyroid
dysfunction and cardiovascular risk factor in an adult population in Obligado,
Paraguay (36), but similar to those found by Maldonado Araque in Spanish adults
(37).
In relation to the diagnosis of thyroid
dysfunctions, the most sensitive methods at present, the so-called third
generation methods, capable of detecting TSH levels of up to 0.01-0.03uIU/ml
(38), have allowed the laboratory to find both the clinical form, but above all
the subclinical ones that could often go unnoticed due to the absence of clear
symptoms. The ranges of these hormones in euthyroid individuals may vary
slightly between different age groups and between different laboratories. In this study, we took as reference values
those recommended by the National Academy of Clinical Biochemistry -NACB (26),
finding a total prevalence of 33% of TD, according to the WHO, between 8 and
10% of the world's population have thyroid function disorders (17). In another study carried out in a Costa
Rican adult population, Guevara et al. found 18.7% of thyroid dysfunctions
(11), while Vera et al. in the national hospital of Itaguá-Paraguay found 34%
of thyroid disorders (51), similar to the data obtained in this study, in
contrast to the 24.4% reported by Kolbe (36).
There are several factors that affect each population
differently and are responsible for the large heterogeneity shown in prevalence
rates between different populations; it should be taken into consideration that thyroid hormone levels vary
with age, method used and population studied, which makes it necessary to have
own reference values, from each laboratory, in different age ranges and from
the indigenous population.
In the
present study, the prevalences of thyroid dysfunctions found were higher than
those observed in a study carried out in the Hospital de Clínicas in
Buenos Aires (39) and similar to the values found in Obligado-Paraguay (36) and
in the Hospital Nacional de Itaguá-Paraguay, but they all coincide in
that the frequency of hypoSC is higher than hypoT, which reflects the need to recognize
these pathologies and establish early treatment, in order to avoid more serious
and costly situations for public health.
Population-based
prevalence studies assessing the frequency of thyroid dysfunction in the
general population, including the NHANES III study (n=16,533), reported a 4.5%
hypoSC and a 0.5% hyperT rate. On the other
hand, the Colorado study (n= 25,862) showed a prevalence of 9.5% and 2.2% of
hypoT and hyperSC (40,41).
The
potentially harmful effects associated with hyperSC are the main reasons why
European guidelines which now recommend initiating treatment of this clinical
condition (42). Recommendations consider
treatment especially for adults with subclinical hyperthyroidism with TSH
levels below 0.1 mIU/L, in order to avoid cardiovascular consequences (42).
Several population-based studies, carried out in asymptomatic groups,
have reported a higher frequency of hypothyroidism in women, especially in the
subclinical form compared to the overt form, with a predominance of women in
our study population, 211 (84%) compared to 39 (16%) men, with a higher
frequency in women in all TDs. Studies
such as Whickham's reported abnormally high TSH in 7.5% of women and 2.8% of
men (43) and in the Birmingham study in women over 60 years of age, hypoT was
found in 2% and mild in 9.6%; furthermore, several studies found a higher
prevalence in women particularly in the sixth decade and up to 16% for hypoSC
(44,45). As women predominate in
our population, as they are the ones who attend more health check-ups, we could
not say that this coincidence with the literature is accurate.
Dyslipidaemia
was found in 34% of the population sample, in which more than half had thyroid
disorders, with a significant association with hypothyroidism (p<0.001). In contrast, no association was found with
hyperthyroidism, which is in agreement with some authors who refer to
hypothyroidism as a recognized cause of secondary dyslipidaemia (46,47). In overt hypothyroidism, the increase in total
cholesterol is above 50% of the values found in euthyroid subjects; This can be
attributed primarily to the increase in LDL-chol and secondarily to the
increase in LDL and VLDL-chol fractions. The main cause of
hypercholesterolaemia in these patients is the decreased clearance of LDL by
its receptor, based on decreased LDL receptor gene expression in fibroblasts,
hepatocytes and other tissues (45).
In hypoT there is a predisposition to cardiovascular problems, as there
is a decrease in myocardial contractility which favors atherosclerotic
processes, there is a reduction in lipolysis and a consequent increase in serum
lipid levels (48). Rodondi et al (49)
have found elevated concentrations of total cholesterol and LDL-cholesterol in
populations with hypoSC compared to euthyroid groups, as in the present study
it was found that hypothyroid patients had a significant difference between the
means and medians of serum levels of total cholesterol, LDL-cholesterol and
VLDL-cholesterol, with higher values than euthyroid patients. Similar results
were reported by Villalba Rinck Hansen et al (47), in a population of
hypothyroid adult women from Posadas. In terms of the comparison of medians
between hyperthyroidism and euthyroidism, significant differences were found
between total cholesterol, LDL cholesterol and TG, but lower serum values were
obtained with respect to euthyroid patients; in hyperthyroidism, an increase in
lipolysis leads to weight loss in patients, while lipolysis leads to lower
concentrations of total cholesterol and LDL cholesterol (46).
Many studies indicate the benefits of
treatment for TD patients, such as improvements in lipid profile, prevention of
early cardiovascular events, reversal of haemodynamic disturbances and
neuropsychiatric symptoms, prevention of atrial fibrillation and development of
osteoporosis with hormone replacement therapy (50). Thyroid hormones play an
important role in lipid synthesis, mobilization and metabolism, as reported in
Colorado (USA), where total cholesterol and LDL-cholesterol were observed to
increase as TSH levels rose (41).
In Paraguay there are few data or studies
on thyroid dysfunction and its relationship with other parameters such as the
lipid profile; one explanation could be the discontinuous supply of reagents
for the determination of the thyroid profile due to a lack of economic
resources, making it difficult to have statistical data for our population.
Consequently, there is a difficulty in early identification of these hormonal
alterations and their subsequent treatment, since the reduction of
comorbidities associated with thyroid dysfunction disorders would contribute to
improving the life quality of these patients, reversing their clinical
manifestations and achieving a longer life expectancy.
Conclusions
·
The prevalence of clinical hypothyroidism
in the studied individuals was 11% and of subclinical hypothyroidism was 19%.
The prevalence of clinical hyperthyroidism was 2% and of subclinical
hyperthyroidism was 1%.
·
When analyzing
hormonal variables, 33% of this population sample had elevated TSH values and
3% had decreased TSH values; the majority had values within the recommended
range, and the most frequently detected thyroid dysfunction was subclinical
hypothyroidism.
·
Hypothyroid
patients have significantly higher serum values of total cholesterol,
LDL-cholesterol and VLDL-cholesterol compared to euthyroid patients.
·
Hyperthyroidism
presents significant differences for total cholesterol, LDL cholesterol and
triglycerides, with respect to euthyroid patients, presenting lower serum
values than euthyroid patients.
·
Dyslipidaemia
is associated with hypothyroidism, so screening for hypothyroidism in patients
with dyslipidaemia is recommended in order to contribute to the reduction of
morbidity and mortality from cardiovascular events.
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