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1.
Arch Iran Med ; 25(7): 417-421, 2022 07 01.
Article in English | MEDLINE | ID: mdl-36404507

ABSTRACT

BACKGROUND: Hypothyroidism is the most common hormonal deficiency worldwide; however, there is limited data about its prevalence in the children and adolescents of the Middle East. METHODS: The prevalence of hypothyroidism were calculated by dividing the number of patients purchasing levothyroxine in 1397 Solar-Hijri year (Correlate with March 2018-February 2019) by the population at risk (per 10000 persons). Data were collected from the Iran health insurance organization registration records and family physician databases of health vice-chancellor of Shiraz University of Medical Sciences. RESULTS: The present study shows that the prevalence of levothyroxine treated population aged under 18 years is 13 in 10000 in the Fars province and it is more common in females (17 in 10000 in females versus 9 in 10000 in males). This study also revealed that the prevalence of hypothyroidism was different in various age groups and increased in older children and adolescents after pubertal ages. Also, an increase in the female: male ratio of prevalence was more obvious during and after puberty. CONCLUSION: Our study showed that the prevalence of congenital hypothyroidism was 3/10000 in southern Iran. Also, the prevalence of hypothyroidism in children and adolescents was totally 13/10000 population, and this prevalence increased in older age and female gender. This prevalence was close to the data from iodine sufficient areas in Europe and the United States.


Subject(s)
Congenital Hypothyroidism , Thyroxine , Humans , Adolescent , Child , Male , Female , Aged , Thyroxine/therapeutic use , Prevalence , Iran/epidemiology , Prescriptions
2.
Iran J Med Sci ; 46(6): 468-474, 2021 11.
Article in English | MEDLINE | ID: mdl-34840387

ABSTRACT

Background: Paricalcitol has been proposed for the treatment of secondary hyperparathyroidism in patients with renal failure and vitamin D deficiency (VDD); however, VDD is related to a range of clinical complaints. We aimed to investigate the effects of paricalcitol on body composition in VDD rats. Methods: Thirty adult male rats aged 10 weeks were randomly divided into three groups of 10, comprising control, VDD, and VDD plus paricalcitol (32 ng/rat intraperitoneal injection) (VDD+P), at the Animal Lab of the Endocrinology and Metabolism Research Center, Shiraz, Iran, in 2020. Body composition was assessed after three weeks via serum biochemical tests and dual-energy X-ray absorptiometry. Finally, the data were analyzed by using the paired-sample t test, the one-way ANOVA, and the Tukey post hoc test. Results: Global lean mass and fat mass were lower in the VDD and VDD+P groups than in the controls (P<0.001). Global fat percentage was reduced significantly in the VDD+P group (P=0.029). Conclusion: Paricalcitol reduced global fat mass and fat percentage in a rat model with VDD. Evaluation of insulin and adiponectin levels is suggested to clarify the physiology of paricalcitol in VDD states.


Subject(s)
Body Composition/drug effects , Ergocalciferols/pharmacology , Vitamin D Deficiency/drug therapy , Vitamin D , Animals , Ergocalciferols/therapeutic use , Male , Rats , Vitamin D Deficiency/complications
3.
Arch Osteoporos ; 16(1): 66, 2021 04 10.
Article in English | MEDLINE | ID: mdl-33837854

ABSTRACT

Insulin resistance may be linked to bone health in young people. This study is the first on adolescents that jointly examined the association of bone health with insulin resistance and body composition. Our results revealed significant negative association between bone parameters and insulin resistance, even after adjustment for confounding factors. PURPOSE: Previous studies are suggestive of the protective role of insulin on bone in adults. Whether this association exists in younger individuals is not clear, yet. This investigation aimed to evaluate the association between insulin resistance, bone parameters, and body composition amongst Iranian adolescentsá¾½ population. METHODS: A cross-sectional study was conducted on 423 participants (224 girls and 199 boys) aged 9-19 years old. Insulin resistance was assessed, using a homeostatic model assessment of insulin resistance (HOMA-IR) and quantitative insulin sensitivity check index (QUICKI). Bone mineral density (BMD), bone mineral content (BMC), total body fat mass (TBFM), and total body lean mass (TBLM) were measured, using dual energy X-ray absorptiometry (DXA), and bone mineral apparent density (BMAD) was calculated. RESULTS: In multiple regression analyses adjusted for potential confounders, the HOMA-IR showed statistically significant negative association with most of the bone parameters (ß = - 1.1 to - 0.002, P = 0.004 to 0.036). On the subject of QUICKI index, this relationship was detected only for lumbar spine (LS) parameters (ß = 0.062 to 37.21, P = 0.0001 to 0.026) and femoral neck bone mineral content (FNBMC) (ß = 1.297, P = 0.013). CONCLUSION: Our results suggest that insulin resistance may be inversely and independently associated with the bone indices in younger individuals. Whether high insulin levels have detrimental effects on growing bone is still unclear and has to be answered.


Subject(s)
Insulin Resistance , Absorptiometry, Photon , Adolescent , Adult , Body Composition , Bone Density , Child , Cross-Sectional Studies , Female , Humans , Iran , Male , Young Adult
4.
Exp Clin Transplant ; 19(9): 928-934, 2021 09.
Article in English | MEDLINE | ID: mdl-31580241

ABSTRACT

OBJECTIVES: Diabetes mellitus is one of the metabolic consequences of solid-organ transplant. Most reports on this condition are from cross-sectional or retrospective studies. In this prospective study, we evaluated the incidence, risk factors, and short-term follow-up of diabetes mellitus in recipients of liver transplant at the Shiraz Liver Transplant Center (Shiraz, Iran). MATERIALS AND METHODS: Recipients of liver transplant who were ≥ 16 year old and were seen from February 2017 until February 2018 were included. Anthropologic measurements and diabetes history were taken between 2 and 4 weeks after transplant. Fasting blood sugar and 75-g oral glucose tolerance test were measured. We diagnosed patients with diabetes mellitus and patients with impaired fasting glucose or impaired glucose tolerance test based on American Diabetes Association criteria. These patients were promptly followed for at least 6 months. RESULTS: Of the 397 recipients who were included in this study, 35.5% were female and 64.5% were male. Overall, the most common reason for transplant was primary sclerosing cholangitis (22.5%). We had 42 living donors and 355 deceased donors, with none being unrelated donors. At first visit (3.8 ± 1.6 wk posttransplant), 20.4% of recipients did not have diabetes, 24.2% were diagnosed with preexisting diabetes mellitus, 31.2% had impaired fasting blood sugar or oral glucose tolerance test, and 24.2% were determined to have posttransplant diabetes mellitus. At last visit (13.6 ± 4.9 mo posttransplant), prevalence for posttransplant diabetes mellitus was 10.8%. Multivariate regression analysis showed that age correlated with development of impaired glucose tolerance test or posttransplant diabetes mellitus (odds ratio 1.060; 95% confidence interval, 1.026-1.095; P < .001). CONCLUSIONS: In this prospective cohort study, we followed recipients posttransplant and reevaluated the prevalence of posttransplant diabetes mellitus. We found significant recovery for this type of diabetes mellitus. Further larger and multicenter studies are necessary to monitor and manage diabetes mellitus posttransplant.


Subject(s)
Diabetes Mellitus , Glucose Intolerance , Liver Transplantation , Adolescent , Blood Glucose/metabolism , Cross-Sectional Studies , Diabetes Mellitus/diagnosis , Diabetes Mellitus/epidemiology , Female , Follow-Up Studies , Glucose Intolerance/complications , Humans , Incidence , Iran/epidemiology , Liver Transplantation/adverse effects , Male , Prospective Studies , Retrospective Studies , Risk Factors , Treatment Outcome
5.
Iran J Child Neurol ; 14(3): 47-56, 2020.
Article in English | MEDLINE | ID: mdl-32952581

ABSTRACT

OBJECTIVES: Previous studies in adults with epilepsy revealed a higher prevalence of metabolic syndrome, resulting in cerebrovascular and cardiovascular events. However, there is insufficient data about body composition and metabolic syndrome in children, especially in the Middle Eastern region. We aimed to investigate metabolic syndrome criteria and body composition in ambulatory children with Epilepsy in Southern Iran. MATERIAL & METHODS: Seventy seven epileptic children with an average age of 11.4 ± 3.2 years and their age-gender-matched controls were included in this study. Anthropometric data, lipid profile, blood glucose, and blood pressure were checked. Body composition was also evaluated by Hologic system dual-energy X-ray absorptiometry. RESULTS: The prevalence of metabolic syndrome as well as the fat mass index in patients were higher than the controls, and p values are 0.032 and 0.012, respectively. Moreover, the lean mass with Bone Mineral Content (BMC) index was detected lower than the controls (P= 0.017).Regarding drugs consumption, serum triglyceride and the blood pressure in patients who receiving carbamazepine was higher than the control individuals with P = 0.019, Beta = 0.379 and P = 0.016, Beta = -0.26, respectively. Fat mass index was also higher in patients using sodium valproate (P = 0.031, Beta = 0.238). CONCLUSION: Our study revealed that children with epilepsy are more prone to metabolic syndrome and higher body fat mass. Therefore, early diagnosis and prevention of metabolic syndrome criteria in patients with epilepsy, With performing regular exercise and having a healthy diet should be encouraged in these children.

6.
Turk J Med Sci ; 49(2): 490-496, 2019 04 18.
Article in English | MEDLINE | ID: mdl-30866603

ABSTRACT

Background/aim: Genetic aspects play a role in insulin resistance in children. In this study, for the first time, the association of LRP5 (rs556442) polymorphism and insulin resistance in Iranian children and adolescents was investigated. Materials and methods: The study population comprises children and adolescents aged 9­18 years. Anthropometric and biochemical parameters were assessed. Insulin resistance/sensitivity was determined by the quantitative insulin sensitivity check index (QUICKI), homeostasis model assessment-insulin resistance (HOMA-IR), insulin-to-glucose ratio, McAuley index, revised McAuley index, fasting insulin resistance index (FIRI), and Bennett's index. LRP5 (rs566442) single nucleotide polymorphism (SNP) was identified using restriction fragment length polymorphism (RFLP). Linear regression analysis was used to determine the association between the LRP5 polymorphism (rs556442) and insulin sensitivity indexes. Results: Significant differences were found between GG genotype vs. AG/AA genotypes for McAuley index (P = 0.049) and revised McAuley index (P = 0.044) when adjusted for interaction factors (age, sex, and puberty) in regression models. No significant association was found between LRP5 (rs566442) and other insulin resistance indexes. Also, LRP5 (rs566442) did not show a significant impact on biochemical parameters. Conclusion: This study showed that LRP5 polymorphism (rs556442) was associated with insulin resistance in Iranian children and adolescents.


Subject(s)
Insulin Resistance/genetics , Low Density Lipoprotein Receptor-Related Protein-5/genetics , Polymorphism, Single Nucleotide/genetics , Adolescent , Child , Cross-Sectional Studies , Female , Genetic Predisposition to Disease , Glucose Tolerance Test , Healthy Volunteers , Homeostasis/genetics , Humans , Iran , Low Density Lipoprotein Receptor-Related Protein-5/physiology , Male , Urban Population
7.
Galen Med J ; 8: e1548, 2019.
Article in English | MEDLINE | ID: mdl-34466525

ABSTRACT

BACKGROUND: Both vitamin D and inflammation were investigated as important players in the pathogenesis of postmenopausal osteoporosis. This study compared vitamin D, inflammatory the biomarkers serum levels and their association with bone mineral density (BMD) in case and control groups to evaluate the possible immune-regulatory effect of vitamin D in this population. MATERIALS AND METHODS: Participants in post-menopausal age, were categorized to 44 osteoporotic vs. 44 healthy aged-matched women according to WHO criteria. Total BMD, T- scores, Z-scores as well as fracture risk were measured in both groups, using Hologic system Dual-energy X-ray absorptiometry (DEXA). Serum 25-OH vitamin D, high sensitive CRP (hs-CRP) and serum amyloid A (SAA) were compared between groups. The association between serum biomarkers level and BMD were also investigated. The same evaluations were performed for vitamin D deficient (<20 ng/mL) and non-deficient (≥20 ng/mL) subgroups. RESULTS: Vitamin D deficiency was higher in the osteoporotic group (32.6%) in comparison with the control group (25.6%), but the differences were not significant (P=0.47). There were no significant differences in serum levels of hs-CRP and SAA (P=0.83 and P=0.39) as well. No significant association between serum inflammatory biomarkers, vitamin D, and BMD were detected (P≥0.05). The results were the same for vitamin D deficient and non-deficient subgroups (P≥0.05). CONCLUSION: In the current study, the beneficial effects of vitamin D as a result of its immune-regulatory mechanisms was not reached. Larger scale studies might pave the way to define vitamin D benefits in postmenopausal osteoporosis.

8.
Bull Emerg Trauma ; 5(1): 29-35, 2017 Jan.
Article in English | MEDLINE | ID: mdl-28246621

ABSTRACT

OBJECTIVE: To determine the prevalence of fractures and associated risk factors in healthy Iranian children and adolescents. METHODS: In this cross sectional population based study, 478 healthy Iranian children and adolescents aged 9-18 years old participated. Baseline data and bone mineral content and density have been determined. One questionnaire was completed for all individuals including previous history of fracture, its location, and level of trauma. Albumin, calcium, phosphorus, alkaline phosphatase, and vitamin D levels were measured. RESULTS: We found a prevalence of 12.9% for fracture. (34.5% for girls and 65.5% for boys); about 71% suffered long bone fracture with distal forearm as the most common site. Totally 58% of the boys and 54% of the girls had fracture with low-energy trauma. The fracture group had lower bone mineral apparent density in the lumbar spine (0.19±0.04 vs. 0.20±0.03, p=0.04), lower serum albumin (4.6±0.5 vs 4.8±0.4, p=0.02), and higher serum alkaline phosphatase level (446±174 vs. 361±188, p=0.02) compared with non-fracture subjects. By logistic regression analysis, we found a significant association for sex, and bone mineral content of the lumbar spine with fracture (p=0.003, p=0.039). CONCLUSION: Compared to other studies, our subjects had lower rate of fracture. We found an association between low bone density and fracture in children and adolescents. This finding has important implications for public health. Further research may contribute to recognition of preventive measures.

9.
Int J Endocrinol Metab ; 15(4): e14099, 2017 Oct.
Article in English | MEDLINE | ID: mdl-29344033

ABSTRACT

BACKGROUND: Improving peak bone mass and bone strength in the first years of life and enhancing it during young adulthood could prevent osteoporosis and fractures in the last years of life. We evaluated the prevalence of low bone mass in the lumbar and femoral neck and its associated factors in southern Iranian children. METHODS: This is a cross-sectional study on healthy Iranian children aged 9 - 18 years old during 2011 - 2012. Dual energy X-ray absorptiometry (DEXA) was used for measuring bone mineral density (BMD). BMD Z-score ≤ -2 was considered as low. Anthropometric data, physical activity, sun exposure, puberty, and mineral biochemical parameters were assessed. Data were analyzed using SPSS v.15. RESULTS: 477 normal children, including 236 (49.5%) girls and 241 (50.5%) boys, aged 13.8 ± 2.7 years were enrolled. Prevalence of low bone mass (LBM) in the femoral and lumbar region was 10.7% and 18.7%, respectively. The prevalence of LBM in femur of girls is twice more than boys. Fat mass index, BMI Z-score, and physical activity were associated with lumbar low bone mass. BMI Z-score and physical activity were associated with femoral low bone mass. CONCLUSIONS: High prevalence of low bone mineral density in children 9 to 18 years in south of the country is concerned and is needed to plan for prevention and treatment. BMI-Z score, fat mass index, and physical activity were the 3 most important preventive factors in developing low bone mass in children.

10.
Int J Endocrinol Metab ; 13(3): e25542, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26401143

ABSTRACT

BACKGROUND: Body weight is made up of lean and fat mass and both are involved in growth and development. Impression of these two components in bone density accrual has been controversial. OBJECTIVES: The aim of this study was to evaluate the relationship between fat and lean mass and bone density in Iranian children and adolescents. PATIENTS AND METHODS: A cross-sectional study was performed on 472 subjects (235 girls, 237 boys) aged 9-18 years old in Fars Province. The participants' weight, height, waist circumference, stage of puberty, and level of physical activity were recorded. Bone Mineral Content (BMC), Bone Mineral Density (BMD), total body fat and lean mass were measured using dual-energy X-ray absorptiometry. RESULTS: Results showed that 12.2% of boys and 12.3% of girls were overweight and 5.5% of boys and 4.7% of girls were obese. Obese individuals had greater total body BMD (0.96 ± 0.11) than normal-weight ones (0.86 ± 0.11) (P < 0.001). We found the greatest correlation between total body BMD and total body lean mass (R = 0.78. P < 0.001) and the least correlation with total body fat percentage (R = 0.03, P = 0.44). Total lean mass in more active boys was 38.1 ± 10.9 and in less active boys was 32.3 ± 11.0 (P < 0.001). The results of multiple regression analysis showed that age and total body lean mass were independent factors of BMD in growing children and adolescents. CONCLUSIONS: These findings suggest that lean mass was the most important predictor of BMD in both genders. Physical activity appears to positively impact on lean mass and needs to be considered in physical education and health-enhancing programs in Iranian school children.

11.
Arch Iran Med ; 17(10): 661-9, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25305764

ABSTRACT

BACKGROUND: The prevalence of childhood obesity has risen greatly worldwide. However, assessment of obesity among children and adolescents is further complicated by the changes occurring in the body composition during the growth. The aim of this study is to create gender-specific percentile curves for total body fat percentage (TBFP), total body fat mass (TBFM), fat mass index (FMI), and fat free mass index (FFMI) in healthy Iranian children and adolescents. METHODS: In this cross-sectional study, 472 healthy Iranian children and adolescents (234 girls and 238 boys) aged 9-18 years old participated. TBFP and TBFM were measured by Dual-Energy X-ray Absorptiometry (DEXA). Weight, height, and waist circumference (WC), pubertal stage and level of physical activity were also recorded. RESULTS: Mean TBFM, TBFP and FMI in girls were significantly more than boys (P < 0.001). The median TBFM in boys increased from 4.8 Kg to 7.5 Kg and in girls from 6.0 Kg to 15.6 Kg. The percentile curves of TBFP in boys were down sloping compared with that in girls (19% increase in girls and 21% decrease in boys from 9-18 years of age). We showed TBFP and FMI had a more complicated relationship with BMI depending on gender and level of BMI, but FFMI consistently increased with BMI in both genders. Also, we found that waist circumference -as a marker of metabolic syndrome-had the greatest correlation with FMI (P < 0.001) between DEXA measured parameters. CONCSLUSION: This study presents normative data for body composition in healthy Iranian children and adolescents and would be useful in adiposity assessment. Our study showed that Iranian children and adolescents had lower total body fat in all age groups and percentiles in comparison with those reported from western children.


Subject(s)
Body Composition , Adipose Tissue/anatomy & histology , Adiposity , Adolescent , Age Factors , Body Mass Index , Child , Cross-Sectional Studies , Female , Humans , Iran/epidemiology , Male , Reference Values , Sex Factors
12.
Arch Iran Med ; 17(5): 347-51, 2014 May.
Article in English | MEDLINE | ID: mdl-24784864

ABSTRACT

BACKGROUND AND OBJECTIVES: Thyroid dysfunction is a common health problem affecting millions of patients worldwide. Autoimmune thyroid disorders are among the most common autoimmune disorders. In this population-based study, we assessed the prevalence of abnormal thyroid function, antithyroid antibodies and the probable relationship between them in Shiraz, southern Iran. METHODS: Serum thyrotropin (TSH) was determined in 981 subjects (66.8% female and 33.2% male; mean age: 39.1 ± 14.3 years), who were selected with stratified random sampling. Because of the preponderance of females over males, we performed the statistical analyses using sex-weighted data (50% for each sex). Also, antithyroid peroxidase antibodies (TPOAb), and antithyroglobulin antibodies (TgAb) were measured in two random subgroups of 376 and 537 patients respectively). Thyromegaly detected on physical examination. RESULTS: In this cross-sectional study, 8.1% of participants had elevated serum TSH level and 3.4% had low serum TSH level. A statistically significant relationship was found between gender and thyromegaly and TSH values. Positive TPOAb and positive TgAb were detected in 17% and 5.1% of participants respectively. In addition, a significant relationship was observed between elevated TSH levels and positive results for both antibodies. Detectable levels of thyroid antibodies correlated with female sex, while no correlation was observed between detectable levels of thyroid antibodies and thyromegaly. CONCLUSION: Thyroid disorders, especially elevated TSH level, are common. It seems that autoimmune mechanisms are strongly involved in the etiology of hypothyroidism in this area.


Subject(s)
Autoantibodies/immunology , Thyroid Diseases/epidemiology , Adolescent , Adult , Autoantibodies/blood , Cross-Sectional Studies , Female , Humans , Iran/epidemiology , Male , Middle Aged , Prevalence , Sex Factors , Thyroid Diseases/immunology , Thyroid Gland/immunology , Thyrotropin/blood , Young Adult
13.
Int J Endocrinol Metab ; 12(4): e19378, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25745488

ABSTRACT

BACKGROUND: Maternal thyroid function alters during pregnancy. Inadequate adaptation to these changes results in thyroid dysfunction and pregnancy complications. OBJECTIVES: This prospective study aimed to evaluate the prevalence of thyroid diseases in pregnancy and its outcomes in south of Iran. MATERIALS AND METHODS: This prospective study was conducted on 600 healthy singleton pregnant women who aged 18 to 35 years old at 15 to 28 weeks of gestation. We investigated the prevalence of thyroid dysfunctions in women. Multivariate analysis was performed to determine the effect thyroid dysfunction on obstetric and neonatal outcome. RESULTS: Thyroid stimulating hormone (TSH) levels of 0.51, 1.18, 1.68, 2.4, and 4.9 mIU/L were at 2.5th, 25th, 50th, 75th, and 97.5th percentile in our population. The prevalence of clinical hypothyroidism, subclinical hypothyroidism, overt hyperthyroidism, and subclinical hyperthyroidism in all pregnant women was 2.4%, 11.3%, 1.2%, and 0.3%, respectively. In addition, 1.4% of patients had isolated hypothyroxinemia. Clinical hypothyroidism was associated with increased risk of preterm delivery (P = 0.045). Subclinical hypothyroidism had a significant association with intrauterine growth restriction (IUGR) (P = 0.028) as well as low Apgar score at first minute (P = 0.022). Maternal hyperthyroidism was associated with IUGR (P = 0.048). CONCLUSIONS: We revealed that thyroid dysfunction during pregnancy was associated with IUGR and low Apgar score even in subclinical forms. Further studies are required to determine whether early diagnosis and treatment of thyroid diseases, even in subclinical form, can prevent their adverse effect on fetus.

14.
Endocrine ; 46(3): 519-25, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24174177

ABSTRACT

Killer cell immunoglobulin-like receptors (KIR) regulate the effector function of natural killer (NK) cells and the subset of T cells with memory phenotype. The number and type of genes that encode KIR receptors substantially varied between individuals and between populations. Specific KIR receptors are known to be associated with certain diseases. The present study was undertaken to investigate if any specific KIR gene(s) is associated with the susceptibility to Hashimoto's thyroiditis (HT), an inflammatory disease characterized by lymphocytic infiltration of the thyroid gland and the presence of autoantibodies directed against thyroglobulin and/or thyroid peroxidase. DNA from 118 patients with HT and 120 healthy controls was characterized for the presence and absence of 11 variable KIR genes using a gene-specific PCR typing system. Although no significant difference in the frequency of individual KIR genes between patients and controls was detected, more patients carry the six activating KIR genes compared with the control group (11.8 vs. 4.1 %, p = 0.032, OR = 3.09, 95 % CI 1.07-8.89). The data suggest that augmented signals from multiple activating KIR receptors might exacerbate the activation of NK cells and T cell subsets against self-antigens, thus contributing to the pathogenesis of HT.


Subject(s)
Genetic Predisposition to Disease , Hashimoto Disease/genetics , Killer Cells, Natural/immunology , Receptors, KIR/genetics , Adult , Autoantigens/genetics , Female , Gene Frequency , Genotype , Hashimoto Disease/immunology , Humans , Male , Middle Aged , Young Adult
15.
Hum Immunol ; 73(10): 1017-22, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22836040

ABSTRACT

Natural killer (NK) cells are key members of innate immunity against tumor and infection. Killer cell immunoglobulin-like receptor (KIR) genes regulates NK cell function, which varies substantially between individuals in the number and type. Specific KIRs are associated with certain diseases. Herein we investigated if KIR genes are associated with thyroid cancer risk. Eighty-five patients with thyroid cancer were characterized for the presence and absence of 11 variable KIR genes using a gene-specific PCR typing system, and compared with our recently published healthy control data. Overall, a trend toward more activating KIR receptors was observed in thyroid cancer patients compared to the healthy controls. Particularly, the activating KIR2DS5 gene was significantly increased in patients compared to the controls. Additionally, three other genes (3DS1-2DL5-2DS1) that are strongly linked to KIR2DS5 at the telomeric region of the KIR gene complex [called Telomeric 4 (T4) gene cluster] were also more predominant in the thyroid cancer patient group than in healthy controls. A similar trend of having more of the T4 gene cluster was also reported in a previous study with cervical neoplasia. Together, these data suggest that specific activating KIR genes in cancer patients could generate a chronic inflammatory condition resulting in a tumor microenvironment that may favor tumor growth.


Subject(s)
Genetic Predisposition to Disease , Receptors, KIR/genetics , Receptors, KIR/metabolism , Thyroid Neoplasms/genetics , Adult , Female , Gene Frequency , Genotype , Humans , Male , Middle Aged , Polymerase Chain Reaction/methods , Risk
16.
Arch Iran Med ; 11(6): 625-8, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18976033

ABSTRACT

BACKGROUND: Behçet's disease is a chronic, multisystemic disease of unknown etiology in which eye involvement is the most common cause of morbidity. In this study, we investigated the possible relation between serum homocysteine level and ocular involvement in patients with Behçet's disease. METHODS: One hundred and fifty patients who fulfilled the criteria of the International Study Group for Behçet's disease (96 females and 54 males) were enrolled. All the patients were evaluated carefully by an experienced ophthalmologist for the diagnosis of ocular involvement. Serum homocysteine, vitamin B12, and folate levels were determined. The patients were categorized according to the presence or absence of uveitis. The data were statistically analyzed by using Student's t-test and P values less than 0.05 were considered statistically significant. RESULTS: Fifty- nine patients (39.3%) had eye involvement, which included anterior uveitis, vitritis, macular damage, optic atrophy, panuveitis, posterior uveitis, retinal vasculitis, and retinal hemorrhage. Serum levels of folate and vitamin B12 were comparable in patients with Behçet's disease. There was no significant correlation between serum homocysteine level in patients with and without eye involvement. CONCLUSION: Our findings suggest that homocysteine level does not have significant effect on eye involvement in patients with Behçet's disease.


Subject(s)
Behcet Syndrome/blood , Behcet Syndrome/epidemiology , Eye Diseases/blood , Eye Diseases/epidemiology , Homocysteine/blood , Adolescent , Adult , Behcet Syndrome/diagnosis , Comorbidity , Eye Diseases/diagnosis , Female , Folic Acid/blood , Humans , Male , Middle Aged , Vitamin B 12/blood , Young Adult
17.
Arch Iran Med ; 11(3): 337-40, 2008 May.
Article in English | MEDLINE | ID: mdl-18426329

ABSTRACT

Barakat syndrome, also known as hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome is an extremely rare congenital disorder. Different etiologies are described for the syndrome but the definite pathophysiology remains unclear. Hereby, we present a case of Barakat syndrome who was diagnosed on the basis of clinical and molecular data.


Subject(s)
Hearing Loss, Sensorineural/congenital , Hypoparathyroidism/congenital , Kidney/abnormalities , Adult , Calcium/blood , Electrocardiography , Epilepsy, Tonic-Clonic/etiology , Female , Humans , Hypertension/etiology , Liver Function Tests , Menstruation Disturbances/etiology , Paresthesia/etiology , Phosphorus/blood , Reflex, Abnormal , Syndrome , Young Adult
18.
Arch Iran Med ; 11(2): 157-61, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18298292

ABSTRACT

BACKGROUND: Iodine deficiency has been identified as a significant public health problem in Iran. The main strategy for controlling iodine deficiency was nationwide salt iodination. Over 10 years after starting this program, goiter is still endemic in school children. Iron deficiency may have interfered with the iodine intervention program. The objective of the present study was to evaluate the relationships between iron status, thyroid hormone profile, and the prevalence of goiter 11 years after implementation of the salt iodination program. METHODS: In this study which was conducted in Marvdasht, Shiraz, 1188 students aged eight to 13 years were enrolled. Goiter was graded according to the classification by the World Health Organization (WHO). Serum concentrations of thyroid hormones and thyroid stimulating hormone were determined using commercial kits. The urinary iodine level was measured using the digestion method. RESULTS: Goiter was endemic (39.6%); the majority of participants had grade 1 thyromegally. Despite the endemic status of goiter in southern Iran, the urine content of iodine reflected a normal iodine intake. The prevalence of iron deficiency was 16.4%. The iron-deficient patients had a significantly higher thyroid stimulating hormone level and lower free T4 concentrations than those with a normal serum ferritin level (P<0.001). CONCLUSION: Iron supplementation may improve thyroid metabolism in children but we still have to investigate the role of other goitrogens in this area.


Subject(s)
Goiter, Endemic/epidemiology , Iron Deficiencies , Adolescent , Analysis of Variance , Child , Female , Humans , Iodine/administration & dosage , Iodine/urine , Iran/epidemiology , Male , Prevalence , Risk Factors , Statistics, Nonparametric , Thyroid Hormones/analysis
19.
Wounds ; 20(4): 101-6, 2008 Apr.
Article in English | MEDLINE | ID: mdl-25942328

ABSTRACT

Collagen constitutes the majority of extracellular matrix in tissues such as bone, cartilage, and especially the skin. Over production and/or decreased degradation of collagen fibers could lead to an abnormal wound healing response resulting in hypertrophic scarring or keloid formation. Recently, angiotensin II has been shown to be present in several cutaneous cells and that it stimulates fibroblast proliferation, collagen synthesis, and suppresses matrix metalloproteinase activity. The following study examines the effect of topical captopril, an inhibitor of angiotensin II production, against hypertrophic scar formation in New Zealand white rabbits.Two dermal wounds were made over the ventral surface of the ears of each rabbit (n = 6). In each animal, separate wounds were treated once per day with either topical 5% captopril or the vehicle alone (70% ethanol and 30% propylene glycol) for 7 consecutive days. Wounds were harvested at postoperative day 28, and the scar elevation index (SEI) as well as collagen organization was evaluated. SEI was reduced from 3.06 in the vehicle-treated group to 1.94 in the captopril treated wounds (P < 0.05). However, an increase in collagen organization was achieved by captopril, while an 8.50% decrease in collagen organization scale was derived by captopril compared to the vehicle. Results of this study show, for the first time, the efficacy of topical captopril as a new agent for the prevention of hypertrophic scar formation in an animal model. Thus, captopril might represent the first angiotensin converting enzyme inhibitor with a novel pharmacologic application in dermatology.

20.
Arch Iran Med ; 10(2): 168-70, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17367218

ABSTRACT

BACKGROUND: Thyroid dysfunction is associated with changes in the appetite. Ghrelin can regulate feeding behavior. The aim of this study was to evaluate whether ghrelin plays a role in the appetite changes in different states of thyroid dysfunction. METHODS: The serum ghrelin levels were measured in 45 newly diagnosed hyperthyroid and 45 newly diagnosed hypothyroid patients before and after medical treatment. Forty-five healthy subjects were also studied as control group. RESULTS: The ghrelin levels did not change significantly in patients with hyperthyroidism or hypothyroidism before and after the treatment. The ghrelin levels were not different from those of the control group. CONCLUSION: Ghrelin is not likely to be the primary determinant of appetite changes in thyroid dysfunction.


Subject(s)
Appetite/physiology , Hyperthyroidism/blood , Hypothyroidism/blood , Peptide Hormones/blood , Adult , Body Mass Index , Female , Ghrelin , Humans , Immunoradiometric Assay , Male , Middle Aged , Radioimmunoassay , Thyroid Hormones/blood
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