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1.
Eye (Lond) ; 37(8): 1602-1607, 2023 06.
Artículo en Inglés | MEDLINE | ID: mdl-35915233

RESUMEN

OBJECTIVES: To detect the serum level of thyroid hormones, vitamin D and vitamin D receptors (VDR) polymorphism in keratoconus (KC) patients and to identify the association between vitamin D deficiency and thyroid dysfunction in KC. METHODS: This cross sectional study included 177 KC patients with no thyroid disorders compared to 85 healthy controls with normal corneal tomography. Measurements of thyroid stimulating hormone (TSH), free triiodothyronine (FT3), free tetraiodothyronine (FT4) and serum 25-OH vitamin D were done using Enzyme linked immusoassay (ELISA test). VDR polymorphisms were tested including [Taq I (rs731236), Apa I (rs7975232) and Bsm I (rs1544410)] using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). RESULTS: An increase in frequency of thyroid disorders (P = 0.04), decrease in serum 25(OH) vitamin D level (P < 0.001), Taq 1 and tt genotype (P < 0.001) were significantly distributed in KC patients. A significantly higher serum 25(OH) vitamin D level was reported in TT genotype, while insufficient level was more common in Tt genotype (P < 0.001). A deficient serum 25(OH) vitamin D level was predominant in tt genotype (P < 0.001). A 95% confidence interval was in TSH (1.603, 2.946), FT4 (24.145, 77.06), hypothyroidism (1.062, 67.63), insufficient (2.936, 11.643) and deficient vitamin D (5.283, 28.704) and all were significant risk factors for KC with (P < 0.05). CONCLUSIONS: Both thyroid disorders and low vitamin D are potential factors for KC development. Studying VDR at the molecular level provides interesting avenues for future research toward the identification of new KC cases.


Asunto(s)
Queratocono , Enfermedades de la Tiroides , Humanos , Receptores de Calcitriol/genética , Queratocono/genética , Estudios Transversales , Genotipo , Polimorfismo Genético , Vitamina D , Tirotropina/genética , Estudios de Casos y Controles , Predisposición Genética a la Enfermedad
2.
Asian Pac J Cancer Prev ; 23(2): 545-552, 2022 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-35225467

RESUMEN

OBJECTIVES: Early diagnosis of cancer remains a great challenge in the field of laboratory medicine. We investigated the ability of ccf DNA and DNA integrity index (DNA II) in differentiating benign from malignant breast diseases. METHODS: Serum samples were collected from 50 patients with benign breast disease (BBD) and 50 newly diagnosed breast cancer (BC) patients, in addition to 50 control women. VEGF was measured by ELISA, while Real-time q-PCR was used to measure ccf DNA concentrations and to assess the concentrations of ALU repeats, both short fragments (115 bp) and long fragments (247 bp), then DNA II was calculated (all were done before and after radical mastectomy). RESULTS: BC group showed significantly higher ccf DNA concentrations and DNA II compared to BBD and control groups, meanwhile, no statistically significant differences were found between BBD and control groups. Ccf DNA concentrations decreased significantly after surgery (P <0.001). Good AUC was found for ccf DNA (AUC=0.860), fair AUC was found for DNA II (AUC=0.727), while VEGF AUC failed to discriminate between BBD and BC cases. CONCLUSION: ccf DNA and DNA II could be used as excellent molecular biomarkers for early diagnosis of BC and for monitoring the efficiency of therapy in such patients. Utilizing these molecular markers would improve both the healthcare and economic burden of malignancy.


Asunto(s)
Enfermedades de la Mama/diagnóstico , Neoplasias de la Mama/diagnóstico , Ácidos Nucleicos Libres de Células/sangre , Pruebas Genéticas/métodos , Factor A de Crecimiento Endotelial Vascular/sangre , Biomarcadores/sangre , Estudios de Casos y Controles , Diagnóstico Diferencial , Femenino , Marcadores Genéticos/genética , Humanos , Mastectomía , Persona de Mediana Edad , Valor Predictivo de las Pruebas
3.
Appl Physiol Nutr Metab ; 41(9): 985-91, 2016 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-27557336

RESUMEN

Vitamin A deficiency (VAD) and altered thyroid function are commonly encountered in patients with liver cirrhosis. The link between vitamin A metabolism and thyroid function has been previously identified. The aim of this study was to explore the association between VAD and the thyroid axis in clinically stable patients with cirrhosis related to hepatitis C virus (HCV). One hundred and twelve patients with clinically stable HCV-related cirrhosis and 56 healthy controls matched for age, sex, and socioeconomic status were recruited for this study. Vitamin A status, liver function, thyroid-stimulating hormone (TSH), free thyroxine (FT4), free triiodothyronine (FT3), reverse triiodothyronine (rT3), anti-thyroid peroxidase antibodies (anti-TPO), and thyroid volume were evaluated. The prevalence of VAD among patients with HCV-related cirrhosis was 62.5% compared with 5.4% among controls (P < 0.001). Patients with HCV-related cirrhosis had significantly higher FT4, FT3, TSH, and thyroid volume than did healthy controls. Of the 112 patients initially recruited, 18 were excluded (patients with subclinical hypothyroidism and/or anti-TPO positive), so a total of 94 patients with HCV-related cirrhosis were divided into 2 groups according to vitamin A status: VAD and normal vitamin A. Patients with VAD had significantly lower vitamin A intake and serum albumin and higher serum bilirubin, FT4, FT3, and TSH than patients with normal vitamin A status. Multiple logistic regression analysis revealed that VAD was associated with Child-Pugh score (ß = 0.11, P = 0.05) and TSH (ß = -1.63, P = 0.02) independently of confounding variables. We conclude that VAD may be linked to central hyperthyroidism in patients with clinically stable HCV-related liver cirrhosis.


Asunto(s)
Hepatitis C/fisiopatología , Hipertiroidismo/etiología , Cirrosis Hepática/etiología , Estado Nutricional , Glándula Tiroides/fisiopatología , Deficiencia de Vitamina A/etiología , Bilirrubina/sangre , Egipto/epidemiología , Femenino , Hepatitis C/sangre , Hepatitis C/patología , Hospitales Universitarios , Humanos , Hipertiroidismo/diagnóstico por imagen , Hipertiroidismo/fisiopatología , Hígado/diagnóstico por imagen , Hígado/fisiopatología , Cirrosis Hepática/diagnóstico por imagen , Masculino , Persona de Mediana Edad , Tamaño de los Órganos , Servicio Ambulatorio en Hospital , Prevalencia , Índice de Severidad de la Enfermedad , Glándula Tiroides/diagnóstico por imagen , Glándula Tiroides/patología , Hormonas Tiroideas/sangre , Tirotropina/sangre , Deficiencia de Vitamina A/epidemiología
4.
Endocr Res ; 41(2): 81-8, 2016 May.
Artículo en Inglés | MEDLINE | ID: mdl-26726735

RESUMEN

OBJECTIVE: to assess the growth and pubertal development among a group of patients with ß-Thalassemia Major (ß-TM) and to evaluate the role of the pituitary gland and liver MRI signal intensity (SI) reduction in assessing and predicting the clinical severity of growth and pubertal dysfunctions. METHODS: Thirty-eight patients with ß-TM were examined and divided into two groups: Group I patients were of normal height and puberty and Group II patients had short statures and hypogonadism. Laboratory investigations included serum ferritin, LH, FSH, prolactin, TSH, and basal and dynamic growth hormones. Pituitary and liver MRIs were performed to assess the pituitary to fat (P/F) and liver to muscle (L/M) signal intensities (SI), respectively. Fifteen healthy and sex- and age-matched subjects were included as controls. RESULTS: Both patient groups had significantly elevated serum ferritin and significantly decreased prolactin and IGF1 compared to control subjects. Group II showed a significant reduction in LH, FSH, and IGF1 and a significant increase in ferritin in comparison with Group I and the control group, and it had a highly significant reduction in both P/F and L/M SI in comparison with Group I (p<0.001 and 0.008, respectively). The reduced P/F ratio was significantly correlated with FSH and LH, and a cutoff for a P/F ratio ≥0.94 was obtained to differentiate between Group I and II. CONCLUSION: MRI in conjunction with the P/F signal intensity ratio is a useful and noninvasive tool for the early diagnosis of pituitary iron overload.


Asunto(s)
Enanismo/diagnóstico , Hipogonadismo/diagnóstico , Sobrecarga de Hierro/diagnóstico , Hígado/diagnóstico por imagen , Hipófisis/diagnóstico por imagen , Talasemia beta/diagnóstico , Adolescente , Adulto , Enanismo/sangre , Enanismo/diagnóstico por imagen , Enanismo/etiología , Femenino , Humanos , Hipogonadismo/sangre , Hipogonadismo/diagnóstico por imagen , Hipogonadismo/etiología , Sobrecarga de Hierro/sangre , Sobrecarga de Hierro/diagnóstico por imagen , Sobrecarga de Hierro/etiología , Imagen por Resonancia Magnética , Masculino , Adulto Joven , Talasemia beta/sangre , Talasemia beta/complicaciones , Talasemia beta/diagnóstico por imagen
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