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Association between primary hypothyroidism and metabolic syndrome and the role of C reactive protein: a cross–sectional study from South India

BACKGROUND: Hypothyroidism (sub-clinical and overt) and metabolic syndrome are recognized risk factors for atherosclerotic cardiovascular disease. This study is an effort to identify the proposed association between these two disease entities and the risk factors involved in this association. METHOD...

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Autores principales: Shantha, Ghanshyam Palamaner Subash, Kumar, Anita A, Jeyachandran, Vijay, Rajamanickam, Deepan, Rajkumar, K, Salim, Shihas, Subramanian, Kuyilan Karai, Natesan, Senthilkumar
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2655275/
https://www.ncbi.nlm.nih.gov/pubmed/19272156
http://dx.doi.org/10.1186/1756-6614-2-2
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author Shantha, Ghanshyam Palamaner Subash
Kumar, Anita A
Jeyachandran, Vijay
Rajamanickam, Deepan
Rajkumar, K
Salim, Shihas
Subramanian, Kuyilan Karai
Natesan, Senthilkumar
author_facet Shantha, Ghanshyam Palamaner Subash
Kumar, Anita A
Jeyachandran, Vijay
Rajamanickam, Deepan
Rajkumar, K
Salim, Shihas
Subramanian, Kuyilan Karai
Natesan, Senthilkumar
author_sort Shantha, Ghanshyam Palamaner Subash
collection PubMed
description BACKGROUND: Hypothyroidism (sub-clinical and overt) and metabolic syndrome are recognized risk factors for atherosclerotic cardiovascular disease. This study is an effort to identify the proposed association between these two disease entities and the risk factors involved in this association. METHODS: A cross – sectional study from a tertiary care teaching hospital in Chennai city, South India. 420 patients with metabolic syndrome (NCEP – ATP III criteria) were included in the study group. 406 appropriately age and sex matched controls having no features of metabolic syndrome (0 out of the 5 criteria) were compared with the study group. The study extended over a 5 year period. TSH, FT4 were measured for both the groups using electrochemiluminescence immuno assay. HsCRP was measured for all the patients in the study group. The baseline characteristics between the groups were compared with Student's't' test. Chi-square test was used to analyze the association between metabolic syndrome and hypothyroidism (overt and sub-clinical). Logistic regression analysis was applied to identify the association between hypothyroidism and the patient characteristics in the study group. RESULTS: Of the 420 patients in the study group, 240 were females (57.1%), 180 were males (42.9%) with mean age 51 ± 9.4 years. Of the 406 patients in the control group, 216 were females (53.2%), 190 males (46.8%) with mean age 49 ± 11.2 years. In the study group, 92 had sub-clinical hypothyroidism (SCH) (21.9%), 31 were overtly hypothyroid (7.4%) and 297 were euthyroid (70.7%). In the control group 27 patients had sub-clinical hypothyroidism (6.6%), 9 patients had overt hypothyroidism (2.2%) and 370 patients were euthyroid (91.2%). On comparison SCH (P < 0.001) and overt hypothyroidism (P < 0.001) were significantly associated with the study group as compared to the control group. Logistic regression analysis recognized the association between female gender (P = 0.021) and HsCRP (P = 0.014) with sub-clinical hypothyroidism and female gender (P = 0.01) with overt hypothyroidism in the study group. CONCLUSION: Hypothyroidism is associated with metabolic syndrome and females are more at risk. Metabolic syndrome patients with a raised HsCRP are at significant risk of having sub-clinical hypothyroidism.
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spelling pubmed-26552752009-03-14 Association between primary hypothyroidism and metabolic syndrome and the role of C reactive protein: a cross–sectional study from South India Shantha, Ghanshyam Palamaner Subash Kumar, Anita A Jeyachandran, Vijay Rajamanickam, Deepan Rajkumar, K Salim, Shihas Subramanian, Kuyilan Karai Natesan, Senthilkumar Thyroid Res Research BACKGROUND: Hypothyroidism (sub-clinical and overt) and metabolic syndrome are recognized risk factors for atherosclerotic cardiovascular disease. This study is an effort to identify the proposed association between these two disease entities and the risk factors involved in this association. METHODS: A cross – sectional study from a tertiary care teaching hospital in Chennai city, South India. 420 patients with metabolic syndrome (NCEP – ATP III criteria) were included in the study group. 406 appropriately age and sex matched controls having no features of metabolic syndrome (0 out of the 5 criteria) were compared with the study group. The study extended over a 5 year period. TSH, FT4 were measured for both the groups using electrochemiluminescence immuno assay. HsCRP was measured for all the patients in the study group. The baseline characteristics between the groups were compared with Student's't' test. Chi-square test was used to analyze the association between metabolic syndrome and hypothyroidism (overt and sub-clinical). Logistic regression analysis was applied to identify the association between hypothyroidism and the patient characteristics in the study group. RESULTS: Of the 420 patients in the study group, 240 were females (57.1%), 180 were males (42.9%) with mean age 51 ± 9.4 years. Of the 406 patients in the control group, 216 were females (53.2%), 190 males (46.8%) with mean age 49 ± 11.2 years. In the study group, 92 had sub-clinical hypothyroidism (SCH) (21.9%), 31 were overtly hypothyroid (7.4%) and 297 were euthyroid (70.7%). In the control group 27 patients had sub-clinical hypothyroidism (6.6%), 9 patients had overt hypothyroidism (2.2%) and 370 patients were euthyroid (91.2%). On comparison SCH (P < 0.001) and overt hypothyroidism (P < 0.001) were significantly associated with the study group as compared to the control group. Logistic regression analysis recognized the association between female gender (P = 0.021) and HsCRP (P = 0.014) with sub-clinical hypothyroidism and female gender (P = 0.01) with overt hypothyroidism in the study group. CONCLUSION: Hypothyroidism is associated with metabolic syndrome and females are more at risk. Metabolic syndrome patients with a raised HsCRP are at significant risk of having sub-clinical hypothyroidism. BioMed Central 2009-03-09 /pmc/articles/PMC2655275/ /pubmed/19272156 http://dx.doi.org/10.1186/1756-6614-2-2 Text en Copyright © 2009 Shantha et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Shantha, Ghanshyam Palamaner Subash
Kumar, Anita A
Jeyachandran, Vijay
Rajamanickam, Deepan
Rajkumar, K
Salim, Shihas
Subramanian, Kuyilan Karai
Natesan, Senthilkumar
Association between primary hypothyroidism and metabolic syndrome and the role of C reactive protein: a cross–sectional study from South India
title Association between primary hypothyroidism and metabolic syndrome and the role of C reactive protein: a cross–sectional study from South India
title_full Association between primary hypothyroidism and metabolic syndrome and the role of C reactive protein: a cross–sectional study from South India
title_fullStr Association between primary hypothyroidism and metabolic syndrome and the role of C reactive protein: a cross–sectional study from South India
title_full_unstemmed Association between primary hypothyroidism and metabolic syndrome and the role of C reactive protein: a cross–sectional study from South India
title_short Association between primary hypothyroidism and metabolic syndrome and the role of C reactive protein: a cross–sectional study from South India
title_sort association between primary hypothyroidism and metabolic syndrome and the role of c reactive protein: a cross–sectional study from south india
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2655275/
https://www.ncbi.nlm.nih.gov/pubmed/19272156
http://dx.doi.org/10.1186/1756-6614-2-2
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