study relationship between the value of 17-ohp and the value of testosterone in monitoring for...

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POSTER PRESENTATION Open Access Study relationship between the value of 17-OHP and the value of testosterone in monitoring for congenital adrenal hyperplasia Ngo Thi Thu Huong 1 , Nguyen Phu Dat 1* , Nguyen Thi Hoan 2 , Bui Phuong Thao 2 , Nguyen Ngoc Khanh 2 , Can Thi Bich Ngoc 2 , Vu Chi Dung 2 From 7th APPES Biennial Scientific Meeting Nusa Dua, Bali. 14-17 November 2012 Deficiency of 21-hydroxylase (21-OHD) is present in 9095% cases of congenital adrenal hyperplasia (CAH), an autosomal recessive disorder. CAH affects severely on the physical development and reproductive function. In monitoring the disease and evaluating treatment out- come, presentation of salt wasting, electrolyte disturbance, androgenism, cushingoid features, plasma levels of 17- OHP, testosterone, Δ 4 -androstenedione, urinary levels of 17-OHCS, 17-CS, and bone age were used. We aimed to study relationship between the value of the plasma 17OHP and the value of the plasma testosterone levels to monitor treatment of CAH. The study was prospective. We collected 82 CAH Vietnamese patients who were diagnosed of 21-OHD. The have been treated and monitored at the Vietnam National Hospital of Pediatrics. Hanoi, Vietnam in the period of 1/2007- 1/2010. The value of plasma levels of 17-OHP and testosterone were measured in combina- tion with clinical symptoms every 6 months. In 82 studys CAH patients aged 1-15 years old, the group aged < 10 years old occupied 82.9%. The salt wasting form occupied 75.6%; the simple virilizing form 24.4%. 59/82 of patients (71.1%) had successful treat- ment with the mean plasma level 17-OHP of 0.02-5.67 nmol/l and the mean levels of testosterone of 0.01- 8.02 nmol/l according to groupsages. The mean levels of plasma 17-OHP and testosterone also increased with age and sex in the group of patients having failed treat- ment. It confirmed a positive relationship between the value of plasma 17 OHP and levels of the testosterone with 95% significant confidence. Each time of patient examination, besides clinical symptoms and plasma levels of 17-OHP should be done to evaluate treatment. Authorsdetails 1 Pediatric Department, Hanoi Medical University,Vietnam. 2 National Hospital of Pediatrics, Hanoi, Vietnam. Published: 3 October 2013 doi:10.1186/1687-9856-2013-S1-P124 Cite this article as: Huong et al.: Study relationship between the value of 17-OHP and the value of testosterone in monitoring for congenital adrenal hyperplasia. International Journal of Pediatric Endocrinology 2013 2013(Suppl 1):P124. Submit your next manuscript to BioMed Central and take full advantage of: Convenient online submission Thorough peer review No space constraints or color figure charges Immediate publication on acceptance Inclusion in PubMed, CAS, Scopus and Google Scholar Research which is freely available for redistribution Submit your manuscript at www.biomedcentral.com/submit 1 Pediatric Department, Hanoi Medical University,Vietnam Full list of author information is available at the end of the article Huong et al. International Journal of Pediatric Endocrinology 2013, 2013(Suppl 1):P124 http://www.ijpeonline.com/content/2013/S1/P124 © 2013 Huong et al; licensee BioMed Central Ltd. 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.

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Page 1: Study relationship between the value of 17-OHP and the value of testosterone in monitoring for congenital adrenal hyperplasia

POSTER PRESENTATION Open Access

Study relationship between the value of 17-OHPand the value of testosterone in monitoring forcongenital adrenal hyperplasiaNgo Thi Thu Huong1, Nguyen Phu Dat1*, Nguyen Thi Hoan2, Bui Phuong Thao2, Nguyen Ngoc Khanh2,Can Thi Bich Ngoc2, Vu Chi Dung2

From 7th APPES Biennial Scientific MeetingNusa Dua, Bali. 14-17 November 2012

Deficiency of 21-hydroxylase (21-OHD) is present in90–95% cases of congenital adrenal hyperplasia (CAH),an autosomal recessive disorder. CAH affects severelyon the physical development and reproductive function.In monitoring the disease and evaluating treatment out-come, presentation of salt wasting, electrolyte disturbance,androgenism, cushingoid features, plasma levels of 17-OHP, testosterone, Δ4-androstenedione, urinary levels of17-OHCS, 17-CS, and bone age were used.We aimed to study relationship between the value of the

plasma 17–OHP and the value of the plasma testosteronelevels to monitor treatment of CAH.The study was prospective. We collected 82 CAH

Vietnamese patients who were diagnosed of 21-OHD.The have been treated and monitored at the VietnamNational Hospital of Pediatrics. Hanoi, Vietnam in theperiod of 1/2007- 1/2010. The value of plasma levels of17-OHP and testosterone were measured in combina-tion with clinical symptoms every 6 months.In 82 study’s CAH patients aged 1-15 years old, the

group aged < 10 years old occupied 82.9%. The salt –wasting form occupied 75.6%; the simple virilizing form24.4%. 59/82 of patients (71.1%) had successful treat-ment with the mean plasma level 17-OHP of 0.02-5.67nmol/l and the mean levels of testosterone of 0.01- 8.02nmol/l according to groups’ages. The mean levels ofplasma 17-OHP and testosterone also increased withage and sex in the group of patients having failed treat-ment. It confirmed a positive relationship between thevalue of plasma 17 – OHP and levels of the testosteronewith 95% significant confidence.

Each time of patient examination, besides clinicalsymptoms and plasma levels of 17-OHP should be doneto evaluate treatment.

Authors’ details1Pediatric Department, Hanoi Medical University,Vietnam. 2National Hospitalof Pediatrics, Hanoi, Vietnam.

Published: 3 October 2013

doi:10.1186/1687-9856-2013-S1-P124Cite this article as: Huong et al.: Study relationship between the valueof 17-OHP and the value of testosterone in monitoring for congenitaladrenal hyperplasia. International Journal of Pediatric Endocrinology 20132013(Suppl 1):P124.

Submit your next manuscript to BioMed Centraland take full advantage of:

• Convenient online submission

• Thorough peer review

• No space constraints or color figure charges

• Immediate publication on acceptance

• Inclusion in PubMed, CAS, Scopus and Google Scholar

• Research which is freely available for redistribution

Submit your manuscript at www.biomedcentral.com/submit1Pediatric Department, Hanoi Medical University,Vietnam

Full list of author information is available at the end of the article

Huong et al. International Journal of Pediatric Endocrinology 2013, 2013(Suppl 1):P124http://www.ijpeonline.com/content/2013/S1/P124

© 2013 Huong et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative CommonsAttribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction inany medium, provided the original work is properly cited.