Increased Abdominal Adiposity in Adolescents and Young Adults With Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Context:Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of cardiovascular disease (CVD). Abdominal adiposity, in particular visceral adipose tissue (VAT), is strongly associated with metabolic syndrome a...
Saved in:
Published in | The journal of clinical endocrinology and metabolism Vol. 100; no. 8; pp. E1153 - E1159 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Oxford University Press
01.08.2015
Copyright by The Endocrine Society Endocrine Society |
Subjects | |
Online Access | Get full text |
ISSN | 0021-972X 1945-7197 1945-7197 |
DOI | 10.1210/jc.2014-4033 |
Cover
Abstract | Context:Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of cardiovascular disease (CVD). Abdominal adiposity, in particular visceral adipose tissue (VAT), is strongly associated with metabolic syndrome and CVD. However, it remains unknown whether VAT is increased in CAH.Objective:The objective of the study was to determine whether adolescents and young adults with classical CAH have more VAT and sc adipose tissue (SAT) than matched controls and whether VAT and SAT are associated with biomarkers of metabolic syndrome, inflammation, and hyperandrogenism in CAH.Design/Setting:This was a cross-sectional study at a tertiary center.Participants:CAH subjects (n = 28; 15.6 ± 3.2 y; 15 females) were matched for age, sex, ethnicity, and body mass index to healthy controls (n = 28; 16.7 ± 2.3 y; 15 females).Main Outcome Measures:VAT and SAT, using computed tomography imaging and serum biomarkers associated with CVD risk, were measured. Data are reported as mean ± SD.Results:Both VAT (43.8 ± 45.5 cm2) and SAT (288.1 ± 206.5 cm2) were higher in CAH subjects than controls (VAT 26.4 ± 29.6 cm2 and SAT 226.3 ± 157.5 cm2; both P < .001). The VAT to SAT ratio was also higher in CAH subjects (0.15 ± 0.07) than controls (0.12 ± 0.06; P < .05). Within CAH, measures of obesity (waist to height ratio, fat mass) and inflammation (plasminogen activator inhibitor-1, high-sensitivity C-reactive protein, leptin) correlated strongly with VAT and SAT. In addition, homeostasis model assessment of insulin resistance, and low-density lipoprotein correlated with abdominal adiposity. There were no sex differences for VAT or SAT in CAH subjects.Conclusions:CAH adolescents and young adults have increased abdominal adiposity, with a higher proportion of proinflammatory VAT than SAT. An improved understanding of the mechanism of obesity in CAH may lead to targeted prevention and therapeutics in this high-risk population. |
---|---|
AbstractList | Context:Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of cardiovascular disease (CVD). Abdominal adiposity, in particular visceral adipose tissue (VAT), is strongly associated with metabolic syndrome and CVD. However, it remains unknown whether VAT is increased in CAH.Objective:The objective of the study was to determine whether adolescents and young adults with classical CAH have more VAT and sc adipose tissue (SAT) than matched controls and whether VAT and SAT are associated with biomarkers of metabolic syndrome, inflammation, and hyperandrogenism in CAH.Design/Setting:This was a cross-sectional study at a tertiary center.Participants:CAH subjects (n = 28; 15.6 ± 3.2 y; 15 females) were matched for age, sex, ethnicity, and body mass index to healthy controls (n = 28; 16.7 ± 2.3 y; 15 females).Main Outcome Measures:VAT and SAT, using computed tomography imaging and serum biomarkers associated with CVD risk, were measured. Data are reported as mean ± SD.Results:Both VAT (43.8 ± 45.5 cm2) and SAT (288.1 ± 206.5 cm2) were higher in CAH subjects than controls (VAT 26.4 ± 29.6 cm2 and SAT 226.3 ± 157.5 cm2; both P < .001). The VAT to SAT ratio was also higher in CAH subjects (0.15 ± 0.07) than controls (0.12 ± 0.06; P < .05). Within CAH, measures of obesity (waist to height ratio, fat mass) and inflammation (plasminogen activator inhibitor-1, high-sensitivity C-reactive protein, leptin) correlated strongly with VAT and SAT. In addition, homeostasis model assessment of insulin resistance, and low-density lipoprotein correlated with abdominal adiposity. There were no sex differences for VAT or SAT in CAH subjects.Conclusions:CAH adolescents and young adults have increased abdominal adiposity, with a higher proportion of proinflammatory VAT than SAT. An improved understanding of the mechanism of obesity in CAH may lead to targeted prevention and therapeutics in this high-risk population. CONTEXT:Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of cardiovascular disease (CVD). Abdominal adiposity, in particular visceral adipose tissue (VAT), is strongly associated with metabolic syndrome and CVD. However, it remains unknown whether VAT is increased in CAH. OBJECTIVE:The objective of the study was to determine whether adolescents and young adults with classical CAH have more VAT and sc adipose tissue (SAT) than matched controls and whether VAT and SAT are associated with biomarkers of metabolic syndrome, inflammation, and hyperandrogenism in CAH. DESIGN/SETTING:This was a cross-sectional study at a tertiary center. PARTICIPANTS:CAH subjects (n = 28; 15.6 ± 3.2 y; 15 females) were matched for age, sex, ethnicity, and body mass index to healthy controls (n = 28; 16.7 ± 2.3 y; 15 females). MAIN OUTCOME MEASURES:VAT and SAT, using computed tomography imaging and serum biomarkers associated with CVD risk, were measured. Data are reported as mean ± SD. RESULTS:Both VAT (43.8 ± 45.5 cm) and SAT (288.1 ± 206.5 cm) were higher in CAH subjects than controls (VAT 26.4 ± 29.6 cm and SAT 226.3 ± 157.5 cm; both P < .001). The VAT to SAT ratio was also higher in CAH subjects (0.15 ± 0.07) than controls (0.12 ± 0.06; P < .05). Within CAH, measures of obesity (waist to height ratio, fat mass) and inflammation (plasminogen activator inhibitor-1, high-sensitivity C-reactive protein, leptin) correlated strongly with VAT and SAT. In addition, homeostasis model assessment of insulin resistance, and low-density lipoprotein correlated with abdominal adiposity. There were no sex differences for VAT or SAT in CAH subjects. CONCLUSIONS:CAH adolescents and young adults have increased abdominal adiposity, with a higher proportion of proinflammatory VAT than SAT. An improved understanding of the mechanism of obesity in CAH may lead to targeted prevention and therapeutics in this high-risk population. Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of cardiovascular disease (CVD). Abdominal adiposity, in particular visceral adipose tissue (VAT), is strongly associated with metabolic syndrome and CVD. However, it remains unknown whether VAT is increased in CAH. The objective of the study was to determine whether adolescents and young adults with classical CAH have more VAT and sc adipose tissue (SAT) than matched controls and whether VAT and SAT are associated with biomarkers of metabolic syndrome, inflammation, and hyperandrogenism in CAH. This was a cross-sectional study at a tertiary center. CAH subjects (n = 28; 15.6 ± 3.2 y; 15 females) were matched for age, sex, ethnicity, and body mass index to healthy controls (n = 28; 16.7 ± 2.3 y; 15 females). VAT and SAT, using computed tomography imaging and serum biomarkers associated with CVD risk, were measured. Data are reported as mean ± SD. Both VAT (43.8 ± 45.5 cm(2)) and SAT (288.1 ± 206.5 cm(2)) were higher in CAH subjects than controls (VAT 26.4 ± 29.6 cm(2) and SAT 226.3 ± 157.5 cm(2); both P < .001). The VAT to SAT ratio was also higher in CAH subjects (0.15 ± 0.07) than controls (0.12 ± 0.06; P < .05). Within CAH, measures of obesity (waist to height ratio, fat mass) and inflammation (plasminogen activator inhibitor-1, high-sensitivity C-reactive protein, leptin) correlated strongly with VAT and SAT. In addition, homeostasis model assessment of insulin resistance, and low-density lipoprotein correlated with abdominal adiposity. There were no sex differences for VAT or SAT in CAH subjects. CAH adolescents and young adults have increased abdominal adiposity, with a higher proportion of proinflammatory VAT than SAT. An improved understanding of the mechanism of obesity in CAH may lead to targeted prevention and therapeutics in this high-risk population. Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of cardiovascular disease (CVD). Abdominal adiposity, in particular visceral adipose tissue (VAT), is strongly associated with metabolic syndrome and CVD. However, it remains unknown whether VAT is increased in CAH.CONTEXTChildhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of cardiovascular disease (CVD). Abdominal adiposity, in particular visceral adipose tissue (VAT), is strongly associated with metabolic syndrome and CVD. However, it remains unknown whether VAT is increased in CAH.The objective of the study was to determine whether adolescents and young adults with classical CAH have more VAT and sc adipose tissue (SAT) than matched controls and whether VAT and SAT are associated with biomarkers of metabolic syndrome, inflammation, and hyperandrogenism in CAH.OBJECTIVEThe objective of the study was to determine whether adolescents and young adults with classical CAH have more VAT and sc adipose tissue (SAT) than matched controls and whether VAT and SAT are associated with biomarkers of metabolic syndrome, inflammation, and hyperandrogenism in CAH.This was a cross-sectional study at a tertiary center.DESIGN/SETTINGThis was a cross-sectional study at a tertiary center.CAH subjects (n = 28; 15.6 ± 3.2 y; 15 females) were matched for age, sex, ethnicity, and body mass index to healthy controls (n = 28; 16.7 ± 2.3 y; 15 females).PARTICIPANTSCAH subjects (n = 28; 15.6 ± 3.2 y; 15 females) were matched for age, sex, ethnicity, and body mass index to healthy controls (n = 28; 16.7 ± 2.3 y; 15 females).VAT and SAT, using computed tomography imaging and serum biomarkers associated with CVD risk, were measured. Data are reported as mean ± SD.MAIN OUTCOME MEASURESVAT and SAT, using computed tomography imaging and serum biomarkers associated with CVD risk, were measured. Data are reported as mean ± SD.Both VAT (43.8 ± 45.5 cm(2)) and SAT (288.1 ± 206.5 cm(2)) were higher in CAH subjects than controls (VAT 26.4 ± 29.6 cm(2) and SAT 226.3 ± 157.5 cm(2); both P < .001). The VAT to SAT ratio was also higher in CAH subjects (0.15 ± 0.07) than controls (0.12 ± 0.06; P < .05). Within CAH, measures of obesity (waist to height ratio, fat mass) and inflammation (plasminogen activator inhibitor-1, high-sensitivity C-reactive protein, leptin) correlated strongly with VAT and SAT. In addition, homeostasis model assessment of insulin resistance, and low-density lipoprotein correlated with abdominal adiposity. There were no sex differences for VAT or SAT in CAH subjects.RESULTSBoth VAT (43.8 ± 45.5 cm(2)) and SAT (288.1 ± 206.5 cm(2)) were higher in CAH subjects than controls (VAT 26.4 ± 29.6 cm(2) and SAT 226.3 ± 157.5 cm(2); both P < .001). The VAT to SAT ratio was also higher in CAH subjects (0.15 ± 0.07) than controls (0.12 ± 0.06; P < .05). Within CAH, measures of obesity (waist to height ratio, fat mass) and inflammation (plasminogen activator inhibitor-1, high-sensitivity C-reactive protein, leptin) correlated strongly with VAT and SAT. In addition, homeostasis model assessment of insulin resistance, and low-density lipoprotein correlated with abdominal adiposity. There were no sex differences for VAT or SAT in CAH subjects.CAH adolescents and young adults have increased abdominal adiposity, with a higher proportion of proinflammatory VAT than SAT. An improved understanding of the mechanism of obesity in CAH may lead to targeted prevention and therapeutics in this high-risk population.CONCLUSIONSCAH adolescents and young adults have increased abdominal adiposity, with a higher proportion of proinflammatory VAT than SAT. An improved understanding of the mechanism of obesity in CAH may lead to targeted prevention and therapeutics in this high-risk population. |
Author | Schrager, Sheree M. Kim, Mimi S. Mittelman, Steven D. Dao-Tran, Anh Gilsanz, Vicente Geffner, Mitchell E. Ryabets-Lienhard, Anna |
AuthorAffiliation | Childrenʼs Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Division of Endocrinology (M.S.K., A.R.-L., A.D.-T., S.D.M., M.E.G.) and Hospital Medicine (S.M.S.); and Department of Radiology (V.G.), Los Angeles, California 90027; and The Saban Research Institute and the University of Southern California (M.S.K., S.D.M., V.G., M.E.G.), Los Angeles, California 90027 |
AuthorAffiliation_xml | – name: Childrenʼs Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Division of Endocrinology (M.S.K., A.R.-L., A.D.-T., S.D.M., M.E.G.) and Hospital Medicine (S.M.S.); and Department of Radiology (V.G.), Los Angeles, California 90027; and The Saban Research Institute and the University of Southern California (M.S.K., S.D.M., V.G., M.E.G.), Los Angeles, California 90027 |
Author_xml | – sequence: 1 givenname: Mimi S. surname: Kim fullname: Kim, Mimi S. email: mskim@chla.usc.edu organization: 1Children's Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Los Angeles, California 90027 – sequence: 2 givenname: Anna surname: Ryabets-Lienhard fullname: Ryabets-Lienhard, Anna organization: 1Children's Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Los Angeles, California 90027 – sequence: 3 givenname: Anh surname: Dao-Tran fullname: Dao-Tran, Anh organization: 1Children's Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Los Angeles, California 90027 – sequence: 4 givenname: Steven D. surname: Mittelman fullname: Mittelman, Steven D. organization: 1Children's Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Los Angeles, California 90027 – sequence: 5 givenname: Vicente surname: Gilsanz fullname: Gilsanz, Vicente organization: 1Children's Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Los Angeles, California 90027 – sequence: 6 givenname: Sheree M. surname: Schrager fullname: Schrager, Sheree M. organization: 1Children's Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Los Angeles, California 90027 – sequence: 7 givenname: Mitchell E. surname: Geffner fullname: Geffner, Mitchell E. organization: 1Children's Hospital Los Angeles (M.S.K., A.R.-L., A.D.-T., S.D.M., V.G., S.M.S., M.E.G.); Los Angeles, California 90027 |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26062016$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kk1v1DAQhi1URD_gxhlF4gAHUmzHH8kFabV8bKVKXEDAyfI6k10vXjvYCSX_gR-N0y0VVKoly_L4eV-NZ-YUHfngAaGnBJ8TSvDrnTmnmLCS4ap6gE5Iw3gpSSOP0AnGlJSNpF-P0WlKO5wxxqtH6JgKLLJInKDfF95E0AnaYrFuw9567YpFa_uQ7DAV1udLcJAM-CEV2rfFtzD6TY6OLge-2GFbLJ1OyZosXAa_AW-Ha48Is9dq6iH2mbC6aEcohlDkpFZTG8OvKYeheAudNRa8mR6jh512CZ7cnGfo8_t3n5ar8vLjh4vl4rI0jJO6rIFy3uo1xabjpAFK2srIThLNoBaCrEXdSdlgWXMKXFO5lrpqG21aLE0NUJ2hNwffflzvoZ3_FrVTfbR7HScVtFX_v3i7VZvwUzFOWdPQbPDyxiCGHyOkQe1tLpFz2kMYkyISU8Epr2VGn99Bd2GMuTJJVUSwSmLBRKae_ZvRbSp_G5WBVwfAxJBShO4WIVjNc6B2Rs1zoOY5yDi9g5vclcGG-T_W3SdiB9FVcAPE9N2NVxDVFrQbtgrnxYSsyyzguM63Mm9RZ9mLgyyM_X1ZXU9n9QcR29LU |
CitedBy_id | crossref_primary_10_1530_EJE_16_0888 crossref_primary_10_3389_fendo_2022_848274 crossref_primary_10_3389_fendo_2022_934675 crossref_primary_10_3390_nu14235184 crossref_primary_10_1530_EJE_17_0154 crossref_primary_10_1002_lipd_12280 crossref_primary_10_1515_jpem_2017_0068 crossref_primary_10_1024_0300_9831_a000274 crossref_primary_10_3389_fendo_2024_1433378 crossref_primary_10_1080_17446651_2025_2450423 crossref_primary_10_1016_j_yhbeh_2020_104908 crossref_primary_10_1111_cen_14967 crossref_primary_10_1159_000514130 crossref_primary_10_3389_fendo_2019_00212 crossref_primary_10_1159_000444169 crossref_primary_10_1210_clinem_dgae563 crossref_primary_10_1007_s40618_022_01824_4 crossref_primary_10_1542_pir_2022_005617 crossref_primary_10_1097_MED_0000000000000545 crossref_primary_10_1186_s12902_023_01499_9 crossref_primary_10_1210_clinem_dgab133 crossref_primary_10_1210_endrev_bnae026 crossref_primary_10_3390_medicina58040500 crossref_primary_10_1111_cen_13313 crossref_primary_10_3389_fped_2022_936944 crossref_primary_10_1093_ejendo_lvae144 crossref_primary_10_3390_metabo15020089 crossref_primary_10_1093_humupd_dmx014 crossref_primary_10_1038_s41431_020_0653_5 crossref_primary_10_1210_jc_2017_00947 crossref_primary_10_4274_jcrpe_galenos_2021_2020_0310 crossref_primary_10_1007_s12020_020_02323_3 crossref_primary_10_1080_07315724_2021_1895902 crossref_primary_10_1159_000537847 crossref_primary_10_1507_endocrj_EJ21_0292 crossref_primary_10_3389_fendo_2019_00681 crossref_primary_10_1210_clinem_dgae718 crossref_primary_10_1097_01_PGO_0001110228_39777_76 crossref_primary_10_1210_js_2019_00123 crossref_primary_10_1210_clinem_dgad628 crossref_primary_10_1002_mgg3_70029 crossref_primary_10_1210_clinem_dgae155 crossref_primary_10_3390_ijns6030068 crossref_primary_10_1017_S1047951124036576 crossref_primary_10_3389_fendo_2021_761258 crossref_primary_10_1016_j_jsbmb_2023_106374 crossref_primary_10_1111_cen_13580 |
ContentType | Journal Article |
Copyright | Copyright © 2015 by the Endocrine Society 2015 Copyright © 2015 by The Endocrine Society Copyright © 2015 by the Endocrine Society |
Copyright_xml | – notice: Copyright © 2015 by the Endocrine Society 2015 – notice: Copyright © 2015 by The Endocrine Society – notice: Copyright © 2015 by the Endocrine Society |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7QP 7T5 7TM H94 K9. 7X8 5PM |
DOI | 10.1210/jc.2014-4033 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Calcium & Calcified Tissue Abstracts Immunology Abstracts Nucleic Acids Abstracts AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) Immunology Abstracts Calcium & Calcified Tissue Abstracts Nucleic Acids Abstracts MEDLINE - Academic |
DatabaseTitleList | AIDS and Cancer Research Abstracts MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1945-7197 |
EndPage | E1159 |
ExternalDocumentID | PMC4524992 26062016 10_1210_jc_2014_4033 00004678-201508000-00068 10.1210/jc.2014-4033 |
Genre | Research Support, Non-U.S. Gov't Journal Article Research Support, N.I.H., Extramural |
GrantInformation_xml | – fundername: NCATS NIH HHS grantid: KL2 TR000131 – fundername: NCRR NIH HHS grantid: UL1 RR031986 – fundername: NCRR NIH HHS grantid: 1UL1RR031986 – fundername: NCATS NIH HHS grantid: KL2TR000131 |
GroupedDBID | --- -~X .55 .XZ 08P 0R~ 18M 1TH 29K 2WC 34G 354 39C 4.4 48X 53G 5GY 5RS 5YH 8F7 AABZA AACZT AAIMJ AAPQZ AAPXW AARHZ AAUAY AAVAP AAWTL ABBLC ABDFA ABEJV ABGNP ABJNI ABLJU ABMNT ABNHQ ABOCM ABPMR ABPPZ ABPQP ABPTD ABQNK ABVGC ABWST ABXVV ACGFO ACGFS ACPRK ACUTJ ACYHN ADBBV ADGKP ADGZP ADHKW ADQBN ADRTK ADVEK AELWJ AEMDU AENEX AENZO AETBJ AEWNT AFCHL AFFZL AFGWE AFOFC AFRAH AFXAL AGINJ AGKRT AGQXC AGUTN AHMBA AHMMS AJEEA ALMA_UNASSIGNED_HOLDINGS APIBT ARIXL ASPBG ATGXG AVWKF AZFZN BAWUL BAYMD BCRHZ BEYMZ BSWAC BTRTY C45 CDBKE CS3 D-I DAKXR DIK E3Z EBS EJD EMOBN ENERS F5P FECEO FHSFR FLUFQ FOEOM FOTVD FQBLK GAUVT GJXCC GX1 H13 HZ~ H~9 KBUDW KOP KQ8 KSI KSN L7B M5~ MHKGH MJL N9A NLBLG NOMLY NOYVH NVLIB O9- OAUYM OBH OCB ODMLO OFXIZ OGEVE OHH OJZSN OK1 OPAEJ OVD OVIDX P2P P6G REU ROX ROZ TEORI TJX TLC TR2 TWZ VVN W8F WOQ X7M YBU YFH YHG YOC YSK ZY1 ~02 ~H1 .GJ 3O- 7X7 88E 8FI 8FJ AAJQQ AAKAS AAPGJ AAQQT AAUQX AAWDT AAYJJ ABDPE ABUWG ABXZS ACFRR ACVCV ACZBC ADMTO ADNBA ADZCM AEMQT AEOTA AERZD AFFNX AFFQV AFKRA AFYAG AGMDO AGORE AHGBF AI. AJBYB AJDVS ALXQX APJGH AQDSO AQKUS AVNTJ BENPR BPHCQ BVXVI CCPQU EIHJH FEDTE FYUFA HMCUK HVGLF IAO IHR INH ITC J5H M1P MBLQV N4W NU- OBFPC PHGZM PHGZT PQQKQ PROAC PSQYO TMA UKHRP VH1 WHG X52 ZGI ZXP AAYXX AEHZK CITATION PJZUB PPXIY PUEGO CGR CUY CVF ECM EIF NPM 7QP 7T5 7TM H94 K9. 7X8 5PM |
ID | FETCH-LOGICAL-c4518-8e255dab20cf519e21d3c7f71a4e8661b68f77907852e5a27b7a3d9acd07c8ee3 |
ISSN | 0021-972X 1945-7197 |
IngestDate | Tue Sep 30 16:59:15 EDT 2025 Tue Sep 30 22:43:49 EDT 2025 Fri Sep 19 20:53:12 EDT 2025 Mon Jul 21 06:03:38 EDT 2025 Wed Oct 01 01:54:04 EDT 2025 Thu Apr 24 23:03:39 EDT 2025 Fri May 16 03:57:52 EDT 2025 Fri Feb 07 10:35:24 EST 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 8 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c4518-8e255dab20cf519e21d3c7f71a4e8661b68f77907852e5a27b7a3d9acd07c8ee3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
PMID | 26062016 |
PQID | 3164370646 |
PQPubID | 2046206 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_4524992 proquest_miscellaneous_1702652587 proquest_journals_3164370646 pubmed_primary_26062016 crossref_primary_10_1210_jc_2014_4033 crossref_citationtrail_10_1210_jc_2014_4033 wolterskluwer_health_00004678-201508000-00068 oup_primary_10_1210_jc_2014-4033 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2015-August |
PublicationDateYYYYMMDD | 2015-08-01 |
PublicationDate_xml | – month: 08 year: 2015 text: 2015-August |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: Washington – name: Chevy Chase, MD |
PublicationTitle | The journal of clinical endocrinology and metabolism |
PublicationTitleAlternate | J Clin Endocrinol Metab |
PublicationYear | 2015 |
Publisher | Oxford University Press Copyright by The Endocrine Society Endocrine Society |
Publisher_xml | – name: Oxford University Press – name: Copyright by The Endocrine Society – name: Endocrine Society |
SSID | ssj0014453 |
Score | 2.4147224 |
Snippet | Context:Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of... CONTEXT:Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of... Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of... |
SourceID | pubmedcentral proquest pubmed crossref wolterskluwer oup |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | E1153 |
SubjectTerms | Abdomen Abdominal Fat - diagnostic imaging Abdominal Fat - pathology Adipose tissue Adiposity Adolescent Adolescents Adrenal Hyperplasia, Congenital - complications Adrenal Hyperplasia, Congenital - epidemiology Adrenal Hyperplasia, Congenital - pathology Adult Biomarkers Body fat Body mass index C-reactive protein Cardiovascular diseases Child Children Computed tomography Cross-Sectional Studies Female Homeostasis Humans Hyperplasia Inflammation Insulin resistance Intra-Abdominal Fat - diagnostic imaging Intra-Abdominal Fat - pathology JCEM Online: Advances in Genetics Leptin Male Metabolic syndrome Obesity Obesity, Abdominal - complications Obesity, Abdominal - epidemiology Obesity, Abdominal - pathology Pediatric Obesity - complications Pediatric Obesity - epidemiology Pediatric Obesity - pathology Plasminogen activator inhibitors Sex differences Subcutaneous Fat - diagnostic imaging Subcutaneous Fat - pathology Teenagers Tomography, X-Ray Computed Young Adult Young adults |
Title | Increased Abdominal Adiposity in Adolescents and Young Adults With Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency |
URI | https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00004678-201508000-00068 https://www.ncbi.nlm.nih.gov/pubmed/26062016 https://www.proquest.com/docview/3164370646 https://www.proquest.com/docview/1702652587 https://pubmed.ncbi.nlm.nih.gov/PMC4524992 |
Volume | 100 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
journalDatabaseRights | – providerCode: PRVBFR databaseName: Free Medical Journals customDbUrl: eissn: 1945-7197 dateEnd: 20241001 omitProxy: true ssIdentifier: ssj0014453 issn: 0021-972X databaseCode: DIK dateStart: 19970101 isFulltext: true titleUrlDefault: http://www.freemedicaljournals.com providerName: Flying Publisher – providerCode: PRVFQY databaseName: GFMER Free Medical Journals customDbUrl: eissn: 1945-7197 dateEnd: 20241001 omitProxy: true ssIdentifier: ssj0014453 issn: 0021-972X databaseCode: GX1 dateStart: 19960101 isFulltext: true titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php providerName: Geneva Foundation for Medical Education and Research |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3bjtMwELXKIiEkhLhTWJCR4KnKKnFuzmO1W6gQ5YVdqW9REjvaLt2kalOh8g38Jv_BjOM6jthKLC9R67hNqzm2Z-xzZgh5n_vcFdKHkVYyPGYEHy7hGXdywIqMoiIvXRQKz75G04vg8zycDwa_LdbStslPip836kr-x6rQBnZFlewtLGu-FBrgNdgXrmBhuP6TjWFwI6ccfMZxLuq2PNdYLBQRS-n5xl2-JnVKoMY2tG6XDRJfUX-E3rMy1GmNMiusIQId1lJlHYYgdb1SQsuR2KoiG8xzpjuB3BdoRs4RZqBA-abt5SL2rJQURn0pK1HDLFV1eZ-uZQMoXO7zGGamvPNscb0YfTsx50E73CLeOF_gWZfZWnMxK7OmnGW1g8tu2262uGeLppHL_SavKuA2Ojuxdzq80PDsNOGoXu3UjgU65vhHJvpHyz3D1Z7okXkSq0rt3UTvuhaiuTVtT8Av9i0fAN8nNy4wECHjAoPJL70Agm_f7xZSQ29UgRd4AQ7-C3TJlXg_4nfIXRZHERba-DQ3TCQIaXWyVP2btT4DxVX2g3qeU0-NaQVFf3N7H_yokXex-a5kF5bzdP6IPNRRDx23EH5MBrJ6Qu7NNK_jKfllkEwNkqlBMl1U1EIyBeBQhWTaIpkikqlBMu2QTDWSqYVkCkimTU37SKYdkp-Ri4-T89Opo-uEOEUQetzhEuJikeXMLUoISCTzhF_EZexlgeTgf-YRLzGtZsxDJsOMxXmc-SLJCuHGBZfSf06OqrqSLwlNco8xmLykV4ggKMGdFUqMXoCjnoVuOSSjvQ3SQifRx1ouyxSDabBYelWkaLEULTYkH0zvVZs85kA_CuY81MVpuxzvbZ3qAbxJfQ-P3SGoiIbknbkN6wMe-mWVrLeb1ItdFoUs5PGQvGihYR7EIjeCJ8Cn4x5oTAfMPd-_Uy0uVQ76IGRBkrAhcXrwSlv1dnpoBLy6Zf_X5H43ExyTo2a9lW8gCmjyt2oM_QHqvgeJ |
linkProvider | Geneva Foundation for Medical Education and Research |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Increased+Abdominal+Adiposity+in+Adolescents+and+Young+Adults+With+Classical+Congenital+Adrenal+Hyperplasia+due+to+21-Hydroxylase+Deficiency&rft.jtitle=The+journal+of+clinical+endocrinology+and+metabolism&rft.au=Kim%2C+Mimi+S.&rft.au=Ryabets-Lienhard%2C+Anna&rft.au=Dao-Tran%2C+Anh&rft.au=Mittelman%2C+Steven+D.&rft.date=2015-08-01&rft.pub=Copyright+by+The+Endocrine+Society&rft.issn=0021-972X&rft.volume=100&rft.issue=8&rft.spage=E1153&rft.epage=E1159&rft_id=info:doi/10.1210%2Fjc.2014-4033&rft.externalDocID=00004678-201508000-00068 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0021-972X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0021-972X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0021-972X&client=summon |