Increased serum osteoprotegerin in disorders characterized by persistent immune activation or glucocorticoid excess--possible role in bone homeostasis
OBJECTIVE: To investigate the possible role of osteoprotegerin (OPG) in bone metabolism in humans by measuring serum levels of OPG in five well-characterized patient populations with known or suspected pathology in bone homeostasis, but with differences in the pathogenesis of these disturbances. DES...
Saved in:
Published in | European journal of endocrinology Vol. 145; no. 6; pp. 685 - 690 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
European Society of Endocrinology
01.12.2001
|
Subjects | |
Online Access | Get full text |
ISSN | 0804-4643 1479-683X |
DOI | 10.1530/eje.0.1450685 |
Cover
Abstract | OBJECTIVE: To investigate the possible role of osteoprotegerin (OPG) in bone metabolism in humans by measuring serum levels of OPG in five well-characterized patient populations with known or suspected pathology in bone homeostasis, but with differences in the pathogenesis of these disturbances. DESIGN: The study comprised 34 patients with Cushing's syndrome (CS), 24 acromegalic patients, 16 patients with growth hormone deficiency (GHD), 29 HIV-infected patients, 25 patients with common variable immunodeficiency (CVI) and 59 age- and sex-matched healthy controls (CTR). METHODS: Serum levels of tumor necrosis factor (TNF)-alpha, OPG, C-terminal telopeptides of Type-I collagen (CTX-I) and osteocalcin were determined in all study subjects as well as cortisol (CS and CTR) and IGF-I (acromegaly, GHD and CTR). RESULTS: OPG levels were significantly elevated in both CVI (median increase approximately 32%, P < 0.05) and HIV-infected patients with especially high levels in the latter group ( approximately 52%, P < 0.001), significantly correlated with increased TNFalpha levels (r = 0.47, P < 0.02). Also CS patients had elevated serum OPG ( approximately 24%, P < 0.01), significantly correlated with increased serum cortisol (r = 0.35, P < 0.05). In contrast, OPG levels in acromegalic and GHD patients were not different from healthy controls. No relationships were found between OPG levels and CTX-I or osteocalcin. CONCLUSIONS: These findings suggest that enhanced OPG levels may be a compensatory response to enhanced osteoclast activity or negative bone remodeling balance in some conditions, but may also be a parameter of enhanced activity in the OPG system possibly correlated to enhanced activity of other members of the TNF family. |
---|---|
AbstractList | To investigate the possible role of osteoprotegerin (OPG) in bone metabolism in humans by measuring serum levels of OPG in five well-characterized patient populations with known or suspected pathology in bone homeostasis, but with differences in the pathogenesis of these disturbances.
The study comprised 34 patients with Cushing's syndrome (CS), 24 acromegalic patients, 16 patients with growth hormone deficiency (GHD), 29 HIV-infected patients, 25 patients with common variable immunodeficiency (CVI) and 59 age- and sex-matched healthy controls (CTR).
Serum levels of tumor necrosis factor (TNF)-alpha, OPG, C-terminal telopeptides of Type-I collagen (CTX-I) and osteocalcin were determined in all study subjects as well as cortisol (CS and CTR) and IGF-I (acromegaly, GHD and CTR).
OPG levels were significantly elevated in both CVI (median increase approximately 32%, P < 0.05) and HIV-infected patients with especially high levels in the latter group ( approximately 52%, P < 0.001), significantly correlated with increased TNFalpha levels (r = 0.47, P < 0.02). Also CS patients had elevated serum OPG ( approximately 24%, P < 0.01), significantly correlated with increased serum cortisol (r = 0.35, P < 0.05). In contrast, OPG levels in acromegalic and GHD patients were not different from healthy controls. No relationships were found between OPG levels and CTX-I or osteocalcin.
These findings suggest that enhanced OPG levels may be a compensatory response to enhanced osteoclast activity or negative bone remodeling balance in some conditions, but may also be a parameter of enhanced activity in the OPG system possibly correlated to enhanced activity of other members of the TNF family. To investigate the possible role of osteoprotegerin (OPG) in bone metabolism in humans by measuring serum levels of OPG in five well-characterized patient populations with known or suspected pathology in bone homeostasis, but with differences in the pathogenesis of these disturbances.OBJECTIVETo investigate the possible role of osteoprotegerin (OPG) in bone metabolism in humans by measuring serum levels of OPG in five well-characterized patient populations with known or suspected pathology in bone homeostasis, but with differences in the pathogenesis of these disturbances.The study comprised 34 patients with Cushing's syndrome (CS), 24 acromegalic patients, 16 patients with growth hormone deficiency (GHD), 29 HIV-infected patients, 25 patients with common variable immunodeficiency (CVI) and 59 age- and sex-matched healthy controls (CTR).DESIGNThe study comprised 34 patients with Cushing's syndrome (CS), 24 acromegalic patients, 16 patients with growth hormone deficiency (GHD), 29 HIV-infected patients, 25 patients with common variable immunodeficiency (CVI) and 59 age- and sex-matched healthy controls (CTR).Serum levels of tumor necrosis factor (TNF)-alpha, OPG, C-terminal telopeptides of Type-I collagen (CTX-I) and osteocalcin were determined in all study subjects as well as cortisol (CS and CTR) and IGF-I (acromegaly, GHD and CTR).METHODSSerum levels of tumor necrosis factor (TNF)-alpha, OPG, C-terminal telopeptides of Type-I collagen (CTX-I) and osteocalcin were determined in all study subjects as well as cortisol (CS and CTR) and IGF-I (acromegaly, GHD and CTR).OPG levels were significantly elevated in both CVI (median increase approximately 32%, P < 0.05) and HIV-infected patients with especially high levels in the latter group ( approximately 52%, P < 0.001), significantly correlated with increased TNFalpha levels (r = 0.47, P < 0.02). Also CS patients had elevated serum OPG ( approximately 24%, P < 0.01), significantly correlated with increased serum cortisol (r = 0.35, P < 0.05). In contrast, OPG levels in acromegalic and GHD patients were not different from healthy controls. No relationships were found between OPG levels and CTX-I or osteocalcin.RESULTSOPG levels were significantly elevated in both CVI (median increase approximately 32%, P < 0.05) and HIV-infected patients with especially high levels in the latter group ( approximately 52%, P < 0.001), significantly correlated with increased TNFalpha levels (r = 0.47, P < 0.02). Also CS patients had elevated serum OPG ( approximately 24%, P < 0.01), significantly correlated with increased serum cortisol (r = 0.35, P < 0.05). In contrast, OPG levels in acromegalic and GHD patients were not different from healthy controls. No relationships were found between OPG levels and CTX-I or osteocalcin.These findings suggest that enhanced OPG levels may be a compensatory response to enhanced osteoclast activity or negative bone remodeling balance in some conditions, but may also be a parameter of enhanced activity in the OPG system possibly correlated to enhanced activity of other members of the TNF family.CONCLUSIONSThese findings suggest that enhanced OPG levels may be a compensatory response to enhanced osteoclast activity or negative bone remodeling balance in some conditions, but may also be a parameter of enhanced activity in the OPG system possibly correlated to enhanced activity of other members of the TNF family. OBJECTIVE: To investigate the possible role of osteoprotegerin (OPG) in bone metabolism in humans by measuring serum levels of OPG in five well-characterized patient populations with known or suspected pathology in bone homeostasis, but with differences in the pathogenesis of these disturbances. DESIGN: The study comprised 34 patients with Cushing's syndrome (CS), 24 acromegalic patients, 16 patients with growth hormone deficiency (GHD), 29 HIV-infected patients, 25 patients with common variable immunodeficiency (CVI) and 59 age- and sex-matched healthy controls (CTR). METHODS: Serum levels of tumor necrosis factor (TNF)-alpha, OPG, C-terminal telopeptides of Type-I collagen (CTX-I) and osteocalcin were determined in all study subjects as well as cortisol (CS and CTR) and IGF-I (acromegaly, GHD and CTR). RESULTS: OPG levels were significantly elevated in both CVI (median increase approximately 32%, P < 0.05) and HIV-infected patients with especially high levels in the latter group ( approximately 52%, P < 0.001), significantly correlated with increased TNFalpha levels (r = 0.47, P < 0.02). Also CS patients had elevated serum OPG ( approximately 24%, P < 0.01), significantly correlated with increased serum cortisol (r = 0.35, P < 0.05). In contrast, OPG levels in acromegalic and GHD patients were not different from healthy controls. No relationships were found between OPG levels and CTX-I or osteocalcin. CONCLUSIONS: These findings suggest that enhanced OPG levels may be a compensatory response to enhanced osteoclast activity or negative bone remodeling balance in some conditions, but may also be a parameter of enhanced activity in the OPG system possibly correlated to enhanced activity of other members of the TNF family. |
Author | Aukrust, P Godang, K Muller, F Bollerslev, J Froland, SS Ueland, T |
Author_xml | – sequence: 1 givenname: T surname: Ueland fullname: Ueland, T – sequence: 2 givenname: J surname: Bollerslev fullname: Bollerslev, J – sequence: 3 givenname: K surname: Godang fullname: Godang, K – sequence: 4 givenname: F surname: Muller fullname: Muller, F – sequence: 5 givenname: SS surname: Froland fullname: Froland, SS – sequence: 6 givenname: P surname: Aukrust fullname: Aukrust, P |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/11720891$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kU9LHjEQxkNR6qvtsdcSL95Wk93sbvZYpFVB6EXB25I_szqyu3mbZMW3H6Sf19FXWygIIRkyv2eGeWaf7cxhBsa-SHEs60qcwD0cU6hq0ej6A1tJ1XZFo6ubHbYSWqhCNaraY_sp3QshKRYf2Z6UbSl0J1fsz8XsIpgEnieIy8RDyhDWMWS4hYgzp-MxheghJu7uTDQuU-I3CeyGr-kXSTFnjtO0zMApjQ8mY5h5iPx2XFxwIWZ0AT2HRwcpFcU6pIR2BB4DXdTC0lD8LkxA7Q1V_MR2BzMm-Pz6HrDrH9-vTs-Ly59nF6ffLgurpMiFHbSCYYDBNNLUvjaNbrWFstbKeyWtLw0ob0oFXvuqlWA7pbRtnak7LaWrDtjRti5N_GuBlPsJk4NxNDOEJfVtWYmqVR2BX1_BxU7g-3XEycRN_-YkAcUWcJGGizD8Q0T_vKmeNtVTuN0U8dV_vMP84luOBsd3VYdblcWQHJLvOKAzf3s9M0-WLKki |
CitedBy_id | crossref_primary_10_1016_j_pnpbp_2013_01_019 crossref_primary_10_1186_s12891_016_1036_5 crossref_primary_10_1161_ATVBAHA_109_184101 crossref_primary_10_1002_jmv_20938 crossref_primary_10_1016_j_bone_2006_06_022 crossref_primary_10_1016_S8756_3282_03_00240_0 crossref_primary_10_1016_j_cytogfr_2004_06_004 crossref_primary_10_1097_01_psy_0000237858_76880_3d crossref_primary_10_1203_01_pdr_0000196375_47889_5b crossref_primary_10_1016_j_coemr_2018_02_009 crossref_primary_10_1016_j_ejim_2012_09_007 crossref_primary_10_1007_s00383_009_2325_y crossref_primary_10_1016_j_ghir_2004_06_002 crossref_primary_10_1093_rheumatology_keq005 crossref_primary_10_1371_journal_pone_0134266 crossref_primary_10_1111_j_1468_1293_2005_00278_x crossref_primary_10_1038_labinvest_3700701 crossref_primary_10_1016_j_jhsa_2024_12_017 crossref_primary_10_1097_MCG_0000000000001032 crossref_primary_10_1016_j_tem_2020_04_004 crossref_primary_10_1359_JBMR_041126 crossref_primary_10_1371_journal_pone_0173034 crossref_primary_10_1186_1546_0096_8_30 crossref_primary_10_1530_EJE_09_0800 crossref_primary_10_1016_j_metabol_2007_01_004 crossref_primary_10_1210_jcem_87_6_8549 crossref_primary_10_1093_alcalc_agl004 crossref_primary_10_1007_BF03346383 crossref_primary_10_1111_j_1365_2265_2005_02221_x crossref_primary_10_1111_j_1365_2796_2011_02393_x crossref_primary_10_1002_cncr_11127 crossref_primary_10_1016_j_fsisyn_2023_100326 crossref_primary_10_1515_CCLM_2002_177 crossref_primary_10_1210_jc_2006_2283 crossref_primary_10_1371_journal_ppat_1004497 crossref_primary_10_1007_s11102_016_0758_6 crossref_primary_10_1016_S0168_8278_02_00435_X crossref_primary_10_1161_01_ATV_0000204334_48195_6a crossref_primary_10_1097_TP_0000000000000227 crossref_primary_10_33549_physiolres_934303 crossref_primary_10_1177_000456320203900602 crossref_primary_10_36290_vnl_2024_067 crossref_primary_10_1111_j_1365_2265_2009_03605_x crossref_primary_10_1111_j_1365_2796_2009_02163_x crossref_primary_10_1038_sj_ki_5002716 crossref_primary_10_1530_eje_1_01874 crossref_primary_10_1016_j_atherosclerosis_2010_06_027 crossref_primary_10_1159_000357787 crossref_primary_10_3389_fendo_2024_1472680 crossref_primary_10_1007_s11102_022_01256_6 crossref_primary_10_1902_jop_2010_100585 crossref_primary_10_1210_jc_2014_2937 crossref_primary_10_1302_0301_620X_90B8_20861 crossref_primary_10_1016_j_jacc_2004_06_076 crossref_primary_10_1111_cen_12189 crossref_primary_10_1097_QAI_0000000000000725 crossref_primary_10_1007_BF03345601 crossref_primary_10_1007_s00223_009_9275_1 crossref_primary_10_1089_aid_2012_0305 crossref_primary_10_1210_clinem_dgac183 crossref_primary_10_36290_vnl_2017_117 crossref_primary_10_1007_s00198_013_2268_y crossref_primary_10_1210_er_2018_00005 crossref_primary_10_1111_j_1478_3231_2005_01073_x crossref_primary_10_1007_s40618_020_01269_7 crossref_primary_10_1097_01_tp_0000209413_45179_f6 crossref_primary_10_1161_CIRCHEARTFAILURE_110_957332 crossref_primary_10_1515_JPEM_2009_22_12_1105 crossref_primary_10_1359_jbmr_2002_17_11_1961 crossref_primary_10_1016_j_bone_2004_04_021 crossref_primary_10_1159_000444638 crossref_primary_10_36290_vnl_2021_073 crossref_primary_10_1016_j_alcohol_2010_09_002 crossref_primary_10_1016_j_metabol_2006_12_018 crossref_primary_10_1016_j_amjcard_2006_08_064 crossref_primary_10_1016_j_maturitas_2006_05_007 crossref_primary_10_1161_01_CIR_0000165119_62099_14 crossref_primary_10_3803_EnM_2023_1782 crossref_primary_10_1186_s12981_017_0162_y crossref_primary_10_1161_JAHA_117_007009 crossref_primary_10_2177_jsci_34_138 crossref_primary_10_5435_JAAOS_D_16_00123 crossref_primary_10_2310_6650_2006_06019 crossref_primary_10_1038_sj_leu_2403429 crossref_primary_10_1097_QAI_0b013e318295eb1d crossref_primary_10_1111_j_1365_2265_2010_03884_x |
ContentType | Journal Article |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
DOI | 10.1530/eje.0.1450685 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic CrossRef |
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 Anatomy & Physiology |
EISSN | 1479-683X |
EndPage | 690 |
ExternalDocumentID | 11720891 10_1530_eje_0_1450685 |
Genre | Journal Article |
GroupedDBID | --- -~X .GJ 08R 0R~ 18M 2WC 3O- 4.4 53G 5GY 5RE 5VS AAPBV AAPXW ABLYK ABOCM ABPTK ABSGY ABSQV ACGFO ACNCT ACPRK ADBBV ADDZX AENEX AFFNX AFHIN AI. ALMA_UNASSIGNED_HOLDINGS BAWUL BCRHZ BTFSW C1A CS3 DIK DU5 E3Z EBS F9R GX1 H13 HZ~ IL9 J5H KQ8 L7B O9- OK1 P2P RHF ROX SJN TBS TEORI TR2 VH1 W8F WOQ ZA5 ZGI ZXP 5WD AABZA AACZT AAUAY AAVAP AAYXX ABDFA ABEJV ABGNP ABJNI ABMNT ABNHQ ABPQP ABPTD ABQNK ABVGC ABWST ABXVV ABXZS ACUTJ ADGKP ADIPN ADNBA ADVEK ADVOB AEMQT AFGWE AFXAL AGORE AGQXC AGUTN AHMMS AJBYB AJEEA AJNCP ALXQX CITATION EMOBN KOP OAUYM OBOKY OCZFY OJZSN OPAEJ OVD OWPYF .55 AAPGJ AARHZ AAWDT ACFRR ADQBN AFYAG ANFBD APJGH ATGXG CGR CUY CVF ECM EIF EJD INIJC NPM PKN TCN TMA VXZ X7M 7X8 NU- |
ID | FETCH-LOGICAL-b410t-bf84effefa61a5d5a6878be2584dd41bd2ae4da24ed8d371eb9448b7ca59811c3 |
ISSN | 0804-4643 |
IngestDate | Fri Jul 11 12:13:24 EDT 2025 Wed Feb 19 02:36:15 EST 2025 Thu Apr 24 22:59:34 EDT 2025 Tue Jul 01 02:38:29 EDT 2025 Tue Apr 04 03:22:32 EDT 2023 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 6 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-b410t-bf84effefa61a5d5a6878be2584dd41bd2ae4da24ed8d371eb9448b7ca59811c3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | https://eje.bioscientifica.com/view/journals/eje/145/6/.xml |
PMID | 11720891 |
PQID | 72303749 |
PQPubID | 23479 |
PageCount | 6 |
ParticipantIDs | proquest_miscellaneous_72303749 pubmed_primary_11720891 crossref_primary_10_1530_eje_0_1450685 crossref_citationtrail_10_1530_eje_0_1450685 bioscientifica_primary_685 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2001-12-01 |
PublicationDateYYYYMMDD | 2001-12-01 |
PublicationDate_xml | – month: 12 year: 2001 text: 2001-12-01 day: 01 |
PublicationDecade | 2000 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | European journal of endocrinology |
PublicationTitleAlternate | Eur J Endocrinol |
PublicationYear | 2001 |
Publisher | European Society of Endocrinology |
Publisher_xml | – name: European Society of Endocrinology |
References | 11720890 - Eur J Endocrinol. 2001 Dec;145(6):681-3 |
References_xml | – reference: 11720890 - Eur J Endocrinol. 2001 Dec;145(6):681-3 |
SSID | ssj0016430 |
Score | 2.013807 |
Snippet | OBJECTIVE: To investigate the possible role of osteoprotegerin (OPG) in bone metabolism in humans by measuring serum levels of OPG in five well-characterized... To investigate the possible role of osteoprotegerin (OPG) in bone metabolism in humans by measuring serum levels of OPG in five well-characterized patient... |
SourceID | proquest pubmed crossref bioscientifica |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 685 |
SubjectTerms | Acromegaly - blood Adult Aged Bone and Bones - metabolism Bone Remodeling Common Variable Immunodeficiency - blood Cushing Syndrome - blood Female Glucocorticoids - metabolism Glycoproteins - blood Glycoproteins - physiology HIV Infections - blood Homeostasis Human Growth Hormone - deficiency Humans Hydrocortisone - blood Immunologic Deficiency Syndromes - blood Insulin-Like Growth Factor I - analysis Male Middle Aged Osteocalcin - blood Osteoclasts - physiology Osteoprotegerin Peptide Fragments - blood Procollagen - blood Receptors, Cytoplasmic and Nuclear - blood Receptors, Cytoplasmic and Nuclear - physiology Receptors, Tumor Necrosis Factor s Tumor Necrosis Factor-alpha - analysis |
Title | Increased serum osteoprotegerin in disorders characterized by persistent immune activation or glucocorticoid excess--possible role in bone homeostasis |
URI | https://eje.bioscientifica.com/view/journals/eje/145/6/.xml https://www.ncbi.nlm.nih.gov/pubmed/11720891 https://www.proquest.com/docview/72303749 |
Volume | 145 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLbKkBBIINi4dNz8gPZSUprEuT0OxDaBxtMq9S2yY2cUrUnVphPbD-En8Ds5x3aSpqMIkKooieKL-n1xjo-_c0zIm8AVOSY1cXKVc4dJIR0e88xhySjzMpFlkYfByadfwpMx-zQJJr3ezzXV0qoSw-z6t3El_4Mq3ANcMUr2H5BtKoUbcA74whEQhuNfYQwvN2rKwWaE5lazAQZslDrzwjlG9Wmlq82uucQQX5ua-dpYnXN0lUGJohpMMUrEJNa4tDbkYqDV7DA5hWbLqRyo7xhR4DjzEl-jCytMhCZECUW_ljMFzfPldLnV2W8NX1XIEsaqrkN_rGqJZaPafo8-DXSqX3aWr45LaX3cn1u21AGNRx0vhruhCGl6U2tVUVZ5ozd2WBwxh4UmudNQmWGbRYkTxnpn4XZcN3kqLYHXR-nQ7BJkP_ih2a_0xrck8FF8qb6pIVywYASlbpHbXhRpOcDxpJESwYxT72nT9MzmcoUK3nWK3yP3xdTkKNVCsA1jaMsMR1s6Zw_JAztFoYeGb49ITxW7ZO-w4FU5u6IHVIuG9d-1S-6cWm3GHvnRsJFqNtINNlL4NWykHTZScUVbNlLDRtqykZYL2mUj3WQjRTZiE8hGusbGx2R89PHsw4ljd_1wBHNHlSPymKGWKeehywMZ8DCOYqE8sJSlZK6QHldMco8pGUs_cpVIGItFlPEgiV0385-QnQKaekaoFyWc5yrwwggexxVuGXlS-HEGcARy1Cf7XTzSuUnxkgJYffK2xibNbL583LblIsV5M2CbArYpnBps--SgebyuZcuDr2ugUxjKcX2OF6pcLdPI8zEbVNInTw3-bUUwzYDeu_t_6vBzcrd9s16QnWqxUi_BYq7EK03XX-qm0RU |
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+serum+osteoprotegerin+in+disorders+characterized+by+persistent+immune+activation+or+glucocorticoid+excess--possible+role+in+bone+homeostasis&rft.jtitle=European+journal+of+endocrinology&rft.au=Ueland%2C+T&rft.au=Bollerslev%2C+J&rft.au=Godang%2C+K&rft.au=Muller%2C+F&rft.date=2001-12-01&rft.pub=European+Society+of+Endocrinology&rft.issn=0804-4643&rft.eissn=1479-683X&rft.volume=145&rft.issue=6&rft.spage=685&rft.epage=690&rft_id=info:doi/10.1530%2Feje.0.1450685 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0804-4643&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0804-4643&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0804-4643&client=summon |