Steroid Screening Tools Differentiating Nonclassical Congenital Adrenal Hyperplasia and Polycystic Ovary Syndrome
© Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissionsoup.com..
PURPOSE: To analyze the performance of basal 17OH-progesterone (17OHP) levels versus the basal 17OHP/cortisol ratio in nonclassical congenital adrenal hyperplasia (NCAH) and polycystic ovary syndrome (PCOS) differential diagnosis. Basal 17OHP levels >10 ng/mL have been used to confirm NCAH diagnosis without the adrenocorticotropic hormone (ACTH) test; however, the optimal cutoff value is a matter of debate.
METHODS: A cross-sectional study was performed at the endocrinology and gynecological endocrinology outpatient clinics of a tertiary hospital. A total of 361 patients with PCOS (age 25.0 ± 5.3 years) and 113 (age 19.0 ± 13.6 years) patients with NCAH were enrolled. Basal and ACTH-17OHP levels were measured by radioimmunoassay, and CYP21A2 molecular analysis was performed to confirm hormonal NCAH diagnosis. Receiver operating characteristic curve analysis compared basal 17OHP levels and the 17OHP/cortisol ratio between NCAH and PCOS patients.
RESULTS: Basal 17OHP levels were higher in NCAH patients than in those with PCOS (8.85 [4.20-17.30] vs 1.00 [0.70-1.50] ng/mL; P < 0.0001), along with 17OHP/cortisol ratio (0.86 [0.47-1.5]) vs 0.12 [0.07-0.19]; P < 0.0001, respectively). Basal 17OHP levels and the 17OHP/cortisol ratio were strongly correlated in both groups (rho = 0.82; P < 0.0001). Areas under the curves for basal 17OHP levels (0.9528) and the 17OHP/cortisol ratio (0.9455) were not different to discriminate NCAH and PCOS (P > 0.05). Basal 17OHP level >5.4 ng/mL and 17OHP/cortisol ratio >2.90 had 100% specificity to identify NCAH.
MAIN CONCLUSIONS: Basal 17OHP levels >5.4 ng/mL can be used to perform differential diagnoses between NCAH and PCOS, dismissing the ACTH test. The basal 17OHP/cortisol ratio was not superior to basal 17OHP levels in this scenario.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:105 |
---|---|
Enthalten in: |
The Journal of clinical endocrinology and metabolism - 105(2020), 8 vom: 01. Aug. |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Maffazioli, Giovana D N [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 08.02.2021 Date Revised 08.02.2021 published: Print Citation Status MEDLINE |
---|
doi: |
10.1210/clinem/dgaa369 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM311096166 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM311096166 | ||
003 | DE-627 | ||
005 | 20231225141523.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2020 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1210/clinem/dgaa369 |2 doi | |
028 | 5 | 2 | |a pubmed24n1036.xml |
035 | |a (DE-627)NLM311096166 | ||
035 | |a (NLM)32530459 | ||
035 | |a (PII)dgaa369 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Maffazioli, Giovana D N |e verfasserin |4 aut | |
245 | 1 | 0 | |a Steroid Screening Tools Differentiating Nonclassical Congenital Adrenal Hyperplasia and Polycystic Ovary Syndrome |
264 | 1 | |c 2020 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 08.02.2021 | ||
500 | |a Date Revised 08.02.2021 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissionsoup.com. | ||
520 | |a PURPOSE: To analyze the performance of basal 17OH-progesterone (17OHP) levels versus the basal 17OHP/cortisol ratio in nonclassical congenital adrenal hyperplasia (NCAH) and polycystic ovary syndrome (PCOS) differential diagnosis. Basal 17OHP levels >10 ng/mL have been used to confirm NCAH diagnosis without the adrenocorticotropic hormone (ACTH) test; however, the optimal cutoff value is a matter of debate | ||
520 | |a METHODS: A cross-sectional study was performed at the endocrinology and gynecological endocrinology outpatient clinics of a tertiary hospital. A total of 361 patients with PCOS (age 25.0 ± 5.3 years) and 113 (age 19.0 ± 13.6 years) patients with NCAH were enrolled. Basal and ACTH-17OHP levels were measured by radioimmunoassay, and CYP21A2 molecular analysis was performed to confirm hormonal NCAH diagnosis. Receiver operating characteristic curve analysis compared basal 17OHP levels and the 17OHP/cortisol ratio between NCAH and PCOS patients | ||
520 | |a RESULTS: Basal 17OHP levels were higher in NCAH patients than in those with PCOS (8.85 [4.20-17.30] vs 1.00 [0.70-1.50] ng/mL; P < 0.0001), along with 17OHP/cortisol ratio (0.86 [0.47-1.5]) vs 0.12 [0.07-0.19]; P < 0.0001, respectively). Basal 17OHP levels and the 17OHP/cortisol ratio were strongly correlated in both groups (rho = 0.82; P < 0.0001). Areas under the curves for basal 17OHP levels (0.9528) and the 17OHP/cortisol ratio (0.9455) were not different to discriminate NCAH and PCOS (P > 0.05). Basal 17OHP level >5.4 ng/mL and 17OHP/cortisol ratio >2.90 had 100% specificity to identify NCAH | ||
520 | |a MAIN CONCLUSIONS: Basal 17OHP levels >5.4 ng/mL can be used to perform differential diagnoses between NCAH and PCOS, dismissing the ACTH test. The basal 17OHP/cortisol ratio was not superior to basal 17OHP levels in this scenario | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Observational Study | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a basal 17OH-progesterone levels | |
650 | 4 | |a diagnosis screening | |
650 | 4 | |a nonclassical congenital hyperplasia | |
650 | 4 | |a polycystic ovary syndrome | |
650 | 7 | |a Biomarkers |2 NLM | |
650 | 7 | |a 17-alpha-Hydroxyprogesterone |2 NLM | |
650 | 7 | |a 68-96-2 |2 NLM | |
650 | 7 | |a Adrenocorticotropic Hormone |2 NLM | |
650 | 7 | |a 9002-60-2 |2 NLM | |
650 | 7 | |a CYP21A2 protein, human |2 NLM | |
650 | 7 | |a EC 1.14.14.16 |2 NLM | |
650 | 7 | |a Steroid 21-Hydroxylase |2 NLM | |
650 | 7 | |a EC 1.14.14.16 |2 NLM | |
650 | 7 | |a Hydrocortisone |2 NLM | |
650 | 7 | |a WI4X0X7BPJ |2 NLM | |
700 | 1 | |a Bachega, Tania A S S |e verfasserin |4 aut | |
700 | 1 | |a Hayashida, Sylvia A Y |e verfasserin |4 aut | |
700 | 1 | |a Gomes, Larissa G |e verfasserin |4 aut | |
700 | 1 | |a Valassi, Helena P L |e verfasserin |4 aut | |
700 | 1 | |a Marcondes, Jose A M |e verfasserin |4 aut | |
700 | 1 | |a Mendonca, Berenice B |e verfasserin |4 aut | |
700 | 1 | |a Baracat, Edmund C |e verfasserin |4 aut | |
700 | 1 | |a Maciel, Gustavo A R |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t The Journal of clinical endocrinology and metabolism |d 1945 |g 105(2020), 8 vom: 01. Aug. |w (DE-627)NLM00001821X |x 1945-7197 |7 nnns |
773 | 1 | 8 | |g volume:105 |g year:2020 |g number:8 |g day:01 |g month:08 |
856 | 4 | 0 | |u http://dx.doi.org/10.1210/clinem/dgaa369 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 105 |j 2020 |e 8 |b 01 |c 08 |