Anti-müllerian hormone compared with other ovarian markers after childhood cancer treatment.


Journal

Acta oncologica (Stockholm, Sweden)
ISSN: 1651-226X
Titre abrégé: Acta Oncol
Pays: England
ID NLM: 8709065

Informations de publication

Date de publication:
Feb 2019
Historique:
pubmed: 19 12 2018
medline: 5 6 2019
entrez: 19 12 2018
Statut: ppublish

Résumé

Gonadal dysfunction is one of the major late complications after cancer diagnosis and treatment. The best markers of ovarian reserve in clinical practice are antral follicle count (AFC) and ovarian volume. We aimed to study the prevalence of premature ovarian insufficiency (POI) and evaluate anti-Müllerian hormone (AMH) and other serum markers for ovarian function in adult women who were childhood cancer survivors (CCS) in comparison with a control group. Altogether, 167 female CCS were compared to 164 matched controls. Prevalence of POI was documented and serum levels of AMH, inhibin B, follicle stimulating hormone (FSH), and estradiol (E2) were compared with AFC and ovarian volume. POI was reported in 22 (13%) of the CCS and in none of the controls. Serum levels of AMH, inhibin B, and FSH, but not E2, correlated significantly with AFC and ovarian volume; AMH showed the highest correlation. There was no difference between CCS and controls regarding the different serum markers as measured by linear regression analysis. ROC curve AUC for primary POI showed the highest values for AMH (0.930) and AFC (0.944). For AFC <10, ROC curve AUC showed highest value for AMH for CCS (0.866) and controls (0.878). In a subgroup of female CCS <40 years (n = 120), the results were similar. We found POI in 13% among CCS, slightly more than in other studies. Serum levels of AMH, inhibin B, and FSH correlated significantly with AFC and ovarian volume, and no difference was noted between CCS and controls. AMH was the most reliable serum marker for ovarian function in terms of POI and low AFC.

Sections du résumé

BACKGROUND BACKGROUND
Gonadal dysfunction is one of the major late complications after cancer diagnosis and treatment. The best markers of ovarian reserve in clinical practice are antral follicle count (AFC) and ovarian volume. We aimed to study the prevalence of premature ovarian insufficiency (POI) and evaluate anti-Müllerian hormone (AMH) and other serum markers for ovarian function in adult women who were childhood cancer survivors (CCS) in comparison with a control group.
MATERIAL AND METHODS METHODS
Altogether, 167 female CCS were compared to 164 matched controls. Prevalence of POI was documented and serum levels of AMH, inhibin B, follicle stimulating hormone (FSH), and estradiol (E2) were compared with AFC and ovarian volume.
RESULTS RESULTS
POI was reported in 22 (13%) of the CCS and in none of the controls. Serum levels of AMH, inhibin B, and FSH, but not E2, correlated significantly with AFC and ovarian volume; AMH showed the highest correlation. There was no difference between CCS and controls regarding the different serum markers as measured by linear regression analysis. ROC curve AUC for primary POI showed the highest values for AMH (0.930) and AFC (0.944). For AFC <10, ROC curve AUC showed highest value for AMH for CCS (0.866) and controls (0.878). In a subgroup of female CCS <40 years (n = 120), the results were similar.
CONCLUSION CONCLUSIONS
We found POI in 13% among CCS, slightly more than in other studies. Serum levels of AMH, inhibin B, and FSH correlated significantly with AFC and ovarian volume, and no difference was noted between CCS and controls. AMH was the most reliable serum marker for ovarian function in terms of POI and low AFC.

Identifiants

pubmed: 30558460
doi: 10.1080/0284186X.2018.1529423
doi:

Substances chimiques

Biomarkers 0
inhibin B 0
Estradiol 4TI98Z838E
Inhibins 57285-09-3
Anti-Mullerian Hormone 80497-65-0
Follicle Stimulating Hormone 9002-68-0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

218-224

Commentaires et corrections

Type : ErratumIn

Auteurs

Anna Nyström (A)

a Department of Clinical Sciences Lund, Pediatrics, Pediatric Endocrinology , Lund University, Skane University Hospital , Lund , Sweden.

Helena Mörse (H)

b Department of Clinical Sciences Lund, Pediatrics, Pediatric Oncology and Hematology , Lund University, Skane University Hospital , Lund , Sweden.

Hanna Nordlöf (H)

c Department of Clinical Sciences Malmö, Reproductive Medicine , Lund University, Skane University Hospital , Malmö , Sweden.

Karin Wiebe (K)

a Department of Clinical Sciences Lund, Pediatrics, Pediatric Endocrinology , Lund University, Skane University Hospital , Lund , Sweden.

Maria Artman (M)

a Department of Clinical Sciences Lund, Pediatrics, Pediatric Endocrinology , Lund University, Skane University Hospital , Lund , Sweden.

Ingrid Øra (I)

b Department of Clinical Sciences Lund, Pediatrics, Pediatric Oncology and Hematology , Lund University, Skane University Hospital , Lund , Sweden.

Aleksander Giwercman (A)

c Department of Clinical Sciences Malmö, Reproductive Medicine , Lund University, Skane University Hospital , Malmö , Sweden.

Emir Henic (E)

c Department of Clinical Sciences Malmö, Reproductive Medicine , Lund University, Skane University Hospital , Malmö , Sweden.

Maria Elfving (M)

a Department of Clinical Sciences Lund, Pediatrics, Pediatric Endocrinology , Lund University, Skane University Hospital , Lund , Sweden.

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Classifications MeSH