Acquired SERPINC1/antithrombin deficiency during oral contraceptive consumption: a case report.


Journal

Journal of medical case reports
ISSN: 1752-1947
Titre abrégé: J Med Case Rep
Pays: England
ID NLM: 101293382

Informations de publication

Date de publication:
28 Jul 2023
Historique:
received: 08 01 2023
accepted: 21 05 2023
medline: 31 7 2023
pubmed: 28 7 2023
entrez: 27 7 2023
Statut: epublish

Résumé

SERPINC1 is a glycoprotein that regulates blood coagulation. SERPINC1 congenital or acquired deficiencies represent a significant risk factor for thromboembolic disease. SERPINC1 acquired defects are observed in very few cases and can occur in many clinical conditions such as treatment with L-asparaginase or oral contraceptive (particularly estrogen derivatives), but these conditions are not routinely investigated. A 50-year-old Caucasian woman who took gestodene 75 µg/ethinylestradiol 20 µg as oral contraceptive, was sent to our thrombophilia clinic because, on thrombophilia testing, a reduction of SERPINC1 (74%) and a slight increase in circulating D-dimer and homocysteine were found. We investigated triggers of such SERPINC1 reduction, and identified gestodene 75 µg/ethinylestradiol 20 µg use as the most likely candidate. Two months after the discontinuation of the oral contraceptive, SERPINC1 value returned to normal (92%) and D-dimer and homocysteine were normalized. Each patient has a different sensitivity to contraceptive use. Genetic (or epigenetic) regulation of anticoagulant proteins might account for a different rate of consumption of anticoagulant proteins as oral contraceptives and probably determine the susceptibility to thrombotic events.

Sections du résumé

BACKGROUND BACKGROUND
SERPINC1 is a glycoprotein that regulates blood coagulation. SERPINC1 congenital or acquired deficiencies represent a significant risk factor for thromboembolic disease. SERPINC1 acquired defects are observed in very few cases and can occur in many clinical conditions such as treatment with L-asparaginase or oral contraceptive (particularly estrogen derivatives), but these conditions are not routinely investigated.
CASE PRESENTATION METHODS
A 50-year-old Caucasian woman who took gestodene 75 µg/ethinylestradiol 20 µg as oral contraceptive, was sent to our thrombophilia clinic because, on thrombophilia testing, a reduction of SERPINC1 (74%) and a slight increase in circulating D-dimer and homocysteine were found. We investigated triggers of such SERPINC1 reduction, and identified gestodene 75 µg/ethinylestradiol 20 µg use as the most likely candidate. Two months after the discontinuation of the oral contraceptive, SERPINC1 value returned to normal (92%) and D-dimer and homocysteine were normalized.
CONCLUSION CONCLUSIONS
Each patient has a different sensitivity to contraceptive use. Genetic (or epigenetic) regulation of anticoagulant proteins might account for a different rate of consumption of anticoagulant proteins as oral contraceptives and probably determine the susceptibility to thrombotic events.

Identifiants

pubmed: 37501065
doi: 10.1186/s13256-023-04038-1
pii: 10.1186/s13256-023-04038-1
pmc: PMC10375737
doi:

Substances chimiques

Contraceptives, Oral 0
Ethinyl Estradiol 423D2T571U
Anticoagulants 0
Antithrombins 0
SERPINC1 protein, human 0
Antithrombin III 9000-94-6

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

323

Informations de copyright

© 2023. The Author(s).

Références

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Auteurs

D Denora (D)

Department of Medical Surgical Ad Health Science, Clinica Medica, Cattinara Hospital, University of Trieste, Trieste, Italy. donatella.denora@libero.it.

M V Di Rosa (MV)

Department of Medical Surgical Ad Health Science, Clinica Medica, Cattinara Hospital, University of Trieste, Trieste, Italy.

N Altamura (N)

Department of Medical Surgical Ad Health Science, Clinica Medica, Cattinara Hospital, University of Trieste, Trieste, Italy.

F Pellicori (F)

Department of Medical Surgical Ad Health Science, Clinica Medica, Cattinara Hospital, University of Trieste, Trieste, Italy.

P Vinci (P)

Department of Medical Surgical Ad Health Science, Clinica Medica, Cattinara Hospital, University of Trieste, Trieste, Italy.

U G Sisto (UG)

SC Pronto Soccorso e Medicina d'urgenza, Cattinara Hospital, Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy.

F Spanò (F)

Department of Medical Surgical Ad Health Science, Clinica Medica, Cattinara Hospital, University of Trieste, Trieste, Italy.

F G Di Girolamo (FG)

SC Assistenza Farmaceutica, Cattinara Hospital, Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy.

N Fiotti (N)

Department of Medical Surgical Ad Health Science, Clinica Medica, Cattinara Hospital, University of Trieste, Trieste, Italy.

G Biolo (G)

Department of Medical Surgical Ad Health Science, Clinica Medica, Cattinara Hospital, University of Trieste, Trieste, Italy.

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