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Kambale-Kombi, P., Marini Djang’eing’a, R., Alworong’a Opara, J., Mbo Mukonkole, J., Bours, V., Mbumba Lupaka, D., et al. (2022) Renal Abnormalities among Sickle Cell Disease Patients in a Poor Management Setting: A Survey in the Democratic Republic of the Congo. Mediterranean Journal of Hematology and Infectious Diseases, 14, e2022046.
https://doi.org/10.4084/mjhid.2022.046

has been cited by the following article:

• TITLE: Assessment of Functional Ovarian Reserve in Homozygous Sickle Cell Patients in Kisangani

  AUTHORS: Junior Lisi-Ankiene Burubu, Jean-Jeannot Sihalikyolo Juakali, Noël Otuli Labama, Jean-Didier Nguma Bosenge, Emmanuel Likwekwe Komanda, Teddy Habiragi Matega, Jérémie Osundja Likilo, Yvette Ufoy Mungu Neema, Jean-Marie Lukangi Demupondo, Patrick Batakuya Magala, Amos Sivulyamwenge Kaghoma, Paul Kombi Kambale, Gédéon Bosunga Katenga

  KEYWORDS: Assessment, Ovarian Reserve, Homozygous Sickle Cell Disease

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.13 No.4, April 22, 2025

  ABSTRACT: Introduction: Sickle cell disease is the most common autosomal recessive genetic haemoglobinopathy in the world. Progress in its management has significantly increased the life expectancy of patients with sickle cell disease, exposing them to age-related complications, including fertility problems. Assessment of ovarian reserve is a key test for estimating fertility potential in women with sickle cell disease. The aim of this study was to determine the ovarian reserve of women with sickle cell disease by measuring antimüllerian hormone and counting antral follicles and identify the associated factors. Material and Methods: This was a cross-sectional analytical study conducted from 5 April to 31 October 2024 in Kisangani, Democratic Republic of the Congo. It enrolled 268 women, categorised into four groups according to their haemoglobin status and the absence or presence of sickle cell crises: HbAA, asymptomatic HbAS (HbASa), symptomatic HbAS (HbASs) and HbSS. Participants with HbAA were grouped with HbASa to form the control group and those with HbSS were grouped with HbASs to form the patient groups. Results: The mean age at menarche was significantly later in the patients in the control group (P-value Conclusion: Sickle cell disease leads to a decrease in ovarian reserve (ORR). This DOR is associated with low BMI, multiple vaso-occlusive and haemolytic crises, low haemoglobin levels and the use of non-steroidal anti-inflammatory drugs.