Sex-based differences in the manifestations and complications of sickle cell disease: Report from the Sickle Cell Disease Implementation Consortium.
Acute Chest Syndrome
/ epidemiology
Adolescent
Adult
Anemia, Sickle Cell
/ complications
Cross-Sectional Studies
Female
Hemoglobin, Sickle
/ genetics
Humans
Male
Pain
/ epidemiology
Patient Admission
/ statistics & numerical data
Self Report
Sex Characteristics
Surveys and Questionnaires
Young Adult
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2021
2021
Historique:
received:
02
03
2021
accepted:
04
10
2021
entrez:
29
10
2021
pubmed:
30
10
2021
medline:
27
11
2021
Statut:
epublish
Résumé
Sex-based clinical outcome differences in sickle cell disease (SCD) remain largely unknown despite evidence that female sex is associated with an increased lifespan. To better characterize sex-based differences in SCD, we assessed pain, treatment characteristics, laboratory measures and complications among males and females currently enrolled in the Sickle Cell Disease Implementation Consortium (SCDIC) registry. The SCDIC consists of eight comprehensive SCD centers and one data coordinating center that received funding from the National Heart Lung and Blood Institute to improve outcomes for individuals with SCD. Eligibility criteria included: 15 to 45 years of age and a confirmed diagnosis of SCD. Self-report surveys were completed and data were also abstracted from the participants' medical records. A total of 2,124 participants were included (mean age: 27.8 years; 56% female). The majority had hemoglobin SS SCD genotype. Females had worse reports of pain severity (mean (SD) T-score 51.6 (9.6) vs 49.3 (10), p<0.001), more vaso-occlusive episodes (p = 0.01) and a higher occurrence of 3 or more hospital admissions in the past year (30.9% vs. 25.5, p = 0.03). On multivariable analysis, males had higher odds of acute chest syndrome (odds ratio (OR) 1.4, p = 0.002), cardiovascular (OR 1.70, p<0.001) and musculoskeletal (OR 1.33, p = 0.0034) complications and lower odds of depression (OR 0.77, p = 0.0381). Females had higher fetal hemoglobin levels with and without hydroxyurea use (9.6% vs 8.5%, p = 0.03 and 3% vs 2.2%, p = 0.0005, respectively). Our data suggests that sex differences in clinical outcomes do occur among individuals with SCD. Future research needs to explore the mechanisms underlying these differences.
Identifiants
pubmed: 34714833
doi: 10.1371/journal.pone.0258638
pii: PONE-D-21-06973
pmc: PMC8555833
doi:
Substances chimiques
Hemoglobin, Sickle
0
Types de publication
Journal Article
Multicenter Study
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0258638Subventions
Organisme : NHLBI NIH HHS
ID : U24 HL133948
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL134042
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL133994
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL133964
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL134007
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL133997
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL134004
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL133990
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL133996
Pays : United States
Déclaration de conflit d'intérêts
Jane S. Hankins receives consultancy fees from Forma Therapeutics, Global Blood Therapeutics and bluebird bio. All other authors have declared that no competing interests exist.
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