Novel Interventions on Comorbidities in Patients with Fetal Alcohol Spectrum Disorder (FASD): An Integrative Review

被引:1
|
作者
Andreu-Fernandez, Vicente [1 ,2 ]
La Maida, Nunzia [3 ]
Marquina, Maribel [2 ]
Mirahi, Afrouz [4 ,5 ]
Garcia-Algar, Oscar [1 ,4 ]
Pichini, Simona [3 ]
Minutillo, Adele [3 ]
机构
[1] Inst Invest Biomed August Pi & Sunyer IDIBAPS, Grup Recerca Infancia & Entorn, Barcelona 08036, Spain
[2] Valencian Int Univ, Biosanit Res Inst, Valencia 46002, Spain
[3] Ist Super Sanita, Natl Ctr Addict & Doping, I-00161 Rome, Italy
[4] BCNatal, Hosp Clin Maternitat, Dept Neonatol, ICGON, Barcelona 08028, Spain
[5] Univ Barcelona, Dept Surg & Med Chirurg Specialties, E-08007 Barcelona, Spain
关键词
prenatal exposure delayed effects; fetal alcohol spectrum disorders; interventions; early diagnosis; follow-up studies; CHOLINE SUPPLEMENTATION; AMELIORATES DEFICITS; RISK-FACTORS; DOUBLE-BLIND; FOLIC-ACID; CHILDREN; EXPOSURE; BEHAVIOR; SYSTEMS; BRAIN;
D O I
10.3390/biomedicines12030496
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prenatal exposure to alcohol can cause Fetal Alcohol Spectrum Disorders (FASDs) after birth, encompassing a spectrum of physical, cognitive, and behavioral abnormalities. FASD represents a severe non-genetic disability avoidable through alcohol abstinence during pregnancy and when planning it. Clinical severity depends on alcohol impact, symptomatology, and resulting disabilities. FASD is a permanent disability with no recognized specific medical care. Conversely, secondary FASD-related disabilities can be symptomatically treated. This integrative review aims to provide information about the novel pharmacological treatments of FASD-associated comorbidities by selecting the last ten years of studies carried out on animals and humans. PRISMA guidelines were followed to search human/animal model studies of pharmacological interventions on FASD comorbidities, using different databases (PubMed, Cochrane, etc.). From 1348 articles, 44 met the criteria after full-text analysis. Firstly, all the reported studies point out that early diagnosis and tailored interventions are the principal tools to reduce FASD-related secondary disabilities, due to the fact that there is currently no approved pharmacological treatment for the tissue damage which produces FASD. Despite limitations in study designs and small sample sizes, these review results highlight how the treatment strategies of children with FASD have changed. In the past, studies focused on treating symptoms, but in the last years, researchers have turned their attention to the prevention targeting central nervous system embryogenesis. Novel treatments like choline and natural antioxidants and nutritional supplements are the most investigated treatments in humans with promising results. More follow-up studies need to be performed, to confirm and generalize reported efficacy to a wide sample size.
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页数:30
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