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Methylenetetrahydrofolate reductase (MTHFR) has various polymorphisms, and the effects of periconceptional folic acid supplementation for decreasing neural tube defects (NTDs) risk differ depending on the genotypes. This study analyzed the effectiveness of multivitamin supplementation on folate insufficiency and hyperhomocysteinemia, depending on MTHFR polymorphisms. Of 205 women, 72 (35.1%), 100 (48.8%) and 33 (16.1%) had MTHFR CC, CT and TT, respectively. Serum folate and homocysteine levels in women with homozygous mutant TT were significantly lower and higher, respectively, than those in women with CC and CT. In 54 women (26.3% of all women) with a risk of NTDs, multivitamin supplementation containing folic acid and vitamin D for one month increased folate level (5.8 ± 0.9 to 19.2 ± 4.0 ng/mL, < 0.0001) and decreased the homocysteine level (8.2 ± 3.1 to 5.8 ± 0.8 nmol/mL, < 0.0001) to minimize the risk of NTDs in all women, regardless of MTHFR genotype. Regardless of MTHFR genotype, multivitamin supplements could control folate and homocysteine levels. Tests for folate and homocysteine levels and optimal multivitamin supplementation in women with risk of NTDs one month or more before pregnancy should be recommended to women who are planning a pregnancy.
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http://dx.doi.org/10.3390/nu13041381 | DOI Listing |
Cochrane Database Syst Rev
August 2025
John Walsh Centre for Rehabilitation Research, Northern Sydney Local Health District and the University of Sydney, St Leonards, Australia.
Rationale: Falls in care facilities are common events, causing considerable morbidity and mortality for older people. This is an update of a review on interventions in care facilities and hospitals first published in 2010 and updated in 2012 and 2018 on interventions in care facilities and hospitals. This review has now been split into separate reviews for each setting.
View Article and Find Full Text PDFPLoS One
August 2025
Institute of Bee Health, Vetsuisse Faculty, University of Bern, Bern, Switzerland.
In managed western honey bee, Apis mellifera, colonies, vitamins are often neglected when it comes to SI feeding despite their importance for health. Moreover, the potential links of vitamin feeding to longevity, food consumption and adult dry weight are poorly understood. Finally, comparative nutritional studies of short-lived summer workers and long-lived winter workers are currently lacking.
View Article and Find Full Text PDFCureus
July 2025
Dermatology, Nicklaus Children's Hospital, Children's Skin Center, Miami, USA.
Nicolaides‑Baraitser syndrome (NBS) is an ultrarare SMARCA2‑related neurodevelopmental disorder, whose cutaneous hallmarks traditionally include early hypotrichosis and coarse, sparse scalp hair. We describe a four‑year‑old girl with genetically confirmed NBS who presented with years‑long, worsening eczematous dermatitis and diffuse, non‑scarring alopecia that far exceeded the baseline hypotrichosis described in the syndrome. Clinical examination revealed erythematous, lichenified patches distributed across the trunk, extremities, and flexural creases, accompanied by generalized scalp thinning without follicular dropout or scarring.
View Article and Find Full Text PDFAnn Med Surg (Lond)
July 2025
Huntsville Hospital, Huntsville, AL, USA.
Introduction And Importance: Vitamin B6 (pyridoxine) deficiency is a rare but reversible cause of seizures in adults, which is often overlooked in post gastrectomy patients. This case highlights the critical role of nutritional supplementation in preventing severe complications such as neuropsychiatric manifestations and seizures, emphasizing the importance of vigilance in postoperative care and patient follow-up.
Case Presentation: A 46-year-old woman with a history of partial gastrectomy presented with intermittent confusion and somnolence for a duration of 6 months.
Front Nutr
August 2025
Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Background: Drug-resistant epilepsy (DRE) is a chronic neurological disorder with somatic impacts and an increased risk of psychiatric comorbidities and cognitive impairment. Previous studies suggested that genomic variants could contribute to the high interindividual variability in epilepsy and in its treatment response, but it remains unclear. Here, we aimed to perform genome-wide association study (GWAS), leverage the enrichment analysis of the genomic variants, and provide the potential molecular signature profiles.
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