1.Research advances in the association of vitamin D with benign paroxysmal positional vertigo and residual dizziness
Xien ZHU ; Shuangmei YAN ; Ping GU
Journal of Apoplexy and Nervous Diseases 2025;42(6):568-572
Benign paroxysmal positional vertigo(BPPV)is a common peripheral vestibular disorder,and at present,otolith shedding and displacement is highly recognized as the main pathological mechanism of BPPV. An increasing amount of evidence has shown that otolith particle shedding is closely associated with vitamin D,and 25-(OH)D is expected to become a potential biomarker for BPPV and an important target for the treatment of BPPV and residual symptoms after successful repositioning. This article reviews the pathophysiological mechanism of vitamin D in BPPV and residual dizziness and summarizes the association of vitamin D with BPPV and residual symptoms based on the treatment methods for vitamin D regulation.
Vitamin D
2.Effects of Vitamin D supplementation on pediatric attention deficit hyperactivity disorder: A meta-analysis and systematic review
Cheska Marie G. Latorre ; Anna Lizza Mañ ; alac
The Philippine Children’s Medical Center Journal 2025;21(1):42-55
OBJECTIVE:
Attention Deficit Hyperactivity Disorder (ADHD) is a common mental disorder in children. It is unclear how nutrition and dietary components relate to ADHD. Some studies suggest that children with ADHD have lower serum levels of vitamin D than healthy controls. In the current study, the effects of Vitamin D supplementation on ADHD were reviewed and analyzed using available literature.
MATERIALS AND METHODS:
A meta-analysis and systematic review were performed. Children less than 18 years old diagnosed with ADHD given Vitamin D supplementation or placebo were included. A search was performed in PubMed/MEDLINE, EMBASE, Scopus, Cochrane, and Google Scholar databases from inception to August 2024 using the MeSH keywords: "Vitamin D" AND (ADHD OR Attention Deficit Hyperactivity Disorder) AND (children OR pediatric OR adolescents) AND randomized controlled trial. Standardized Mean Difference (SMD) was used as an effect measure and pooled using random effects meta-analysis.
RESULTS:
The pooled SMS showed significantly lower ADHD scores (SMD=-0.59, 95%CI=-1.06 to -0.11, p=0.01), lower inattentive scores (SMD=-0.61, 95%CI=-1.00 to -0.23, p=0.002), and lower hyperactivity scores (SMD=-0.64, 95%CI=-1.08 to -0.20, p=0.004) in children given Vitamin D supplementation. The adverse events reported were minor only and did not vary significantly between intervention and control groups.
CONCLUSION
Vitamin D treatment as an adjuvant to methylphenidate alleviated ADHD symptoms without significant adverse effects, correlating with enhanced vitamin D levels. Given the robust evidence and well-structured randomized controlled trials, we strongly advocate for the integration of vitamin D supplementation with ADHD treatment.
Human
;
Male,Female
;
Adolescent: 13-18 yrs old
;
Child Preschool: 2-5 yrs old
;
Child: 6-12 yrs old
;
Vitamin D
;
meta-analysis
;
systematic review
3.Sensory peripheral neuropathy aggravated by vitamin B12 in elder patient. A case report
Lobaina Abozaid ; Selma Mohammed Taha
Philippine Journal of Internal Medicine 2024;62(1):331-333
Background:
Vitamin B12 is one of the common drugs used by physicians to treat peripheral neuropathy (PN), although
many patients have a good response, however, overdose and toxicity aggravate the condition and worsen the patient’s
symptoms. The purpose of this paper is to highlight association between Vitamin B12 toxicity and deterioration of PN
symptoms.
Case Summary:
An elder Sudanese man with acute onset of sensory PN, the patient’s symptoms started by tingling
sensations and paresthesia affecting both hands and feet. After patient received cobalamin (vitamin B 12) prescribed by
his doctor, the patient symptoms were markedly aggravated and his condition worsened to extend that impaired the
normal patient ordinary work. No symptoms related to motor system. Other possible etiologies were studied and excluded.
Investigations of his condition revealed blood level of B12 was 1900 pg/mL, the patient condition improved dramatically
with discontinuation of the drug.
Conclusion
Cobalamin toxicity aggravate sensory PN symptoms. Clinicians are advised to adjust the dose and check
Cobalamin level before and during treatment to avoid its toxicity.
Peripheral Nervous System Diseases
;
Vitamin B 12
4.Isotretinoin-induced gouty arthritis in a 26-year-old Filipino female patient with acne vulgaris: A case report
Charlene Lorraine A. Elio ; Ma. Dulce Amor Vivian F. Galang
Journal of the Philippine Dermatological Society 2024;33(Suppl 1):1-1
INTRODUCTION
Oral isothretinoin is the treatment of choice in moderate to severe acne vulgaris. The most common adverse effect is mild mucocutaneous symptoms and the most seious risk is related to teratogenecity. Hyperuricemia and gouty arthritis are rarely associated with isotretinoin therapy.
CASE REPORTWe report a case of a 26-year-old female patient with no known comorbidities who was started on isotretinoin therapy for acne vulgaris. The patient presented with baseline hyperuricemia with no joint pains or swelling. Two and a half weeks later after initiation of isotretinoin therapy, the patient developed pain and swelling on the left wrist, hence was started on urate-lowering medications and maintained on isotretinoin tharapy. The patient had no recurrence of joint pains and remains symptom-free for six months later.
Human ; Female ; Adult: 25-44 Yrs Old ; Acne Vulgaris ; Arthritis, Gouty ; Hyperuricemia ; Isotretinoin ; Retinoids
5.Olmsted syndrome in a 12-year-old Filipino male: A case report and future directions.
Aznaida T. Pandapatan ; Cindy J. Tan ; Joyce Anne S. Tan
Acta Medica Philippina 2024;58(17):83-87
We report a case of a Filipino child who presented with yellowish hyperkeratotic plaques on the palms and soles with palmar transgredient extension to the wrists, a yellowish hyperkeratotic plaque over the coccygeal area, and brownish-black hyperkeratotic perianal plaques. Patient had delayed physical development and short stature, but no intellectual disability. Histopathologic examination showed palmoplantar keratoderma. These clinical findings of symmetrical palmoplantar keratoderma with periorificial keratotic plaques were consistent with Olmsted Syndrome. Oral retinoids with topical keratolytics afforded significant improvement with increased hand mobility. Although there is no curative management for these patients, current experimental therapies like epidermal growth factor receptor (EGFR) inhibitors and Transient Receptor Potential Vanilloid-3 (TRPV3) antagonists are promising. Olmsted Syndrome is a rare genodermatosis with 73 cases officially reported as of this writing. This is the first case to be reported from the Philippines.
Human ; Male ; Child: 6-12 Yrs Old ; Keratoderma, Palmoplantar ; Acitretin
6.A case of systematized epidermal nevus (Nevus Unius Lateris) in a 20-year-old Filipino female treated with ablative CO2 laser and topical tretinoin
Maria Emilia Ruth V. Eusebio ; Emy Christine C. Onishi-Limchoa ; Doha Mae Laurisse M. Manalo-Legas
Acta Medica Philippina 2024;58(17):88-93
This is a case of a 20-year-old female with no known comorbidities presenting with verrucous plaques arranged in a unilateral blaschkoid distribution at birth. Biopsy was consistent with epidermal nevus hence patient was diagnosed as systematized epidermal nevus, Nevus Unius Lateris type. Gold standard treatment is full thickness surgical excision however, due to the extensive involvement, treatment of this condition remains a challenge. Hence, non-surgical combination of ablative CO2 laser and topical tretinoin 0.1% were done. Thinner lesions (1-3 mm) showed lower recurrence (50%) as compared to thicker lesions (>3 mm) showing 100% recurrence after six months. Hence, another CO2 laser session is needed. Quality of life was measured using the Dermatologic Life Quality Index (DLQI) with noted 35% improvement post-treatment.
CO2 laser
;
lasers, gas
;
tretinoin
;
retinoids
7.A tale of scales: Siblings with lamellar ichthyosis treated with acitretin.
Patricia Anne Nicole O. RAMIREZ-ECARMA ; Jerlyn Maureen P. SERVAS ; Alexis Paula D. IBAÑEZ ; Patricia Ysabel G. ORETA-ARBOLEDA ; Ma. Angela M. LAVADIA ; Lily Lyralin L. TUMALAD
Journal of the Philippine Medical Association 2024;103(1):94-104
INTRODUCTION
Lamellar ichthyosis (LI) is an inherited rare disorder characterized by generalized scaling presenting at birth and persisting throughout life. It presents at birth with a collodion membrane, later developing into large, brown scales across the skin. LI requires ongoing treatment and monitoring due to physical and psychosocial impacts. This study highlights siblings who showed substantial quality-of-life improvements with oral retinoid therapy.
OBJECTIVETo present and discuss a detailed case summary, explore management options, and evaluate the treatment outcomes.
CASE SUMMARYWe report on a pair of siblings, a 24-year-old male and a 19-year-old female, who were born encased in a collodion membrane, and later presented with large, brown, plate-like scales all over the body. Skin changes were accompanied by intermittent heat intolerance and mild ectropion, which subsequently caused impaired quality of life while growing up. Histopathology results were consistent with lamellar ichthyosis. Both siblings responded well to oral Acitretin at 0.5 mglkglday, showing significant shedding of thick scales and a reduction of ectropion within the first two weeks of therapy.
CONCLUSIONLamellar ichthyosis, a severe, lifelong disorder with psychosocial repercussions, requires long-standing, continual therapy. Maximizing treatment options with oral acitretin, addressing the psychosocial implications of the disease and getting patients actively involved in its management results in better treatment outcomes.
Human ; Male ; Female ; Young Adult: 19-24 Yrs Old ; Ichthyosis, Lamellar ; Acitretin
9.An Artificial Neural Network Model Combined with Dietary Retinol Intake from Different Sources to Predict the Risk of Nonalcoholic Fatty Liver Disease.
Can LIU ; Shi Hui ZHOU ; Hong SU ; Wen Qin YANG ; Jiao LU
Biomedical and Environmental Sciences 2023;36(12):1123-1135
OBJECTIVE:
This study aimed to develop an artificial neural network (ANN) model combined with dietary retinol intake from different sources to predict the risk of non-alcoholic fatty liver disease (NAFLD) in American adults.
METHODS:
Data from the 2007 to 2014 National Health and Nutrition Examination Survey (NHANES) 2007-2014 were analyzed. Eligible subjects ( n = 6,613) were randomly divided into a training set ( n 1 = 4,609) and a validation set ( n 2 = 2,004) at a ratio of 7:3. The training set was used to identify predictors of NAFLD risk using logistic regression analysis. An ANN was established to predict the NAFLD risk using a training set. Receiver operating characteristic (ROC) curve analysis was performed to evaluate the accuracy of the model using the training and validation sets.
RESULTS:
Our study found that the odds ratios ( ORs) and 95% confidence intervals ( CIs) of NAFLD for the highest quartile of plant-derived dietary retinol intake (i.e., provitamin A carotenoids, such as β-carotene) ( OR = 0.75, 95% CI: 0.57 to 0.99) were inversely associated with NAFLD risk, compared to the lowest quartile of intake, after adjusting for potential confounders. The areas under the ROC curves were 0.874 and 0.883 for the training and validation sets, respectively. NAFLD occurs when its incidence probability is greater than 0.388.
CONCLUSION
The ANN model combined with plant-derived dietary retinol intake showed a significant effect on NAFLD. This could be applied to predict NAFLD risk in the American adult population when government departments formulate future health plans.
Adult
;
Humans
;
Vitamin A
;
Non-alcoholic Fatty Liver Disease/epidemiology*
;
Nutrition Surveys
;
Diet
;
Neural Networks, Computer
10.Loss of RBFOX2 inhibits meiotic initiation in male mice.
Lin YAN ; Jian CHEN ; Yan NING ; Chunsheng HAN
Chinese Journal of Biotechnology 2023;39(10):4108-4122
Meiotic initiation is a critical step in gametogenesis. Recently, some genes required for meiotic initiation have been identified. However, meiosis-initiating factors and the underlying mechanisms are far from being fully understood. We have established a long-term culture system of spermatogonial stem cells (SSCs) and an in vitro model of meiotic initiation using mouse SSCs. Our previous study revealed that the RNA-binding protein RBFOX2 may regulate meiotic initiation, but the role and the mechanism need to be further elucidated. In this study, we constructed RBFOX2 knockdown SSC lines by using lentivirus-mediated gene delivery method, and found that the knockdown SSCs underwent normal self-renewal, mitosis and differentiation. However, they were unable to initiate meiosis when treated with retinoic acid, and they underwent apoptosis. These results indicate that RBFOX2 plays an essential role in meiotic initiation of spermatogonia. This work provides new clues for understanding the functions of RNA-binding proteins in meiotic initiation.
Mice
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Male
;
Animals
;
Spermatogonia/metabolism*
;
Meiosis/genetics*
;
Cell Differentiation
;
Tretinoin/pharmacology*
;
Mitosis
;
Testis/metabolism*


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