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Vitamin D deficiency in patients with cystic fibrosis: a systematic review and meta-analysis.
Farahbakhsh, Nazanin; Fatahi, Somaye; Shirvani, Armin; Motaharifard, Monireh Sadat; Mohkam, Masoumeh; Tabatabaii, Seyed Ahmad; Khanbabaee, Ghamartaj; Yaghoobpoor, Shirin; Davoodi, Seyedeh Zahra; Hosseini, Amir Hossein.
  • Farahbakhsh N; Department of Pediatric Pulmonology, Mofid Pediatrics Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Fatahi S; Department of Clinical Nutrition and Dietetics, Faculty of Nutrition and Food Technology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Shirvani A; Pediatric Gastroenterology, Hepatology, and Nutrition Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Motaharifard MS; Faculty of Medical Education, Shahid Beheshty University of Medical Sciences, Tehran, Iran.
  • Mohkam M; Pediatric Nephrology Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Tabatabaii SA; Pediatric Nephrology Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Khanbabaee G; Department of Pediatric Pulmonology, Mofid Pediatrics Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Yaghoobpoor S; Department of Pediatric Pulmonology, Mofid Pediatrics Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Davoodi SZ; Student Research Committee, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Hosseini AH; Student Research Committee, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
J Health Popul Nutr ; 43(1): 11, 2024 Jan 17.
Article en En | MEDLINE | ID: mdl-38233891
ABSTRACT

AIM:

Vitamin D is a prominent modulator of immunity and respiratory function. It plays a vital role in respiratory diseases such as cystic fibrosis (CF). S. However, there is a dearth of information on patients with CF. The purpose of the meta-analysis is to highlight the importance of following the existing guidelines regarding maintenance of Vitamin D serum levels in patients with CF.

METHODS:

The systematic search was conducted without utilizing any time or language limitations in original database from the beginning until March 2022. The meta-analysis was performed using a random-effects model. Heterogeneity was determined by I2 statistics and Cochrane Q test.

RESULTS:

Pooled analysis using the random-effects model of the 8 case-control studies with 13 effect sizes revealed that the serum 25-OH-vitamin D in participants with cystic fibrosis was significantly lower than controls in pediatrics and adolescences (WMD - 3.41 ng/ml, 95% CI - 5.02, - 1.80, p = < 0.001) and adults (WMD - 2.60 ng/ml, 95% CI - 4.32, - 0.89, p = 0.003). Based on data from 12 studies (21 effect sizes) with a total of 1622 participants, the prevalence of vitamin D levels of 20-30 ng/ml in CF patients was 36% among pediatrics/adolescents and 63% among adults. In addition, 27% of pediatric/adolescent CF patients and 35% of adult CF patients had vitamin D levels of below 20 ng/ml.

CONCLUSIONS:

As a result, according to the existing guidelines, our results proved the need to pay attention to the level of vitamin D in these patients.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Deficiencia de Vitamina D / Fibrosis Quística Tipo de estudio: Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Adolescent / Adult / Child / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Deficiencia de Vitamina D / Fibrosis Quística Tipo de estudio: Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Adolescent / Adult / Child / Humans Idioma: En Año: 2024 Tipo del documento: Article