Literature DB >> 17412651

Hypomagnesaemia in cystic fibrosis patients referred for lung transplant assessment.

A Gupta1, K M Eastham, N Wrightson, D A Spencer.   

Abstract

BACKGROUND: Hypomagnesaemia in patients with cystic fibrosis (CF) is under-recognized although the true incidence is unknown. Many patients are asymptomatic, although severe deficiency may be associated with muscle weakness, cramps and tetany. Hypomagnesaemia may be a risk factor for post-transplant complications including convulsions, which may be exacerbated by the use of calcineurin inhibitors. The aims of the present study were to describe serum magnesium levels and to investigate the relationship between magnesium levels and age, and renal function measurements in patients with CF referred to a transplant centre for lung transplant assessment.
METHODS: We reviewed the data of all 106 CF patients referred for transplant assessment from January 1995 to December 2003. Demographic and biochemical data were recorded and the explanatory variables were subjected to univariate analysis and linear regression analysis.
RESULTS: Mean serum magnesium level was 0.75 mmol/L (range 0.46-1.03, normal range 0.74-1.1). 57% of patients had hypomagnesaemia. Serum magnesium levels were not associated with age, serum creatinine or GFR.
CONCLUSIONS: Hypomagnesaemia is a common finding in patients with CF referred for lung transplant assessment. Serum magnesium levels should be monitored in all CF patients being referred for lung transplant irrespective of the results of other renal function tests.

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Year:  2007        PMID: 17412651     DOI: 10.1016/j.jcf.2007.01.004

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  8 in total

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Journal:  J Bacteriol       Date:  2017-10-31       Impact factor: 3.490

2.  Magnesium Status and Calcium/Magnesium Ratios in a Series of Cystic Fibrosis Patients.

Authors:  Marlene Fabiola Escobedo-Monge; Enrique Barrado; Joaquín Parodi-Román; María Antonieta Escobedo-Monge; Marianela Marcos-Temprano; José Manuel Marugán-Miguelsanz
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3.  A neutrophil intrinsic impairment affecting Rab27a and degranulation in cystic fibrosis is corrected by CFTR potentiator therapy.

Authors:  Kerstin Pohl; Elaine Hayes; Joanne Keenan; Michael Henry; Paula Meleady; Kevin Molloy; Bakr Jundi; David A Bergin; Cormac McCarthy; Oliver J McElvaney; Michelle M White; Martin Clynes; Emer P Reeves; Noel G McElvaney
Journal:  Blood       Date:  2014-06-16       Impact factor: 22.113

4.  Function and regulation of TRPM7, as well as intracellular magnesium content, are altered in cells expressing ΔF508-CFTR and G551D-CFTR.

Authors:  F Huguet; M L Calvez; N Benz; S Le Hir; O Mignen; P Buscaglia; F D Horgen; C Férec; M Kerbiriou; P Trouvé
Journal:  Cell Mol Life Sci       Date:  2016-02-13       Impact factor: 9.207

Review 5.  Mg2+ Transporters in Digestive Cancers.

Authors:  Julie Auwercx; Pierre Rybarczyk; Philippe Kischel; Isabelle Dhennin-Duthille; Denis Chatelain; Henri Sevestre; Isabelle Van Seuningen; Halima Ouadid-Ahidouch; Nicolas Jonckheere; Mathieu Gautier
Journal:  Nutrients       Date:  2021-01-13       Impact factor: 5.717

6.  Magnesium Status and Ca/Mg Ratios in a Series of Children and Adolescents with Chronic Diseases.

Authors:  Marlene Fabiola Escobedo-Monge; Enrique Barrado; Joaquín Parodi-Román; María Antonieta Escobedo-Monge; María Carmen Torres-Hinojal; José Manuel Marugán-Miguelsanz
Journal:  Nutrients       Date:  2022-07-18       Impact factor: 6.706

Review 7.  Update on the management of vitamins and minerals in cystic fibrosis.

Authors:  Senthilkumar Sankararaman; Sara J Hendrix; Terri Schindler
Journal:  Nutr Clin Pract       Date:  2022-08-23       Impact factor: 3.204

8.  Stenotrophomonas maltophilia virulence and specific variations in trace elements during acute lung infection: implications in cystic fibrosis.

Authors:  Arianna Pompilio; Domenico Ciavardelli; Valentina Crocetta; Ada Consalvo; Roberta Zappacosta; Carmine Di Ilio; Giovanni Di Bonaventura
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  8 in total

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