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Long term magnesium supplementation influences favourably the natural evolution of neuropathy in Mg-depleted type 1 diabetic patients (T1dm)

De Leeuw I, Engelen W, De Block C, Van Gaal L

Magnesium research · 18 citas

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Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación no declarada

Publicación

Publicado
2004-06-01 · Magnes Res · vol. 17 · número 2 · págs. 109–14
Editorial
National Institutes of Health
Citado
39 citas · más que el 80% de estudios similares · 1.4× el promedio de su campo
Referencias
0 trabajos
Acceso
De pago
Áreas de investigación
Magnesium in Health and Disease · Peripheral Neuropathies and Disorders · Alcoholism and Thiamine Deficiency
Palabras clave
magnesium supplementation, type 1 diabetes, diabetic polyneuropathy, hypomagnesemia, erythrocyte magnesium, long-term glycemic control, disease progression, diabetes duration, diabetic ketoacidosis
MeSH
humans, diabetic neuropathies, diabetes mellitus, type 1, magnesium, dietary supplements, adult, female, male

4 autores

  • Ivo De Leeuw🇧🇪Antwerp University Hospital
  • Wendy Engelen
  • Christophe E.M. De Block
  • Luc Van Gaal

Resumen

El texto original del estudio, en el idioma en que se publicó.

Chronic Mg depletion in T1dm has been linked to polyneuropathy (PNP). Short term Mg supplementation has suggested a decrease in pathological EMG signs typical for PNP. The aim of this study is to determine if long term supplementation under stable metabolic control can normalize the Mg status and influence the natural evolution of PNP. 110 T1dm (60 M,50 W) with chronic Mg depletion (erythrocyte Mg < 2.3 mMol/l) were randomised to receive 300 mg Mg++ daily or no supplement for a period of 5 years. Follow-up was organized by the same diabetologist: HbA1c, renal function and Mg status every 3 months, electromyography (EMG) and clinical neurological control with staging every year. Drop-out was decided for recurrent DKA, diseases or drugs interfering with Mg status or side-effects of Mg treatment. 97 patients (53 M,44 W) finished the study: 49 (27 M,22W) were supplemented (group A) and 48 (26 M,22 W) served as controls (group B). At the start there were no significant differences between both groups. HbA1c after 5 years (A:7.80% sd 0.80, B:7.75% sd 0.75) was not significantly different from the start. Erythrocyte Mg (Mg rbc) rose significantly (p < 0.0001) in group A to normal levels but remained low in group B. Staging of PNP after 5 years shows a decrease in 39%, statu quo in 49% and a worsening in 12% in group A and 8,31 and 61% respectively in group B (Fisher Exact test: p < 0.0001). Normalization of EMG signs was only seen in incipient PNP. Logistic regression analysis shows that longer duration of diabetes (p < 0.006) and low Mgrbc (p < 0.05) are the major determinants of PNP evolution. Under stable metabolic control long term Mg supplementation is able to restore a normal Mg status and influence favourably the natural evolution of PNP as compared to non supplemented T1dm controls.

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