Meta menu:

From here, you can access the Emergencies page, Contact Us page, Accessibility Settings, Language Selection, and Search page.

  • Go to Emergencies.
  • Current language selection: EN

    Change language selection to:

  • Contact us:

    Campus Charité MitteCharitéplatz 1 (local address: Luisenstraße 13)
    10117 Berlin

    Campus Virchow-KlinikumAugustenburger Platz 1 (local address: Südring 4)
    13353 Berlin

    Campus Benjamin FranklinHindenburgdamm 30 (local address: Haus V, Eingang West)
    12203 Berlin

  • Accessibility:
    Contrast Settings Change contrast
    Font size
    Font size bigger: STRG+ Font size smaller: STRG-

    You can enlarge or reduce the browser window. Please use CTRL and + to zoom in or CTRL and - to zoom out. Press CTRL and 0 to reset your browser window to normal size.

Open Menu
© Charité | Wiebke Peitz

Press release

15.03.2011

Magnesium deficiency: not always a nutritional problem

Back to Overview

You are here:

Scientists of the Charité decipher genetic defect

Researchers and scientists of the Charité – Universitätsmedizin Berlin, in cooperation with the Max Delbrück Center for Molecular Medicine, and colleagues from the Netherlands, Belgium, Switzerland and the Czech Republic have succeeded in identifying a genetic cause of magnesium deficiency. The study from Dr. Dominik Müller of the Department of Pediatric Nephrology, ascertained changes in a gene which is involved in the regulation of magnesium processes involved in the kidney. This research which is published in the current issue of the journal "American Journal of human genetics", opens the way for possible future medicinal treatment of genetically caused magnesium deficiencies.

A magnesium deficiency, with symptoms of fatigue and muscle weakness up to severe seizures and heart rhythm disturbances, may also be associated with diabetes and high blood pressure and have up till now been mostly explained by dietary insufficiencies. Dr. Müller and his team have now shown that an altered gene may be the cause for this deficiency. Changes in a gene (Cnnm2), entail changes in the human blueprint and thus in the structure and function of protein sequence. In this case, the change affects a protein that is anchored in the membrane of kidney cells and intestinal cells and is responsible for the absorption of magnesium in the blood stream. Since this process no longer works in the defective protein, the magnesium is not put into the blood stream but excreted through the intestine and the urine and therefore forfeited. Dr. Mueller commented on his research results as follows: "Our results provide us with a number of new insights into magnesium metabolism in the body. In the end, following further research and development, we see the possibility to deal with such deficiencies medicinally "

Stuiver et al., CNNM2, Encoding a Basolateral Protein Required for Renal Mg2+ Handling, Is Mutated in Dominant Hypomagnesemia, The American Journal of Human Genetics (2011), doi:10.1016/j.ajhg.2011.02.005

Contact

Priv.-Doz. Dr. Dominik Müller
Klinik für Pädiatrie mit Schwerpunkt Nephrologie
Campus Virchow-Klinikum
t: +49 30 450 616 147



Back to Overview