EMBO: Researchers from the University of Helsinki, Finland, found that diet
could have a strong impact on the progression of mitochondrial disease.
In their study, published in EMBO Molecular Medicine,
low-carbohydrate diet aggravated muscle damage in patients with a
mitochondrial muscle disease called “progressive external
ophthalmoplegia” (PEO). However, damage was not permanent. The patients
recovered quickly and short-term muscle damage eventually resulted in a
modest improvement of muscle strength in the long run. However, more
research is needed before diet change is used as a tool in therapeutic
strategy.
Mitochondrial diseases are a group of disorders that result from
defects in mitochondria, specialized cellular compartments that convert
nutrition into chemical energy the cell can use. In PEO, the muscles of
the eyes are affected, leading to limitations in eye movement and
drooping eyelids. In addition, patients often suffer from weakness of
muscles in the arms or legs, particularly during exercise.
“Since mitochondria turn the food we eat into energy, we expected
that diet should have an impact on disease progression,” said Anu
Suomalainen, senior author of the publication. After promising results
from mouse experiments, Suomalainen and her colleagues set out to test
this notion in a small pilot trial comprising five PEO patients and ten
control subjects.
All participants were switched to a high-fat, low-carbohydrate
“modified Atkins” diet. Contrary to the researchers’ expectations, the
primary reaction of the patients to the diet was detrimental. They
suffered from progressive muscle pain and showed signs of muscle damage
so that the trial was prematurely discontinued after a maximum of 11
days on the diet. However, the patients recovered quickly and 2.5 years
later, they had actually gained in muscle strength as compared to
pre-diet state. Apparently, the short-term muscle damage induced by diet
had a modest beneficial impact in the long run.
A thorough examination of the patients allowed the researchers to
explain this devious route to improvement. They showed that modified
Atkins diet selectively kills muscle fibers that were already damaged
through disease-related mitochondrial dysfunction. Whereas most body
cells can use a broad range of biomolecules as fuel, pre-damaged fibers
apparently depend on carbohydrates. If carbohydrates are not provided in
the diet the fibers die, explaining the short-term adverse reactions of
the patients. The scientists speculate that this could stimulate muscle
regeneration: healthy satellite cells - muscle stem cells - are
activated; they divide and eventually fuse with existing muscle fibers,
supplying them with healthy mitochondria.
The results point to the potential of using dietary change as a
therapeutic strategy, although in a carefully controlled clinical
setting. In fact, caution is required. Low-carbohydrate diet can lead to
long-term improvement but can also cause muscle damage. This
observation also casts light on the alleged safety of low-carbohydrate
diets as a means of weight loss. For some people with subclinical
mitochondrial diseases, it may have adverse side effects on muscles.
Modified Atkins diet induces subacute selective ragged-red-fiber-lysis in mitochondrial myopathy patients
Ahola
S, Auranen M, Isohanni P, Niemisalo S, Urho N, Buzkova J, Velagapudi V,
Lundbom N, Hakkarainen A, Muurinen T, Piirilä P, Pietiläinen KH,
Suomalainen A.
Read the paper:
doi: 10.15252/emmm.201606592