Abnormal lipid metabolism in fat cells predicts future weight gain and diabetes in women
The inefficient breakdown
of fats foretells later metabolic complications such as type 2 diabetes in
women and weight gain. Low levels of hormone-stimulated lipolysis -- a
biochemical process by which triglycerides (Cholesterol, lipid) are broken down
into energy-rich fatty acids -- were related with weight gain and metabolic
problems in future. To detect impedances in hormone-stimulated
lipolysis, researchers created an algorithm using clinical and blood
measures.
Researchers believed that their
proposed algorithm could be helpful in identifying subjects with a high risk of
becoming overweight or obese. These findings may well be utilized by clinicians
to determine who would benefit the most from intensified lifestyle
interventions such as physical activity, which improves hormone-stimulated
lipolysis and may therefore prevent metabolic disturbances and fat accumulation.
Researchers took biopsies of
subcutaneous fat tissue from healthy and non-obese 89 women, and followed up 13
years later. The women who gained weight within the between times showed a 50% diminish
in hormone-stimulated lipolysis and a 50% increment in spontaneous lipolysis compared
with weight-stable individuals. Moreover, lower expression of genes involved in
regulating lipolysis was related with later weight gain.
Therefore it can be concluded
that insufficient lipolysis which cannot be satisfactorily quickened by hormone
stimulation, may shift the balance in lipid turnover towards uptake, which
facilitates fat mass accumulation.
Instead of tissue biopsies, the
researchers next constructed an algorithm to estimate hormone-stimulated
lipolysis based on clinical and blood measures. To distinguish parameters for
this metabolic measure, researchers analysed information from 1,045 subjects.
They found six parameters which included fasting plasma HDL
cholesterol, waist circumference, fasting plasma adrenaline, fasting serum
insulin, body weight and fasting plasma glycerol divided by total body fat.
In a subset of 226 subjects, the
algorithm predicted high or low lipolytic activity with approximately 75%
specificity and greater than 80% sensitivity. When tested in a separate group
of 14 individuals, the algorithm corresponded well with measured levels of
hormone-stimulated lipolysis and predicted weight changes over time.
These results suggest that the
algorithm could be used to estimate hormone-stimulated lipolysis rather than tissue
biopsies in a routine clinical practice. However, future studies are needed to implement
the algorithm in larger groups of people and to decide whether the findings of
this study also apply to men.
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