Sunday, February 8, 2015

Cooking Food at High Temperatures Ups Dangerous AGEs

A new study demonstrates that cooking foods at high temperatures increases the risk of Alzheimer's. The study looked at the Advanced Glycation End products (AGEs) in national diets, then compared total AGEs to Alzheimer's disease rates. Find out more.



A new paper published in the Journal of Alzheimer's Disease provides evidence that cooking foods at high temperatures increases the risk of Alzheimer's disease. This study looked at the content of Advanced Glycation End products (AGEs) in national diets and clinical studies, and compared total AGEs to Alzheimer's disease rates.

AGEs are a group of compounds that are combinations of sugars and proteins and other large molecules. They can be formed in the body, and there is a large body of literature on AGEs and Alzheimer's disease. However, AGEs are also formed when food is cooked at high temperatures or aged for a long time such as in hard cheese. AGEs increase the risk of various chronic diseases through several mechanisms including increased inflammation and oxidative stress.

Our newly published paper is the first that estimated the AGE content of diets from observational studies in various countries, which estimated the link between dietary factors and risk of Alzheimer's disease. For this purpose, the values for AGE for many types of food were taken from a study by researchers at the Mount Sinai School of Medicine in New York. They cooked 549 foods by different methods and measured the AGE content of the cooked food. They found that the higher the cooking temperature, the higher the AGE content. For example, 100 grams of raw beef had 707 kU of AGEs, but 100 grams of roast beef had 6071 kU.

To use their findings in our study, we obtained information from observational studies in which diet was assessed using food frequency questionnaires or from national dietary supply values from the Food and Agriculture Organization of the United Nations. We then used either a range of cooking temperatures or methods for the observational studies or an estimate of average cooking methods and temperatures for the national dietary supply data.

In typical national diets, we found that meat made the highest contribution of AGEs, followed by vegetable oils, cheese, and fish. Foods such as cereals/grains, eggs, fruit, legumes, milk, nuts, starchy roots, and vegetables generally make low contributions to the total amount of AGEs in a diet, either because they are generally prepared at low temperatures or since they comprise smaller portions of diets.

According to Drs. Jaime Uribarri and Weijing Cai of The Icahn School of Medicine at Mount Sinai, "This epidemiological study supports our previous findings in animals and humans of an important role for dietary AGEs in Alzheimer's disease. We found that mice kept on a diet high in AGEs, similar to Western diet, had high levels of AGEs in their brains together with deposits of amyloid-β, a component of the plaques characteristic of Alzheimer's disease, while at the same time developed declines in cognitive and motor abilities. The mice fed a low AGE diet remained free of these conditions. In addition, clinical studies have shown that subjects with higher blood AGE levels, in turn resulting from high AGE diets, are more likely to develop cognitive decline on follow up.

The findings point to an easily achievable goal that could reduce the risk of dementia through the consumption of non-AGE-rich foods, for example, foods that cooked or processed under lower heat levels and in the presence of more water, raising the importance of not just what we eat, but also how we prepare what we eat."

Source:


Journal Reference:
  1. Perrone L, Grant WB. Observational and ecological studies of dietary advanced glycation end products in national diets and Alzheimer’s disease incidence and prevalence. Journal of Alzheimer’s Disease, February 2015 DOI: 10.3233/JAD-140720

1 comment:

  1. L-carnosine is a antiglicating, or Anti Advanced End Products(anti-A.G.E. supplements),and is a heavy metal chelators,peroxinitrite scavengers ,etc.About Carnosine , we can read that : 1) Journal PLoS One. 2013 Jul.title:Anti-aggregating effect of the naturally occurring dipeptide carnosine on aβ1-42 (betamyloid) fibril formation. Authors : professor Aloisi A and colleagues from the National Nanotechnology Laboratory , Istituto Nanoscienze Lecce,Italy.In the article we can read that : Overall, our results suggest an effective role of Carnosine against Aβ1-42 (betamyloid) aggregation. 2) Journal of Dermatological Treatment. 2012 October , with the title : Skin Beautification With Oral Non-Hydrolized Versions of Carnosine and Carcinine: Effective Therapeutic Management and Cosmetic Skincare Solutions Against Oxidative Glycation and Free-Radical Production as a Causal Mechanism of Diabetic Complications and Skin Aging , where we can read that : Advanced glycation Maillard reaction end products (AGEs) are causing the complications of diabetes and skin aging, primarily via adventitious and cross-linking of proteins… The finding that already-formed AGE cross-links can be pharmacologically severed and attendant pathology thereby reversed by non-hydrolized carnosine…”
    3) Journal of Alzheimers Disease . 2007 May. ” Could Carnosine or Related Structures Suppress Alzheimer's Disease?” author:professor Hipkiss ,from the Centre for Experimental Therapeutics, the London Queen Mary's School of Medicine and Dentistry, England , where we can read that : “These observations suggest that carnosine and related structures should be explored for therapeutic potential towards AD and other neurodegenerative disorders.”
    The interesting is that the very small doses , as 60(sixty)mg. to 80(eighty) miligrams three times a day(Only under physician prescription) looks to gives the best results.

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