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Aging Genetics Genomics Longevity

Genetic “Ageotypes” predict health as we age

Stanford’s Michael Snyder has categorized how humans age into different classes called “ageotypes”: metabolic, immune, hepatic and nephrotic.

43 healthy men and women between the ages of 34 and 68 were profiled, with extensive measurements of certain microbes and biological molecules, such as proteins, metabolites and lipids, taken at least five times over two years.

Snyder said that the study enabled the researchers to see clear patterns of how individuals experience aging on a molecular level and help them focus on health-risk factors and find the areas in which they’re most likely to encounter problems in the future.

For example, those who are metabolic agers might be at a higher risk for diabetes or show signs of elevated hemoglobin A1c as they grow older. Immune agers might generate higher levels of inflammatory markers or be more prone to immune-related diseases as they age. The ageotypes are not mutually exclusive. They signify the pathways in which increases in aging biomarkers are most pronounced

Differences in aging between healthy and insulin resistant participants were studied for the first time. Snyder discovered 10 molecules that significantly differed between insulin-sensitive and insulin-resistant people as they age. Many of those markers were involved in immune function and inflammation.

In some people, their markers decreased, at least for a short period, when they changed their behavior. The overall rate at which they aged declined, and in some cases aging markers decreased. This occured in molecules including hemoglobin A1c and creatine, a marker for kidney function, among a small subset of participants.

In that subset, Snyder said, there were individuals who made lifestyle changes to slow their aging rate. Among those who exhibited decreased levels of hemoglobin A1c, many had lost weight, and one made dietary changes. Some who saw a decrease in creatine, indicating improved kidney function, were taking statins. In other cases, exactly why rates of aging markers waned was unclear. For some people, there were no obvious behavioral changes, yet the team still saw a decreased rate of aging along their ageotype pathways. There was also a handful of people that maintained a slower-than-average aging rate throughout the entire study.

Prof Snyder was a speaker at the 2019 ApplySci conference at Stanford.


Join ApplySci at the 13th Wearable Tech + Digital Health + Neurotech Silicon Valley conference on February 11-12, 2020 at Quadrus Sand Hill Road.  Speakers include:  Zhenan Bao, Stanford – Vinod Khosla, Khosla Ventures – Mark Chevillet, Facebook – Shahin Farshchi, Lux Capital – Carla Pugh, Stanford – Nathan Intrator, Tel Aviv University | Neurosteer – Wei Gao, Caltech – Sergiu Pasca, Stanford – Walter Greenleaf, Stanford – Sheng Xu, UC San Diego – Dror Ben-Zeev, University of Washington – Mikael Eliasson, Roche  – Unity Stoakes, StartUp Health – Garth Smith, Ontario Brain Institute – Erika Ross, Abbott Neuromodulation

Categories
Featured Genomics Longevity

George Church on reversing aging | ApplySci @ Harvard

George Church again keynoted the ApplySci Boston conference, this year at Harvard Medical School on November 14, 2019.

Click to view his groundbreaking talk on reversing aging.


Join ApplySci at the 13th Wearable Tech + Digital Health + Neurotech Silicon Valley conference on February 11-12, 2020 at Quadrus Sand Hill Road.  Speakers include:  Zhenan Bao, Stanford – Vinod Khosla, Khosla Ventures – Mark Chevillet, Facebook – Shahin Farshchi, Lux Capital – Carla Pugh, Stanford – Nathan Intrator, Tel Aviv University | Neurosteer – Wei Gao, Caltech – Sergiu Pasca, Stanford – Walter Greenleaf, Stanford – Sheng Xu, UC San Diego – Dror Ben-Zeev, University of Washington – Mikael Eliasson, Roche  – Unity Stoakes, StartUp Health – Garth Smith, Ontario Brain Institute

Categories
Brain Longevity Seniors

Biological age blood test could identify dementia risk

King’s College London professor James Timmons has developed a gene signature blood test that he believes could be used to predict Alzheimer’s disease.  His goal is early detection and preventative treatment. The test is the first to  measure biological age.

Researchers analyzed  thousands of blood, brain and muscle samples to find 150 markers of gene activity associated with good health at age 65.  This produced a rating system that could be incorporated into a blood test.

700 healthy 70 year olds had widely varied healthy aging scores. Higher scores were associated with better mental ability, kidney function and longevity over 12 years. Low scores were linked to Alzheimer’s.

According to Timmons, “This is the first blood test of its kind that has shown that the same set of molecules are regulated in both the blood and the brain regions associated with dementia, and it can help contribute to a dementia diagnosis. This also provides strong evidence that dementia in humans could be called a type of ‘accelerated ageing’ or ‘failure to activate the healthy aging program’.”

Categories
Longevity

Algorithm identified genes could be “turned off” for anti aging effect

http://www.cs.tau.ac.il/~ruppin/mta_aging.pdf

Tel Aviv University Professor Eytan Ruppin‘s lab has developed an algorithm to predict which genes can be “turned off” to create the same anti-aging effect as calorie restriction.

“Most algorithms try to find drug targets that kill cells to treat cancer or bacterial infections,” said Keren Yizhak, lead researcher. “Our algorithm is the first in our field to look for drug targets not to kill cells, but to transform them from a diseased state into a healthy one.”

Professor Ruppin is a leader in genomic scale metabolic monitoring, which describes the metabolism of living cells.  Yizhak’s “metabolic transformation algorithm” can take information about any two metabolic states and predict environmental or genetic changes required to go from one to the other.

Categories
Data Longevity

Protective genes vs lifestyle for longevity

http://ngm.nationalgeographic.com/2013/05/longevity/hall-text

Scientists studying longevity have begun using powerful genomic technologies, basic molecular research, and, most important, data on small, genetically isolated communities of people to gain increased insight into the maladies of old age and how they might be avoided.