In this issue

Jonathan Tobin: Defending the Right to a Jewish State

Heather Hale: Compliment your kids without giving them big heads

Megan Shauri: 10 ways you are ruining your own happiness

Carolyn Bigda: 8 Best Dividend Stocks for 2015

Kiplinger's Personal Finance editors: 7 Things You Didn't Know About Paying Off Student Loans

Samantha Olson: The Crucial Mistake 55% Of Parents Are Making At Their Baby's Bedtime

Densie Well, Ph.D., R.D. Open your eyes to yellow vegetables

The Kosher Gourmet by Megan Gordon With its colorful cache of purples and oranges and reds, COLLARD GREEN SLAW is a marvelous mood booster --- not to mention just downright delish
April 18, 2014

Rabbi Yonason Goldson: Clarifying one of the greatest philosophical conundrums in theology

Caroline B. Glick: The disappearance of US will

Megan Wallgren: 10 things I've learned from my teenagers

Lizette Borreli: Green Tea Boosts Brain Power, May Help Treat Dementia

John Ericson: Trying hard to be 'positive' but never succeeding? Blame Your Brain

The Kosher Gourmet by Julie Rothman Almondy, flourless torta del re (Italian king's cake), has royal roots, is simple to make, . . . but devour it because it's simply delicious

April 14, 2014

Rabbi Dr Naftali Brawer: Passover frees us from the tyranny of time

Greg Crosby: Passing Over Religion

Eric Schulzke: First degree: How America really recovered from a murder epidemic

Georgia Lee: When love is not enough: Teaching your kids about the realities of adult relationships

Cameron Huddleston: Freebies for Your Lawn and Garden

Gordon Pape: How you can tell if your financial adviser is setting you up for potential ruin

Dana Dovey: Up to 500,000 people die each year from hepatitis C-related liver disease. New Treatment Has Over 90% Success Rate

Justin Caba: Eating Watermelon Can Help Control High Blood Pressure

The Kosher Gourmet by Joshua E. London and Lou Marmon Don't dare pass over these Pesach picks for Manischewitz!

April 11, 2014

Rabbi Hillel Goldberg: Silence is much more than golden

Caroline B. Glick: Forgetting freedom at Passover

Susan Swann: How to value a child for who he is, not just what he does

Cameron Huddleston: 7 Financial Tasks You Should Tackle Right Now

Sandra Block and Lisa Gerstner: How to Profit From Your Passion

Susan Scutti: A Simple Blood Test Might Soon Diagnose Cancer

Chris Weller: Have A Slow Metabolism? Let Science Speed It Up For You

The Kosher Gourmet by Diane Rossen Worthington Whitefish Terrine: A French take on gefilte fish

April 9, 2014

Jonathan Tobin: Why Did Kerry Lie About Israeli Blame?

Samuel G. Freedman: A resolution 70 years later for a father's unsettling legacy of ashes from Dachau

Jessica Ivins: A resolution 70 years later for a father's unsettling legacy of ashes from Dachau

Kim Giles: Asking for help is not weakness

Kathy Kristof and Barbara Hoch Marcus: 7 Great Growth Israeli Stocks

Matthew Mientka: How Beans, Peas, And Chickpeas Cleanse Bad Cholesterol and Lowers Risk of Heart Disease

Sabrina Bachai: 5 At-Home Treatments For Headaches

The Kosher Gourmet by Daniel Neman Have yourself a matzo ball: The secrets bubby never told you and recipes she could have never imagined

April 8, 2014

Lori Nawyn: At Your Wit's End and Back: Finding Peace

Susan B. Garland and Rachel L. Sheedy: Strategies Married Couples Can Use to Boost Benefits

David Muhlbaum: Smart Tax Deductions Non-Itemizers Can Claim

Jill Weisenberger, M.S., R.D.N., C.D.E : Before You Lose Your Mental Edge

Dana Dovey: Coffee Drinkers Rejoice! Your Cup Of Joe Can Prevent Death From Liver Disease

Chris Weller: Electric 'Thinking Cap' Puts Your Brain Power Into High Gear

The Kosher Gourmet by Marlene Parrish A gift of hazelnuts keeps giving --- for a variety of nutty recipes: Entree, side, soup, dessert

April 4, 2014

Rabbi David Gutterman: The Word for Nothing Means Everything

Charles Krauthammer: Kerry's folly, Chapter 3

Amy Peterson: A life of love: How to build lasting relationships with your children

John Ericson: Older Women: Save Your Heart, Prevent Stroke Don't Drink Diet

John Ericson: Why 50 million Americans will still have spring allergies after taking meds

Cameron Huddleston: Best and Worst Buys of April 2014

Stacy Rapacon: Great Mutual Funds for Young Investors

Sarah Boesveld: Teacher keeps promise to mail thousands of former students letters written by their past selves

The Kosher Gourmet by Sharon Thompson Anyone can make a salad, you say. But can they make a great salad? (SECRETS, TESTED TECHNIQUES + 4 RECIPES, INCLUDING DRESSINGS)

April 2, 2014

Paul Greenberg: Death and joy in the spring

Dan Barry: Should South Carolina Jews be forced to maintain this chimney built by Germans serving the Nazis?

Mayra Bitsko: Save me! An alien took over my child's personality

Frank Clayton: Get happy: 20 scientifically proven happiness activities

Susan Scutti: It's Genetic! Obesity and the 'Carb Breakdown' Gene

Lecia Bushak: Why Hand Sanitizer May Actually Harm Your Health

Stacy Rapacon: Great Funds You Can Own for $500 or Less

Cameron Huddleston: 7 Ways to Save on Home Decor

The Kosher Gourmet by Steve Petusevsky Exploring ingredients as edible-stuffed containers (TWO RECIPES + TIPS & TECHINQUES)

Jewish World Review

Saving Sight From Macular Degeneration: New Therapies Show Promise

By Claire Ainsworth

AMD is a disease of the macula, a pea-sized patch in the center of the retina

JewishWorldReview.com | It starts with a barely perceptible blurring of vision from time to time -- the sort of thing you might chalk up to getting older. But when you get it checked out, there's disturbing news: You have a disease called age-related macular degeneration, or AMD.

AMD can progress slowly or quickly, but there's no cure. Your hopes for an idyllic retirement -- reading all those books, driving to new places, or just enjoying a carefree independence -- are now clouded by uncertainty.

It's a depressing picture, and the odds are that one day it will happen to you or someone you know. People typically develop AMD after the age of 50, and it affects nearly 1 in 10 people over the age of 80. It's the most common cause of blindness in the West.

That picture may be about to change, however. A decade ago, an important insight into the biology of AMD led to an explosion of new strategies to treat it. And thanks to several anatomical peculiarities of the eye, it's an ideal test bed for therapies that would be riskier in other parts of the body.

As a result, AMD has been the focus of several high-tech approaches, ranging from RNA interference to gene therapy and stem cells. Some of the most promising will soon be tested in people and could become established therapies in the next decade.


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As its name suggests, AMD is a disease of the macula, a pea-sized patch in the center of the retina. Its high acuity allows you to see fine detail, such as the letters on a page.

The retina has several layers. Incoming light first reaches the photoreceptor cells, which turn it into electrical impulses. Underneath is a layer of supporting cells called the retinal pigmented epithelium, or RPE, which nourish the photoreceptors and clean up their waste. Below the RPE are the capillaries that form the retina's blood supply, but between blood and RPE is a thin layer called the blood-retinal barrier. Like the blood-brain barrier, this is only selectively permeable, keeping any toxins in the blood from reaching the delicate photoreceptors. It also helps to keep out the immune system and means that anything put into the eye is more likely to stay there.

The exact causes of AMD are still unclear, but the RPE cells appear to wither and die first. With their support system deteriorating, the photoreceptors die, too. People retain their fuzzier peripheral vision, but as the disease progresses, their central vision goes and with it the ability to read, drive or even recognize facial expressions.

"That is very isolating for people," says Barbara McLaughlan of the UK's Royal National Institute of Blind People. People with AMD in both eyes will typically become classed as legally blind between five and 10 years after the first symptoms appear.

For about 1 in 10 people with AMD, though, the disease suddenly progresses with terrifying speed. New blood vessels sprout under the retina, leaking blood and fluid. The macula swells and becomes scarred, and central vision can be lost in weeks. This form is known as wet AMD, while the slower version is the dry form.

Until recently, people with AMD had few options. They are advised to avoid smoking and eat a diet rich in zinc, beta-carotene and vitamins C and E, but that can only slow things down. Various forms of eye surgery and laser or light therapies are used to treat wet AMD but these are either risky or of limited help.

In the 1990s, however, studies of eye tissue taken at autopsy led to a key insight. The maculas of people with wet AMD had high levels of a signaling molecule called vascular endothelial growth factor (VEGF), which triggers the growth of new blood vessels.

The idea of blocking the action of this molecule has generated a host of treatment strategies. The most successful so far is an antibody fragment that binds to VEGF. Called Lucentis, it halts vision loss in about 95 percent of people with wet AMD, and restores some sight in more than a third.

"We had never seen anything like it," says Daniel Martin of the Cole Eye Institute, Cleveland, Ohio.

This approach is no panacea, though. For one thing the treatment must be injected into the eye every 4 to 6 weeks, and this occasionally triggers retinal detachment or an eye infection that can lead to blindness. It's also expensive: Lucentis, which is the only antibody-based drug approved to treat wet AMD, costs $2,000 a shot, although some clinics provide a cheaper unlicensed alternative.

Still, now that the principle of blocking VEGF has been established, various groups are working on improved therapies. The next treatment to reach the clinic might be VEGF Trap-Eye, a protein that binds to VEGF more tightly than Lucentis as well as mopping up another molecule involved in blood vessel growth -- placental growth factor. Developer Regeneron says this might make it more potent, or require less frequent injections, perhaps every 8 weeks. The first results from large trials comparing VEGF Trap-Eye with Lucentis are due by the end of the year.

A completely different approach is to use RNA interference, a relatively new technique for switching off individual genes by delivering short stretches of RNA. So far the main hurdle has been getting RNA into the target cells, but the eye's accessibility means this is not so much of a problem. A few RNA-based drugs designed to block AMD are in the early stages of development.

The first to be tested in people was one called bevasiranib, though so far results have been poor. Other firms are looking beyond directly blocking VEGF, and are using RNA interference to target other molecules in its signaling pathway, either upstream or downstream. Merck and Pfizer have already bought rights to such agents, and each has a drug in early trials in people.

Like VEGF antibodies, RNA drugs would still entail regular eye injections. What's needed is a longer-lasting approach, which might come in the form of gene therapy.

The idea of permanently inserting new genes into cells has generated great hopes in the past few decades but it's a risky path to tread. In 1999, U.S. teenager Jesse Gelsinger died after a massive immune reaction against the virus used to deliver a gene. In 2002, a different virus triggered leukemia in several children.

The eye might be a safer testing ground for gene therapies. It's enclosed by the blood-retina barrier, keeping viruses in and the immune system mostly out. Side effects should be limited to the eye, and in a worst-case scenario, the organ could be removed without endangering life. Researchers can peer inside for easy delivery of the therapy and to monitor progress, and the other, untreated eye is the perfect experimental control. There are also simple and safe ways to test the retina's functioning. Partly thanks to work in the eye, gene therapy is seeing something of a renaissance.

Proof of principle came in 2000 when a team led by Robin Ali at the Institute of Ophthalmology in London restored vision in mice with an inherited form of blindness. They delivered a gene with a virus called AAV -- a different one to those that caused Gelsinger's death and the leukemia cases.

Slowly and cautiously, Ali's group and others have been trying out an AAV-based gene therapy in people with an inherited form of blindness. There has been some vision improvement in most of the people who have received it so far. After just one treatment, benefits can persist for two years, according to Ali's latest, unpublished results.

"This gave a huge boost to the field, because it showed it can be safe and effective," says Ali.

Work has now begun to find out whether gene therapy could provide a long-lasting treatment for AMD. U.S. firm Genzyme has started recruiting for a trial involving a gene therapy designed to mop up VEGF. And this year, UK firm Oxford Biomedica plans to carry out trials in people of a therapy that delivers two other genes to block blood vessel growth.

All this is a long way from becoming an established therapy, however. In the meantime, faster progress may come via lower-tech drugs, with molecules small enough to diffuse through the tissues of the eye, so they could be given as eye drops. For example, a group of drugs called kinase inhibitors block the signals involved in blood vessel growth. Some are already used as cancer treatments and several are now in clinical trials for wet AMD, where they look promising.

Yet all these approaches have a major drawback. Because they work by blocking abnormal blood vessel growth, they would be no help for the 85 percent of AMD patients who have the dry form of the disease.

Now, however, a possible treatment for dry AMD is on the horizon. Instead of tinkering with molecules or genes, the strategy is to entirely replace the problem RPE layer with a new one grown from stem cells.

In theory, stem cells offer the hope of growing new tissues to order, yet in reality, many challenges remain. At the moment human embryonic stem cells usually come from surplus IVF embryos. Tissues derived from these would be rejected unless the patient takes lifelong immunosuppressive drugs, as after an organ transplant. But again, the eye has a unique advantage. Because it's relatively shielded from the immune system, only low doses of immunosuppressants should be needed to prevent rejection.

One of the pioneering groups in this field is led by Pete Coffey at University College London. They have grown tiny sheets of RPE cells in the lab and have shown these can restore vision in rats and pigs. They hope to start the first trials in people early next year.

"It could be an immense step," says Coffey. "No one has yet gone into the clinic with a human embryonic stem cell therapy."

U.S. firm Pfizer has teamed up with Coffey, and has made RPE cells the main focus of its new regenerative medicine unit in Cambridge, UK. "We are trying to make the production of RPE more commercial," says Ruth Mackernon, chief scientific officer at the Cambridge unit.

U.S. company ACT is also developing stem-cell RPE transplants, which have been successfully tested in animals. The company is now in talks with the U.S. Food and Drug Administration about trials in people with an inherited form of macular degeneration.

RPE transplants would only be helpful for people who still have some photoreceptors left to salvage, but one day even people beyond this stage may benefit. In 2006, Ali's team announced that they had taken photoreceptor cells from a young mouse and transplanted them into an adult mouse retina (Nature). The team is now working on doing the same with human embryonic stem cells.

It is fair to say that in the next few years the eye will see a host of pioneering therapies. Hopefully they will mean more of us can look forward to that idyllic retirement after all.

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