NEWS & COMMENT

 

2008
2007

2006
2005
2004

 

Architect/Adventurer Philippe Rahm speaks at Harvard on environmental therapeutics

January, 2008.  Maybe he didn't mean it this way, but his concepts surely jibe with our thrust.  In English -- with a French accent -- a remarkable Harvard lecture that addresses light, dark, humidity and oxygen concentration as driving forces in our lives.  (Reserve an hour for this lecture.)

Watch and listen with .mov software on your computer.


 

Letter to the New York Times on sleep and light

New York, December 2, 2007. Did Thomas Edison’s invention of the electric light wreak havoc on heliocentric sleep behavior, or did our society always cut sleep short? . . . Neuroscientists now know that light, natural or synthetic, is the most potent stimulus for the body’s circadian system. It deeply influences our ability to sleep. In fact, light is so important to our sleep-wake behavior that our brains contain a special pathway, called the retinohypothalamic tract, that delivers information from the eye to the brain’s circadian circuitry. So when the eye is exposed to light, it signals to the brain: The sun is up, you should be, too. Today’s challenge is to engineer environments that take advantage of our biology. . . . One way is to be more sophisticated about our use of light.

Jeffrey M. Ellenbogen, M.D., Director, Sleep Medicine Program, Massachusetts General Hospital, Boston



 

Major new compilation on chronobiology in psychiatry

December 1, 2007. We celebrate the publication of a pace-setting set of research and clinical articles that define the state of the art in our favorite field, chronobiology in psychiatry, in the December issue of Sleep Medicine Reviews. We celebrate doubly, because the issue is dedicated to our director, Dr. Anna Wirz-Justice, at the culmination of her remarkably productive career at the Center for Chronobiology, Psychiatric University Hospitals, Basel, Switzerland. Three of the most relevant pieces for CET are available for free download from our site. Francesco Benedetti’s article lays out the program for CET’s newly-established Chronotherapeutics Consultants group.

Wirz-Justice A. Chronobiology and psychiatry.
Terman M. Evolving applications of light therapy.
Benedetti F, et al. Chronotherapeutics in a psychiatric ward.


 

Consumers Union weighs in on drugs vs. light for SAD

November 1, 2007. With completion over a year ago of a drug company study of Wellbutrin to “prevent” SAD by beginning treatment early in autumn, Consumer Reports has considered whether or not this provides a meaningful advance over light therapy. They point out that the response to light therapy is faster than with drugs, and that light can also be used as a prophylactic. “The best strategy is to watch for early warning signs, including fatigue, oversleeping, carbohydrate cravings, and weight gain. They tend to creep up weeks before your mood actually plummets, says Michael Terman, Ph.D. [CET’s president]. . . . ‘Clinically, there’s nothing special about the efficacy of Wellbutrin relative to other common antidepressants for the treatment of SAD,’ says Terman.”

Read the whole story.

 


 

Douglas Holmes, 1933-2007

We record with great sorrow the death of one of our founding Board members, Dr. Doug Holmes. Doug had a formative vision for CET and was a supreme guide from our start in 1993. Excelsior, Doug!

From the New York Times, May 25, 2007: "Dr. Holmes was emeritus director of the research division and national Alzheimer’s center at the Hebrew Home for the Aged in the Bronx; he had founded the research division there in the mid-1980s. He was also affiliated for many years with the Resource Center for Minority Aging Research at Columbia University. Dr. Holmes’s best-known research centered on the delivery of services to elderly people. Among the subjects he investigated were dementia care, sexuality among the elderly, meal-delivery programs for the homebound and the need to improve services for aging members of minority groups. With his wife and frequent collaborator, Monica Bychowski Holmes, he published the 'Handbook of Human Services for Older Persons' (Human Sciences Press) in 1979. Although Dr. Holmes came to be identified most prominently with his work on aging, he began his career studying child welfare. His research interests included early-childhood education and child-abuse treatment programs, among other subjects. He was a co-author of a book about adolescent drug use, 'The Language of Trust: Dialogue of the Generations' (Science House, 1971), written with his wife and Lisa Appignanesi. Dr. Holmes’s other books include 'The Therapeutic Classroom' (Aronson, 1974; with Dr. Bychowski Holmes and Judith Field). Douglas Holmes was born on Dec. 7, 1933, in Washington, Conn. He earned a bachelor’s degree in economics from Tufts University in 1958 and a doctorate in psychology from New York University in 1963."



 


Psychiatric News picks up on negative air ionization

January 5, 2007. Psychiatric News, the monthly organ of the American Psychiatric Association, finds the latest results on negative air ionization of particular interest for psychiatrists. Their article recounts the evolving research story in detail, and even recommends a trip to Niagara Falls! . . . Dr. Ray Lam of the University of British Columbia provides the concluding comment: "There has, regretfully, been less [commercial] interest in these new noninvasive biological treatments" because, as writer Joan Arehart-Treichel notes, "there is no huge profit to be made from them as from, say, psychotropic medication."

Negative Ions May Offer Unexpected MH Benefit

 


 

Reuters Health reviews the latest Columbia study of treatments for SAD

January 3, 2007. After a year and a half in a publication queue, and just in time for winter, the American Journal of Psychiatry has issued CET president Michael Terman and Jiuan Su Terman’s report on a 6-year NIH-sponsored clinical trial of dawn simulation and negative air ionization, both compared with standard bright light therapy. Reuters summarizes the results . . . and points readers to CET.org for our self-assessment of seasonal depression.

The Reuters news release
The study
The PIDS self-assessment

 


National Public Radio interviews a light and ion therapy patient

December 21, 2006. André Pennycook, a graphics designer, is a veteran user of bright light therapy, dawn simulation and negative air ionization. Health Reporter Allison Aubrey probes him for a first-hand compare and contrast.

Read this improtant story and listen to André’s words to the wise

listen to the audio file: listen to the audio file

 


 

Jane Brody points New York Times readers to CET

December 5, 2006. The Personal Health columnist and guru provides an update on SAD research, theorizing and clinical practice – specifically, environmental therapeutics, not meds. We’re delighted that she recommends the same light box and ionizer we selected for the CET Store. And the article made it onto the Times’ most-emailed list!

“Getting a Grip on the Winter Blues”

 


 

Gauging depression severity: AutoSIGH update

November 2006. We launched our automated questionnaire for current depression severity, the AutoSIGH, in 2005. Our goal was to help people gauge the seriousness of their current situation, monitor changes whether on or off treatment, and seek professional help if indicated. (The AutoSIGH delivers individualized, confidential recommendations, and the user remains anonymous.) In developing the AutoSIGH, we had in mind especially people without ready access to mental health providers, or people who fear telling doctors, clergy, family or friends about their problem. More than 1000 people have accessed the AutoSIGH so far. Highlights: (a) Of those who completed all the questions, 36% reported suicidal thinking short of taking action; we referred them to help centers and urged them to tell someone close. (b) 1% reported making a suicide attempt in recent days; we urged them promptly to call their doctor and, if unavailable, go to an emergency room or call 911. We do not know whether these people sought help beyond the AutoSIGH, but we are gratified they came to us for guidance.

 


 

“The Morning Person Solution”

November 2006. If you feel sluggish when you wake up, perhaps you envy morning chronotypes – the “larks” of our world, who spring out of bed smiling, and get to work in time…. MSN.com has a feature story about how to get there, and cet.org is very happy about that!

The Morning Person Solution


 

On About.com: “The Top 5 Things You Should Know About SAD Research”

November 2006. This popular informational website, which is produced by the New York Times, provides readers with CET president Dr. Michael Terman’s report, “Winter 2006-2007 SAD Treatment Update.” Read about the latest drug, light and negative air ion studies.

 


 

Ionizing large spaces: two groundbreaking museum exhibits

 

September 2006 – February 2007. Architect Philippe Rahm does it again, but this time with negative air ions! (See our reports on his earlier lighting installations, below.) Rahm’s idea was to ionize entire exhibition spaces at Kusthaus Graz, Austria, and at the MAK Center’s Schindler House in Los Angeles, to see if visitors’ moods would be enhanced with negative, but not positive air ionization. The notion stems from clinical research on the antidepressant effect of negative air ionization and a recent study of college students who showed quick enhancement even though they were not clinically depressed. The underlying message is clear enough: we should be considering this technology for living and working spaces that are vulnerable to low ambient ion levels.

Architects’ workshop at Graz
MAK exhibit podcast (video .m4v)
College student study

(See our website for clinical information about negative air ionization.)

 


 

Wikipedia weighs in on light therapy

August 2006. We're happy to note that the free, online encyclopedia Wikipedia (http://en.wikipedia.org) has added notes, references and weblinks on our topic of interest, which is bringing many new visitors to CET.org. Their section on seasonal affective disorder badly needs editing (we will try), but their notes on newer applications are right on the mark:

Non-seasonal depression: Only recently have clinical studies been conducted which specifically excluded all patients with any degree of seasonality. Before these studies, there was suspicion that any depressed patients who benefitted from light treatment were really only having the SAD component of their depression treated. However, light therapy is now an established treatment for depression, regardless of seasonality, and has certain advantages over drugs, in that it might take less time to see a benefit (typically antidepressant drugs take several weeks to reach full effectiveness).

Delayed sleep phase syndrome: When treating delayed sleep phase syndrome, the timing of the exposure is critical. The light must be provided as soon after arising as possible to achieve any effect. Some users have reported success with lights that turn on shortly before waking (dawn simulation).


 

Major new lighting effect may regularize menstruation and promote ovulation

Quebec, July 2006. At the Society for Light Treatment and Biological Rhythms 18th annual meeting, Dr. Konstantin Danilenko of the Russian Academy of Medical Sciences reported that morning light therapy taken 7-14 days after menstruation onset (in the follicular phase) significantly increased ovulation in women with cycles longer than 28 days. Moreover, sex hormone levels and ovary follicle growth were enhanced. This simple, non-drug treatment may have major benefits for women aiming to conceive (. . . or not).

 


 

More news on the purported clinical efficacy of blue light (see our earlier items below)

We have reported our great concern over so-called blue light therapy, which has been widely marketed without FDA regulatory approval, adequate tests of long-term safety for the eyes, and indeed clinical trials demonstrating benefit for the treatment of depression. Now, the latest:

Quebec, July 2006. At the Society for Light Treatment and Biological Rhythms 18th annual meeting, Dr. Marijke Gordijn of the University Medical Centre Groningen (The Netherlands) reported the first head-to-head clinical trial of standard bright white light therapy and white light with added short-wavelength (blue) “enrichment” (the manufacturer’s term). There were no significant differences between the two treatments – that is, no advantage of added blue. Our no-brainer conclusion: stick with standard white light therapy and avoid the exacerbated visual glare and possible cumulative retinal damage of excessive short-wavelength exposure.

 


 

The Sleeping Pill/Antidepressant Brouhaha


March 19, 2006. Media attention has suddenly soared concerning side effects of psychotropic medication heretofore unreported and possibly undetected. The New York Times has been publishing news items, editorials, op-eds and letters almost daily. The latest focus is on Ambien (the popular sleeping pill), with stories of inexplicable nighttime eating binges, cooking and sleep walking – all forgotten and mystifying by wake-up time the next morning. Within the psychiatric community, clinicians have begun sharing a long list of case episodes, thus far unpublished. They are debunking the notion that the side effects are due simply to overdosing; indeed, some are saying, underdosing with inadequate sleep onset is most risky. Author/editor Lauren Slater notes in today’s Times, “psychotropics rise to prominence in ways that are distressingly familiar, with pixie dust and promise. . . . If we are smart, we will see that disappointment is built into each drug's birth and is inevitable in its lifetime.” This is perhaps overstatement, given the life-saving benefits of some antidepressants, antipsychotics and mood stabilizers. But fact is, psychoactive drug discovery has been largely serendipitous – spin-offs of drugs designed for other medical conditions – rather than the outcome of cumulative, purposeful research that translates basic science into clinical application. Where’s the notable exception? Light therapy. As CET director Anna-Wirz Justice and colleagues have written in Science Magazine, “Light therapy is the only treatment in psychiatry that evolved directly out of neurobiological models of behavior.” With its favorable side-effect profile and demonstrated efficacy for treatment of both depression and sleep-onset insomnia, it is a natural nonpharmacologic alternative to psychotropic medication. So why does light therapy remain largely invisible? Partly, 40 years of psychopharmacology ethos in psychiatry. Partly, the Food and Drug Administration’s hands-off attitude, which serves to discourage insurance reimbursement and sustain reliance on drugs. Partly, the investment motives of Big Pharma. Lauren Slater concludes, again with some overstatement, “It is up to us, the consumers, to disregard the hype that too often infuses harmacological findings — to know that the pill we cradle in our palm may ease our pain, but will just as surely take its toll.”

 


A case history of general interest: light therapy for treatment-resistant nonseasonal depression


Lancaster, PA, December 29, 2005. Andrea Gregg suffered major depression for many years without significant relief from a series of standard medications. Hospitalized, after she began treatment with an alternate drug class (the monoamineoxidase inhibitor Parnate) and morning light therapy, her symptoms lifted. In a year since returning home, she has remained much improved -- except when she skips light therapy. Read her story and a discussion by talented journalist Linda Espenshade about the wider implications of this treatment strategy .


Click here for the full text.



Consumer Reports on Health weighs in . . .

December, 2005. This no-nonsense health newsletter published by Consumers Union writes -- in its second major story on SAD -- that if extra outdoor exposure doesn't work, "consider bright light therapy. Choose a light box that's specifically designed to treat SAD and that shines slightly down and delivers white light, not blue. . . . If you have severe symptoms or if light therapy doesn't work, causes persistent side effects, or is too risky for you, consult your physician or a mental-health professional." Amen. We are also delighted that they refer readers to CET's Personalized Inventory for Depression and SAD (AutoPIDS), "which can help you determine if you have SAD and can try treating yourself or if you should consult a mental-health professional."

Read the article.



Added risk factor for people with SAD and winter doldrums: tanning salons!


November, 2005. Concerned about the growing evidence that artificial indoor tanning devices cause skin cancer, Tennessee psychologist Joel Hillhouse and colleagues surveyed 126 females for their tanning habits and evidence of seasonal depression (as can also obtained from CET's Automated Personalized Inventory for Depression and SAD). Although a large minority (44%) were healthful non-tanners, tanners were twice as likely to report seasonal mood cycles than not: 66% vs. 34%! CET's strong advice: to combat SAD, use non-UV light therapy to the eyes rather than UV tanning devices. Bright white light therapy has been demonstrated to be safe and effective, while the use of tanning devices is self-destructive. SAD sufferers have enough burden to bear without adding the cancer risk of tanning.


The study is reported in the Archives of Dermatology (2005;141:1465), published by the American Medical Association.




Clinical service for light therapy established at New York-Presbyterian Hospital

November, 2005. In a hospital-first for the US, New York-Presbyterian -- the primary teaching hospital of Columbia and Cornell -- has established a Center for Light Treatment and Biological Rhythms following the recent consensus recommendations of the American Psychiatric Association. Treatment foci are seasonal and nonseasonal depression, and circadian rhythm sleep disorders. Designed for outpatients in the NYC metro area, and others who can travel to NYC for a single in-depth evaluation session, the program provides monitoring and guidance as patients take treatment at home. The service also coordinates with patients' primary providers, facilitating combination treatment with light and antidepressant medications when indicated. Inpatient supervision of light therapy is also offered at the hospital's Columbia University Medical Center campus.

Check the Center's website.



"Artificial Lighting and the Blue Light Hazard," a talk and demo by Dan Roberts

October, 2005. This is a must hear-see. Roberts, who heads the nonprofit, Macular Degeneration Support, exposes fallacious claims about full-spectrum lighting and lays out the known and potential dangers of extended exposure to blue-enriched lighting of any kind. He proposes a warning label for use by the (unregulated) lighting industry, for attention of everyone over age 55 as well as those with or at risk for age-related macular degeneration. The presentation will come up on your screen without the need for player software.

Click here for the presentation.



Light and ions shown to work without seasonality

Cambridge, England, May 2005. OK -- we know that depressed patients who do not have SAD can respond to light therapy. However, it has never been shown that such patients are truly nonseasonal, since studies have included patients with winter worsening, even though they also suffered depression at other times of year. Now, a Wesleyan-Columbia team has published a study in which seasonality was absolutely ruled out: all patients were continuously depressed for at least two years (most often longer), and their suffering was no worse in winter than at other times. Modeled on a previous study of SAD by Terman and colleagues, patients received either morning bright light therapy, high-density negative air ions or a low-density ion placebo. The antidepressant response was remarkable, with 50% of light and high-density ion patients showing complete symptom remission within 5 weeks, while none of the patients on placebo showed remission. Considering that these patients had previously shown inadequate response to drugs, both light and ions for chronic depression should now go high on the list of alternate treatments.

Goel N, Terman M, Terman JS, Macchi MM, Stewart JW. Controlled trial of bright light and negative air ions for chronic depression. Psychological Medicine 2005;35 (e-published May 2005, print issue July 2005).


European Medicines Agency (EMEA) concludes against antidepressant drugs for children and teens

London, April 25, 2005. EMEA's Committee for Medicinal Products for Human Use has reviewed the experience with 12 of the most common antidepressant drugs and found "increased risk of side-effects such as suicide attempt, suicidal thoughts and hostility (predominantly aggression, oppositional behaviour and anger) in children and adolescents." The warning goes a step further than an earlier British warning that had exempted Prozac, and includes both serotonin-norepinephrine reputake inihibitors and selective serotonin reuptake inhibitors in the Prozac family. In planning discontinuation of the drugs for their children, parents are warned that this must be done gradually -- under a doctor's supervision -- to avoid withdrawal effects like dizziness, sleep problems and anxiety. CET urges the field to consider proven non-drug alternatives like bright light therapy and dawn simulation (the latter administered automatically during sleep without any compliance problems or competition with the daily schedule of activities).

Download the EMEA press release and Q&A.


"Mood Brighteners: Light Therapy Gets Nod as Depression Buster" by Bruce Bower

Science News, April 23, 2005. A new scientific era may have dawned for light therapy, a potential depression fighter that has languished in the shadows of antidepressant medication and psychotherapy for the past 20 years. A research review commissioned by the American Psychiatric Association in Washington, D.C., concludes that in trials, daily exposure to bright light is about as effective as antidepressant drugs in quelling seasonal affective disorder (SAD), or winter depression, and other forms of depression. "I now tell my patients that light therapy is a reasonable depression treatment, even if the data base for this approach is relatively small," says psychiatrist Robert N. Golden of the University of North Carolina at Chapel Hill. Golden directed the new statistical review, which appears in the April American Journal of Psychiatry. . . . To Golden's surprise, pooled data from the acceptable investigations showed markedly eased SAD symptoms from both bright-light exposure after awakening and dawn simulation, in which a light box each morning provides a sleeping person with gradually intensifying illumination. Moreover, light therapy yielded substantial relief for outpatients with mild-to-moderate depression unrelated to any season. Such therapy also magnified the depression-fighting effects of antidepressants in these individuals.

View the whole article.


International review committee endorses chronotherapeutics

Cambridge, England, March 2005. Last year, the International Society for Affective Disorders (ISAD) formed a Committee on Chronotherapeutics chaired by CET Board member Anna Wirz-Justice. First on their agenda was to evaluate two non-drug methods that have shown promise for seriously depressed patients, regardless of seasonality – light therapy and wake therapy. Light therapy, of course, is the major focus of CET's website. Wake therapy involves skipping all sleep for one night, which surprisingly can result in instantaneous mood improvement. Problem is, blue mood returns with sleep the next night. By combining wake therapy with daily light therapy, however, the mood improvement can be maintained, even while antidepressant medications slowly build up to therapeutic blood levels. The report, to be published in the July issue of Psychological Medicine (but already available to subscribers on-line) concludes: "The public zeitgeist favours non-pharmaceutical treatments. Patients accept and often prefer them. Unlike many touted remedies, however, wake and light therapy are not alternative, unproved, or soft. Wake and light therapy provide flexible opportunities for multimodal treatment as adjuvants with negligible side-effects or untoward interactions with ongoing medication. . . . It is time for wake and light therapy to be incorporated into mainstream psychiatry. To consider them mere curiosities outside the paradigm wastes resources and prolongs suffering. Building on the example of the American Psychiatric Association [see our News item below], national psychiatric associations should exert clinical leadership and develop standards of practice for chronotherapeutics. It would be a shame to wait for the insurance industry to impose these measures based purely on the cost considerations of managed care.” CET is following through with the establishment of Chonotherapeutics Consultants, under Dr. Wirz-Justice, which will offer guidance to hospitals in administering these procedures.

Wirz-Justice A, Benedetti F, Berger M, Lam RW, Martiny K, Terman M, Wu J. Chronotherapeutics (light and wake therapy) in affective disorders. Psychological Medicine 2005;35 (e-published March 2005, print issue July 2005).


More about blue light hazard. . . .

April 2005. Following our note on recently marketed blue light boxes (two items below), we Googled "blue light" hazard eyes retina and came up with more than 10,000 citations, many of them relevant to the development of light therapy standards, and representing all points of view. We draw special attention to MDsupport.org (in this case, MD = macular degeneration), with a broad overview by director Dan Roberts titled Artificial Lighting and the Blue Light Hazard. As the site explains, "Age-related macular degeneration is the leading cause of legal blindness in senior citizens. An estimated fifteen million people in the United States have it, and approximately two million new cases are diagnosed annually. . . . [It] is a progressive disease of the retina wherein the light-sensing cells in the central area of vision (the macula) stop working and eventually die. The disease is thought to be caused by a combination of genetic and environmental factors, and it is most common in people who are age sixty and over. . . . What kind of lighting is best for people with retinal diseases like macular degeneration? Researchers tell us that ultraviolet (UV) and blue light rays may be harmful to those of us with retinal disease, while marketers tell us that lamps with enhanced UV and blue will help us to see better and stay healthier. Advertisers tell us that the intensity and range of colors offered by lamps that replicate sunshine and daylight are necessary for best vision and visual health. At the same time, doctors admonish us to wear blue-blocking, UV-protective sunglasses when we go outdoors. What's going on? What should we believe? How can light hurt our retinas? What are the differences between fluorescent, halogen, neodymium, and regular incandescent light bulbs? What do they mean by labels such as 'full spectrum' and 'daylight'?" To this, we add the questions, What is the effect of long-term cumulative exposure to blue light, even at moderate intensity? Does it raise the likelihood of accelerating macular degeneration in vulnerable people as they grow older?

Read on.


American Psychiatric Association task force weighs in on light therapy

April 2005. The long-awaited, important report is out! The group's exhaustive analysis of the literature "revealed that a significant reduction in depression symptom severity was associated with bright light treatment and dawn simulation in seasonal affective disorder and with bright light treatment in nonseasonal depression." They conclude that clinical trials suggest these treatments "are efficacious, with effect sizes equivalent to those in most antidepressant pharmacotherapy trials." The number of adequate light therapy trials, however, was small, underscoring the need for further research. Very much in line with CET's analysis of the situation, the report editorializes: "The pharmaceutical industry, which has considerable resources devoted to research and development activities, funds much of the clinical trial research for potential new antidepressant pharmacotherapies. In contrast, there has not been a similarly endowed industry nor as sizable a market in place to support the development and testing of light therapy treatments." Coming from a prominent group of psychopharmacologists, we can only say, "Amen and amen."

Golden RN, Gaynes BN, Ekstrom RD, Hamer RM, Jacobsen FM, Suppes T, Wisner KL, Nemeroff CB. The efficacy of light therapy in the treatment of mood disorders: a review and meta-analysis of the evidence. American Journal of Psychiatry 2005;182:656-662.


Concern over recently marketed blue light boxes

April 2005. CET's Ask the Doctor forum has begun to receive numerous experessions of concern from consumers about a small, blue lighting device that has recently been mass-marketed. The issue is important enough that we post the last interchange here. The questioner asks: "New light boxes are beginning to appear on the market that tote around superiority because the light emitted is in the blue range (470 nm) of the light spectrum. They even claim that research has now shown that 470 nm light is the 'action mechanism' in treating circadian rhythm disorders such as SAD. What is your take on all of this? Advertising gimmick or really clinically supported? Thank you for your help." Our response: Yes, there have been recent unconscionable commercial initiatives. Narrow-band blue light has been shown to suppress melatonin hormone production and to elicit circadian rhythm phase shifts in physiology research experiments that are based on a single light exposure. These studies are important to understand nervous system mechanisms of circadian light input. However, a distinction must be made for any jump to multiple treatment exposures as an antidepressant. The clinical utility, safety and tolerability of blue light have definitely not been established. Indeed, there is widespread concern in the ophthalmology community about potential phototoxic reactions in the retina resulting from prolonged blue light exposure. For example, a Japanese study of rhesus monkeys found that focused LED blue light produced a grey, discolored region in the retina, abnormal electroretinogram, a marked disruption of the disks of photoreceptor cells, damage in the retinal pigment epithelium, among other severe consequences. The investigators concluded that this damage “may impair function and continuous exposure to blue light is potentially dangerous to vision” (Koide R, et al. Nippon Ganka Gakkai Zasshi. 2001;105:687-695). While the particular exposure conditions for the monkeys undoubtedly differed from the exposure conditions of the recently marketed blue light device, the latter has not been adequately evaluated for safety, and consumers should avoid the risk. Furthermore, there has been no clinical study showing blue light superior to the balanced white light from well-tested light boxes. The claims you cite are far more than an 'advertising gimmick', as you put it. They spell potential danger for the user. This is a particular worry for long-term treatment applications. Previously published hazard functions for blue light probably do not apply here. Consumers are urged to contact the FDA in the U.S. if they have concern. The phones and addresses of regional offices are listed at www.fda.gov/opacom/backgrounders/complain.html.



Springtime light simulation goes architectural

Winter 2005, Paris. Based on the dusk-to-dawn simulation algorithm CET president Michael Terman developed for treatment of depression and circadian rhythm sleep disorders, prize-winning architect Philipe Rahm designed a perpetual spring equinox for a courtyard display at the Swiss Cultural Institute in Paris. Rahm writes: "Going back several hours, several months, a season, finding this moment of comfort that we lost as the year advanced, going back from winter to fall, from night to afternoon. Architecture as constructed temporalities.” In preparation: an eternal summer day for a large cluster of trees in Jöss, Austria.

Visit Rahm's adventurous site.



"All Sleepless and Light" by Joe Studwell

Financial Times, October 22, 2004. A new article by Joe Studwell (see also "Oh, Behave!" below) documents major recent successes of combined light therapy, wake therapy, and medication in patients hospitalized with major depression. This is watershed news for environmental therapeutics. We're delighted that Studwell points FT readers to cet.org and our Automated Morningness-Eveningess Questionnaire, which provides guidance for the optimum scheduling of light therapy according to the internal circadian clock. "There is little doubt among key researchers that sleep deprivation, light therapy and the action of SSRI drugs are synergistically linked in some unknown but fundamental way," he writes. "For both political and financial reasons, however, the breakthrough research on these connections has been done at small private clinics . . . rather than in the big US teaching hospitals or in Europe's massive public health systems. . . . SSRI drugs take from two to four weeks to have any effect. Psychotherapy typically requires three months to show results. In the meantime, a proportion of patients kill themselves (acute bipolar patients have a lifetime suicide risk of one in five). By contrast, sleep deprivation works for most patients in 24 hours, and the effect can then be sustained with light therapy and drugs. . . . In most circumstances patients are quick to choose combination therapy over the more expensive and slow-acting alternatives." Citing Joseph Wu, M.D., of the University of California, Studwell notes that "Wu has been somewhat surprised that the US's 'managed care' providers, in their relentless drive to control costs, have not taken more notice of the new combination therapies. 'This has been a tragically ignored and neglected area that can have a real impact in clinical management,' he says. One possible explanation, according to Wu, is that the inundation of marketing [by the giant pharmaceutical companies] drowns out ideas that don't have that kind of massive advertising.'" CET has become a prime, non-profit resource for this nonpharmaceutical initiative, and will now offer hospitals and the managed care industry guidance in setting up the procedures at individual sites. For institutional inquiries, please contact our Chronotherapeutics Consultants at cc@cet.org.

Download the full article.




"Stronger Warning Urged on Antidepressants for Teenagers" by Erica Goode

New York Times, February 2, 2004. A scientific advisory panel urged the Food and Drug Administration . . . to issue stronger warnings to doctors now about the possible risks to children of a newer generation of antidepressant drugs, rather than wait until the agency's review of the drugs was completed. "Our sense is that we would like in the interim for the F.D.A. to go ahead and issue stronger warning indications to clinicians" about the chance that the antidepressants might be linked to suicidal thinking and behavior, hostility or other forms of violent behavior, said Dr. Matthew Rudorfer, a scientist at the National Institute of Mental Health and the chairman of the F.D.A. advisory committee. . . . Dr. Thomas Laughren, the team leader for the F.D.A.'s division of neuropharmacological drug products, said that the agency took the panel's recommendation "very seriously" and that it would probably issue such a warning "sooner rather later." . . . Dr. Rudorfer said the committee was struck by the fact that in some cases described at the hearing doctors had seemingly prescribed antidepressants casually and failed to monitor the children closely while they were taking them. "We were all concerned about the stories we heard," Dr. Rudorfer said, noting that the drugs were "very powerful but also potentially very effective." . . . The F.D.A. has asked researchers at Columbia University to trace the data used in the drugs' clinical trials to make sure that behaviors coded in the trials as suicidal in fact represent suicidal thoughts or actions. . . . Dr. Laughren . . . said there was "a suggestion from that data that there is a signal of something, there is an excess of something occurring." But trying to figure out what that "something" is, Dr. Laughren said, is enormously complicated.
CET comments: We have long thought that dawn simulation in the bedrooms of depressed, oversleeping teenagers could be a boon. This deserves a sponsored clinical trial.



“Oh, Behave!” by Joe Studwell

Financial Times, January 24, 2004. Big Pharma [the pharmaceutical industry] can't sell us things we do not want. We possess an irrepressible belief that chemical solutions exist to life's problems: this is what makes the business so big. . . . But the very scale of such success underscores why medical ethicists, police and parents are wringing their hands about diversion and abuse of behavioural drugs. . . . Sales trends suggest that US versus European differences of opinion over behavioural drugs will continue to see Americans consume more than Europeans. But there is one point on which everyone – chief executives, doctors, pundits and consumers – on both sides of Atlantic agreed: people would prefer non-pharmaceutical alternatives to cope with their problems if they were available. . . . The US system tends to militate against non-drug therapies in primary care. . . . Americans get an average of seven minutes of their GP's time per visit. “Our system creates an ironic incentive,” says Katharine Greider. “You're under pressure from insurers to keep costs down but there's a contradictory pressure to prescribe. Writing a prescription is an office-terminating event. It signals to the patient: `It's time to go away now'.” . . . As behavioural science brings us new possibilities in mental as well as physical health, personal choice is more important than ever and consumers should be fully informed. [Emphases ours.]

View the full article.



"Brightening Depression" by Dr. Anna Wirz-Justice and colleagues

Science Magazine, January 23, 2004. Light therapy cannot be patented, and . . . will not bring profits to the conventional psychopharmacology industry, but can help the patient in a shorter time and with fewer side effects than drugs and can be easily and successfully combined with medication. Given the psychological suffering that depression inflicts – including the danger of suicide – and the financial pressures to minimize the duration of hospitalization, it is surprising how little notice is taken of [this] remarkable chronobiological intervention. We must include [it] in the therapeutic armamentarium. . . . An American Psychiatric Association task force recently has concluded the same.

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Shedding light on depression, no matter the season

Light therapy, the primary treatment for winter depression, may offer a drug-free way to treat nonseasonal depression as well. Clinical trials have demonstrated similar levels of improvement with light therapy and antidepressant drugs. However, light therapy worked faster, with gains starting within one week. Medications took up to eight weeks to achieve similar results. Several European hospitals are routinely administering light therapy to depressed patients. The U.S. badly needs to catch up.

Kripke DF. Light treatment for nonseasonal depression: speed, efficacy, and combined treatment. Journal of Affective Disorders. 1998;49:109-117.



Individualized timing is key to successful light therapy for winter depression

For several years, clinical researchers have debated the necessity of using light therapy at a particular time of day. In 1998, three independent research groups convincingly demonstrated that most people with winter depression experience greatest relief with morning light. Now the prescription has been further refined: the best response to morning light is obtained by tailoring treatment to each individual's sleep cycle at a time roughly equivalent to 2.5 hours after the midpoint of sleep, or 8.5 hours after the onset of melatonin secretion by the pineal gland. Since some people begin to secrete melatonin – and go to sleep -- much later than others, the optimum time of morning treatment can vary by up to four hours from one person to the next. Furthermore, while short sleepers (about 6 hours per night) will use the lights around their normal wake-up time, long sleepers will have to wake up earlier to gain this advantage. For example, an 8-hour sleeper who goes to bed at 11:30 p.m. and wakes up at 7:30 a.m. when depressed would begin treatment at 6:30 a.m. This individually tailored approach promises to further enhance the efficacy of light therapy.

Terman JS, Terman M, Lo ES, Cooper TB. Circadian time of morning light administration and therapeutic response in winter depression. Archives of General Psychiatry 2001;58:69-75.

Wirz-Justice A. Beginning to see the light. Archives of General Psychiatry 1998;55:861-862.



Is light therapy safe?

The light therapy industry has been inconsistent -- even slack -- in establishing standards for light therapy devices, and the physical properties of light from their devices vary widely, causing concern among ophthalmologists. Use of poorly made apparatus carries a risk of excessive ultraviolet radiation (UV), even when a manufacturer states that the light is "UV-reduced" or "UV-free." Inappropriate exposure is sometimes immediately apparent in skin reddening and puffiness. This may be more likely in patients who are using photosensitizing medications (which include certain antidepressants), but it is also seen in unmedicated patients with high skin sensitivity. Longer-term consequences for the cornea and lens of the eye have not been systematically measured, although they might be suspected. Recently, a group including lighting specialists (not commercially affiliated), an ophthalmologist and a mental health expert collaborated on a study comparing a wide range of lamps and filters. They found major differences in UV lamp emission and filter transmission and identified specific components that optimize the safety factor. Interestingly, "museum light" technology -- designed to prevent fading of pigments in artwork -- won out on all fronts. Of special interest was a clear plastic material used instead of glass in picture frames. Following the researchers' recommendations, two companies in Canada and the U.S. have integrated this material into a diffusing screen for 10,000 lux light boxes.

Remé C, Rol P, Kaase H, Terman M. Bright light therapy in focus: Lamp emission spectra and ocular safety. Technology and Health Care 1996;4:403-413.



Depressed and pregnant

Depressed women who are pregnant face special treatment challenges. While postpartum depression has been widely publicized, about 1 in 10 women suffer from depressive episodes during pregnancy, a time when medications need to be strictly controlled in order to protect the fetus. Furthermore, because depression during pregnancy increases the likelihood of a postpartum depression, every effort should be made to treat the depression immediately. Might lights work here? Investigators at three major centers think so, and they have completed a pilot to demonstrate it. They are currently inviting pregnant women to join a clinical trial at the University of Pittsburgh. If you are a potential volunteer or interested clinician, send them a message.

Epperson CN, Terman M, Terman JS, Hanusa BH, Oren DA, Peindl KS, Wisner KL. Randomized clinical trial of bright light therapy for antepartum depression: preliminary findings. Journal of Clinical Psychiatry, 2004;65:421-425.



Melatonin stabilizes sleep cycles in blind people

Use of melatonin as a sleeping pill is controversial, and there have been no definitive clinical trials. Melatonin supplements may help some insomniacs fall asleep earlier if taken before the body begins secrete its own melatonin in the evening, but there is little evidence that overnight sleep quality is improved for people who experience nighttime disruptions. Blind people face a unique challenge. Because they lack the feedback from the daily light-dark cycle that controls sleep timing in sighted people, their body clocks tend to drift out of synch with day and night. This leads to sleeping at inappropriate hours and waking when others sleep. In a major study reported in the New England Journal of Medicine, blind people were given melatonin pills in the evening. Nearly all of them eventually began to sleep normally; their body clocks stopped drifting. Although the optimum dose of melatonin remains to be determined, further clinical trials may prove an enormous boon for blind people.

Sack RL, Brandes RW, Kendall AR, Lewy AJ. Entrainment of free-running circadian rhythms by melatonin in blind people. New England Journal of Medicine 2000;343:1070-1077.



On the horizon: lights for chronic fatigue syndrome?

CFS involves far more than fatigue: patients often experience headache, sore throat, pain (in lymph nodes, muscles and joints), and low-grade fevers, which can continue for years. Perhaps it is not surprising that CFS sufferers often become depressed. In a recent study of more than 100 patients, those who identified winter difficulties in their history were significantly more likely to develop major depression than those who identified no particular season as worse than the others. Furthermore, the affected group -- about 1/3 of the total -- experienced excessive sleep, difficulty awakening, carbohydrate cravings and weight gain that were indistinguishable from healthy SAD patients. Scientists think that SAD may overlay CFS, and that some CFS symptoms might be effectively treated with artificial light. Although CFS patients often receive multiple medications, effective treatment has been elusive. Case studies have shown light therapy to alleviate depression, sleeping problems, and in one case, even joint pain. Clinical trials of light therapy now become a priority.

Lam RW. Seasonal affective disorder presenting as chronic fatigue syndrome. Canadian Journal of Psychiatry 1991;36: 680-682.

Terman M, Levine SM, Terman JS, Doherty S. Chronic fatigue syndrome and seasonal affective disorder: comorbidity, diagnostic overlap, and implications for treatment. American Journal of Medicine 1998;105:115S-124S.



Human circadian rhythm gene discovered

For the first time, researchers have identified a genetic mutation that speeds up the circadian clock in humans, causing them to fall asleep and wake up extremely early (for example, falling asleep at 7 p.m. and waking spontaneously at 2 a.m.). Although this kind of “early bird” pattern is relatively common among the elderly, researchers have finally discovered an inheritable genetic mutation that corresponds to sleeping problems in other segments of the population. Although the finding may offer an explanation to people suffering from early bird syndrome (known technically as “familial advanced sleep-phase syndrome”), it does not mean that any specific gene therapy is at hand. And while the media has touted the findings as offering hope to jet lag sufferers and shift workers, there is no evidence that the identified gene affects the dynamics of the sleep-wake cycle given such man-made disruptions. On the other hand, light therapy offers the promise of adjusting the internal circadian clock to normalize sleep cycles whether or not the abnormality has a genetic or man-made origin. Early sleepers, for example, have shown improvement given regular exposure to bright evening light.

Toh KL, Jones CR, He Y, Eide EJ, Hinz WA, Virshup DM, Ptacek LJ, Fu YH. An hPer2 phosphorylation site mutation in familial advanced sleep-phase syndrome. Science 2001;291:1040-1043.

Jones CR, Campbell SS, Zone SE, Cooper F, DeSano A, Murphy PJ, Jones B, Czajkowski L, Ptacek LJ. Familial advanced sleep-phase syndrome: A short-period circadian rhythm variant in humans. Nature Medicine1999;9:1062-1065.

Murphy PJ, Campbell SS. Enhanced performance in elderly subjects following bright light treatment of sleep maintenance insomnia. Journal of Sleep Research 1996;3:165-172.