Wednesday, November 18, 2009

One Pill Makes Your Libido Larger

It's every man's dream - a pill to make women want more sex. According to Boehringer Pharmaceuticals, that dream could be a reality in a few years, in the form of the strangely-named flibanserin. But is it the latest wonder-drug or just a glorified sleeping pill? Read on.

Flibanserin was originally developed as an antidepressant, but in clinical trials against depression it reportedly failed to perform better than placebo. The standard for getting approved as an antidepressant is low, so this is quite an achievement.

The BBC today described flibanserin as the "Female Viagra", which is rather confusing, because it's meant to increase sexual desire, which is one thing Viagra (sidenafil) doesn't do. The reason for the Female Viagra headline is that, as Professor John Thorp says:
"It's essentially a Viagra-like drug for women in that diminished desire or libido is the most common feminine sexual problem, like erectile dysfunction is in men"
Yes, one in ten women suffer apparently from "Hypoactive Sexual Desire Disorder" (HSDD) as Boehringer Pharmaceuticals helpfully informs us. And “As many as two out of every 10 women describe some degree of decreased sexual desire" according to the unfortunately named Dr Charles de Wet, Boehringer medical director for the UK.

HSDD is a diagnosis in the DSM-IV, the American Psychiatric Association's listing of psychiatric illnesses, and it's been recognised as a disorder since 1980. It is not, however, a very popular diagnosis yet. There are only 60,000 Google hits for it, as opposed to 1,600,000 for "major depression" and, er, 90,000 for "neuroskeptic". Odd for a disorder apparently plaguing at least 10% of women.

Indeed, some people say that it's no more than a label invented by psychiatrists who didn't understand women and then promoted by drug companies in order to sell drugs. This is almost certainly true, but it's also a bit simplistic, because there are people who perceive themselves as suffering from low libido, and if flibanserin really helps them, that's surely a good thing.

How is flibanserin supposed to work? According to a paper on the Pharmacology of Flibanserin, it's a serotonin receptor 5HT1A agonist and a 5HT2A antagonist. This makes it a kind of cross between the antidepressants nefazadone and buspirone. Neither of these are widely used as antidepressants because they're not considered highly effective. Flibanserin is also a weak dopamine D4 receptor partial agonist. This might underlie its aphrodisiac properties, because drugs which increase dopamine levels are known to enhance motivation and libido (or indeed cause problematic hypersexuality.) In rats and mice, flibanserin has sedative effects and enhances the effects of other sedatives. It also has antidepressant-like effects in some tests but not all. Drug geeks can click the image on the left for more details.

*

Now for the big question - does it actually work? Well, there have been no published clinical trials yet. At all. The trials in depression, where it failed to work, have never been published. Hmm. However, four trials in "Hypoactive Sexual Desire Disorder" were recently completed and the results were presented yesterday at a sexual medicine conference in Europe (ESSM) in the form of three posters (1,2,3). The trials were known as - groan - VIOLET, ORCHID, DAISY and DAHLIA. I probably don't have to tell you that they were all funded by Boehringer Pharmaceuticals.

The main poster is Efficacy of flibanserin 100 mg qhs as a potential treatment for Hypoactive Sexual Desire Disorder in premenopausal women which pools the data from three trials with a total of about 1,400 women. They found that taking flibanserin 100 mg every night had small beneficial effects. Relative to placebo, it increased the number of "satisfying sexual encounters" by 0.7 per month. It also improved scores on questionnaire measures of sexual function, a bit.

In any trial like this you have to ask whether there is result cherry-picking going on. Maybe they asked dozens of questions about the women's sex lives, and they're only telling us about the minority where the drug seemed to work? People often do that but in this case, the Clinical Trials Register suggests there was no funny business of that kind. It also shows that there have been no trials using 100mg which weren't included in the poster, so the trials themselves weren't cherry picked either. That's reassuring. But it looks like the effects were only significant when all three trials were pooled - one poster shows the results of the ORCHID trial alone, and most were non-significant.




What about the side effects? There's a whole poster about them. 100 mg flibanserin nightly caused 14% of patients to drop out due to side effects, vs 7% in the placebo group - so an extra 7% decided it wasn't worth it. It caused dizziness, nausea, fatigue, somnolence - and bizarrely, also insomnia. Notably, 50mg daily was much worse than 100 mg nightly, which suggests that taking this at night, rather than in the morning, is a good idea. But given what it is meant to treat, you'd want to do that anyway, right?

But this leads onto my biggest problem with these findings. It's obvious from the side effects data that this drug is a sedative - it makes you tired and sleepy. The animal data confirm this. It's much more likely to put you to sleep than it is to make you enjoy sex in any given month. Off the top of my head, I suspect its sedative properties are a result of its 5HT2A antagonism.

Any sedative can increase sexual desire, as anyone who has ever been to a bar will know. So whether this drug actually has an aphrodisiac effect, as opposed to just being a sleeping pill, is anyone's guess. To find out, you'd need to compare it to a sleeping pill, say, Valium. Or a couple of glasses of wine. Until someone does that, we don't know if this drug is destined to be the next big thing or a big disappointment.

Edit: Just noticed that Dr Petra Boynton has a fantastic post about the background to flibanserin and the manufacturer's apparent attempt to recruit her to write about HSDD.

[BPSDB]

ResearchBlogging.org

Borsini F, Evans K, Jason K, Rohde F, Alexander B, Pollentier S (2002). Pharmacology of flibanserin. CNS drug reviews, 8 (2), 117-42 PMID: 12177684

One Pill Makes Your Libido Larger

It's every man's dream - a pill to make women want more sex. According to Boehringer Pharmaceuticals, that dream could be a reality in a few years, in the form of the strangely-named flibanserin. But is it the latest wonder-drug or just a glorified sleeping pill? Read on.

Flibanserin was originally developed as an antidepressant, but in clinical trials against depression it reportedly failed to perform better than placebo. The standard for getting approved as an antidepressant is low, so this is quite an achievement.

The BBC today described flibanserin as the "Female Viagra", which is rather confusing, because it's meant to increase sexual desire, which is one thing Viagra (sidenafil) doesn't do. The reason for the Female Viagra headline is that, as Professor John Thorp says:
"It's essentially a Viagra-like drug for women in that diminished desire or libido is the most common feminine sexual problem, like erectile dysfunction is in men"
Yes, one in ten women suffer apparently from "Hypoactive Sexual Desire Disorder" (HSDD) as Boehringer Pharmaceuticals helpfully informs us. And “As many as two out of every 10 women describe some degree of decreased sexual desire" according to the unfortunately named Dr Charles de Wet, Boehringer medical director for the UK.

HSDD is a diagnosis in the DSM-IV, the American Psychiatric Association's listing of psychiatric illnesses, and it's been recognised as a disorder since 1980. It is not, however, a very popular diagnosis yet. There are only 60,000 Google hits for it, as opposed to 1,600,000 for "major depression" and, er, 90,000 for "neuroskeptic". Odd for a disorder apparently plaguing at least 10% of women.

Indeed, some people say that it's no more than a label invented by psychiatrists who didn't understand women and then promoted by drug companies in order to sell drugs. This is almost certainly true, but it's also a bit simplistic, because there are people who perceive themselves as suffering from low libido, and if flibanserin really helps them, that's surely a good thing.

How is flibanserin supposed to work? According to a paper on the Pharmacology of Flibanserin, it's a serotonin receptor 5HT1A agonist and a 5HT2A antagonist. This makes it a kind of cross between the antidepressants nefazadone and buspirone. Neither of these are widely used as antidepressants because they're not considered highly effective. Flibanserin is also a weak dopamine D4 receptor partial agonist. This might underlie its aphrodisiac properties, because drugs which increase dopamine levels are known to enhance motivation and libido (or indeed cause problematic hypersexuality.) In rats and mice, flibanserin has sedative effects and enhances the effects of other sedatives. It also has antidepressant-like effects in some tests but not all. Drug geeks can click the image on the left for more details.

*

Now for the big question - does it actually work? Well, there have been no published clinical trials yet. At all. The trials in depression, where it failed to work, have never been published. Hmm. However, four trials in "Hypoactive Sexual Desire Disorder" were recently completed and the results were presented yesterday at a sexual medicine conference in Europe (ESSM) in the form of three posters (1,2,3). The trials were known as - groan - VIOLET, ORCHID, DAISY and DAHLIA. I probably don't have to tell you that they were all funded by Boehringer Pharmaceuticals.

The main poster is Efficacy of flibanserin 100 mg qhs as a potential treatment for Hypoactive Sexual Desire Disorder in premenopausal women which pools the data from three trials with a total of about 1,400 women. They found that taking flibanserin 100 mg every night had small beneficial effects. Relative to placebo, it increased the number of "satisfying sexual encounters" by 0.7 per month. It also improved scores on questionnaire measures of sexual function, a bit.

In any trial like this you have to ask whether there is result cherry-picking going on. Maybe they asked dozens of questions about the women's sex lives, and they're only telling us about the minority where the drug seemed to work? People often do that but in this case, the Clinical Trials Register suggests there was no funny business of that kind. It also shows that there have been no trials using 100mg which weren't included in the poster, so the trials themselves weren't cherry picked either. That's reassuring. But it looks like the effects were only significant when all three trials were pooled - one poster shows the results of the ORCHID trial alone, and most were non-significant.




What about the side effects? There's a whole poster about them. 100 mg flibanserin nightly caused 14% of patients to drop out due to side effects, vs 7% in the placebo group - so an extra 7% decided it wasn't worth it. It caused dizziness, nausea, fatigue, somnolence - and bizarrely, also insomnia. Notably, 50mg daily was much worse than 100 mg nightly, which suggests that taking this at night, rather than in the morning, is a good idea. But given what it is meant to treat, you'd want to do that anyway, right?

But this leads onto my biggest problem with these findings. It's obvious from the side effects data that this drug is a sedative - it makes you tired and sleepy. The animal data confirm this. It's much more likely to put you to sleep than it is to make you enjoy sex in any given month. Off the top of my head, I suspect its sedative properties are a result of its 5HT2A antagonism.

Any sedative can increase sexual desire, as anyone who has ever been to a bar will know. So whether this drug actually has an aphrodisiac effect, as opposed to just being a sleeping pill, is anyone's guess. To find out, you'd need to compare it to a sleeping pill, say, Valium. Or a couple of glasses of wine. Until someone does that, we don't know if this drug is destined to be the next big thing or a big disappointment.

Edit: Just noticed that Dr Petra Boynton has a fantastic post about the background to flibanserin and the manufacturer's apparent attempt to recruit her to write about HSDD.

[BPSDB]

ResearchBlogging.org

Borsini F, Evans K, Jason K, Rohde F, Alexander B, Pollentier S (2002). Pharmacology of flibanserin. CNS drug reviews, 8 (2), 117-42 PMID: 12177684

AMIGOS PÉROLAS!!!



QUERO DEMONSTRAR A FORMA DO MEU CARINHO POR VOCÊ CONSIDERANDO UMA PÉROLA. VOCÊ, SIM VOCÊ! QUE PASSA POR AQUI TODAS AS MANHÃS BEM CEDINHO.

QUERO LHE HOMENAGEAR COM ESTE LINDO SELO DE:
" AMIGOS PÉROLAS".
ÉS O MEU MAR, O MEU ACONCHEGO E A MINHA TERNURA.

AMIGO MARAVILHOSO, GUARDADO NA CONCHA DO MEU CORAÇÃO.
A TI DEDICO ESTE LINDO SELO.
FIZ PENSANDO EM VOCÊ, MEU AMIGO DE FÉ, MEU IRMÃO CAMARADA. SÃO PALAVRAS QUE SAÍRAM DE UM CORAÇÃO E FELIZ E AMADO.
OBRIGADO PELO CARINHO. ESSAS PALAVRAS, NÃO SÃO PALAVRAS QUALQUER, MAS, SÃO PALAVRAS VINDAS DO CORAÇÃO, QUE ESTÁ MUITO FELIZ COM A SUA AMIZADE.
RECEBA ESTE SELO QEU FIZ COM O CORAÇÃO PARA LHE MOSTRAR O MEU AFETO.
PARA VOCÊ MEU QUERIDO AMIGO(A), SEGUIDORA.
QUE TODAS AS MANHÃS ESTÃO AQUI, JUNTINHO DE MIM!!!
DEDICO PRIMEIRAMENTE EM ESPECIAL PARA:

ANA- DO BLOG PELOS CAMINHOS DA VIDA- QUE BATE PONTO TODOS OS DIAS.
FAÇA SOL OU FAÇA CHUVA. AMO VOCÊ MINHA AMIGA/IRMÃ VIRTUAL

MARCIA- MEUS PENSAMENTOS- MINHA MADRINHA DE BLOG- TAMBÉM IRMA/AMIGA VIRTUAL. TAMBÉM TE AMO.

ISA DO BLOG MOMENTOS MEUS- QUE QUANDO OUBE DA MINHA CIRURGIA, FOI ATÉ FÁTIMA E TROUXE UMA VELA DA SORTE, PARA MINHA PROTEÇÃO.- MUITO OBRIGADA AMIGA.


PARA MYLLA- UMA PESSOA MARAVILHOSA, QUE ME LEVOU PARA ESTE MUNDO VIRTUAL, ONDE GANHEI MUITOS AMIGOS, PRINCIPALMENTE: VOCÊ!

FERNANDA E POEMAS, GRAÇA DO BLOG ZAMBEZIANA, ANNA LUISA
MARIA, MONIQUINHA, ALVARO, ANDREIA, DANIEL, EMANUEL, CHICA
, PARA MINHA QUERIDA MARI AMORIM, NEIDE

REPASSO A TODOS OS MEUS DEMAIS, QUERIDOS AMIGOS(A) QUE SEMPRE ESTÃO AQUI, ME ACOMPANHANDO E CONTRIBUINDO PARA AS MELHORIAS DESTE BLOG.

PARA QUEM FOR REPASSAR ADINATE TERÁ QUE CUMPRIR REGRINHAS:

1) INDICAR O BLOG QUE PRESENTEOU...

2)-INDICAR 05 BLOGS AMIGOS PÉROLAS,

3) DIZER PORQUE PRESENTEOU COM ESTE SELO.

AGORA DEIXO UM CARINHO MUITO ESPECIAL A TODOS, E QUE DEUS LHE ACOMPANHE NESTE LINDO DIA, DE SOL ENSOLARADO.


http://3.bp.blogspot.com/_vzrlnu76oJw/SwLuPTOB3mI/AAAAAAAACbU/Inhys3fT97g/S220/DSC01050.JPG
com muito carinho
Sandra

Tuesday, November 17, 2009

UM LINDO PRESENTE DA MARI AMORIM....

ONTEM AO PASSAR PELOS BLOGS, POR CAUSA DA COLETIVA, REFERENTE A GINCANA, ENCONTREI UM LINDO PRESENTE A MINHA ESPERA.
QUASE TIVE UM COISA.
A MARI AMORIM DO BLOG BRINCANDO COM AS RIMAS, ME PRESENTEOU COM ESTE LINDO PORTA RETRATO.
É MARAVILHOSO. MUITO OBRIGADA AMIGA...
VOCÊ É SIMPLESMENTE DEMAIS.
É O QUE EU SEMPRE DIGO. AMIGOS SE CONQUISTAM.
SÃO AS NOSSAS PÉROLAS.

SÃO NOSSOS BOTÕES DE ROSAS!!!

VEJAM QUE LINDO.
VEJAM QUE LINDO.
EM DEMBRO ESTAREMOS COMPLETANDO UM ANO!!!

MUITO OBRIGADA AMIGA. VOCÊ É MARAVILHOSA.
VENHAM CONHECER ESTE LINDO BLOG. http://felinodamadrugada1.blogspot.com/


APROVEITO AINDA, PARA AGRADECER A TODOS QUE COM PARTILHARAM DA FESTA SURPRESA DO QUERIDO AMIGO JOÂO.

NÃO DEIXE DE CONHECER ESTES LINDOS CANTINHOS

Poetas-Um Vôo Livre
(Tem Amor)


Sinal de Liberdade-uma expressão de sentimento
(Tem Sentimentos)

Blog Coletivo-Uma Interação de Amigos
(tem debate e presentes..Vá nas postagens)

Meus Mimos!
(Tem presentes: Vários, veja nas postagens, siga a lista, vai descendo..)


Te espero lá. Se você ainda pegou seu presenta, corre lá.

Monday, November 16, 2009

B-Movie Medicine

We all know about movies that are so bad, they're good. But could the same thing apply to doctors?

As I described last week, Desiree Jennings is a young woman from Virginia who developed horrible symptoms, including muscle spasms and convulsions, after getting a flu vaccine. It looked a bit like a form of brain damage called dystonia.

Numerous neurologists concluded that her illness was mostly or entirely psychogenic. A certain Dr Rashid Buttar, however, said that she was suffering from neurological damage caused by toxins in the flu vaccine.

Buttar gave her chelation therapy to flush the toxins out. Within 15 minutes, she was cured. Biologically speaking, this is ludicrous. It's flat-out impossible that chelation could reverse brain damage in 15 minutes, even if Jennings did have brain damage in the first place.

But Buttar's treatment worked, amazingly well by all accounts. This is not surprising, because the illness was psychological in nature, and Dr Buttar's treatment was, psychologically, very effective. Jennings was admitted to Dr Buttar's private clinic; she had IV lines put in to her arm; Dr Buttar attached the chelation treatment to the IV drip and, in a textbook example of how to produce a placebo effect:
I told her "Now the magic should start", prepared her for what I expected to happen. (interview with Dr Buttar, 05:30 onwards)
The magic did indeed happen, precisely because Dr Buttar convinced Jennings that it would.

*

What would have happened to Jennings if there were no Dr Buttars in the world? Her doctors would have run scans and tests to check if Jennings had any neurological damage. The results would have been normal. Jennings would probably have interpreted this as "We don't know what's wrong with you", although experts would have suspected that the symptoms were most likely psychogenic.

At some point, someone would have had to raise that possibility with her. But the point about psychogenic illness is that it's not "faking", "acting" or "made up" - the patient believes they are ill. The symptoms don't feel psychogenic. This is why people often interpret the suggestion that symptoms are psychogenic as saying "you're not really ill" and hence "you're either lying, or crazy". Of course, patients suffering from psychogenic illness are neither, and they know it.

So, without complementary and alternative medicine, Jennings might have ended up believing herself to be suffering from an illness so obscure that doctors were unable to diagnose it, and hence, unable to cure it. A hopeless situation. A worse thing for someone with psychogenic symptoms to believe is hard to imagine.

Dr Buttar's treatment was psychologically very powerful - precisely because he believed in it, so he was able to convince Jennings to believe in it. A doctor who realized that Jennings' symptoms were psychogenic would have found it much harder to achieve the same result. In order to do so, they would have to lie to her, by pretending to believe in a treatment which they knew was just a placebo. This is hard - the doctor would need to be an excellent actor as well as a medic - not to mention ethically tricky.

Interestingly, 100 years ago, this problem wouldn't have arisen. Doctors knew much less about diagnosis and there were few laboratory tests or scans in those days, so there was usually no way to prove that some symptoms were organic and others were psychogenic. Everyone got the same treatment. Of course, the treatments back then were less good at treating organic illnesses, but that wouldn't necessarily have made them any worse as placebos. Ironically, as mainstream medicine gets better and better at diagnosing and treating disease, it may be getting worse at dealing with psychogenic symptoms.

[BPSDB]

B-Movie Medicine

We all know about movies that are so bad, they're good. But could the same thing apply to doctors?

As I described last week, Desiree Jennings is a young woman from Virginia who developed horrible symptoms, including muscle spasms and convulsions, after getting a flu vaccine. It looked a bit like a form of brain damage called dystonia.

Numerous neurologists concluded that her illness was mostly or entirely psychogenic. A certain Dr Rashid Buttar, however, said that she was suffering from neurological damage caused by toxins in the flu vaccine.

Buttar gave her chelation therapy to flush the toxins out. Within 15 minutes, she was cured. Biologically speaking, this is ludicrous. It's flat-out impossible that chelation could reverse brain damage in 15 minutes, even if Jennings did have brain damage in the first place.

But Buttar's treatment worked, amazingly well by all accounts. This is not surprising, because the illness was psychological in nature, and Dr Buttar's treatment was, psychologically, very effective. Jennings was admitted to Dr Buttar's private clinic; she had IV lines put in to her arm; Dr Buttar attached the chelation treatment to the IV drip and, in a textbook example of how to produce a placebo effect:
I told her "Now the magic should start", prepared her for what I expected to happen. (interview with Dr Buttar, 05:30 onwards)
The magic did indeed happen, precisely because Dr Buttar convinced Jennings that it would.

*

What would have happened to Jennings if there were no Dr Buttars in the world? Her doctors would have run scans and tests to check if Jennings had any neurological damage. The results would have been normal. Jennings would probably have interpreted this as "We don't know what's wrong with you", although experts would have suspected that the symptoms were most likely psychogenic.

At some point, someone would have had to raise that possibility with her. But the point about psychogenic illness is that it's not "faking", "acting" or "made up" - the patient believes they are ill. The symptoms don't feel psychogenic. This is why people often interpret the suggestion that symptoms are psychogenic as saying "you're not really ill" and hence "you're either lying, or crazy". Of course, patients suffering from psychogenic illness are neither, and they know it.

So, without complementary and alternative medicine, Jennings might have ended up believing herself to be suffering from an illness so obscure that doctors were unable to diagnose it, and hence, unable to cure it. A hopeless situation. A worse thing for someone with psychogenic symptoms to believe is hard to imagine.

Dr Buttar's treatment was psychologically very powerful - precisely because he believed in it, so he was able to convince Jennings to believe in it. A doctor who realized that Jennings' symptoms were psychogenic would have found it much harder to achieve the same result. In order to do so, they would have to lie to her, by pretending to believe in a treatment which they knew was just a placebo. This is hard - the doctor would need to be an excellent actor as well as a medic - not to mention ethically tricky.

Interestingly, 100 years ago, this problem wouldn't have arisen. Doctors knew much less about diagnosis and there were few laboratory tests or scans in those days, so there was usually no way to prove that some symptoms were organic and others were psychogenic. Everyone got the same treatment. Of course, the treatments back then were less good at treating organic illnesses, but that wouldn't necessarily have made them any worse as placebos. Ironically, as mainstream medicine gets better and better at diagnosing and treating disease, it may be getting worse at dealing with psychogenic symptoms.

[BPSDB]

FESTA SURPRESA PARA VOCÊ AMIGO!!




HOJE É UM DIA MUITO ESPECIAL PARA M
IM...
QUERO JUNTO COM ESTE LINDO AMIGO, COMEMORAR MAIS UMA DATA MUITO ESPECIAL: SEU ANIVERSÁRIO.
PARABÉNS JOÃO MENERÉS. PARA VOCÊ, TODO ESTE CARINHO


NÃO ACHOU QUE EU IRIA DEIXAR PASSAR, NÃO É????

AMIGOS É PARA SEREM GUARDADOS NO LADO ESQUERDO DO CORAÇÃO.

(Tomei a liberdade e trouxe do blog da Luisa)

PESSOA MARAVILHOSA. AMA A VIDA, LEVANTA CEDO E SAI PELAS RUAS A FOTOGRAFAR A VIDA.
ESTE É O MEU QUERIDO AMIGO JOÃO.
SEMPRE BEM COM A VIDA!

SEJA MUITO FELIZ HOJE AMIGO.

LINDA PORTUGAL QUE TEM VOCÊ...
UM CORAÇÃO CHEIO DE AMOR E PACIÊNCIA.
PARABÉNS AMIGO!!!
http://1.bp.blogspot.com/_TPh_fZjUkQk/SrJ82MWY8BI/AAAAAAAAA0Q/2M5Lie_-4JM/s400/JM_RETRATO_para_LA_VANU.13.09.2009.jpg





Recado Para Orkut - Aniversário: 3

CONVIDO VOCÊ MEU AMIGO SEGUIDOR E VISITANTE PARA JUNTOS IRMOS ATÉ LÁ PRESTAR ESTA HOMENAGEM SURPRESA PARA MEU QUERIDO JOÃO.


VAMOS BRINDAR COM CHAMPANHE BEM GELADINHA, ESTA LINDA DATA.

COMER BOLO....

CLICK NESTE ENDEREÇO E VAMOS

http://grifoplanante.blogspot.com/