ChemicalBeauty
Bluelighter
2nd worst article ever.
qwe said:how do they know that the pills were usually mostly MDMA?
felixdahousekat said:I would like to see it compared to alcohol use, to put things into perspective.![]()
lifeisforliving said:*shrug* I look back at my use of MDMA, which was usually 400 to 600mg a night (once a month or so, off and on for 8 years), and then look at my grades in university... it sure hasn't hurt my intellect as measured by my GPA. I definitely experienced symptoms which only abated after 6 months of stopping MDMA, but I haven't noticed any permanent changes in my personality or memory...
The war has been set, the sides are clearly defined and its the dark side that is using misinformation and emotional headlines against our cold hard logic.
I exercise a healthy dose of skepticism when concerning these recent scientific discoveries about the "dangers" of illicit drugs. At one point, the article maintains that the drug is dangerous in excessive volume. It went on to say that heavy and consistent dosage can incur damage to neurons and severe mood fluctuations. I believe this is fundamental reasoning concerning any substance--be it intoxicating, mind-altering or simply nourishing (i.e. the exhausted old platitude, "All Things In Moderation").
Rated E said:They didn't claim the test was about MDMA. Look at the title, it says "ecstasy use".
^ Yep, you got me.go-ee said:While I appreciate the fact that you guys are scrutinizing the article (which should be done upon presentation of any scientific paper). I think many of you are missing the point and trying to justify your usage of MDMA.
Church said:Bahahaha! You're joking, right? 8(
To study the causal nature of ecstasy use on neuroimaging, neurocognitive, and clinical abnormalities observed in ecstasy users and to determine the effect of relatively low cumulative dosages of ecstasy, a sample of 188 ecstasy-naive young adults (aged 18 to 35 years) with a relatively high probability to start using ecstasy in near future was followed during a period of 12 to 24 months (Figure 2). They were actively recruited between March 2002 and April 2004, using a combination of targeted site sampling at locations such as dance events, discotheques, youth fairs, universities, colleges, and parks; advertisement through a Web site on the project and an Internet campaign; and snowball sampling referrals. Main criteria for inclusion were intent (probable or certain) to use ecstasy for the first
time in the near future (3-5 points on a 5-points scale; 1 = certainly not; 2 = probably not; 3 = undecided; 4 = probably yes; 5 = certainly yes) and/or having one or more friends who already use ecstasy.
After baseline examination subjects had to complete questionnaires sent to them by mail about their drug use every 3 months during a follow-up period of 1 year.
Besides assessing drug use through these questionnaires, the main outcome parameters were assessed up to three times: (Tl) directly following recruitment, i.e. before first ecstasy use, in the total cohort (N = 188); (T2) soon after first ecstasy use in the first 30 incident ecstasy users; (T3) between 12 and 24 months after baseline assessment in (T3a) all incident ecstasy users (N = 50-60), and in (T3b) an individually matched (gender, age, DART-IQ, cannabis use) control group of persistent ecstasy-naive subjects (N = 50-60). Single photon emission computed tomography (SPECT) imaging was only performed twice because of radiation exposure (at the first and third session). Follow-up measurements were finished in June 2005.
To study whether a low dose of ecstasy use is neurotoxic, outcome parameters of neurotoxicity will be compared between the first follow-up session soon after first ecstasy use in 30 incident cases (T2) and their baseline sessions before first ecstasy use (Tl). We
will also investigate whether ecstasy users differ from ecstasy-naive subjects on indicators of neurotoxicity and if so, whether differences were present before or developed after the first use of ecstasy. In order to examine this, indicators of neurotoxicity of incident ecstasy users (T3a) will be compared with persistent ecstasy-naive subjects (T3b) and both groups will be compared with their own baseline data (Tl).
Moreover, to assess whether certain variables (such as higher levels of depression, impulsivity and sensation seeking) can be considered as risk-factors for future ecstasy use in ecstasy-naive young adults, baseline data of incident ecstasy users (i.e. before first ecstasy use)
will be compared with baseline data of persistent ecstasy-naive subjects. Finally, dopamine transporter (DAT) densities will be compared before and after ecstasy use in a subgroup of incident ecstasy users to specify possible effects of ecstasy use on the dopamine
neurotransmitter system.
I don't think he was joking.
mdma = mdma
ecstacy = sometimes mdma, sometimes meth, sometimes mda, mde, ketamine etc etc etc
I have no cognitive impairment from light E use over a 2 year period 4-6 years ago. I used approximately 20 pills over 12 experiences in that 2 year period. I used moderately at times and binged at others (4 pills in a night at one point and 3 in 2 days at another, while only taking 1/2 a pill in a 6 month period at others). I have limited experience with other drugs but overall have maintained a relatively healthy diet and exercise program over the course of those 6 years.
I feel completely fine. I feel I have the same intellectual capacity and actualy an improved ability to recall certain events than I did prior to use.
I don't know all the details of the study but I think the long term effects of ecstasy use is going to be extremely hard to quantitize. Every user has a different history. Some used lightly, some moderly, and some just went crazy. Some people used a lot of other drugs in conjunction with ecstasy, some did not. Some abused their body by maintaining an unhealthy diet throghout their period of use, worsening the side effects. Some people pre and post load and space their rolls to maximize the body's regenerative capacities.
Lastly, the brain regrows. You have to use it though! If you challenge yourself intellectually you will always be improving your cognitive function. If you binge hard on drugs, fall into a lifestyle devoid of intellectual stimulation, and have a terrible diet, is it any surprise your brain will atrophy? Any brain would in such a situation, with or without the ecstasy.
Anyway that's just how I feel about the subject. I never felt like ecstasy impaired me long term but it did leave me feeling emotionally fragile for a few weeks after use and I think it has a higher potential for damage than say, marijuana or alcohol or even cocaine.
go-ee said:I have a copy of the full actual article (it is in several journals) and here is the design section for the sub-section we are talking about. The actual experiment is very large and had several sub-sections. More so, it controls for a huge variety of factors. The section we are talking about (and is the focus in the BBC study) is the prospective substudy. I have no idea what you are talking about Vecktor, your idea of what they did in the experiment is not what was performed.