- Joined
- Sep 21, 2016
- Messages
- 1,243
- Reaction score
- 2,336
- Points
- 5,596
- Location
- Kier, PE
- Fellow [Any Field]
There's emerging evidence that vitamin D levels are the reason why MS goes up in the more extreme lattitudes. As we know several neurological and psychiatric disorders, prevention is probably the best step. Better to not get MS at all since there's no cure. Same with schizophrenia. For this reason I'm pretty loose with recommending patients get Vitamin D levels, and consistent with recent data almost all my patients have Vitamin D deficiencies.
I'm suspecting Vitamin D could be a potential and exploitable factor in preventing Schizophrenia and Bipolar Disorder.
Heh I just saw a patient who had this work done, shiesta city. I guess they sleep at night on their yachts because I don't otherwise know how you could be a physician, do that work, and sleep at night.Lots of "integrative, holistic" clinics around here offering a urine neurotransmitter metabolite testing panel which is sold by the company that also sells the supplements to correct those levels to the "recommended" (rather than lab ref normal) value (as if there's any useful correlation or treatment function with either.) Nothing to see regarding kickbacks or conflicts of interest there...
Heh I just saw a patient who had this work done, shyster city. I guess they sleep at night on their yachts because I don't otherwise know how you could be a physician, do that work, and sleep at night.
Repleting is probably protective for bone health and reduces thinning but the prevailing thinking seems to be that low vitamin D levels are a marker or correlate with ill health, rather than playing a causal role.
I always ask for TSH labs if they've been done and will ask for them if there's associated physical symptoms with the depression or anxiety to suggest an abnormality. I haven't had too many patients whose mood symptoms resolved or dramatically improved with treatment, but I have had quite a few patients who needed adjustments to their meds who may not have gotten them otherwise who did feel better when it was addressed. I don't regularly order Vitamin D on an outpatient basis, but may throw it on if they're getting other labs drawn, especially if it's been low previously and they're not on a supplement.How often are you all checking vitamin D, B12, folate, TSH levels? I don't get it unless there's something on the history on the ROS to make me suspicious enough of it. I'm not getting everyone with treatment resistant depression to get the labs, but I feel like this is more common practice. I just think the pretest probability would be low. In my area, it seems like everyone would be low on Vitamin D for half if not most of the year based on the amount of sun we get regardless of their depression status.
I feel like I keep getting asked by patients about magnesium, 5HTP, GABA, inositol, ashwagandha, theanine, fish oil, coenzyme q10, and all these other supplements that don't seem to have much evidence base, but I also haven't searched it myself for any RCTs or data on it for the most part. I have seen the RCT on Silexan but haven't used it in my practice. I also don't know how they interact with the meds I'm prescribing since most people don't tell me they are taking them, when they're starting or stopping them, and I'm not asking every appointment outside of the intake if they are.
This is the right answer. Us primary care types went through the same thing with HDL and niacin.The problem is whenever we look at whether repleting Vit D actually alleviates most of the negative conditions it is associated with, the answer is usually "no." Repleting is probably protective for bone health and reduces thinning but the prevailing thinking seems to be that low vitamin D levels are a marker or correlate with ill health, rather than playing a causal role.
That's pretty huge if you could use a supplement to the point where around 6 of your patients no longer want a benzo. I'll use it for every patient with an anxiety disorder who wants a benzo if that's the case if I can even reduce a % of them, even if it isn't the majority. I feel like SSRIs also don't help completely resolve depression/anxiety in a majority of patients anyways. Are there any risks to using Silexan?There is evidenced based data that Silexan (found in lavender) can work well for anxiety. I've told patients to try it. So far about of 20 patients, 1/3 reported significant benefit (like they don't want to take a benzo anymore kind of improvement). Now while that benefit was significant this was below the majority so don't go there expecting this to work.
That's pretty huge if you could use a supplement to the point where around 6 of your patients no longer want a benzo. I'll use it for every patient with an anxiety disorder who wants a benzo if that's the case if I can even reduce a % of them, even if it isn't the majority. I feel like SSRIs also don't help completely resolve depression/anxiety in a majority of patients anyways. Are there any risks to using Silexan?
Has anyone else noticed that basically everyone who has vitamin D levels drawn are somehow deficient in vitamin D?
This is a feature of moderity not a problem with the lab draws. When we were hunting/gathering/farming outside as a species it would not be a problem. Many people aspire to avoid time outside these days...Has anyone else noticed that basically everyone who has vitamin D levels drawn are somehow deficient in vitamin D?
Seems a bit paranoid to me. What could possibly be the motivation fot SDN to remove a post mentioning a brand of this stuff? This forum is meant for us to collaborate and share knowledge, even if that's suggesting one drug or brand over another.If I mention the name this post will likely get struck down.
Seems a bit paranoid to me. What could possibly be the motivation fot SDN to remove a post mentioning a brand of this stuff? This forum is meant for us to collaborate and share knowledge, even if that's suggesting one drug or brand over another.
That's pretty huge if you could use a supplement to the point where around 6 of your patients no longer want a benzo. I'll use it for every patient with an anxiety disorder who wants a benzo if that's the case if I can even reduce a % of them, even if it isn't the majority. I feel like SSRIs also don't help completely resolve depression/anxiety in a majority of patients anyways. Are there any risks to using Silexan?
I think Carlat has covered this fairly extensively. Reportedly, in the right ratio (EPA > DHA), the effect size is pretty remarkable with regard to mood lability in borderline.Isn't there somewhat reasonable evidence for Omega-3 fatty acids as well? I've seen some data in borderline personality, as well as depression.
There’s evidence for omega 3 in schizophrenia and the APA has even recommended all psychotic people be on omega 3s
But doesn’t the APA recommend them for all psychotic patients?There was a time when omega-3s looked like they made a big difference in first episode psychosis, but the big international multi-center trial was a total bust, with the caveat that the control condition was also receiving CSC-style care. This would be unremarkable in a FEP program but doesn't really happen outside of them.
No, definitely not. The practice guidelines don't mention anything about omega-3s. Years ago, there was an APA omega-3 subcommittee that said there was evidence supporting the use of omega-3s for mood disorders but said the evidence was less clear for psychosis. In addition, the committee was formed with several integrative psychiatrists and one now known sex offender. But the APA never recommend omega-3s for all patients- psychotic or otherwise.But doesn’t the APA recommend them for all psychotic patients?
It seems like there was a recommendation at one point in time I guess it’s been revisedNo, definitely not. The practice guidelines don't mention anything about omega-3s. Years ago, there was an APA omega-3 subcommittee that said there was evidence supporting the use of omega-3s for mood disorders but said the evidence was less clear for psychosis. In addition, the committee was formed with several integrative psychiatrists and one now known sex offender. But the APA never recommend omega-3s for all patients- psychotic or otherwise.
This article is inaccurateIt seems like there was a recommendation at one point in time I guess it’s been revised
Trim the fat: the role of omega-3 fatty acids in psychopharmacology - PMC
The American Psychiatric Association (APA) currently recommends the use of omega-3 fatty acid supplementation for depressive disorders, impulse-control disorders, and psychotic disorders in treatment guidelines. This review examines the evidence for ...www.ncbi.nlm.nih.gov
Yes have also had responses to Silexan 80 mg nightly. Good effect size and side effect profile, appeals to a lot of people due to its supplement-esque nature. Certainly higher on my list than Buspar for unspecified anxiety at this point. And 40 cents a capsule on Amazon.I have now had a few patient's report positive results with Silexan, and it's certainly been well tolerated even among my patients who did not benefit. I would say this should be pretty high up on treatment algorithms for anxiety and the very top for patient's who are worried about pharmaceuticals (of course I would much rather have the pharmaceutical version from Europe but you can get the proprietary blend on Amazon for a very reasonable price).
I have now had a few patient's report positive results with Silexan, and it's certainly been well tolerated even among my patients who did not benefit. I would say this should be pretty high up on treatment algorithms for anxiety and the very top for patient's who are worried about pharmaceuticals (of course I would much rather have the pharmaceutical version from Europe but you can get the proprietary blend on Amazon for a very reasonable price).
I'll add a 3rd data point for Silexan. Have had a few patients do great with this and given how benign it is (most common side effect is lavender burps!) seems like a fantastic option.Yes have also had responses to Silexan 80 mg nightly. Good effect size and side effect profile, appeals to a lot of people due to its supplement-esque nature. Certainly higher on my list than Buspar for unspecified anxiety at this point. And 40 cents a capsule on Amazon.
I am suprised to see this. I've been concerned by the likely at least partial GABAergic mechanism, hepatotoxicity, and med interaction concerns particularly in the setting of few trials looking at ashwaganda, but an openevidence search suggests there's been some reassuring findings re: CYP interactions at least.I'll add a 3rd data point for Silexan. Have had a few patients do great with this and given how benign it is (most common side effect is lavender burps!) seems like a fantastic option.
I'll also add a plug for Ashwagandha for some patients. Biggest thing I educate them on there is that the recommended dose is a lot lower than what some supplements have (recommended is 200-300mg BID vs supplements with 1,000mg+ per capsule) and that higher doses can increase GI issues. I have a few patients that have switched to it as an alternative to their cannabis which imo is a big win for those I was otherwise unable to convince to drop the weed.
Agreed, I would also be concerned recommending ashwaganda.I am suprised to see this. I've been concerned by the likely at least partial GABAergic mechanism, hepatotoxicity, and med interaction concerns particularly in the setting of few trials looking at ashwaganda, but an openevidence search suggests there's been some reassuring findings re: CYP interactions at least.
I am suprised to see this. I've been concerned by the likely at least partial GABAergic mechanism, hepatotoxicity, and med interaction concerns particularly in the setting of few trials looking at ashwaganda, but an openevidence search suggests there's been some reassuring findings re: CYP interactions at least.