I have noticed that everytime I take a supplement that increases dopamine (for example l-tyrosine, NADH) I get the dopamine boost after one hour of taking the supplement but it takes 5-6 hours to increase noradrenaline. I think I'm low in noradrenaline as it usually has so pronounced effects on me, like it relieves my fatigue and brain fog, makes me calmer and less depressed, helps with POTS and makes me warmer (I'm always cold).
Conversion from dopamine to noradrenaline needs vitamin c and copper. I have supplemented both of these but haven't noticed any benefits concerning this issue.
I tried loading up on precursors, cofactors, and methylation support, but to no avail. That seems like the place to start, it just that my body still wouldn't convert to norepi. I now take Droxidopa, which is extremely helpful. Strattera is also helpful. Here is a thread which discusses both:
https://forums.phoenixrising.me/thr...wisdom-regarding-this-med.42680/#post-2410381
My 23andme report uploaded to one of the gene sites also shows a lot of polymorphisms in the DBH gene--10 of them out of a total of 17 show on the report.
I have 29 variants that were tested for DBH on my 23andMe raw data, no sure why I have more tested. Anyhow, about 17 show homo or heterozygous for the minor allele, but to be honest, I don't think it has any clinical significance. Most (all?) of the SNPs list are not clinically significant and/or the allele variants occur at a close to 50/50 ratio in the population.
It looks like DBH deficiency is diagnosed by clinical symptoms, serum catecholamine levels (high dopamine, low epi and norepi) and serum levels of DBH. The genetics are still being worked out. This paper identifies several DBH polymorphisms that are associated with DBH deficiency:
https://www.ncbi.nlm.nih.gov/books/NBK1474/. Unfortunately, none of them are included in the 23andMe data.
I wonder if a person with DBH defiency has noradrenaline defiency symptoms always since birth. I didn't have any before I got sick with CFS.
I think I may have had some symptoms early on like poor exercise tolerance (but I could still do it), apathy, low energy, and low blood pressure (but not incapacitating), but I was still a functional human. I certainly didn't have these symptoms to the extent described in the literature for DBH deficiency.
Now, my blood pressure can drop to less than 80 systolic without compression and medication, but I don't have ptosis (drooping eyelids), nausea, vomiting, or some of the other symptoms described in DBH deficiency. A urinary neurotransmitter profile showed I have low catecholamines, including dopamine, but I am waiting on results from a fractionated serum catecholamine test (dopamine, epi, norepi), so hoping that will tell me more. Testing for BH4 did show any problems there.
I don't think I have classical DBH deficiency, but maybe I have a SNP in DBH that is not yet recognized that causes it to function slower than normal. Or I may have a CNS dysautonomia in the hypothalamus or brainstem causing my body to be unable to regulate blood pressure. It remains a mystery.