Gerovital: Difference between revisions

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[Addendum: It is of the opinion of this editor it is not a coincidence that the actual studies are simply not even mentioned. The actual evidence shows that GH3 as a reversible monoamine oxidase inhibitor i.e. it increases the availability of neurotransmitters such as serotonin and dopamine, together with lowering cortisol, is a potential treatment for anxiety, depression, which can, in turn, improve outcome, thus might, in fact, have "any health benefit" as our sycophants for the war on drugs are all too quick to allege. We see in one study in 2015 that:
[Addendum: It is of the opinion of this editor it is not a coincidence that the actual studies are simply not even mentioned. The actual evidence shows that GH3 as a reversible monoamine oxidase inhibitor i.e. it increases the availability of neurotransmitters such as serotonin and dopamine, together with lowering cortisol, is a potential treatment for anxiety, depression, which can, in turn, improve outcome, thus might, in fact, have "any health benefit" as our sycophants for the war on drugs are all too quick to allege. We see in one study in 2015 that:


"Participants were men and women between 50 and 89 years of age, with a median of 62.53 years. Before the intervention, the demographic characteristics and the baseline SF-36 scores, low mood, and anxiety statuses were comparable (p > 0.05). After the 12-week intervention, the scores of role-physical (RP), bodily pain (BP), general health (GH), vitality (VT), mental health (MH) and health transition (HT), mental composite score (MCS) of the G.H.3. group were higher than the placebo group (p < 0.05), There were no significant differences in other domains in SF-36 and PCS between the two groups(p > 0.05), the scores of SDS and SAS in the G.H.3. group were both lower than the placebo group(p < 0.01), the prevalence rates of low moods in the G.H.3. group and the placebo group were 20.8 % and 34.0 % respectively, no significant difference was found (χ2 =2.127,p = 0.145), while the prevalence rate of clinical anxiety concerns in the G.H.3. group was 2.1 %, which was significantly lower than the placebo group, 22.0 % (χ2 =9.040,p < 0.001)." <ref name="Gang Xu, Zhaochun Cao, Mina Shariff, Pingping Gu, Tuong Nguyen, Tian Zhou, Rong Shi & Jianyu Rao">{{cite journal |title=Effects of G.H.3. On mental symptoms and health-related quality of life among older adults: results of a three-month follow-Up study in Shanghai, China |url=https://nutritionj.biomedcentral.com/articles/10.1186/s12937-016-0133-5 |journal=Nutrition Journal |year=2015 |access-date=26 January 2016 |location=Shanghai, China|doi=10.1186/s12937-016-0133-5 |last1=Xu |first1=Gang |last2=Cao |first2=Zhaochun |last3=Shariff |first3=Mina |last4=Gu |first4=Pingping |last5=Nguyen |first5=Tuong |last6=Zhou |first6=Tian |last7=Shi |first7=Rong |last8=Rao |first8=Jianyu |volume=15 |page=9 |pmid=26813677 |pmc=4729140 }}</ref>]
"Participants were men and women between 50 and 89 years of age, with a median of 62.53 years. Before the intervention, the demographic characteristics and the baseline SF-36 scores, low mood, and anxiety statuses were comparable (p > 0.05). After the 12-week intervention, the scores of role-physical (RP), bodily pain (BP), general health (GH), vitality (VT), mental health (MH) and health transition (HT), mental composite score (MCS) of the G.H.3. group were higher than the placebo group (p < 0.05), There were no significant differences in other domains in SF-36 and PCS between the two groups(p > 0.05), the scores of SDS and SAS in the G.H.3. group were both lower than the placebo group(p < 0.01), the prevalence rates of low moods in the G.H.3. group and the placebo group were 20.8 % and 34.0 % respectively, no significant difference was found (χ2 =2.127,p = 0.145), while the prevalence rate of clinical anxiety concerns in the G.H.3. group was 2.1 %, which was significantly lower than the placebo group, 22.0 % (χ2 =9.040,p < 0.001)." <ref name="Gang Xu, Zhaochun Cao, Mina Shariff, Pingping Gu, Tuong Nguyen, Tian Zhou, Rong Shi & Jianyu Rao">{{cite journal |title=Effects of G.H.3. On mental symptoms and health-related quality of life among older adults: results of a three-month follow-Up study in Shanghai, China |url= |journal=Nutrition Journal |year=2015 |access-date=26 January 2016 |location=Shanghai, China|doi=10.1186/s12937-016-0133-5 |last1=Xu |first1=Gang |last2=Cao |first2=Zhaochun |last3=Shariff |first3=Mina |last4=Gu |first4=Pingping |last5=Nguyen |first5=Tuong |last6=Zhou |first6=Tian |last7=Shi |first7=Rong |last8=Rao |first8=Jianyu |volume=15 |page=9 |pmid=26813677 |pmc=4729140 }}</ref>]


==Development and marketing==
==Development and marketing==

Revision as of 09:53, 24 April 2021

Original presentation of Gerovital

Gerovital H3 (or procaine hydrochloride and products known as GH3 and other variants which may or may not be identical to Gerovital H3) is a preparation developed during the 1950s and promoted by its advocates as an effective anti-aging treatment. In the United States, the FDA bans Gerovital H3 from interstate commerce as an unapproved drug and, since 1982, has prohibited its importation.

Gerovital is promoted with false claims [according to whom?] of its curative abilities for a wide range of human ailments; research has found no evidence that it has any health benefit [citation needed][the claim that research has found no evidence that it has any health benefit -- is not backed by any citation of a study or review. In fact, there are studies that show evidence for a benefit - albeit not for the dubious purpose of 'anti-aging' which is itself a straw-man of an absurd type.] or "anti-aging" [citation needed] [who is making that claim other than a single article cited over and over again from 2013?] properties.[1]

[Addendum: It is of the opinion of this editor it is not a coincidence that the actual studies are simply not even mentioned. The actual evidence shows that GH3 as a reversible monoamine oxidase inhibitor i.e. it increases the availability of neurotransmitters such as serotonin and dopamine, together with lowering cortisol, is a potential treatment for anxiety, depression, which can, in turn, improve outcome, thus might, in fact, have "any health benefit" as our sycophants for the war on drugs are all too quick to allege. We see in one study in 2015 that:

"Participants were men and women between 50 and 89 years of age, with a median of 62.53 years. Before the intervention, the demographic characteristics and the baseline SF-36 scores, low mood, and anxiety statuses were comparable (p > 0.05). After the 12-week intervention, the scores of role-physical (RP), bodily pain (BP), general health (GH), vitality (VT), mental health (MH) and health transition (HT), mental composite score (MCS) of the G.H.3. group were higher than the placebo group (p < 0.05), There were no significant differences in other domains in SF-36 and PCS between the two groups(p > 0.05), the scores of SDS and SAS in the G.H.3. group were both lower than the placebo group(p < 0.01), the prevalence rates of low moods in the G.H.3. group and the placebo group were 20.8 % and 34.0 % respectively, no significant difference was found (χ2 =2.127,p = 0.145), while the prevalence rate of clinical anxiety concerns in the G.H.3. group was 2.1 %, which was significantly lower than the placebo group, 22.0 % (χ2 =9.040,p < 0.001)." [2]]

Development and marketing

The impetus for developing the drug is sometimes alleged to have come from Nicolae Ceaușescu, who funded the establishment of a research organization, the National Institute of Geriatrics, in Bucharest, Romania, headed by Ana Aslan (1897–1988).[1]

From the 1950s until her death in 1988, Aslan promoted Gerovital H3 with great success. In the 1960s and 1970s her Romanian clinic, the Parhon Institute, became a mecca for celebrities seeking treatment, and an upscale tourist attraction. The New York Times referred to Gerovital's "jet-set aura," noting that Aslan had been covered in "society columns where such public figures as Nikita S. Khrushchev, Konrad Adenauer, and Ibn Saud have been listed among the multitudes said to have taken the drug." As late as 1988 an advertisement by the Romanian National Tourist Office lauded "the picturesque and exciting cities, scenic delights, famous resorts (including Gerovital H3 treatment centers), cultural and historic treasures that await the traveler to Romania."[3]

With the rise of the Web Gerovital has enjoyed a new lease of promotional life as it is promoted by many sites with claims of its "cure-all" abilities.[1]

Denouncement

A 1973 New York Times[medical citation needed] article said "cold water was thrown on [Gerovital]'s reputation years ago" by "three reports published simultaneously in British Medical Journal [that said it] found no merit for procaine hydrochloride for any of the problems of aging."[4]

Some clinical trials in the mid-to-late 1970s suggested that Gerovital H3 acts as a weak, competitive, reversible MAO inhibitor, and so may have some antidepressant value, but otherwise has a negligible effect on disease. In 1994, the U.S. FDA Consumer magazine said: "No health claims for Gerovital have been substantiated, and FDA considers it an unapproved new drug. It has caused low blood pressure, respiratory difficulties, and convulsions in some users."[5] Suppliers assert that the product is safe, and one cites a brief quotation from a newspaper article that says "while as early as 1973 Elmer Gardner of the FDA's Bureau of Drugs stated 'There is no safety problem with Gerovital H-3.'"[6]

Effectiveness

There is no evidence that Gerovital is helpful in slowing aging or treating illness.[1]

Drug or nutrient?

Procaine itself is often considered to be a drug. Earlier references by advocates of Gerovital H3 refer to it as a drug. Hoffer and Walker (1980) call it a "youth drug." Mircea Dumitru, Aslan's colleague and personal physician, describes it as "a complex drug acting like the procaine molecule ... The addition of benzoic acid, potassium and disodium phosphate increase the effects of Gerovital-H3 biotrophic treatment."[7]

FDA ban

As of 2004, the FDA's 1982 automatic detention alert is still in effect and bans the import of Gerovital H3 into the U.S. as "a new drug within the meaning of 201(p), without an approved new drug application [Unapproved New Drug, Section 505(a)]."[8]

The ban covers:

  • Gerovital, GH3, KH3, Zell H3, GH3 etc. This order was rescinded for GEROVITAL Cosmetics Lines, not containing procaine.
  • finished injectable or oral Procaine Hydrochloride

References

  1. ^ a b c d Perls T (June 2013). "The reappearance of procaine hydrochloride (Gerovital H3) for antiaging". J Am Geriatr Soc. 61 (6): 1024–5. doi:10.1111/jgs.12278. PMID 23772727. S2CID 41813351.
  2. ^ Xu, Gang; Cao, Zhaochun; Shariff, Mina; Gu, Pingping; Nguyen, Tuong; Zhou, Tian; Shi, Rong; Rao, Jianyu (2015). "Effects of G.H.3. On mental symptoms and health-related quality of life among older adults: results of a three-month follow-Up study in Shanghai, China". Nutrition Journal. 15. Shanghai, China: 9. doi:10.1186/s12937-016-0133-5. PMC 4729140. PMID 26813677. {{cite journal}}: |access-date= requires |url= (help)CS1 maint: unflagged free DOI (link)
  3. ^ "Our colorful TOUROMANIA booklet has it all". New York Times. 1988-03-06.
  4. ^ Harold M. Schmeck Jr (1973-03-18). "Disputed Drug Is Restudied for Use in Geriatrics". New York Times.
  5. ^ Jed Disbennett (March 1994). "Unproven Medical Treatments Lure Elderly". FDA Consumer Magazine. Archived from the original on 2004-12-11.
  6. ^ "FDA Quotes". Tierra Mega-Nutrients. Archived from the original on 2006-06-20. Retrieved 2006-11-28.
  7. ^ Dumitru M.D. Ph. D., Mircea. "Professor Ana Aslan and Gerovital-H3, the Original and First Anti-Aging Medicine". International Antiaging Systems. Archived from the original on 2006-05-18. Retrieved 2006-12-02.
  8. ^ "Automatic Detention [for Gerovital] (IA#61-01)". U.S. Food and Drug Administration. Archived from the original on 2006-09-30. Retrieved 2006-11-28.