Microsoft word - hrt & hearing loss.doc

PRESERVING SIGHT, SOUND AND OTHER SENSES:
The abstracts below show that testosterone, estrogen, aldosterone, cortisone /prednisone, melatonin
and antioxidants/ insulin sensitizers have significant protective benefits on hearing and sight, whether
longterm or acutely.
The Frisinas' work (Univ Rochester) showing that estrogen protects but progestin worsens hearing is
news, brought to our attention by Dr Joe Mercola's email. Another nail in the coffin of the synthetic
progestins.
The Frisinas stress that age-related hearing loss (presbycusis) is the number one
communication disorder, and it is one of the top three chronic medical conditions of elderly
persons.

Invariable simultaneous age-related hearing and sight loss associate with massive global impairment
and early mortality.
Does human progesterone, and the aldosterone mimic Florinef have adverse or protective effect
on hearing? Considering that all studies show largely opposite none-gyne effects of human vs
synthetic progestins, androgens and estrogens, such discordance seems unlikely.
These questions have huge implications for the better-off, since tens of millions are using
progestins/ progesterone (for both contraception and HT) without objective evidence of need or
benefit: risk;
and millions are using prednisone (or nonsteroidal anti-inflammatories) where androgen +-
cortisone/ aldosterone might be much better.

The internet does not reveal whether aldosterone is available for oral use (as opposed to Florinef).
Contrary to the media hype on the web claiming that progesterone was the problem in the
Frisina study -
Dr Frisina confirms that in his cross-sectional observational study, users were on the usual
megadose xenohormones. They recruited 124 well American women aged at least 60 yrs (60-86) ie
mean around ?72yrs, ie born between ?1920 and 1945? virtually all HT users (for 5-35yrs mean ?
20y) were on oral xenohormones-
n=30 - post hysterectomy currently on premarin equivalent mean ?+- 0.625mg/d
likely for ~30yrs
n=32 - on premarin ? 0.625mg dly for 22d/mo; + cyclic provera 5mg/d for 12d/mo -
likely for ~20yrs.
Thus their subjects were diehards - either (despite the WHI hysteria) 62 stubborn HT users
(healthy
user bias) or
62 healthy never-users ie who never had persistent hormone-deficiency symptoms.
Unfortunately one cannot guess the % effect of HT - but they showed that the hearing damage in the
progestin+ estrogen group (vs nonusers) was significant p<0.01, whereas estrogen alone apparently
did not associate with adverse effect
.
The most remarkable study is the PROSPECTIVE 50 year old RCT by Dr TE Weston
PRESBYACUSIS: A STUDY
: 1964:
400 well elderly men and women in London with or without presbyacusis (age-related hearing loss)
in London were randomised to placebo, vitamin B, a bendrofluazide diuretic or xenoHT oral estrogen
(Estinyl 30mcg)-methyltestosterone 12.5mg/d . This RCT showed that, comparing baseline with end-
audiometry after between 3 months and 3 years, only Vit BCo, and HT,
significantly improved hearing. (whereas a diuretic, or vasodilator, had no benefit). The incidence of
presbyacusis increased with age to a peak at about 65 and then gradually fell away again. Most of
those likely to be seriously affected present before the age of 70
. Females are liable to develop
presbyacusis earlier and ultimately more severely than males. Half of those suffering from presbyacusis
had tinnitus as well, a third vertigo, and a fifth both tinnitus and vertigo. Vitamin B had the most

extensive and the most generalized ameliorating effect, closely followed by the androgen-
oestrogen combination.
Previous acoustic trauma increased the ultimate severity of presbyacusis, but
was not a key factor in its overall incidence or severity. Regular smoking, arteriosclerosis and
hypertension
were most associated with early and ultimately severe presbyacusis, A history of
circulatory disturbance was the commonest factor in the history, and arteriosclerosis the commonest
factor in the examination of all groups. It was particularly common among those with the profoundest
hearing loss. Amongst those with an early or severe loss of hearing there was a high incidence of
deterioration in the other special senses. ( 1964;7:191-8 .free fulltext article on line.)
.

We will (and colleagues elsewhere should) ask our local ENT and eye colleagues
(doctors/ audiometry / optician) to collect HRT/no HRT and other drug/ supplement use with
height, weight, bloodpressure in their patients in future, to correlate hormone and other
metabolic parameters. Audiometry and expert eye (optometric) screening is costly, so it will be
easier to get data together (by questionnaire) from ENT & ophthalmology practitioners than
from our apparently
hearing- and vision-unimpaired patients - although we are seeing a rash of
vertigo-hearing loss patients lately.
We try to get all patients to go for regular eye if not ear tests, but not many “well” people do.
This data will strengthen the already overwhelming evidence for appropriate hormone and
other natural multisupplements in both men and women; and that progestins (and possibly
progesterone) should be avoided;
since men (in whom relative androgen deficiency is present in half by late life) make needed
estrogen from testosterone,
and women do best (since HRT suppresses androgen production), with appropriate combined
testosterone-estradiol replacement (which based on 60year old trials and our current evidence
obviates the need for progestin protection of the breasts and endometrium).,
Overweight-related diabetes is especially associated with both early visual and hearing loss, but
it’s incidence and mortality easily halved by appropriate safe natural supplements.
A >50strong -strong battery of long- proven natural safe supplements that preserve/ prolong/
improve hearing, sight , brain, circulation, immunity, joints. mood, brawn and bones is available
everywhere – but denied, neglected by most doctors because it is lowcost, and studiously avoided by
drug companies, private medical schemes, politicians and most researchers and academics.
Drug companies (and thus the organised disease industry they control via massive income for
shareholders, lobbyists, regulators, researchers, universities, hospitals, pharmacists, and disease
awareness groups ) promote only patentable designer products ie registerable and thus profitable
synthetics- what they mendaciously choose to call “medicines”, “drugs” - as opposed to the natural
proven freely available supplements, the real original medicines that they want to suppress, subject to
far more rigorous control than patent chronic drugs that regulators allow to be launched on the public
with as little as three months small “trials”.
No such patent chronic drugs of the past 40 years have been shown to do what natural
supplements do ie safely halve all-cause mortality and morbidity. .
We can prophesy that with the drastic fall in use, strength and degree of infections,
neuro- and eye-toxic drugs, smoking and permitted alcohol and noise pollution, and with early
and permanent physiological testo-esto replacement plus insulin sensitizers and vitamins B and
antioxidants ( rather than mega-HRT), the results will be far better today than in Weston’s time.

NDB

Source: http://healthspanlife.files.wordpress.com/2008/01/microsoft-word-hrt-hearing-loss.pdf

Effect of silicon supplement on osteopenia induced by ovariectomy in rats

© 2000 Springer-Verlag New York Inc. Effect of Silicon Supplement on Osteopenia Induced by Ovariectomy in Rats H. Rico, J. L. Gallego-Lago, E. R. Herna´ndez, L. F. Villa, A. Sanchez-Atrio, C. Seco, J. J. Ge´rvas Departamento de Medicina, Universidad de Alcala´, 28801, Madrid, SpainReceived: 15 February 1999 / Accepted: 25 June 1999 Abstract. The effect of silicon (Si) supplement on

2917_a02_p35-44

AIDS RESEARCH AND HUMAN RETROVIRUSES Volume 17, Number 1, 2001, pp. 35–43 Mary Ann Liebert, Inc. The Antiviral Drug Docosanol as a Treatment for Kaposi’sSarcoma Lesions in HIV Type 1-Infected Patients: MICHAEL J. SCOLARO,1 LUCY B. GUNNILL,2 LAURA E. POPE,2 M.H. KHALIL,2 ABSTRACT Docosanol inhibits a broad spectrum of lipid-enveloped viruses in vitro including HSV-1, HSV-2, VZV, CM

Copyright © 2010-2018 Pharmacy Drugs Pdf