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  • Warning about AS

    As some of you know, I reported to you that my red blood count was significantly up and have been treating with a Hemotologist since November.....Well I was diagnosed with Polycythemia and now require week phlebotomies (drawing of blood) in order to keep my red count within normal limits. Having said that, the AMA just published a paper indicating that AS can be significant factor in the development of the disease, and since I have been a long time user that makes sence. Now instead of injecting oils each week, I am giving a pint of blood. This will most likely occur for the rest of my life, or until I develop other egregious problems. The one problem that really scares me is leukemia.

    So along with all the other concerns Users have about AS, this is now something new to think about while you are injecting or poping pills....

  • #2
    Why should anyone believe you when you copied and pasted all those FAQ writtings and said you wrote them?

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    • #3
      I dont see how this could happen with aas use. Also, Bouncer is right. You are going to have to give us some hard proof, b4 anyone should believe u.

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      • #4
        There is a ton of evidence that some AAS can raise red blood cell levels but all the articles I have read point to this being a temporary phenomenon. I have never read or heard of AAS being linked to Polycythemia.

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        • #5
          I thought raising red blood cell count was a good thing in that it enables better transportation of oxygen

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          • #6
            no, high count of red blood cell is bad. can cause leukemia, thickens the blood that leads to heart attacks or strokes.

            Comment


            • #7
              Originally posted by spidey
              There is a ton of evidence that some AAS can raise red blood cell levels but all the articles I have read point to this being a temporary phenomenon. I have never read or heard of AAS being linked to Polycythemia.
              OK, I take that back. I just did a PUBMED search on Polycythemia and steroids and found a few articles. Note that the Polycythemia in question was temporary however and reversed upon cessation of testosterone replacement. Also, note that it is quite rare for test replacement to cause Polycythemia as evidenced by the physician's statement that they were unaware of any other publications at the time making that connection.

              POLYCYTHAEMIA AS A COMPLICATION OF TRANSDERMAL TESTOSTERONE THERAPY
              As the population of Western developed countries becomes
              older, the well-being of elderly citizens is an emerging
              challenge. Hormonal replacement therapy is being prescribed
              ever more frequently for the elderly, but the clinical
              consequences of these treatments are not fully understood.
              A 73-year-old man was hospitalized for evaluation of an
              8-kg weight loss, sweats and redness of facial skin. His past
              medical history included asthma and hypertension for
              which he received fluticasone and losartan respectively.
              The symptoms developed 10 months after beginning daily
              transdermal testosterone therapy with 10 mg of androstanolone.

              This drug was prescribed within the context of a
              protocol to slow the natural ageing process, even though
              the patient had low±normal serum testosterone levels. One
              year before admission, the haemogram was normal and his
              pulse was 100 beats/min and regular. The patient had no
              fever and no hepatosplenomegaly, but he was hypertensive
              (170/95 mmHg). Results of blood analyses were white
              blood cells (WBCs) 6  109/l (62% granulocytes and 22%
              lymphocytes), red blood cells (RBCs) 5´870  1012/l,
              haemoglobin (Hb) 17´8 g/dl, haematocrit 56%, mean
              corpuscular volume 95 fl (normal range 85±95 fl), platelet
              count 176  109/l, serum B12 0´45 ng/l (normal range
              250±750 ng/l), serum erythropoietin 1´07 U/l (normal
              range 1´9±13´7 U/l) and red cell volume 52 ml/kg. Histological
              examination of bone marrow aspirate and biopsy
              samples demonstrated hyperplasia of the three cell lines
              without dystrophy and fibrosis; bone marrow cells were
              cytogenetically normal. Abdominal computerized tomography
              scan detected no enlarged spleen or tumoral mass. The
              diagnosis was consistent with secondary polycythaemia and
              transdermal testosterone was stopped.
              Three months later,
              the patient had gained 4 kg, Hb was 14´6 g/dl, haematocrit
              was 45%, serum erythropoietin was 7´5 U/l and red cell
              volume had decreased (40 ml/kg); the last was completely
              normalized 9 months after testosterone withdrawal.

              Serum androgen levels decline with age in normal men,
              such that most men over 60 years of age have mean serum
              total testosterone levels near the low end of the normal
              adult range. It is not known whether lower testosterone in
              older men has an effect on androgen-responsive organ
              systems, such as muscle, bone and prostate. Consequently,
              in Western countries, current studies are trying to evaluate
              the relative benefits and risks of testosterone supplementation
              in older men. Testosterone has been touted by some
              members of the alternative medicine community as a sexual
              potency enhancer, energy stimulator and all-round fountain
              of youth. However, haematocrits and RBC volumes have
              Correspondence 237
              q 2000 Blackwell Science Ltd, British Journal of Haematology 110: 234±243
              been shown to rise significantly during testosterone
              replacement therapy and the stimulatory effects of androgens
              on erythropoiesis are well documented
              (Shahidi, 1973;
              Krauss et al, 1991; Tenover, 1992). Drinka et al (1995)
              recently reported two cases of polycythaemia in two men,
              one aged 66 and one aged 73 years old who had,
              respectively, received intramuscular testosterone (150 mg/
              70 kg every 2 weeks) for 14 and 17 weeks.
              The risk of
              haemoconcentration during testosterone therapy might be
              greater if the patient also has a condition considered as a
              risk factor for polycythaemia, such as sleep apnoea
              syndrome (Drinka et al, 1995). Although elevated haematocrits
              have been reported for parenteral testosterone
              supplementation (Tenover, 1992; Drinka et al, 1995), we
              are unaware of reports linking topical testosterone with the
              development of polycythaemia.
              We describe the first case in
              which the transdermal delivery of testosterone across nonscrotal
              skin of a male patient probably induced supraphysiological
              concentrations of testosterone. Androstanolone
              withdrawal led to the normalization of the red cell
              volume, suggesting that the drug was responsible for the
              appearance of polycythaemia.
              Testosterone is able to
              increase erythropoiesis by stimulating the kidney to
              produce erythropoietin but in our patient the serum
              erythropoietin level was low, suggesting an erythropoietinindependent
              mechanism of polycythaemia induction
              (Shahidi, 1973). Thus, during testosterone replacement
              therapy, haematocrit monitoring should be standard
              practice in medical centres and older men should be tested
              periodically throughout therapy.

              1Clinique de MeÂdecine Interne
              et Maladies Infectieuses, and
              2Service d'HeÂmatologie,
              HoÃpital Haut-LeÂveÃque,
              Avenue de Magellan,
              33604 Pessac, France.
              E-mail:
              [email protected]
              J. F. Viallard1
              G. Marit2
              P. MercieÂ1
              B. Leng1
              J. Reiffers2
              J. L. Pellegrin1
              REFERENCES
              Drinka, P.J., Jochen, A.L., Cuisinier, M., Bloom, R., Rudman, I. &
              Rudman, D. (1995) Polycythemia as a complication of testosterone
              replacement therapy in nursing home men with low testosterone
              levels. Journal of the American Geriatric Society, 43, 899±900.
              Krauss, D.J., Taub, H.A., Lantinga, L.J., Dunsky, M.H. & Kelly, C.M.
              (1991) Risks of blood volume changes in hypogonadal men
              treated with testosterone enanthate for erectile impotence. Journal
              of Urology, 146, 1566±1570.
              Shahidi, N.T. (1973) Androgens and erythropoiesis. New England
              Journal of Medicine, 289, 72±80.
              Tenover, J.S. (1992) Effects of testosterone supplementation in the
              aging male. Journal of Clinical Endocrinology and Metabolism, 75,
              1092±1098.
              Keywords: polycythaemia, transdermal testosterone, elderly.


              POLYCYTHEMIA IN A PHYSICIAN SECONDARY
              TO SELF-ADMINISTERED GROWTH HORMONE,
              TESTOSTERONE, AND DEHYDROEPIANDROSTERONE
              TO PREVENT AGING
              To the Editor: Recently, the use of hormonal supplementation
              in healthy elderly subjects to prevent the effects of
              aging has generated much interest in the lay and medical
              literature.1,2 During normal aging, there is progressive
              decline in growth hormone (GH) secretion (somatopause),
              impairment of ovarian and testicular function, and reduced
              adrenal androgen secretion. GH supplementation increases
              lean body mass, skin thickness, and bone density and
              decreases adipose tissue in normal elderly people.1 Testosterone
              administration in elderly men might improve lean
              body mass and sexual function.3 Dehydroepiandrosterone
              (DHEA) administration might also have beneficial effects
              on some age-related bodily changes.4 Nevertheless, the side
              effects and long-term safety of hormonal supplementation
              remain unknown.
              A healthy 65-year-old physician practicing family
              medicine decided to self-administer a combination of GH,
              testosterone, and DHEA to maintain vigor and prevent
              aging.
              Before commencement of treatment, his blood
              counts were hemoglobin (Hb) 16.8 g/dL, white blood cell
              (WBC) 7.7  109/L, and platelet (plt) 238  109/L. He had
              not undergone endocrinological evaluations. The treatment
              consisted of four units of recombinant human GH
              subcutaneously every week, testosterone 250 mg intramuscularly
              every month, and oral DHEA 50 mg every day.
              After
              3 months of hormonal administration, a blood count
              showed Hb519.8 g/dL, WBC55.9  109/L, and plt5
              189  109/L. The treatment was stopped and venesection
              Figure 1. Power flow Doppler ultrasound reveals no flow
              through the external carotid artery.
              LETTERS TO THE EDITOR 1031 JAGS JUNE 2004–VOL. 52, NO. 6
              of two units of blood performed. Physical examination was
              normal. Ultrasonogram of the abdomen and kidneys were
              normal. Plasma erythropoietin was suppressed to an
              undetectable level. A diagnosis of hormone-induced polycythemia
              was made.
              He was reassured but advised to stop the
              medication. Two months after cessation of treatment, his
              blood counts had returned to normal
              (Hb515.4 g/dL,
              WBC56.6  109/L, and plt5182  109/L). Plasma erythropoietin
              level had risen to 5.9 mU/mL (reference range5
              2.9–24.5). His latest blood counts and erythropoietin levels
              have remained normal, nearly 1 year afterward.
              None of the hormones used in this case has been
              reported to give rise to polycythemia when administered at
              the dose described. Therefore, the development of polycythemia
              was likely due to the synergistic interactions of the
              three hormonal supplements.
              Neither the benefits nor the
              long-term safety of hormonal supplementation are known.
              In elderly subjects, concerns have been raised about the
              possibility of increased cancer risks with GH administration.
              2 This case showed that even physicians might find it
              difficult to determine the risk and benefits from the existing
              literature. The medical profession and the lay public should
              wait for future clinical and laboratory research to determine
              the role of hormonal supplementation in the elderly
              population.
              Yok L. Kwong, MD
              Department of Medicine
              Clarence C. K. Lam, FRC Path
              Department of Pathology
              Queen Mary Hospital
              Hong Kong
              REFERENCES
              1. Rudman D, Feller AG, Nagraj HS et al. Effects of human growth hormone in
              men over 60 years old. N Engl J Med 1990;323:1–6.
              2. Vance ML. Can growth hormone prevent aging? N Engl J Med 2003;348:779–
              780.
              3. Steidle C, Schwartz S, Jacoby K et al. AA2500 testosterone gel normalizes
              androgen levels in aging males with improvements in body composition and
              sexual function. J Clin Endocrinol Metab 2003;88:2673–2681.
              4. Baulieu EE, Thomas G, Legrain S et al. Dehydroepiandrosterone (DHEA),
              DHEA sulfate, and aging: Contribution of the DHEAge study to a sociobiomedical.
              Proc Natl Acad Sci U S A 2000;97:4279–4284.
              Last edited by spidey; 01-28-05, 10:15 AM.

              Comment


              • #8
                FYR

                My doc told me of the AMA findings yesterday and it was not based on HRT....it was based on AS used 7 to 10 higher ......which is about what I was taking, and probably what many of the board members are taking....I will ask her for the article and post it asap. There is no cure for polycythemia if you have it...you can only control the symtoms, and at any time your bone marrow can decide to stop producing red blood cells, causeing the spleen to take over....all this leads to disaster and leukemia.....as a matter of fact, if bleeding you does not work, the medical profession introduces chemotherapy into your system to slow down the production of RBC...after 15-20 years of this stuff you stand a 78% chance of leukemia.....

                Comment


                • #9
                  Originally posted by therock
                  I dont see how this could happen with aas use. Also, Bouncer is right. You are going to have to give us some hard proof, b4 anyone should believe u.
                  I take this statement back bro. After reading what Spidey put and doing my own research, I come to the conclusion that you are in fact telling the truth. Also keep us posted bro, and what the hell were you on and at what dosage if you dont mind me asking.

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                  • #10
                    you the man spidey

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                    • #11
                      nice stuff spidey

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                      • #12
                        bump

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                        • #13
                          sorry to hear that man, thanks for posting and letting everyone know. Good luck and keep us updated on your condition.

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                          • #14
                            therock

                            for the last 6 years I have been on a variety of AS....including Deca, Cyp test, Enan test, sust, fina, dbol and a50.......I would take about 1200-1600 mg per week of the injectibles and run the orals for about 4-6 weeks during the 12 week cycle.....According to my doctor, its not the amount you take.....Polycythemia can strike anyone one at anytime.....my dad passed away 10 years ago with luekemia so I am assuming that at some point in my life the disease will develop into that....thanks for asking.....this is a source of deep concern for me and a source of depression. It's nice to be in your 50's an have a 224lb body of a 20 y.o., but it's nicer to have your health.......be careful gentlemen.....don'
                            t be in denial......this can happen to you..........bob

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                            • #15
                              How old are you?

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