Article Data

  • Views 1017
  • Dowloads 119

Editorial

Open Access

Predictive factors for elevated prostate specific antigen and hematocrit levels during testosterone replacement therapy in patients with testosterone deficiency

  • Chung Heon Ryu1,†
  • Sun Gu Park1,†
  • Jeong Kyun Yeo2
  • Min Gu Park2,*,

1Department of Clinical Laboratory Science, Daejeon Health Institute of Technology, 34504 Daejeon, Republic of Korea

2Department of Urology, College of Medicine, Inje University, Seoul Paik Hospital, 04551 Seoul, Republic of Korea

DOI: 10.31083/j.jomh1804099 Vol.18,Issue 4,April 2022 pp.1-10

Submitted: 30 November 2021 Accepted: 24 January 2022

Published: 30 April 2022

*Corresponding Author(s): Min Gu Park E-mail: uromgpark@gmail.com uromgpark@paik.ac.kr

† These authors contributed equally.

Abstract

Objective: We examined risk factors associated with prostate specific antigen (PSA) and hematocrit (hct) elevation during testosterone replacement therapy (TRT) in patients with testosterone deficiency (TD). Methods: We retrospectively analyzed the medical records of patients receiving TRT for ≥3 months. We investigated the following parameters: age, body mass index, comorbidities, TRT type, TRT duration, pre-TRT prostate volume, pre- and post-TRT serological tests, prostate biopsies, prostate cancer diagnoses, pre- and post-TRT aging male symptom scale scores, hct elevation, and PSA elevation. The patients were divided into two groups based on the PSA elevation status for comparison, following which we analyzed the predictive factors for PSA elevation. They were also divided into two groups based on hct elevation status. Results: The PSA elevation group showed a statistically significantly higher mean age, pre-TRT prostate volume, and PSA level compared to the non-elevation group. The PSA non-elevation group showed a significantly higher percentage of smokers, while the PSA elevation group showed a statistically significantly higher prevalence of benign prostatic hyperplasia (BPH_LUTS). The results demonstrated that a large pre-TRT prostate volume, high pre-TRT PSA levels, BPH_LUTS, and being a non-smoker were the contributing factors for PSA elevation. The hct elevation group showed statistically significantly higher pre-TRT Hb, hct, and post-TRT testosterone levels, and dyslipidemia rates, as well as a non-statistically significant prevalence of testosterone enanthate (TE) and testosterone undecanoate (TU) intramuscular injection. The pre-TRT Hb and hct levels were contributing factors for hct elevation during TRT. TE injection showed marginal statistical significance. Conclusions: We identified large prostate volumes, high PSA levels, BPH_LUTS, and being non-smokers prior to TRT as risk factors for PSA elevation during TRT. Interestingly, we found that TRT-induced hct elevation was likely to occur in patients with high pre-TRT Hb and hct levels. Additionally, the hct levels should be monitored when using TE for TRT.

Keywords

testosterone; testosterone deficiency; testosterone replacement therapy; prostate specific antigen (PSA); hematocrit

Cite and Share

Chung Heon Ryu,Sun Gu Park,Jeong Kyun Yeo,Min Gu Park. Predictive factors for elevated prostate specific antigen and hematocrit levels during testosterone replacement therapy in patients with testosterone deficiency. Journal of Men's Health. 2022. 18(4);1-10.

References

[1] Hackett G, Cole N, Mulay A, Strange RC, Ramachandran S. Long-Term Testosterone Therapy in Type 2 Diabetes Is Associ-ated with Decreasing waist circumference and improving erec-tile function. The World Journal of Men’s Health. 2020; 38: 68–77.

[2] Bhasin S, Brito JP, Cunningham GR et al. Testosterone Ther-apy in Men With Hypogonadism: An Endocrine Society Clin-ical practice guideline. The Journal of Clinical Endocrinology and Metabolism. 2018; 103: 1715–1744.

[3] Kim M, Byun SS, Hong SK. Testosterone Replacement Therapy in Men with Untreated or Treated Prostate Cancer. The World Journal of Mmen’s Health 2021; 39: 705–723.

[4] Wang C, Nieschlag E, Swerdloff R, Behre HM, Hellstrom WJ, Gooren LJ, et al. Investigation, treatment, and monitoring of late-onset hypogonadism in males: ISA, ISSAM, EAU, EAA, and ASA recommendations. European Journal of Endocrinol-ogy. 2008; 159: 507–514.

[5] Morgentaler A. Testosterone and prostate cancer: an historical perspective on a modern myth. European Urology. 2006; 50: 935–939.

[6] Morgentaler A, Traish AM. Shifting the paradigm of testos-terone and prostate cancer: the saturation model and. The lim-its of androgen-dependent growth. European Urology. 2009; 55: 310–320.

[7] Mulhall JP, Trost LW, Brannigan RE, Kurtz EG, Redmon JB, Chiles KA, et al. Evaluation and Management of Testosterone Deficiency: AUA Guideline. The Journal of Urology. 2018; 200: 423–432.

[8] Rhoden EL, Morgentaler A. Influence of demographic factors and biochemical characteristics on the. prostate-specific antigen (PSA) response to testosterone replacement therapy. Inter-national Journal of Impotence Research. 2006; 18: 201–205.

[9] Coward RM, Simhan J, Carson CC, 3rd. Prostate-specific anti-gen changes and prostate cancer in hypogonadal men treated with testosterone replacement therapy. BJU International. 2009; 103: 1179–1183.

[10] Ohlander SJ, Varghese B, Pastuszak AW. Erythrocytosis Fol-lowing Testosterone Therapy. Sexual Medicine Reviews. 2018; 6: 77–85.

[11] Mirone V, Debruyne F, Dohle G, et al. European Association of Urology Position Statement on the Role of the Urologist in the management of male hypogonadism and testosterone therapy. European Urology. 2017; 72: 164–167.

[12] Hayden RP, Bennett NE, Tanrikut C. Hematocrit Response and Risk Factors for Significant Hematocrit Elevation with im-plantable testosterone pellets. The Journal of Urology. 2016; 196: 1715–1720.

[13] Lee DS, Park HJ. Efficacy and Safety of Testosterone Therapy Based on Guideline Recommendations; re: Clinical Practice Guideline by the American College of Physicians. The World Journal of Men’s Health. 2020; 38: 397.

[14] Shahidi NT. Androgens and erythropoiesis. The New England Journal of Medicine. 1973; 289: 72–80.

[15] Keohane C, McMullin MF, Harrison C. The diagnosis and man-agement of erythrocytosis. BMJ. 2013; 347: f6667.

[16] Braekkan SK, Mathiesen EB, Njølstad I, Wilsgaard T, Hansen JB. Hematocrit and risk of venous thromboembolism in a gen-eral population. The Tromso study. Haematologica. 2010; 95: 270–275.

[17] Ip FF, di Pierro I, Brown R, Cunningham I, Handelsman DJ, Liu PY. Trough serum testosterone predicts the development of polycythemia in hypogonadal men treated for up to 21 years with subcutaneous testosterone pellets. European Journal of En-docrinology. 2010; 162: 385–390.

[18] Pastuszak AW, Gomez LP, Scovell JM, Khera M, Lamb DJ, Lip-shultz LI. Comparison of the Effects of Testosterone Gels, In-jections, and Pellets on Serum hormones, erythrocytosis, lipids, and prostate‐specific antigen. Sexual Medicine Reviews. 2015; 3: 165–173.

[19] Schubert M, Minnemann T, Hübler D, et al. Intramuscular testosterone undecanoate: pharmacokinetic aspects of a novel testosterone formulation during long-term treatment of men with hypogonadism. The Journal of Clinical Endocrinology and Metabolism. 2004; 89: 5429–5434.

[20] Swerdloff RS. Long-term pharmacokinetics of transdermal testosterone gel in hypogonadal men. Journal of Clinical Endocrinology & Metabolism. 2000; 85: 4500–4510.

[21] Patnaik MM, Tefferi A. The complete evaluation of erythrocy-tosis: congenital and acquired. Leukemia. 2009; 23: 834–844.

[22] Montero D, Lundby C. Red cell volume response to exer-cise training: Association with aging. Scandinavian Journal of Medicine & Science in Sports. 2017; 27: 674–683.

[23] Bohnen AM, Groeneveld FP, Bosch JL. Serum prostate-specific antigen as a predictor of prostate volume in the community. Eu-ropean Urology. 2007; 51: 1645–1652.

[24] Roehrborn CG, Boyle P, Gould AL, Waldstreicher J. Serum prostate-specific antigen as a predictor of prostate volume in men with benign prostatic hyperplasia. Urology. 1999; 53: 581–589.

[25] Mochtar CA, Kiemeney LA, van Riemsdijk MM et al. Prostate-specific antigen as an estimator of prostate volume in the man-agement of patients with symptomatic benign prostatic hyper-plasia. European Urology. 2003; 44: 695–700.

[26] Shoskes DA, Barazani Y, Fareed K, Sabanegh E, Jr. Outcomes of Prostate Biopsy in Men with Hypogonadism Prior or During Testosterone replacement therapy. International Brazilian Jour-nal of Urology. 2015; 41: 1167–1171.

[27] Zhao J, Stockwell T, Roemer A, Chikritzhs T. Is alcohol con-sumption a risk factor for prostate cancer? A systematic review and meta–analysis. BMC Cancer. 2016; 16: 1–13.

[28] Li J, Thompson T, Joseph DA, Master VA. Association between smoking status, and free, total and percent free prostate specific antigen. The Journal of Urology. 2012; 187: 1228-1233.

[29] Kristal AR, Chi C, Tangen CM, Goodman PJ, Etzioni R, Thomp-son IM. Associations of demographic and lifestyle characteris-tics with prostate-specific antigen (PSA) concentration and rate of PSA increase. Cancer. 2006; 106: 320–328.

[30] Gelmann EP, Chia D, Pinsky PF et al. Relationship of demo-graphic and clinical factors to free and total prostate-specific antigen. Urology. 2001; 58: 561–566.

[31] Field AE, Colditz GA, Willett WC, Longcope C, McKinlay JB. The relation of smoking, age, relative weight, and dietary in-take to serum adrenal steroids, sex hormones, and sex hormone-binding globulin in middle-aged men. The Journal of Clinical Endocrinology and Metabolism. 1994; 79: 1310–1316.

[32] Koc G, Akgul K, Yilmaz Y, Dirik A, Un S. The effects of cigarette smoking on prostate-specific antigen in two different age groups. Canadian Urological Association Journal. 2013; 7: E704.

[33] Moreira DM, Nickel JC, Gerber L, et al. Smoking Is Associated with Acute and Chronic Prostatic Inflammation: Results from the REDUCE study. Cancer Prevention Research. 2015; 8: 312–317.

Abstracted / indexed in

Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,200 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.

Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.

Directory of Open Access Journals (DOAJ) DOAJ is a unique and extensive index of diverse open access journals from around the world, driven by a growing community, committed to ensuring quality content is freely available online for everyone.

SCImago The SCImago Journal & Country Rank is a publicly available portal that includes the journals and country scientific indicators developed from the information contained in the Scopus® database (Elsevier B.V.)

Publication Forum - JUFO (Federation of Finnish Learned Societies) Publication Forum is a classification of publication channels created by the Finnish scientific community to support the quality assessment of academic research.

Scopus: CiteScore 0.9 (2023) Scopus is Elsevier's abstract and citation database launched in 2004. Scopus covers nearly 36,377 titles (22,794 active titles and 13,583 Inactive titles) from approximately 11,678 publishers, of which 34,346 are peer-reviewed journals in top-level subject fields: life sciences, social sciences, physical sciences and health sciences.

Norwegian Register for Scientific Journals, Series and Publishers Search for publication channels (journals, series and publishers) in the Norwegian Register for Scientific Journals, Series and Publishers to see if they are considered as scientific. (https://kanalregister.hkdir.no/publiseringskanaler/Forside).

Submission Turnaround Time

Conferences

Top