N-Terminal Propeptide of Type III Procollagen as a Biomarker of Anabolic Response to Recombinant Human GH and Testosterone
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CONTEXT: Biomarkers that predict musculoskeletal response to anabolic therapies should expedite drug development. During collagen synthesis in soft lean tissue, N-terminal propeptide of type III procollagen (P3NP) is released into circulation. We investigated P3NP as a biomarker of lean body mass (LBM) and muscle strength gains in response to testosterone and GH. DESIGN: Community-dwelling older men received GnRH agonist plus 5 or 10 g testosterone gel plus 0, 3, or 5 microg recombinant human GH daily. P3NP levels were measured at baseline and wk 4, 8, 12, and 16. LBM and appendicular skeletal muscle mass (ASM) were measured by dual-energy x-ray absorptiometry. RESULTS: One hundred twelve men completed treatment; 106 underwent serum P3NP measurements. P3NP levels were higher at wk 4 than baseline (6.61 +/- 2.14 vs. 4.51 +/- 1.05, P < 0.0001) and reached plateau by wk 4 in men receiving testosterone alone. However, wk 8 P3NP levels were higher than wk 4 levels in men receiving testosterone plus recombinant human GH. Increases in P3NP from baseline to wk 4 and 16 were significantly associated with gains in LBM (r = 0.26, P = 0.007; r = 0.53, P < 0.001) and ASM (r = 0.17, P = 0.07; r = 0.40, P < 0.0001). Importantly, for participants receiving only testosterone, P3NP increases at wk 4 and 16 were related to muscle strength gains (r = 0.20, P = 0.056 and r = 0.36, P = 0.04). In stepwise regression, change in P3NP explained 28 and 30% of the change in ASM and LBM, respectively, whereas change in testosterone but not IGF-I and age provided only small improvements in the models. CONCLUSION: Early changes in serum P3NP levels are associated with subsequent changes in LBM and ASM during testosterone and GH administration. Serum P3NP may be a useful early predictive biomarker of anabolic response to GH and testosterone.
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Increase in PIIINP levels is known to be associated with increases in lean body mass and appendicular skeletal mass in the elderly.
“Increase in PIIINP levels is known to be associated with increases in lean body mass and appendicular skeletal mass in the elderly. 40”
From A Phase 1 study for safety and pharmacokinetics of BIO101 (20‐hydroxyecdysone) in healthy young and older adults (2023) · cites this paper as [40]
The Abstract and Discussion report that increases in P3NP were associated with gains in lean body mass and appendicular skeletal muscle mass. The study involved community-dwelling older men receiving testosterone with or without recombinant human GH, so it does not establish the association for elderly people generally. Passage page numbers were not supplied. (LLM, conf=0.85)
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Cardiac cachexia - Up-to-date 2015
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- Authors
- Bhasin, S., He, E. J., Kawakubo, M., Schroeder, E. T., Yarasheski, K., Opiteck, G. J., Reicin, A., Chen, F., Lam, R., Tsou, J. A., Castaneda-Sceppa, C., Binder, E. F., Azen, S. P., & Sattler, F. R.
- Affiliations
- Boston University (US)
- School of Dentistry (E.J.H.), University of Southern California, Los Angeles, California 90089
- University of Southern California (US)
- Washington University in St. Louis (US)
- Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
- Jean Mayer U.S. Department of Agriculture Human Nutrition Research Center on Aging (C.C.-S.), Tufts University, Boston, Massachusetts 02111
- Corresponding author
- Bhasin, Shalender
- ORCID
- Venue
- The Journal of Clinical Endocrinology & Metabolism
- Publisher
- The Endocrine Society
- Published
- 2009-11-01
- Volume
- 94
- Issue
- 11
- Pages
- 4224-4233
- ISSN
- 0021-972X (ISSN-L)
- 1945-7197
- PMC
- PMC2775648
- OpenAlex
- W1970823846
- Cited by
- 62
- References
- 44
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 5 · 2023: 3 · 2022: 2 · 2021: 6 · 2020: 5 · 2019: 3 · 2018: 2 · 2017: 2 · 2016: 4 · 2015: 9 · 2014: 4 · 2013: 3 · 2012: 5
- FWCI
- 2.19
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Digital Repository Service (Northeastern University) (submittedVersion)
- Funders
- U.S. Department of Agriculture (58-1950-9-001)
- University of Southern California
- National Institutes of Health (58-1950-9-001, 5p41rr000954-34, 5P30AG031679, 5p30ag031679-15)
- Genentech
- National Institute on Aging (5 P30 AG031679, R01 AG18169, R01AG018169, P30-AG031679, 1R01AG22356)
- National Institute of Diabetes and Digestive and Kidney Diseases (R21DK074345, R56DK049393, R01DK054163, R01DK049393, P30DK056341)
- National Center for Research Resources (P41-RR000954, M0I RR000043, M01RR000054, RR000054, M01RR000043, M01RR000036)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
- Health Sciences › Medicine › Physiology › Nutrition and Health in Aging
- Keywords
- recombinant human growth hormone, testosterone, lean body mass, appendicular skeletal muscle mass, muscle strength, older men, GnRH agonist, insulin-like growth factor I, collagen synthesis, sarcopenia prevention, osteoporosis prevention
- MeSH terms
- Aged, Aged, 80 and over, Body Weight, Hematocrit, Humans, Insulin-Like Growth Factor I, Male, Peptide Fragments, Procollagen, Recombinant Proteins, Regression Analysis, Growth Hormone, Testosterone, Time Factors, Biomarkers, Leuprolide, Human Growth Hormone, Muscle Strength
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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