Lifestyle
- Regular weight-bearing exercise
- Adequate sun exposure
- Smoking cessation
Procollagen Type I N-Terminal Propeptide · PINP
P1NP quantifies the synthesis of type I collagen, indicating bone formation rates.
Age Group
Levels vary by age and sex; higher in children and adolescents due to growth.
Procollagen Type I N-Terminal Propeptide (P1NP) is a biomarker that reflects the synthesis of type I collagen, the predominant collagen in bone. It is released into the bloodstream during the formation of new bone matrix, making it a useful indicator of bone formation rates. Clinically, P1NP is significant in the diagnosis and management of osteoporosis, as elevated levels can indicate high bone turnover, which is associated with increased fracture risk. It is also used to monitor the effectiveness of osteoporosis treatments, as changes in P1NP levels can reflect treatment response. In the context of athletic performance, P1NP can provide insights into bone health, particularly in athletes at risk of bone stress injuries due to conditions like Relative Energy Deficiency in Sport (REDs). Monitoring P1NP can help in assessing bone formation and the risk of stress fractures. However, P1NP levels can be influenced by factors such as renal function, circadian rhythms, and nutritional status. Researchers recommend standardized sample collection protocols to minimize variability and improve the reliability of P1NP measurements.
Klinische Bedeutung
Elevated P1NP levels suggest increased bone turnover, often seen in osteoporosis or metabolic bone diseases. Reduced levels may indicate suppressed bone formation, potentially due to nutritional deficiencies or hormonal imbalances.
Rising P1NP values suggest increased bone turnover, possibly due to osteoporosis or fracture healing. Re-test in 3-6 months.
Falling P1NP values may indicate effective treatment response or reduced bone formation.
Re-test Interval
6 months if outside optimal range
Note:
Consult a healthcare provider before starting any supplementation, especially if you have underlying health conditions.
Draw samples at the same time of day due to circadian variations.
Testing Frequency
Every 6-12 months for osteoporosis management.
May affect
Current research suggests that reference ranges for P1NP may vary significantly by age, sex, and ethnicity, particularly in pediatric populations, indicating a need for standardized protocols. Researchers have not yet established optimal target levels for P1NP in various clinical contexts, such as chronic kidney disease or relative energy deficiency in sport. Additionally, the interaction of P1NP with other risk factors in fracture risk algorithms remains inadequately explored, leaving clinical implications uncertain.
1,864
Total Citations
28
Human/RCT
9.5
Avg. Influence
2024
Latest
Researchers found that P1NP and CTX are recommended as reference markers for assessing bone turnover and predicting fracture risk in osteoporosis. The study highlighted the need for international standards to enhance the reliability of these biomarkers in clinical practice. It also noted that treatment-induced changes in these markers are significant for monitoring therapy effectiveness.
This study examined the effects of a single intravenous infusion of zoledronic acid compared to weekly oral alendronate in postmenopausal women with low bone density. Researchers found that the infusion maintained bone mineral density for 12 months and that patients preferred the yearly infusion over weekly oral therapy. Additionally, biomarkers related to bone turnover showed different patterns between the two treatment groups.
Researchers found that bone turnover markers, including P1NP, can predict fracture risk and monitor responses to osteoporosis treatments. The study emphasized the need for standardized protocols for measuring these markers due to their variability. It also discussed the critical roles of calcium and phosphate in bone metabolism.
Researchers developed a highly sensitive mass spectrometry-based assay for measuring rat P1NP levels to study bone formation. The study demonstrated that this new assay could effectively monitor changes in P1NP levels in response to treatments affecting bone metabolism. The findings indicate its potential utility in preclinical bone research.
Researchers reviewed the role of biomarkers, including PINP, in detecting bone metastasis in prostate cancer. They highlighted the limitations of traditional diagnostic methods and the potential of biomarkers to improve early detection and management of bone metastases.
Researchers observed that a lower serum P1NP/βCTX ratio and hypoalbuminemia are independently associated with an increased prevalence of nonvertebral fractures in older adults. The study indicated that these markers could serve as useful prognostic tools for fracture risk stratification in the elderly population.
This multicenter study evaluated the harmonization of assays for measuring P1NP in clinical laboratories. Researchers found that both serum and plasma samples are suitable for P1NP determination, and they identified significant biases between different assay methods. The study concluded that harmonization efforts could improve the reliability of P1NP measurements across laboratories.
This study established reference levels for P1NP and osteocalcin in healthy Korean children and adolescents. Researchers observed significant age- and sex-related variations in P1NP levels, with the highest levels occurring in infancy. The findings indicate the necessity of age-specific reference data for pediatric bone health assessments.
Researchers found that bone turnover markers (BTMs) in children and adolescents differ from adults due to growth and remodeling processes. This study highlighted the limited clinical use of BTMs in pediatrics due to age- and gender-specific challenges. It also discussed the physiological and pathological modifications of BTMs in younger populations.
Researchers highlighted the challenges and potential of using bone turnover markers (BTMs) in pediatric clinical settings. The study emphasized that BTMs can provide valuable insights into bone development and metabolic disorders in children. It called for more research to establish reliable reference intervals for BTMs in pediatric populations.
22
Total Trials
1,585
Total Enrolled
Iuliu Hatieganu University of Medicine and Pharmacy
40
2026
Change from baseline in serum procollagen type I N-terminal propeptide (P1NP)
Mansoura University
60
2025
Improvement in Bone-Specific Biomarkers (BALP, P1NP, TRAP-5b)
Odense University Hospital
12
2025
Change in serum bone formation marker P1NP
Odense University Hospital
136
2024
Procollagen type 1 N-terminal propeptide (P1NP)
Odense University Hospital
64
2024
Procollagen type 1 N-terminal propeptide (P1NP)
Memorial Sloan Kettering Cancer Center
10
2023
Percent change in bone formation marker, P1NP
Bursa Yuksek Ihtisas Training and Research Hospital
45
2022
The serum levef of Procollagen type 1 N-terminal propeptide (P1NP) (ng/ml)
University of Colorado, Denver
20
2022
Difference in change in propeptide of type 1 procollagen (P1NP)
University of Colorado, Denver
59
2021
Difference in change of propeptide of type 1 procollagen (P1NP) over 1 year
Morten Frost
64
2021
Procollagen type 1 N-terminal propeptide (P1NP)
Shenzhen People's Hospital
90
2020
Procollagen type 1 n-terminal propeptide (P1NP)
Columbia University
55
2018
Bone formation in serum by P1NP
Ioannis K. Triantafyllopoulos, MD,MSci,PhD
51
2017
Comparison of %-changes of P1NP and CTX levels from baseline to 3 months of supplementation between the two groups.
University of California, San Diego
48
2014
Change in Total Procollagen Type 1 N-terminal Propeptide (a Marker of Bone Formation) [P1NP] Levels
University of Pittsburgh
26
2013
Change From Baseline of Systemic Markers of Bone Metabolism (C-terminal Peptide of Type 1 Collagen (CTx) and Amino-terminal Propeptide of Type-1 Procollagen (P1NP))
Sheffield Children's NHS Foundation Trust
20
2012
Serum bone turnover marker concentrations: P1NP and CTX (ng/ml)
Takeda
115
2010
Percent Change From Baseline to Week 26 in Bone Formation Marker Aminoterminal Propeptide of Type 1 Collagen (P1NP)
University of Pittsburgh
58
2009
Measurements of amino-terminal telopeptides of procollagen 1 (P1NP), a marker of bone formation, in lactating and non-lactating post-partum African-American women both at 6-8 and at 12-14 weeks post-partum and normal controls
TransPharma Medical
104
2008
Change from baseline to endpoint 96 days in procollagen 1 N-terminal propeptide (P1NP)
Société des Produits Nestlé (SPN)
144
2007
Percentage change from baseline for bone formation (serum P1NP & osteocalcin) and bone resorption (urinary NTX & serum CTX) markers
Sanofi
290
2004
Compare the PTH-associated change from baseline at Month 3 of procollagen peptide P1NP, in subjects previously treated with Risedronate or Alendronate
University of Tennessee
74
2002
Biomarkers bone turnover (P1NP and CTX)
Research publications about P1NP over time
9totalLog lab results, track trends and optimize your biomarkers over time.
This page is for informational and research purposes only. All information is based on published scientific literature and does not constitute medical advice, diagnosis, or treatment recommendations. Many substances listed may not be approved for human use and may be subject to drug regulation laws (e.g., AMG in Germany, FDA in the US). PepStack does not encourage the use of any substance on humans. Always consult a qualified healthcare professional before making any health-related decisions. Use of this information is entirely at your own risk. PepStack assumes no liability for the accuracy, completeness, or timeliness of the content provided. Full disclaimer