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It is untrue that one needs to cycle creatine as it does not result in any process "fatigue"
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Creatine is often taken by athletes to help as a [[bodybuilding supplements|supplement]] for those wishing to gain muscle mass ([[bodybuilding]]). There are a number of forms but the most common are creatine monohydrate (creatine complexed with a molecule of [[water]]) and [[creatine ethyl ester]] (CEE). A number of methods for ingestion exist: as a powder mixed into a drink, or as a capsule or caplet. Once ingested, creatine is highly [[Bioavailability|bioavailable]], whether it is ingested as the crystalline monohydrate form, the free form in solution, or even in meat. Creatine salts will become the free form when dissolved in aqueous solution. Conventional wisdom recommends the consumption of creatine with high [[glycemic index]] [[carbohydrate]]s.<ref>{{cite journal |author=Steenge GR, Simpson EJ, Greenhaff PL |title=Protein- and carbohydrate-induced augmentation of whole body creatine retention in humans |journal=J. Appl. Physiol. |volume=89 |issue=3 |pages=1165–71 |date=1 September 2000|pmid=10956365 |url=http://jap.physiology.org/cgi/content/full/89/3/1165 }}</ref>
Creatine is often taken by athletes to help as a [[bodybuilding supplements|supplement]] for those wishing to gain muscle mass ([[bodybuilding]]). There are a number of forms but the most common are creatine monohydrate (creatine complexed with a molecule of [[water]]) and [[creatine ethyl ester]] (CEE). A number of methods for ingestion exist: as a powder mixed into a drink, or as a capsule or caplet. Once ingested, creatine is highly [[Bioavailability|bioavailable]], whether it is ingested as the crystalline monohydrate form, the free form in solution, or even in meat. Creatine salts will become the free form when dissolved in aqueous solution. Conventional wisdom recommends the consumption of creatine with high [[glycemic index]] [[carbohydrate]]s.<ref>{{cite journal |author=Steenge GR, Simpson EJ, Greenhaff PL |title=Protein- and carbohydrate-induced augmentation of whole body creatine retention in humans |journal=J. Appl. Physiol. |volume=89 |issue=3 |pages=1165–71 |date=1 September 2000|pmid=10956365 |url=http://jap.physiology.org/cgi/content/full/89/3/1165 }}</ref>


Endogenous serum or plasma creatine concentrations in healthy adults are normally in a range of 2–12&nbsp;mg/L. A single 5&nbsp;g (5000&nbsp;mg) oral dose in healthy adults results in a peak plasma creatine level of approximately 120&nbsp;mg/L at 1–2 hours post-ingestion. Creatine has a fairly short elimination half-life, averaging just less than 3 hours, so to maintain an elevated blood plasma level it would be necessary to take small oral doses every 3–6 hours throughout the day. There are two scientifically proven ways to supplement with creatine. The first is through a loading phase, in which 20&nbsp;grams is taken for 5–7 days, followed by a maintenance phase of 3-5&nbsp;grams a day for periods of 2–3 months at a time. The second consists of taking 3-10&nbsp;grams of creatine per day for a period of 2–3 months with no loading phase. It is generally recommended to take at least 1–2 weeks off from creatine supplementation in order to maintain a proper response mechanism in the body.<ref>{{cite web|url= http://www.exrx.net/Nutrition/Supplements/Creatine.html |title=Creatine |accessdate=2010-03-29}}</ref> After the "loading dose" period (1–2 weeks, 12-24&nbsp;g a day), it is no longer necessary to maintain a consistently high serum level of creatine. As with most supplements, each person has their own genetic "preset" amount of creatine they can hold. The rest is eliminated out of the body as waste. Creatine is consumed by the body fairly quickly, and if one wishes to maintain the high concentration of creatine, Post-loading dose, 2-5&nbsp;g daily is the standard amount to intake.<ref>Kamber M, Koster M, Kreis R, Walker G, Boesch C, Hoppeler H. Creatine supplementation--part I: performance, clinical chemistry, and muscle volume. Med. Sci. Sports Exer. 31: 1763-1769, 1999.</ref><ref>Deldicque L, Décombaz J, Zbinden Foncea H, Vuichoud J, Poortmans JR, Francaux M. Kinetics of creatine ingested as a food ingredient. Eur. J. Appl. Physiol. 102: 133-143, 2008.</ref><ref>R. Baselt, ''Disposition of Toxic Drugs and Chemicals in Man'', 8th edition, Biomedical Publications, Foster City, CA, 2008, pp. 366-368.</ref>
Endogenous serum or plasma creatine concentrations in healthy adults are normally in a range of 2–12&nbsp;mg/L. A single 5&nbsp;g (5000&nbsp;mg) oral dose in healthy adults results in a peak plasma creatine level of approximately 120&nbsp;mg/L at 1–2 hours post-ingestion. Creatine has a fairly short elimination half-life, averaging just less than 3 hours, so to maintain an elevated blood plasma level it would be necessary to take small oral doses every 3–6 hours throughout the day. There are two scientifically proven ways to supplement with creatine. The first is through a loading phase, in which 20&nbsp;grams is taken for 5–7 days, followed by a maintenance phase of 3-5&nbsp;grams a day for periods of 2–3 months at a time. The second consists of taking 3-10&nbsp;grams of creatine per day for a period of 2–3 months with no loading phase. Contrary to popular belief, due to its nature, creatine does not need to be cycled.<ref>{{cite web|url= http://examine.com/supplements/Creatine/#main_dosage |title=Creatine |accessdate=2012-02-07}}</ref> After the "loading dose" period (1–2 weeks, 12-24&nbsp;g a day), it is no longer necessary to maintain a consistently high serum level of creatine. As with most supplements, each person has their own genetic "preset" amount of creatine they can hold. The rest is eliminated out of the body as waste. Creatine is consumed by the body fairly quickly, and if one wishes to maintain the high concentration of creatine, Post-loading dose, 2-5&nbsp;g daily is the standard amount to intake.<ref>Kamber M, Koster M, Kreis R, Walker G, Boesch C, Hoppeler H. Creatine supplementation--part I: performance, clinical chemistry, and muscle volume. Med. Sci. Sports Exer. 31: 1763-1769, 1999.</ref><ref>Deldicque L, Décombaz J, Zbinden Foncea H, Vuichoud J, Poortmans JR, Francaux M. Kinetics of creatine ingested as a food ingredient. Eur. J. Appl. Physiol. 102: 133-143, 2008.</ref><ref>R. Baselt, ''Disposition of Toxic Drugs and Chemicals in Man'', 8th edition, Biomedical Publications, Foster City, CA, 2008, pp. 366-368.</ref>


===Creatine ethyl ester===
===Creatine ethyl ester===

Revision as of 20:47, 7 February 2012

Creatine supplements are athletic aids used to increase high-intensity athletic performance. Though researchers have known of the use of creatine as an energy source by skeletal muscles since the beginning of the 20th century, they were popularized as a performance-enhancing supplement in 1992.

History of creatine supplements

In 1912, Harvard University researchers Otto Folin and Willey Glover Denis found proof that ingesting creatine can dramatically boost the creatine content of the muscle.[1] In the late 1920s, after finding that the intramuscular stores of creatine can be increased by ingesting creatine in larger than normal amounts, scientists discovered creatine phosphate, and determined that creatine is a key player in the metabolism of skeletal muscle. The substance creatine is naturally formed in vertebrates.

While creatine's influence on physical performance has been well documented since the early twentieth century, it came into public view following the 1992 Olympics in Barcelona. An August 7, 1992 article in The Times reported that Linford Christie, the gold medal winner at 100 meters, had used creatine before the Olympics. An article in Bodybuilding Monthly named Sally Gunnell, who was the gold medalist in the 400-meter hurdles, as another creatine user. In addition, The Times also noted that 100 meter hurdler Colin Jackson began taking creatine before the Olympics.[2][3]

At the time, low-potency creatine supplements were available in Britain, but creatine supplements designed for strength enhancement were not commercially available until 1993 when a company called Experimental and Applied Sciences (EAS) introduced the compound to the sports nutrition market under the name Phosphagen.[4] Research conducted afterward showed that the consumption of high glycemic carbohydrates in conjunction with creatine increases creatine muscle stores.[5] In 1998, MuscleTech Research and Development launched Cell-Tech, the first creatine-carbohydrate-alpha lipoic acid supplement.[6] Alpha lipoic acid has been demonstrated to enhance muscle phosphocreatine levels and total muscle creatine concentrations. This approach to creatine supplementation was supported by a study performed in 2003.[7]

Creatine and athletic performance

There is scientific evidence that short term creatine use can increase maximum power and performance in high-intensity anaerobic repetitive work (periods of work and rest) by 5 to 15%. This is mainly bouts of running/cycling sprints and multiple sets of low RM weightlifting. Single effort work shows an increase of 1 to 5%. This refers mainly to single sprints and single lifting of 1-2RM weights. However, some studies show no ergogenic effect at all.[8] Studies in endurance athletes have been less than promising, most likely because these activities are sustained at a given intensity and thus do not allow for significant intra-exercise synthesis of additional creatine phosphate molecules. Ingesting creatine can increase the level of phosphocreatine in the muscles up to 20%. It must be noted creatine has no significant effect on aerobic endurance, though it will increase power during short sessions of high-intensity aerobic exercise.[9][10]

Since body mass gains of about 1 kg can occur in a week's time, many studies suggest that the gain is simply due to greater water retention inside the muscle cells.[11] Other studies, however, have shown that creatine increases the activity of satellite cells, which make muscle hypertrophy possible. Creatine supplementation appears to increase the number of myonuclei that satellite cells will 'donate' to damaged muscle fibers, which increases the potential for growth of those fibers. This increase in myonuclei probably stems from creatine's ability to increase levels of the myogenic transcription factor MRF4.[12][13]

In another study, researchers concluded that changes in substrate oxidation may influence the inhibition of fat mass loss associated with creatine after weight training when they discovered that fat mass did not change significantly with creatine but decreased after the placebo trial in a 12-week study on ten active men. The study also showed that 1-RM bench press and total body mass increased after creatine, but not after placebo.[14] The underlying effect of creatine on body composition has yet to be determined, as another study with a similar timeframe suggests no effect on body composition, but had less overall emphasis on metabolic effects.[15]

Creatine use is not considered doping and is not banned by the majority of sport-governing bodies. However, in the United States, the NCAA recently ruled that colleges could not provide creatine supplements to their players, though the players are still allowed to obtain and use creatine independently.

Endocrine effects

Increase in dihydrotestosterone

A 2009 study[16] showed that after a 7 day loading phase of creatine supplementation, followed by a further 14 days of creatine maintenance supplementation, while testosterone levels in blood serum were unchanged, levels of dihydrotestosterone increased by 56% after the initial 7 days of creatine loading and remained 40% above baseline after 14 days maintenance. The ratio of dihydrotestosterone to testosterone was also increased by 36% after 7 days creatine supplementation and remained elevated by 22% after the maintenance dose.[16] This could explain the fact that creatine users tend to report a slight onset of acne after starting creatine supplementation.[citation needed] It could also be a factor when it comes to the increased athletic performance that has been correlated with creatine supplemenation, although dihydrotestosterone has only minor anabolic effects compared to testosterone.[citation needed]

Increase in muscle insulin-like growth factor-I (IGF-I)

One study done in 2008 showed that levels of insulin-like growth factor-1 (IGF-I) in muscle increased by 24% compared to placebo after resistance training for 8 weeks.[17]

Creatine ingestion

Creatine is often taken by athletes to help as a supplement for those wishing to gain muscle mass (bodybuilding). There are a number of forms but the most common are creatine monohydrate (creatine complexed with a molecule of water) and creatine ethyl ester (CEE). A number of methods for ingestion exist: as a powder mixed into a drink, or as a capsule or caplet. Once ingested, creatine is highly bioavailable, whether it is ingested as the crystalline monohydrate form, the free form in solution, or even in meat. Creatine salts will become the free form when dissolved in aqueous solution. Conventional wisdom recommends the consumption of creatine with high glycemic index carbohydrates.[18]

Endogenous serum or plasma creatine concentrations in healthy adults are normally in a range of 2–12 mg/L. A single 5 g (5000 mg) oral dose in healthy adults results in a peak plasma creatine level of approximately 120 mg/L at 1–2 hours post-ingestion. Creatine has a fairly short elimination half-life, averaging just less than 3 hours, so to maintain an elevated blood plasma level it would be necessary to take small oral doses every 3–6 hours throughout the day. There are two scientifically proven ways to supplement with creatine. The first is through a loading phase, in which 20 grams is taken for 5–7 days, followed by a maintenance phase of 3-5 grams a day for periods of 2–3 months at a time. The second consists of taking 3-10 grams of creatine per day for a period of 2–3 months with no loading phase. Contrary to popular belief, due to its nature, creatine does not need to be cycled.[19] After the "loading dose" period (1–2 weeks, 12-24 g a day), it is no longer necessary to maintain a consistently high serum level of creatine. As with most supplements, each person has their own genetic "preset" amount of creatine they can hold. The rest is eliminated out of the body as waste. Creatine is consumed by the body fairly quickly, and if one wishes to maintain the high concentration of creatine, Post-loading dose, 2-5 g daily is the standard amount to intake.[20][21][22]

Creatine ethyl ester

CEE is a form of commercially available creatine touted to have higher absorption rates and a longer serum half-life than regular creatine monohydrate by several supplement companies. However, no peer-reviewed studies have emerged on creatine ethyl ester which conclusively prove these claims. A study presented at the 4th International Society of Sports Nutrition (ISSN) annual meeting demonstrated that the addition of the ethyl group to creatine actually reduces acid stability and accelerates its breakdown to creatinine. The researchers concluded that creatine ethyl ester is inferior to creatine monohydrate as a source of creatine.[23]

As a supplement, the compound was patented, and licensed through UNeMed, the technology transfer entity of the University of Nebraska Medical Center.[24]

Creatine hydrochloride

CrHCl is a hydrochloride salt patented in 2009 and marketed as an athletic and bodybuilding supplement. A study by Vireo Systems (commissioned by supplement manufacturer ProMera Health) found CrHCl to be 59 times more soluble in water than creatine monohydrate.[25] Due to its higher solubility, the recommended dosage for CrHCl is much lower than that for creatine monohydrate.

Manufacture

Synthetic creatine is usually made from sarcosine (Sarcosine salts) and cyanamide. Sarcosine is a naturally occurring amino acid like creatine, but manufacturers use a synthetic version. Sarcosine is usually made from chloroacetic acid. Sarcosine is N-methylglycine (H3C-NH-CH2-COOH) which is also an endogenous antagonist of glycine transporter-1. Cyanamide is an amide of cyanogen, and has white crystalline composition.

The creatine made from sarcosine and cyanamise is made in a glass-lined vat called a reactor. Because of the cost of manufacturing reactors and the need for specialist technicians, most synthetic creatine is made by a few firms, which resell to a number of retailers. The reactor has a big rod-like whisk that shoots into the mix to agitate it. The reactor is filled with water, the sarcosine and cyanamide are put in with catalyst compounds. The reactor is heated and pressurized, causing synthetic creatine crystals to form.[26] The crystalline creatine is then centrifuged to spin out undesirable by-products like creatinine and di-cyandiamide and subsequently vacuum dried. The dried creatine compound is milled into a fine powder for improved bioabsorption. Milling techniques differ, resulting in final products of varying solubility and bioabsorbability. For instance, creatine compounds milled to 200 mesh are referred to as micronized.

Safety

Current studies indicate that short-term creatine supplementation in healthy individuals is safe, although those with renal disease should avoid it due to possible risks of renal dysfunction, and before using it healthy users should bear these possible risks in mind.[10][27][28][29] Small-scale, longer-term studies have been done and seem to demonstrate its safety.[30][31] There have been reports of muscle cramping with the use of creatine, though a study showed no reports of muscle cramping in subjects taking creatine on a 15-item panel of qualitative urine markers. Creatine did not cause any clinically significant changes in serum metabolic markers, muscle and liver enzyme efflux, serum electrolytes, blood lipid profiles, red and white whole blood cell hematology, or quantitative and qualitative urinary markers of renal function.[32]

In addition, experiments have shown that creatine supplementation improved the health and lifespan of mice.[33] Whether these beneficial effects would also apply to humans is still uncertain.

Studies have not yet determined if creatine supplementation will accelerate the growth of cysts in humans with Polycystic Kidney Disease. PKD is prevalent in approximately 1 in 1000 people and may not be detectable until affected individuals reach their thirties.

In 2004 the European Food Safety Authority (EFSA) published a record that stated that oral long-term intake of 3 g pure creatine per day is risk-free.[34] The reports of damage to the kidneys or liver by creatine supplementation have been scientifically refuted.[35][36][37]

Creatine and mental performance

Creatine administration was shown to significantly improve performance in cognitive and memory tests in vegetarian individuals involved in double-blind, placebo-controlled cross-over trials.[38] Vegetarian supplementation with creatine seems to be especially beneficial as they appear to have lower average body stores, since meat is a primary source of dietary creatine.[38] This study did not, however, compare the differing effects of creatine on vegetarians and non-vegetarians.

References

  1. ^ Folin O, Denis W (1912). "Protein metabolism from the standpoint of blood and tissue analysis. Third paper, Further absorption experiments with especial reference to the behavior of creatine and creatinine and to the formation of urea". Journal of Biological Chemistry. 12 (1): 141–61.
  2. ^ "Supplement muscles in on the market". National Review of Medicine. 204-07-30. Retrieved 2011-05-25. {{cite web}}: Check date values in: |date= (help)
  3. ^ Passwater, Richard A. (2005). Creatine. p. 9. ISBN 0-87983-868-x. Retrieved 2011-05-25. {{cite book}}: Check |isbn= value: invalid character (help); Cite has empty unknown parameter: |coauthors= (help)
  4. ^ Stoppani, Jim (May, 2004). Creatine new and improved: recent high-tech advances have made creatine even more powerful. Here's how you can take full advantage of this super supplement. Muscle & Fitness. Retrieved 2010-03-29. {{cite book}}: Check date values in: |date= (help)
  5. ^ Green AL, Hultman E, Macdonald IA, Sewell DA, Greenhaff PL (1996). "Carbohydrate ingestion augments skeletal muscle creatine accumulation during creatine supplementation in humans". Am. J. Physiol. 271 (5 Pt 1): E821–6. PMID 8944667. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  6. ^ Profiles of Drug Substances, Excipients and Related Methodology By Harry G. Brittain
  7. ^ Burke DG, Chilibeck PD, Parise G, Tarnopolsky MA, Candow DG (2003-09-01). "Effect of alpha-lipoic acid combined with creatine monohydrate on human skeletal muscle creatine and phosphagen concentration". International Journal of Sport Nutrition and Exercise Metabolism. 13 (3). Human Kinetics Publishers: 294–302. PMID 14669930.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  8. ^ Kreider R, Rasmussen C, Ransom J, Almada AL. (1998). "Effects of creatine supplementation during training on the incidence of muscle cramping, injuries and GI distress". Journal of Strength Conditioning Research. 12 (275).{{cite journal}}: CS1 maint: multiple names: authors list (link)
  9. ^ Engelhardt, M (1998-07-01). "Creatine supplementation in endurance sports". Medicine & Science in Sports & Exercise. 30 (7). Lippincott Williams & Wilkins: 1123–9. doi:10.1097/00005768-199807000-00016. PMID 9662683. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  10. ^ a b Graham AS, Hatton RC (1999). "Creatine: a review of efficacy and safety". J Am Pharm Assoc (Wash). 39 (6): 803–10, quiz 875–7. PMID 10609446.
  11. ^ Powers, M; et al. (2003). "Creatine Supplementation Increases Total Body Water Without Altering Fluid Distribution". Journal of Athletic Training. 38 (Jan–Mar). National Athletic Trainers' Association, Inc: 44–50. PMC 155510. PMID 12937471. {{cite journal}}: Unknown parameter |author-separator= ignored (help)
  12. ^ Hespel, P (2001). "Creatine supplementation: exploring the role of the creatine kinase/phosphocreatine system in human muscle". Canadian Journal of Applied Physiology. 26 (Suppl.). Human Kinetics Publishers, Inc.: S79–102. PMID 11897886. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  13. ^ Olsen, S; Aagaard P; et al. (2006). "Creatine supplementation augments the increase in satellite cell and myonuclei number in human skeletal muscle induced by strength training". The Journal of Physiology. 573 (Jun 1): 525–34. doi:10.1113/jphysiol.2006.107359. PMC 1779717. PMID 16581862. {{cite journal}}: Unknown parameter |author-separator= ignored (help)
  14. ^ Huso, ME (2002-08-16). "Creatine supplementation influences substrate utilization at rest". Journal of Applied Physiology. 93 (6): 2018–22. doi:10.1152/japplphysiol.01170.2001. PMID 12391059. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  15. ^ Huso, ME (2007-12-01). "Effect of in-season creatine supplementation on body composition and performance in rugby union football players". Applied physiology, nutrition, and metabolism. 32 (6): 1052–7. doi:10.1139/H07-072. PMID 18059577. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  16. ^ a b Van der Merwe, Johann; Brooks, Naomi E; Myburgh, Kathryn H (2009). "[Three Weeks of Creatine Monohydrate Supplementation Affects Dihydrotestosterone to Testosterone Ratio in College-Aged Rugby Players]". Clinical Journal of Sport Medicine. 19 (5): 399–404. doi:10.1097/JSM.0b013e3181b8b52f. PMID 19741313.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  17. ^ http://www.ncbi.nlm.nih.gov/pubmed/18708688
  18. ^ Steenge GR, Simpson EJ, Greenhaff PL (1 September 2000). "Protein- and carbohydrate-induced augmentation of whole body creatine retention in humans". J. Appl. Physiol. 89 (3): 1165–71. PMID 10956365.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  19. ^ "Creatine". Retrieved 2012-02-07.
  20. ^ Kamber M, Koster M, Kreis R, Walker G, Boesch C, Hoppeler H. Creatine supplementation--part I: performance, clinical chemistry, and muscle volume. Med. Sci. Sports Exer. 31: 1763-1769, 1999.
  21. ^ Deldicque L, Décombaz J, Zbinden Foncea H, Vuichoud J, Poortmans JR, Francaux M. Kinetics of creatine ingested as a food ingredient. Eur. J. Appl. Physiol. 102: 133-143, 2008.
  22. ^ R. Baselt, Disposition of Toxic Drugs and Chemicals in Man, 8th edition, Biomedical Publications, Foster City, CA, 2008, pp. 366-368.
  23. ^ Child, R. & Tallon, M.J. (2007). Creatine ethyl ester rapidly degrades to creatinine in stomach acid. International Society of Sports Nutrition 4th Annual Meeting
  24. ^ UNeMed 2003 Annual Report, p.4
  25. ^ ProMera Health. "CON-CRĒT: FAQ". Retrieved 19 February 2011.
  26. ^ http://tnation.t-nation.com/free_online_forum/diet_performance_nutrition_supplements/how_is_creatine_made Creatine Manufacture Process
  27. ^ Creatine's Side Effects. Fact or Fiction?, An interview of Professor Jacques R. Poortmans
  28. ^ Poortmans J. R., Francaux, M. (2000). "Adverse effects of creatine supplementation. Fact or Fiction?". Sports Medicine. 30 (3): 155–70. doi:10.2165/00007256-200030030-00002. PMID 10999421. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  29. ^ Robinson, T.M. (2000). "Dietary creatine supplementation does not affect some haematological indices, or indices of muscle damage and hepatic and renal function". British Journal of Sports Medicine. 34 (4): 284–288. doi:10.1136/bjsm.34.4.284. PMC 1724224. PMID 10953902. Retrieved 2007-04-12. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  30. ^ Mayhew DL, Mayhew JL, Ware JS (2002). "Effects of long-term creatine supplementation on liver and kidney functions in American college football players". Int J Sport Nutr Exerc Metab. 12 (4): 453–60. PMID 12500988.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  31. ^ Poortmans, J.R. (2003). "Long-term oral creatine supplementation does not impair renal function in healthy athletes| jou22469320296". Molecular and Cellular Biochemistry. 244 (1–2): 95–104. doi:10.1023/A:1022469320296. PMID 12701816. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help); Unknown parameter |month= ignored (help)
  32. ^ Kreider, R.B. (2004-11-01). "Long-term creatine supplementation does not significantly affect clinical markers of health in athletes". Molecular and Cellular Biochemistry. 244 (1–2). Springer Netherlands: 95–104. doi:10.1023/A:1022469320296. PMID 12701816. Retrieved 2007-04-12. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  33. ^ Bender A; Beckers J; Schneider I; et al. (2008). "Creatine improves health and survival of mice". Neurobiol. Aging. 29 (9): 1404–11. doi:10.1016/j.neurobiolaging.2007.03.001. PMID 17416441. {{cite journal}}: Unknown parameter |author-separator= ignored (help); Unknown parameter |month= ignored (help)
  34. ^ http://www.efsa.europa.eu/EFSA/efsa_locale-1178620753824_1178620761727.htm
  35. ^ Gualano, Bruno; Ugrinowitsch, Carlos; Novaes, Rafael Batista; Artioli, Guilherme Gianini; Shimizu, Maria Heloisa; Seguro, Antonio Carlos; Harris, Roger Charles; Lancha, Antonio Herbert (2008). "Effects of creatine supplementation on renal function: A randomized, double-blind, placebo-controlled clinical trial". European Journal of Applied Physiology. 103 (1): 33–40. doi:10.1007/s00421-007-0669-3. PMID 18188581.
  36. ^ Kreider, Richard B.; Melton, Charles; Rasmussen, Christopher J.; Greenwood, Michael; Lancaster, Stacy; Cantler, Edward C.; Milnor, Pervis; Almada, Anthony L. (2003). "Long-term creatine supplementation does not significantly affect clinical markers of health in athletes". Molecular and Cellular Biochemistry. 244 (1–2): 95–104. doi:10.1023/A:1022469320296. PMID 12701816.
  37. ^ Buford, Thomas W; Kreider, Richard B; Stout, Jeffrey R; Greenwood, Mike; Campbell, Bill; Spano, Marie; Ziegenfuss, Tim; Lopez, Hector; Landis, Jamie (2007). "International Society of Sports Nutrition position stand: Creatine supplementation and exercise". Journal of the International Society of Sports Nutrition. 4: 6. doi:10.1186/1550-2783-4-6. PMC 2048496. PMID 17908288.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  38. ^ a b Rae C, Digney AL, McEwan SR, Bates TC (2003). "Oral creatine monohydrate supplementation improves brain performance: a double-blind, placebo-controlled, cross-over trial". Proc Biol Sci. 270 (1529): 2147–50. doi:10.1098/rspb.2003.2492. PMC 1691485. PMID 14561278. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)