Difference between revisions of "Lactate Threshold"
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Some of the tests could be "p-hacking", where the study looks at a sufficiently large number of variables that some correlation occurs randomly<ref name="HeadHolman2015"/>. | Some of the tests could be "p-hacking", where the study looks at a sufficiently large number of variables that some correlation occurs randomly<ref name="HeadHolman2015"/>. | ||
[[File:LactateComp.jpg|none|thumb|500px|The correlation (or lack thereof) between MLSS and the lactate levels at the MLSS intensity seen during 3 or 5 minute incremental power tests<ref name="Heck-1985"/>.]] | [[File:LactateComp.jpg|none|thumb|500px|The correlation (or lack thereof) between MLSS and the lactate levels at the MLSS intensity seen during 3 or 5 minute incremental power tests<ref name="Heck-1985"/>.]] | ||
− | = | + | ==Lactate Threshold And Near Infrared Spectroscopy== |
+ | A promising technology for measuring Lactate Threshold is Near-infrared spectroscopy (NIRS) which shines infrared light into the skin above an active muscle and measures the reflected light. NIRS measures the oxygen saturation in the capillaries of the muscle and has the potential to test for Lactate Threshold without any blood sampling. Because NIRS can monitor continually, it is possible that it may be able to determine the Lactate Threshold during an incremental test rather than requiring the multiple tests of MLSS. | ||
+ | ===Introduction to NIRS and SmO2=== | ||
+ | Near-infrared spectroscopy (NIRS) has been shown to measure the oxygen saturation of blood in muscle (SmO<sub>2</sub>) or other body tissues (StO<sub>2</sub>)<ref name="Kek-2008"/><ref name="Torricelli-2004"/><ref name="Mancini-1994"/>. (This works on similar principles to a [[Pulse Oximeter]].) Medical NIRS systems for monitoring StO<sub>2</sub> use Infrared LED or Lasers at 2, 3, or 4 frequencies<ref name="Hyttel-Sorensen-2011"/>. SmO<sub>2</sub> reflects the balance of oxygen delivery and consumption during exercise<ref name="Chance-1992"/> and there are some initial indications that relative SmO<sub>2</sub> may reflect changes in performance capacity<ref name="Neary-2005"/>. There is generally a four phase response of smo2 during incremental exercise from rest to maximum intensity and the following recovery<ref name="Belardinelli-1995a"/>: | ||
+ | # An initial increase in SmO<sub>2</sub> above resting levels to supply the now active muscles. (This may be due to increased blood flow<ref name="Bhambhani-1997"/>, but computer models do not support this<ref name="Fuglevand-1997"/>.) | ||
+ | # SmO<sub>2</sub> decreases linearly or exponentially with increasing intensity, followed by a leveling off as the subject approaches maximum intensity. There is some evidence of a breakpoint where the rate of decline increases (see below). | ||
+ | # During the first 1-2 minutes of recovery there is a rapid increase in SmO<sub>2</sub> which usually exceeds resting levels. | ||
+ | # SmO<sub>2</sub> then declines to resting levels over a further few minutes. | ||
+ | Skin should not impact SmO<sub>2</sub> readings more than 5%<ref name="Hampson-1988"/>, but surface fat can interfere with smo2<ref name="van Beekvelt-2001"/><ref name="Homma1996"/><ref name="BenaronMatsushita1998"/><ref name="BenaronYamamoto1998"/>. Because the penetration depth of NIRS is about 50-60% of the distance between the emitter and receiver, the site must be selected so that the fat layer is much thinner than this depth<ref name="Bhambhani-2004"/>. | ||
+ | ===SmO<sub>2</sub> Breakpoint=== | ||
+ | As the intensity increases during incremental exercise SmO<sub>2</sub> will remain constant or decline, with the rate of decline being greater near the Lactate Threshold<ref name="Belardinelli-1995a"/><ref name="Bhambhani-2004"/><ref name="Belardinelli-1995b"/>. This has led to several studies using the concept of an SmO<sub>2</sub> "breakpoint"<ref name="Grassi-1999"/>. This breakpoint is a change in the slope of the line plotting SmO<sub>2</sub> against work intensity in an incremental intensity test. This increase in the rate of desaturation can either be visually determined or based on bilinear regression. (The bilinear regression iterates over different combinations of two regression lines to find the lowest sum of squares of the residuals. I could not find the details of the constraints placed on this approach.) | ||
+ | [[File:SmO2 Breakpoint1.jpg|none|thumb|500px|A graph showing the SmO<sub>2</sub> breakpoint.]] | ||
+ | ===SmO<sub>2</sub> and Lactate Threshold=== | ||
+ | A number of studies have looked at the relationship between SmO<sub>2</sub> and Lactate or Lactate Threshold | ||
+ | * A study of five mountain climbers found a relationship between the "point of inflection of lactate" and the SmO<sub>2</sub> breakpoint during an incremental cycling test<ref name="Grassi-1999"/>. The definition they were using for the inflection of lactate was a blood lactate reading that is more than 0.5 below the subsequent value, with typical lactate levels below 2 mmol/l. This is closer to the "aerobic threshold" concept than the typical Lactate Threshold. The study did not find any correlation between the SmO<sub>2</sub> breakpoint and the 4 mmol/l value of blood lactate. The breakpoint was determined from bi-linear regression. | ||
+ | * A study of 40 sedentary undergraduates showed a correlation between SmO<sub>2</sub> returning to resting levels and Ventilatory Threshold (VT) in 65% of subjects during an incremental cycling test<ref name="Bhambhani-1997"/>. While the text refers to Lactate Threshold as the point at which Lactate rises above resting levels (aerobic threshold) the method used to determine VT appears to be the anaerobic threshold. This study did not use the breakpoint mentioned above, but the point where the SmO<sub>2</sub> drops below the level detected at rest. | ||
+ | * A study of 11 subjects of varying fitness levels showed a correlation between SmO<sub>2</sub> breakpoint determined visually and Ventilatory Threshold (VT) during an incremental cycling test<ref name="Belardinelli-1995a"/>. | ||
+ | * A comparison between 12 healthy subjects and 7 suffering from chronic heart failure (CHF) showed a correlation between the SmO<sub>2</sub> breakpoint and Ventilatory Threshold (VT) during an incremental cycling test<ref name="Belardinelli-1995c"/>. | ||
+ | * A 2012 study compared the results from NIRS on the calf (Gastrocnemius Lateralis) and quads (Vastus Lateralis) in 31 active but not highly trained college students during an incremental cycling test<ref name="Wang-2012"/>. The study found a correlation between Lactate Threshold (determined from the log-log method<ref name="Davis-2007"/>) and the SmO<sub>2</sub> breakpoint (determined from bi-linear regression) in both locations, but the quads corresponded better. (I suspect the results from running could be quite different.) | ||
+ | * A 2009 study used MLSS (the gold standard for Lactate Threshold) with running to evaluate NIRS<ref name="Snyder-2009"/>. The 16 athletes performed between 2 and 5 tests of 30 minutes each to determine MLSS, separated by at least 48 hours each. The subjects then performed an incremental treadmill test using 6 minute stages with the 4th stage at the pace they estimated they could maintain for an hour (around Lactate Threshold). The first 3 stages where then 0.66, 0.44, & 0.22 meter/second slower, and the subsequent stages were 0.22 meters/second faster each time. SmO<sub>2</sub> breakpoint was defined as the workload immediately prior to a drop of 15% that lead to a continuous decline in smo2. A Lactate breakpoint was also determined based on the incremental test using the workload prior to an increase of 1 mmol/l as the criteria. Both the SmO<sub>2</sub> and Lactate breakpoint were determined visually. Of the 16 subjects, 1 did not reach MLSS, 2 did not have both a SmO<sub>2</sub> breakpoint or a Lactate breakpoint (based on the criteria used) and 1 did not have either. The study found that SmO<sub>2</sub> is as effective as Lactate breakpoint tests for determining true Lactate Threshold (MLSS). The table below shows the values for each of 12 subjects, with the paces shown as KPH, then min/mile, then the error as a percentage. This shows that while smo2 is as good as the lactate breakpoint, the individual differences from MLSS are not insignificant. For instance, subject 5 had an MLSS of 6:21, but an SmO<sub>2</sub> breakpoint of 6:57 and lactate breakpoint of 6:59, which is a big difference. | ||
+ | {| class="wikitable" | ||
+ | ! Subject | ||
+ | ! MLSS | ||
+ | ! SmO<sub>2</sub> | ||
+ | ! Lb | ||
+ | ! MLSS | ||
+ | ! SmO<sub>2</sub> | ||
+ | ! Lb | ||
+ | ! SmO<sub>2</sub> err | ||
+ | ! Lb err | ||
+ | |- | ||
+ | | 1 | ||
+ | | 13.5 | ||
+ | | 12.9 | ||
+ | | 13.7 | ||
+ | | 7:09 | ||
+ | | 7:29 | ||
+ | | 7:03 | ||
+ | | 4.4% | ||
+ | | -1.5% | ||
+ | |- | ||
+ | | 2 | ||
+ | | 14.3 | ||
+ | | 14.2 | ||
+ | | 13.4 | ||
+ | | 6:45 | ||
+ | | 6:48 | ||
+ | | 7:12 | ||
+ | | 0.7% | ||
+ | | 6.3% | ||
+ | |- | ||
+ | | 3 | ||
+ | | 9 | ||
+ | | 9.5 | ||
+ | | 9.5 | ||
+ | | 10:44 | ||
+ | | 10:10 | ||
+ | | 10:10 | ||
+ | | -5.6% | ||
+ | | -5.6% | ||
+ | |- | ||
+ | | 4 | ||
+ | | 13.4 | ||
+ | | 12.9 | ||
+ | | 12.9 | ||
+ | | 7:12 | ||
+ | | 7:29 | ||
+ | | 7:29 | ||
+ | | 3.7% | ||
+ | | 3.7% | ||
+ | |- | ||
+ | | 5 | ||
+ | | 15.2 | ||
+ | | 13.9 | ||
+ | | 13.8 | ||
+ | | 6:21 | ||
+ | | 6:57 | ||
+ | | 6:59 | ||
+ | | 8.6% | ||
+ | | 9.2% | ||
+ | |- | ||
+ | | 6 | ||
+ | | 12.9 | ||
+ | | 12.7 | ||
+ | | 13.5 | ||
+ | | 7:29 | ||
+ | | 7:36 | ||
+ | | 7:09 | ||
+ | | 1.6% | ||
+ | | -4.7% | ||
+ | |- | ||
+ | | 7 | ||
+ | | 15.4 | ||
+ | | 14.5 | ||
+ | | 15.3 | ||
+ | | 6:16 | ||
+ | | 6:40 | ||
+ | | 6:19 | ||
+ | | 5.8% | ||
+ | | 0.6% | ||
+ | |- | ||
+ | | 8 | ||
+ | | 11.5 | ||
+ | | 11.7 | ||
+ | | 10.9 | ||
+ | | 8:24 | ||
+ | | 8:15 | ||
+ | | 8:52 | ||
+ | | -1.7% | ||
+ | | 5.2% | ||
+ | |- | ||
+ | | 9 | ||
+ | | 10.8 | ||
+ | | 10.9 | ||
+ | | 10.8 | ||
+ | | 8:56 | ||
+ | | 8:52 | ||
+ | | 8:56 | ||
+ | | -0.9% | ||
+ | | 0.0% | ||
+ | |- | ||
+ | | 10 | ||
+ | | 14.2 | ||
+ | | 14.2 | ||
+ | | 13.2 | ||
+ | | 6:48 | ||
+ | | 6:48 | ||
+ | | 7:19 | ||
+ | | 0.0% | ||
+ | | 7.0% | ||
+ | |- | ||
+ | | 11 | ||
+ | | 11.6 | ||
+ | | 12.2 | ||
+ | | 12.2 | ||
+ | | 8:19 | ||
+ | | 7:55 | ||
+ | | 7:55 | ||
+ | | -5.2% | ||
+ | | -5.2% | ||
+ | |- | ||
+ | | 12 | ||
+ | | 14.8 | ||
+ | | 14.6 | ||
+ | | 13.8 | ||
+ | | 6:31 | ||
+ | | 6:37 | ||
+ | | 6:59 | ||
+ | | 1.4% | ||
+ | | 6.8% | ||
+ | |- | ||
+ | | Mean | ||
+ | | 13.05 | ||
+ | | 12.85 | ||
+ | | 12.75 | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | |- | ||
+ | | SD | ||
+ | | 1.88 | ||
+ | | 1.51 | ||
+ | | 1.55 | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | |} | ||
+ | ===Thoughts on SmO2 and Lactate Threshold=== | ||
+ | I think that the currently available research indicates that NIRS and SmO<sub>2</sub>hold promise for simplifying the measurement of Lactate Threshold. However, the research is at a fairly early stage, with only one study using the gold standard of MLSS. There are also indications in the research that the indicators of Lactate Threshold are not always evident in all subjects. There is no indication if this is a problem that occurs in specific subjects so that they will never get a valid test result, or if it's a problem that simply occurs randomly. Currently there are two consumer products available; [[BSX]] and [[Moxy]]. BSX is a fully automated approach to analyzing the data and estimating Lactate Threshold, whereas the Moxy is intended to provide the end-user with the underlying data to evaluate. | ||
+ | =Factors That May Influence Lactate Threshold= | ||
There are a few factors that may change the Lactate Threshold (other than training) | There are a few factors that may change the Lactate Threshold (other than training) | ||
* Because lactate is produced from the metabolism of carbohydrate, a reduction in carbohydrate intake (or [[Glycogen]] depletion) will shift the lactate curve to the right<ref name="Reilly-1999"/><ref name="Yoshida-1984"/><ref name="Maassen-1989"/><ref name="McLellan-1989"/>. | * Because lactate is produced from the metabolism of carbohydrate, a reduction in carbohydrate intake (or [[Glycogen]] depletion) will shift the lactate curve to the right<ref name="Reilly-1999"/><ref name="Yoshida-1984"/><ref name="Maassen-1989"/><ref name="McLellan-1989"/>. | ||
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<ref name="Lehmann-1983">M. Lehmann, A. Berg, R. Kapp, T. Wessinghage, J. Keul, Correlations between laboratory testing and distance running performance in marathoners of similar performance ability., Int J Sports Med, volume 4, issue 4, pages 226-30, Nov 1983, doi [http://dx.doi.org/10.1055/s-2008-1026039 10.1055/s-2008-1026039], PMID [http://www.ncbi.nlm.nih.gov/pubmed/6654546 6654546]</ref> | <ref name="Lehmann-1983">M. Lehmann, A. Berg, R. Kapp, T. Wessinghage, J. Keul, Correlations between laboratory testing and distance running performance in marathoners of similar performance ability., Int J Sports Med, volume 4, issue 4, pages 226-30, Nov 1983, doi [http://dx.doi.org/10.1055/s-2008-1026039 10.1055/s-2008-1026039], PMID [http://www.ncbi.nlm.nih.gov/pubmed/6654546 6654546]</ref> | ||
<ref name="Allen-1985">WK. Allen, DR. Seals, BF. Hurley, AA. Ehsani, JM. Hagberg, Lactate threshold and distance-running performance in young and older endurance athletes., J Appl Physiol (1985), volume 58, issue 4, pages 1281-4, Apr 1985, PMID [http://www.ncbi.nlm.nih.gov/pubmed/3988681 3988681]</ref> | <ref name="Allen-1985">WK. Allen, DR. Seals, BF. Hurley, AA. Ehsani, JM. Hagberg, Lactate threshold and distance-running performance in young and older endurance athletes., J Appl Physiol (1985), volume 58, issue 4, pages 1281-4, Apr 1985, PMID [http://www.ncbi.nlm.nih.gov/pubmed/3988681 3988681]</ref> | ||
+ | <ref name="Kek-2008">KJ. Kek, R. Kibe, M. Niwayama, N. Kudo, K. Yamamoto, Optical imaging instrument for muscle oxygenation based on spatially resolved spectroscopy., Opt Express, volume 16, issue 22, pages 18173-87, Oct 2008, PMID [http://www.ncbi.nlm.nih.gov/pubmed/18958095 18958095]</ref> | ||
+ | <ref name="Torricelli-2004">A. Torricelli, V. Quaresima, A. Pifferi, G. Biscotti, L. Spinelli, P. Taroni, M. Ferrari, R. Cubeddu, Mapping of calf muscle oxygenation and haemoglobin content during dynamic plantar flexion exercise by multi-channel time-resolved near-infrared spectroscopy., Phys Med Biol, volume 49, issue 5, pages 685-99, Mar 2004, PMID [http://www.ncbi.nlm.nih.gov/pubmed/15070196 15070196]</ref> | ||
+ | <ref name="Hyttel-Sorensen-2011">S. Hyttel-Sorensen, LC. Sorensen, J. Riera, G. Greisen, Tissue oximetry: a comparison of mean values of regional tissue saturation, reproducibility and dynamic range of four NIRS-instruments on the human forearm., Biomed Opt Express, volume 2, issue 11, pages 3047-57, Nov 2011, doi [http://dx.doi.org/10.1364/BOE.2.003047 10.1364/BOE.2.003047], PMID [http://www.ncbi.nlm.nih.gov/pubmed/22076266 22076266]</ref> | ||
+ | <ref name="Chance-1992">B. Chance, MT. Dait, C. Zhang, T. Hamaoka, F. Hagerman, Recovery from exercise-induced desaturation in the quadriceps muscles of elite competitive rowers., Am J Physiol, volume 262, issue 3 Pt 1, pages C766-75, Mar 1992, PMID [http://www.ncbi.nlm.nih.gov/pubmed/1312785 1312785]</ref> | ||
+ | <ref name="Bhambhani-2004">YN. Bhambhani, Muscle oxygenation trends during dynamic exercise measured by near infrared spectroscopy., Can J Appl Physiol, volume 29, issue 4, pages 504-23, Aug 2004, PMID [http://www.ncbi.nlm.nih.gov/pubmed/15328597 15328597]</ref> | ||
+ | <ref name="Belardinelli-1995a">R. Belardinelli, TJ. Barstow, J. Porszasz, K. Wasserman, Changes in skeletal muscle oxygenation during incremental exercise measured with near infrared spectroscopy., Eur J Appl Physiol Occup Physiol, volume 70, issue 6, pages 487-92, 1995, PMID [http://www.ncbi.nlm.nih.gov/pubmed/7556120 7556120]</ref> | ||
+ | <ref name="Belardinelli-1995b">R. Belardinelli, TJ. Barstow, J. Porszasz, K. Wasserman, Skeletal muscle oxygenation during constant work rate exercise., Med Sci Sports Exerc, volume 27, issue 4, pages 512-9, Apr 1995, PMID [http://www.ncbi.nlm.nih.gov/pubmed/7791581 7791581]</ref> | ||
+ | <ref name="Belardinelli-1995c">R. Belardinelli, D. Georgiou, TJ. Barstow, Near infrared spectroscopy and changes in skeletal muscle oxygenation during incremental exercise in chronic heart failure: a comparison with healthy subjects., G Ital Cardiol, volume 25, issue 6, pages 715-24, Jun 1995, PMID [http://www.ncbi.nlm.nih.gov/pubmed/7649420 7649420]</ref> | ||
+ | <ref name="Neary-2005">JP. Neary, DC. McKenzie, YN. Bhambhani, Muscle oxygenation trends after tapering in trained cyclists., Dyn Med, volume 4, issue 1, pages 4, Mar 2005, doi [http://dx.doi.org/10.1186/1476-5918-4-4 10.1186/1476-5918-4-4], PMID [http://www.ncbi.nlm.nih.gov/pubmed/15790400 15790400]</ref> | ||
+ | <ref name="Grassi-1999">B. Grassi, V. Quaresima, C. Marconi, M. Ferrari, P. Cerretelli, Blood lactate accumulation and muscle deoxygenation during incremental exercise., J Appl Physiol (1985), volume 87, issue 1, pages 348-55, Jul 1999, PMID [http://www.ncbi.nlm.nih.gov/pubmed/10409594 10409594]</ref> | ||
+ | <ref name="Bhambhani-1997">YN. Bhambhani, SM. Buckley, T. Susaki, Detection of ventilatory threshold using near infrared spectroscopy in men and women., Med Sci Sports Exerc, volume 29, issue 3, pages 402-9, Mar 1997, PMID [http://www.ncbi.nlm.nih.gov/pubmed/9139181 9139181]</ref> | ||
+ | <ref name="Wang-2012">B. Wang, G. Xu, Q. Tian, J. Sun, B. Sun, L. Zhang, Q. Luo, H. Gong, Differences between the Vastus Lateralis and Gastrocnemius Lateralis in the Assessment Ability of Breakpoints of Muscle Oxygenation for Aerobic Capacity Indices During an Incremental Cycling Exercise., J Sports Sci Med, volume 11, issue 4, pages 606-13, 2012, PMID [http://www.ncbi.nlm.nih.gov/pubmed/24150069 24150069]</ref> | ||
+ | <ref name="Mancini-1994">DM. Mancini, L. Bolinger, H. Li, K. Kendrick, B. Chance, JR. Wilson, Validation of near-infrared spectroscopy in humans., J Appl Physiol (1985), volume 77, issue 6, pages 2740-7, Dec 1994, PMID [http://www.ncbi.nlm.nih.gov/pubmed/7896615 7896615]</ref> | ||
+ | <ref name="Fuglevand-1997">AJ. Fuglevand, SS. Segal, Simulation of motor unit recruitment and microvascular unit perfusion: spatial considerations., J Appl Physiol (1985), volume 83, issue 4, pages 1223-34, Oct 1997, PMID [http://www.ncbi.nlm.nih.gov/pubmed/9338432 9338432]</ref> | ||
+ | <ref name="Hampson-1988">NB. Hampson, CA. Piantadosi, Near infrared monitoring of human skeletal muscle oxygenation during forearm ischemia., J Appl Physiol (1985), volume 64, issue 6, pages 2449-57, Jun 1988, PMID [http://www.ncbi.nlm.nih.gov/pubmed/3403428 3403428]</ref> | ||
+ | <ref name="Homma1996">Sachiko Homma, Influence of adipose tissue thickness on near infrared spectroscopic signal in the measurement of human muscle, Journal of Biomedical Optics, volume 1, issue 4, 1996, pages 418, ISSN [http://www.worldcat.org/issn/10833668 10833668], doi [http://dx.doi.org/10.1117/12.252417 10.1117/12.252417]</ref> | ||
+ | <ref name="van Beekvelt-2001">MC. van Beekvelt, MS. Borghuis, BG. van Engelen, RA. Wevers, WN. Colier, Adipose tissue thickness affects in vivo quantitative near-IR spectroscopy in human skeletal muscle., Clin Sci (Lond), volume 101, issue 1, pages 21-8, Jul 2001, PMID [http://www.ncbi.nlm.nih.gov/pubmed/11410110 11410110]</ref> | ||
+ | <ref name="BenaronMatsushita1998">David A. Benaron, Kenichi Matsushita, Sachiko Homma, Eiji Okada, Britton Chance, Marco Ferrari, <title>Influence of adipose tissue on muscle oxygenation measurement with an NIRS instrument</title>, volume 3194, 1998, pages 159–165, ISSN [http://www.worldcat.org/issn/0277786X 0277786X], doi [http://dx.doi.org/10.1117/12.301048 10.1117/12.301048]</ref> | ||
+ | <ref name="BenaronYamamoto1998">David A. Benaron, Katsuyuki Yamamoto, Masatsugu Niwayama, Ling Lin, Toshikazu Shiga, Nobuki Kudo, Makoto Takahashi, Britton Chance, Marco Ferrari, <title>Accurate NIRS measurement of muscle oxygenation by correcting the influence of a subcutaneous fat layer</title>, volume 3194, 1998, pages 166–173, ISSN [http://www.worldcat.org/issn/0277786X 0277786X], doi [http://dx.doi.org/10.1117/12.301049 10.1117/12.301049]</ref> | ||
+ | <ref name="Davis-2007">JA. Davis, R. Rozenek, DM. DeCicco, MT. Carizzi, PH. Pham, Comparison of three methods for detection of the lactate threshold., Clin Physiol Funct Imaging, volume 27, issue 6, pages 381-4, Nov 2007, doi [http://dx.doi.org/10.1111/j.1475-097X.2007.00762.x 10.1111/j.1475-097X.2007.00762.x], PMID [http://www.ncbi.nlm.nih.gov/pubmed/17944661 17944661]</ref> | ||
+ | <ref name="Snyder-2009">AC. Snyder, MA. Parmenter, Using near-infrared spectroscopy to determine maximal steady state exercise intensity., J Strength Cond Res, volume 23, issue 6, pages 1833-40, Sep 2009, doi [http://dx.doi.org/10.1519/JSC.0b013e3181ad3362 10.1519/JSC.0b013e3181ad3362], PMID [http://www.ncbi.nlm.nih.gov/pubmed/19675475 19675475]</ref> | ||
</references> | </references> |
Revision as of 15:20, 16 September 2015
Lactate Threshold is a key component of running performance, and is a better predictor of race performance than V̇O2max. Lactate Threshold can be thought of a reflecting a change from largely aerobic exercise to largely anaerobic exercise. Lactate Threshold is often used to determine the correct pace for Tempo Runs, though the science indicates such training is ineffective at best. However, Lactate Threshold provides an excellent way of monitoring the effectiveness of your training, and provides an objective estimate of your race pace. Unfortunately, measuring Lactate Threshold is time consuming and expensive, with the gold standard MLSS test requiring three to five 30 minute tests on separate days.
Contents
- 1 What is Lactate?
- 2 What is the Lactate Threshold?
- 3 Lactate Threshold Training
- 4 The Usefulness of Lactate Threshold
- 5 Lactate Curve
- 6 Determining Lactate Threshold
- 7 Factors That May Influence Lactate Threshold
- 8 Aerobic Threshold
- 9 References
1 What is Lactate?
Main article: Lactate
At one time Lactate was viewed as a harmful waste product due anaerobic exercise, but research since the early 2000s has shown that Lactate is an intermediate fuel in the metabolism of carbohydrates. Muscles will burn Lactate in preference to Glucose, and will convert Lactate back to Glucose at rest. The level of Lactate in the blood is primarily dependent on exercise intensity, rather like Heart Rate. Lactate is used as a fuel source by working muscles, and injecting extra lactate into the blood results in increased lactate metabolism and carbohydrate sparing[1] without impairing performance[2]. Note that Lactate forms Lactic Acid in the blood, and the terms are used interchangeably.
2 What is the Lactate Threshold?
The Lactate Threshold (LT) is the point at which the lactate level in the blood will rise even if the work intensity is kept constant. This is sometimes referred to as the Anaerobic Threshold (AT), or the Onset of Blood Lactate Accumulation (OBLA), though the most accurate term is Maximal Lactate Steady State (MLSS). Even within the scientific community terminology is confusing[3]. It is sometimes believed that the MLSS represents the maximum clearance of Lactate, but this may not be the case[2]. Note that Lactate is normally measured in the blood stream, so the Lactate level reflects the net of the muscles releasing and absorbing Lactate. Lactate Threshold is important as it is an excellent good predictor of race performance[4][5][6][7][8][9], and may be a better predictor than V̇O2max[10]. Lactate Threshold can be thought of as the percentage of VO2max that can be maintained for a protracted time[11], though it's not clear what the limiting factor is for exercise above the Lactate Threshold[12].
3 Lactate Threshold Training
Main article: Tempo Runs
There is good evidence that endurance training changes Lactate Threshold. However, the idea that training at threshold intensity, such as Tempo Runs, is particularly effective has no evidence[13]"/>[14], and polarized training is a better approach[15][16]. For trained athletes, Tempo runs are ineffective[17] and may actually be counterproductive[18][14]. See Tempo Runs for more details. Detraining shifts will reduce the Lactate Threshold[19], and Lactate levels can be higher at a given intensity after just a few days without training[20], suggesting rapid detraining effects.
4 The Usefulness of Lactate Threshold
One of the primary goals of Lactate Threshold testing is to determine the correct pace for Tempo Runs. However, even if Tempo training is ineffective there are two good reasons for knowing your Lactate Threshold. Firstly, monitoring Lactate Threshold is a great way of evaluating the effectiveness of a training regime. Secondly, Lactate Threshold can be used to validate race pace goals. If your Lactate Threshold suggests a much faster race pace than you've been able to achieve, it suggests either a lack of resistance to muscular damage or a lack of mental fortitude. If the Lactate Threshold suggests a race pace that is slower than your target goal, it suggests you objective is wrong and you should aim for a slower finish time. This is especially important in the marathon, where "hitting the wall" is a common issue.
5 Lactate Curve
It is common to plot exercise intensity against lactate level to produce a blood lactate curve similar to the one below, showing an exponential rise in lactate level with intensity. It's generally accepted that a shift of the curve to the right indicates an improved athletic performance[21][22], and training can improve performance because of this shift without a change in aerobic capacity (V̇O2max)[23]. There is some limited evidence from radio-isotope studies in animals that a benefit of endurance training may be in Lactate clearance[24]. Note that above the Lactate Threshold the Lactate level is not at a steady state, but rises even though the intensity remains constant, so the typical curve that is shown is rather misleading. Some Lactate Curves are plotting Blood Lactate against time during an Incremental Power Test (see below), which is more reasonable, but can still be rather misleading.
6 Determining Lactate Threshold
There are various ways of determining the Lactate Threshold, each with their own problems.
- MLSS. The gold standard test (and the only one that appears to be valid) is to measure Maximal Lactate Steady State (MLSS). The test requires 3 to 5 constant intensity trials of at least 30 minutes' duration, each performed on separate days. Each test is at a different exercise intensity, and the highest intensity that does not have a rise in blood lactate in the last 20 minutes is the MLSS. While this is the best way of determining Lactate threshold, it's obviously time consuming and interferes with the athlete's regular training. Because of the effort of MLSS testing, various shortcuts have been tried.
- Fixed Blood Lactate Accumulation. A simple approach is to assume that Lactate Threshold always occurs at the same Lactate level. Sadly, this assumption is wrong, as Lactate Threshold can occur at vastly different levels.
- Lactate Patterns. There are various approaches that look at the pattern of change in Lactate in an attempt to create a simple test. So far, I've seen little evidence to support any of these approaches.
- Heart Rate Deflection. An indirect way of finding Lactate Threshold is to look for the Heart Rate Deflection, sometimes called the "Conconi test". This test only requires a heart rate monitor to perform rather than blood draws, so it is much easier than the above approaches. However, the validity of the Conconi test has many issues and seems of dubious value[25]. See Heart Rate Deflection for details.
- Respiratory gasses. Another method for estimating Lactate Threshold is to measure the respiratory gasses[3][26], but given this is impractical for most athletes, it's not covered here.
6.1 Lactate Threshold & Maximal Lactate Steady State
The best approach to determine Lactate Threshold is to measure the Maximal Lactate Steady State (MLSS)[27]. The test is actually several constant load trials of at least 30 minutes' duration on different days at various exercise intensities (in the range of 50–90% V̇O2max. The highest workload that results in an increase of less than 1 mmol/L of lactate between the 10 and 30 minute mark defines the MLSS[28][29][30]. Lactate is typically measured using a blood sample, either using a pinprick or a catheter. Note that MLSS for a given individual will vary by sport[31], probably based on the mass of muscle engaged[32][33]. The difficulty of performing this test makes it impractical in most situations.
6.2 Lactate Threshold & Incremental Power Test
A common approach to determine the Lactate Threshold is the Incremental Power Test. The subject exercises in stages of increasing intensity, with lactate measured at the end of each stage, with stages typically lasting 3 to 10 minutes. However, blood lactate takes 20-30 minutes to stabilize for a given intensity[4]. This means that the incremental power test tends to be of limited value[34], with 3 minute stages giving low reproducibility[35], the stage length changing the lactate values[27], and even longer stages lengths of 8 minutes having low reproducibility[36]. The lactate level can drop between the 4th and 12th minute of exercise at a constant intensity[37]. Some have suggested using the lactate value measured as an indication of the prior stage's intensity, as it takes more than 3 minutes for lactate to stabilize[38], but this rather arbitrary approach can be used as a guideline (at best)[6]. For running, it is common to pause the exercise for 30 seconds to take a blood sample. These breaks only make a non-significant difference to the testing, though the slight difference tends to be greater at higher intensities[39].
6.3 Lactate Threshold & Fixed Blood Lactate Accumulation
Because MLSS is time consuming and expensive, a shortcut is often used to estimate MLSS by assuming that it occurs at a fixed Lactate Level (Fixed Blood Lactate Accumulation, or FBLA)[29], unusually 4.0 mmol/l[40] though sometimes 3.5 mmol/l[41][42]. However, while the MLSS may average around 4.0 mmol/l[42], there are significant differences for individuals[43], with variations between 3.0 and 5.5 in small sample sizes[40] and has been shown to have a range as wide as 2.0 to 10.0 mmol/l[27][44]. This approach also typically uses a blood test, but in some sports (like running), the athlete has to pause to have a pinprick blood sample taken, further confusing the test[40]. The term "Individual Anaerobic Threshold" (IAT) has been used to emphasize that the Lactate Threshold is specific to each individual rather than using a FBLA, though this can refer to a specific protocol for estimating MLSS[44]. The Fixed Blood Lactate Accumulation is sometimes called "Onset of Blood Lactate Accumulation" (OBLA)[43], a particularly misleading term in this context.
6.4 Lactate Threshold Estimation From Lactate Patterns
There have been several approaches to determining MLSS without the difficulty of the full protocol[45][46][5][47][48][28], but their validity is limited[49][29][50][51]. These approaches generally look for some pattern in the change of Lactate level. For example, one approach called the "Lactate Minimum Speed Test" (LMST) uses an initial sprint to elevate blood lactate followed by an incremental power test[52][53][54]. However, the effectiveness of the LMST is profoundly impacted by the starting speed of the incremental portion of the test[55]and so the results may be coincidence[56]. This is not entirely surprising given the initial sprint phase disrupts the metabolism[56]. Some trivial approaches have been tried, such as looking for a 1 mmol/l increase followed by another 1 mmol/l increase[57]. So for an athlete performing an incremental load test with Lactate readings of 1.7, 2.3, 2.6, 3.7, & 5.6 the conclusion would be their Lactate Threshold is 3.7 (3.7 is more than 1.0 more than 2.6 and followed by another increment of more than 1.0.) However, given that most portable Lactate meters have a Typical Error of 0.4-1.0 mmol/l[58], a fractional error in the reading gives a different result. In the previous example, if the 2.6 reading was 2.8, then the Lactate Threshold would jump from 3.7 to 5.6. Part of the problem with these approaches may be that MLSS may not represent the point of maximum lactate clearance[33], as injecting additional lactate into the blood of athletes exercising above MLSS did not significantly increase lactate levels[2]. Some of the tests could be "p-hacking", where the study looks at a sufficiently large number of variables that some correlation occurs randomly[59].
6.5 Lactate Threshold And Near Infrared Spectroscopy
A promising technology for measuring Lactate Threshold is Near-infrared spectroscopy (NIRS) which shines infrared light into the skin above an active muscle and measures the reflected light. NIRS measures the oxygen saturation in the capillaries of the muscle and has the potential to test for Lactate Threshold without any blood sampling. Because NIRS can monitor continually, it is possible that it may be able to determine the Lactate Threshold during an incremental test rather than requiring the multiple tests of MLSS.
6.5.1 Introduction to NIRS and SmO2
Near-infrared spectroscopy (NIRS) has been shown to measure the oxygen saturation of blood in muscle (SmO2) or other body tissues (StO2)[60][61][62]. (This works on similar principles to a Pulse Oximeter.) Medical NIRS systems for monitoring StO2 use Infrared LED or Lasers at 2, 3, or 4 frequencies[63]. SmO2 reflects the balance of oxygen delivery and consumption during exercise[64] and there are some initial indications that relative SmO2 may reflect changes in performance capacity[65]. There is generally a four phase response of smo2 during incremental exercise from rest to maximum intensity and the following recovery[66]:
- An initial increase in SmO2 above resting levels to supply the now active muscles. (This may be due to increased blood flow[67], but computer models do not support this[68].)
- SmO2 decreases linearly or exponentially with increasing intensity, followed by a leveling off as the subject approaches maximum intensity. There is some evidence of a breakpoint where the rate of decline increases (see below).
- During the first 1-2 minutes of recovery there is a rapid increase in SmO2 which usually exceeds resting levels.
- SmO2 then declines to resting levels over a further few minutes.
Skin should not impact SmO2 readings more than 5%[69], but surface fat can interfere with smo2[70][71][72][73]. Because the penetration depth of NIRS is about 50-60% of the distance between the emitter and receiver, the site must be selected so that the fat layer is much thinner than this depth[74].
6.5.2 SmO2 Breakpoint
As the intensity increases during incremental exercise SmO2 will remain constant or decline, with the rate of decline being greater near the Lactate Threshold[66][74][75]. This has led to several studies using the concept of an SmO2 "breakpoint"[76]. This breakpoint is a change in the slope of the line plotting SmO2 against work intensity in an incremental intensity test. This increase in the rate of desaturation can either be visually determined or based on bilinear regression. (The bilinear regression iterates over different combinations of two regression lines to find the lowest sum of squares of the residuals. I could not find the details of the constraints placed on this approach.)
6.5.3 SmO2 and Lactate Threshold
A number of studies have looked at the relationship between SmO2 and Lactate or Lactate Threshold
- A study of five mountain climbers found a relationship between the "point of inflection of lactate" and the SmO2 breakpoint during an incremental cycling test[76]. The definition they were using for the inflection of lactate was a blood lactate reading that is more than 0.5 below the subsequent value, with typical lactate levels below 2 mmol/l. This is closer to the "aerobic threshold" concept than the typical Lactate Threshold. The study did not find any correlation between the SmO2 breakpoint and the 4 mmol/l value of blood lactate. The breakpoint was determined from bi-linear regression.
- A study of 40 sedentary undergraduates showed a correlation between SmO2 returning to resting levels and Ventilatory Threshold (VT) in 65% of subjects during an incremental cycling test[67]. While the text refers to Lactate Threshold as the point at which Lactate rises above resting levels (aerobic threshold) the method used to determine VT appears to be the anaerobic threshold. This study did not use the breakpoint mentioned above, but the point where the SmO2 drops below the level detected at rest.
- A study of 11 subjects of varying fitness levels showed a correlation between SmO2 breakpoint determined visually and Ventilatory Threshold (VT) during an incremental cycling test[66].
- A comparison between 12 healthy subjects and 7 suffering from chronic heart failure (CHF) showed a correlation between the SmO2 breakpoint and Ventilatory Threshold (VT) during an incremental cycling test[77].
- A 2012 study compared the results from NIRS on the calf (Gastrocnemius Lateralis) and quads (Vastus Lateralis) in 31 active but not highly trained college students during an incremental cycling test[78]. The study found a correlation between Lactate Threshold (determined from the log-log method[79]) and the SmO2 breakpoint (determined from bi-linear regression) in both locations, but the quads corresponded better. (I suspect the results from running could be quite different.)
- A 2009 study used MLSS (the gold standard for Lactate Threshold) with running to evaluate NIRS[80]. The 16 athletes performed between 2 and 5 tests of 30 minutes each to determine MLSS, separated by at least 48 hours each. The subjects then performed an incremental treadmill test using 6 minute stages with the 4th stage at the pace they estimated they could maintain for an hour (around Lactate Threshold). The first 3 stages where then 0.66, 0.44, & 0.22 meter/second slower, and the subsequent stages were 0.22 meters/second faster each time. SmO2 breakpoint was defined as the workload immediately prior to a drop of 15% that lead to a continuous decline in smo2. A Lactate breakpoint was also determined based on the incremental test using the workload prior to an increase of 1 mmol/l as the criteria. Both the SmO2 and Lactate breakpoint were determined visually. Of the 16 subjects, 1 did not reach MLSS, 2 did not have both a SmO2 breakpoint or a Lactate breakpoint (based on the criteria used) and 1 did not have either. The study found that SmO2 is as effective as Lactate breakpoint tests for determining true Lactate Threshold (MLSS). The table below shows the values for each of 12 subjects, with the paces shown as KPH, then min/mile, then the error as a percentage. This shows that while smo2 is as good as the lactate breakpoint, the individual differences from MLSS are not insignificant. For instance, subject 5 had an MLSS of 6:21, but an SmO2 breakpoint of 6:57 and lactate breakpoint of 6:59, which is a big difference.
Subject | MLSS | SmO2 | Lb | MLSS | SmO2 | Lb | SmO2 err | Lb err |
---|---|---|---|---|---|---|---|---|
1 | 13.5 | 12.9 | 13.7 | 7:09 | 7:29 | 7:03 | 4.4% | -1.5% |
2 | 14.3 | 14.2 | 13.4 | 6:45 | 6:48 | 7:12 | 0.7% | 6.3% |
3 | 9 | 9.5 | 9.5 | 10:44 | 10:10 | 10:10 | -5.6% | -5.6% |
4 | 13.4 | 12.9 | 12.9 | 7:12 | 7:29 | 7:29 | 3.7% | 3.7% |
5 | 15.2 | 13.9 | 13.8 | 6:21 | 6:57 | 6:59 | 8.6% | 9.2% |
6 | 12.9 | 12.7 | 13.5 | 7:29 | 7:36 | 7:09 | 1.6% | -4.7% |
7 | 15.4 | 14.5 | 15.3 | 6:16 | 6:40 | 6:19 | 5.8% | 0.6% |
8 | 11.5 | 11.7 | 10.9 | 8:24 | 8:15 | 8:52 | -1.7% | 5.2% |
9 | 10.8 | 10.9 | 10.8 | 8:56 | 8:52 | 8:56 | -0.9% | 0.0% |
10 | 14.2 | 14.2 | 13.2 | 6:48 | 6:48 | 7:19 | 0.0% | 7.0% |
11 | 11.6 | 12.2 | 12.2 | 8:19 | 7:55 | 7:55 | -5.2% | -5.2% |
12 | 14.8 | 14.6 | 13.8 | 6:31 | 6:37 | 6:59 | 1.4% | 6.8% |
Mean | 13.05 | 12.85 | 12.75 | |||||
SD | 1.88 | 1.51 | 1.55 |
6.5.4 Thoughts on SmO2 and Lactate Threshold
I think that the currently available research indicates that NIRS and SmO2hold promise for simplifying the measurement of Lactate Threshold. However, the research is at a fairly early stage, with only one study using the gold standard of MLSS. There are also indications in the research that the indicators of Lactate Threshold are not always evident in all subjects. There is no indication if this is a problem that occurs in specific subjects so that they will never get a valid test result, or if it's a problem that simply occurs randomly. Currently there are two consumer products available; BSX and Moxy. BSX is a fully automated approach to analyzing the data and estimating Lactate Threshold, whereas the Moxy is intended to provide the end-user with the underlying data to evaluate.
7 Factors That May Influence Lactate Threshold
There are a few factors that may change the Lactate Threshold (other than training)
- Because lactate is produced from the metabolism of carbohydrate, a reduction in carbohydrate intake (or Glycogen depletion) will shift the lactate curve to the right[81][82][83][84].
- It's not clear if Delayed Onset Muscle Soreness changes the lactate curve as there are reports that it does[85] and reports that it does not[86].
- Lactate Threshold will vary by sport, probably based on the mass of muscle engaged[32], or because the inactive muscles consume more lactate as the concentration rises[38]. MLSS may also vary with environmental conditions, with a lower lactate levels at MLSS in hotter conditions[87].
8 Aerobic Threshold
There is a related concept called "Aerobic Threshold" that is generally used to mean the exercise intensity at which Lactate levels rise above resting baselines[27]. This threshold is believed to be the upper limit of nearly exclusive use of aerobic metabolism that can be sustained for many hours. Intensities just above the aerobic threshold can be maintained for prolonged periods (~4 hours)[88]. This aerobic threshold can be hard to determine in untrained subjects as it occurs at very low intensities[89]. Unfortunately, the term "Lactate Threshold" is sometimes used to mean this point where lactate rises above resting levels[82].
9 References
- ↑ Benjamin F. Miller, Jill A. Fattor, Kevin A. Jacobs, Michael A. Horning, Franco Navazio, Michael I. Lindinger, George A. Brooks, Lactate and glucose interactions during rest and exercise in men: effect of exogenous lactate infusion, The Journal of Physiology, volume 544, issue 3, 2002, pages 963–975, ISSN 00223751, doi 10.1113/jphysiol.2002.027128
- ↑ 2.0 2.1 2.2 Darren Ellis, Catherine Simmons, Benjamin F. Miller, Sodium lactate infusion during a cycling time-trial does not increase lactate concentration or decrease performance, European Journal of Sport Science, volume 9, issue 6, 2009, pages 367–374, ISSN 1746-1391, doi 10.1080/17461390903009158
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<ref>
tag; name "Palmer-1999" defined multiple times with different content - ↑ 6.0 6.1 C. Baldari, L. Guidetti, A simple method for individual anaerobic threshold as predictor of max lactate steady state., Med Sci Sports Exerc, volume 32, issue 10, pages 1798-802, Oct 2000, PMID 11039656
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