Many performance labs and coaches determine the anaerobic threshold based on a lactate concentration of 4 mmol/l during an incremental test. This article answers whether that is a valid method of assessing the anaerobic- or lactate threshold.

By Loek Vossen

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Where does the 4 mmol/l theory come from?

The 4 mmol/l mark is widely known and used to determine the anaerobic threshold. But why? Let’s have a look at the origin of the 4 mmol/l theory.

In 1976, INSCYD’s advisory board member Alois Mader and his colleagues introduced the terms “lactate threshold” and “aerobic-anaerobic threshold”. Mader, who was working in Cologne (Germany), found that a blood lactate concentration of 4 mmol/l can be a criterion for the assessment of these thresholds, during an incremental lab test. His work was published in German.

In 1981, Bertil Sjödin and his colleagues introduced the English term “Onset of blood lactate accumulation” or “OBLA”. They also used a blood lactate concentration of 4 mmol/l to determine their exercise intensity: OBLA.

In more recent scientific publications, the 4 mmol/l lactate threshold mark is referred to as LT4.

Why 4 mmol/l lactate does not necessarily equal MLSS

As mentioned, Mader and his colleagues (also referred to as the Cologne group) used the 4 mmol/l mark in an incremental lab test. Soon other scientists started to demonstrate that the Individual Anaerobic Threshold (IAT) did not always occur at a blood lactate concentration of 4 mmol/l, when using an incremental lab test that was different from the original protocol.

To solve this problem, Mader and his team worked on a new test to determine the anaerobic threshold. They asked volunteers to exercise at a constant intensity (at the expected threshold intensity) for ~30 minutes. They then identified whether this intensity was indeed the maximal intensity at which blood lactate concentration remained stable. The highest intensity at which lactate remained stable was called “maxLass” or “MLSS”. To this day, this method is considered the “gold standard” method of assessing the anaerobic threshold.

Example maximal lactate steady state
An example of 3 maximal lactate steady state (MLSS) tests. The blue and green line both show lactate steady states, while the red line does not. The green line is the maximal lactate steady state in this example.

Because the MLSS test takes a lot of time (you have to do multiple ~30 min tests), interest in determining the anaerobic threshold via an incremental test remained. One way to solve this problem was by comparing the MLSS tests with incremental lab tests.

In 1985, Mader and Heck published their new findings in a scientific paper called: Justification of the 4-mmol/l Lactate Threshold. There are two important conclusions in this paper:

  1. A 4 mmol/l blood lactate concentration indeed correlates with the “gold standard” MLSS test in the original incremental lab test of Mader (see image below, R2 = 0,98).
  2. If you change the original protocol, you cannot use the 4 mmol/l mark anymore for determining the anaerobic threshold.
Regression between treadmill speed in graded exercise tests at the 4-mmol/l threshold (x-axis) and the speed at the maximal lactate steady state, MLSS (y-axis). N=16, R2=0,98, Bias=0,12 m/s
Regression between treadmill speed in graded exercise tests at the 4-mmol/l threshold (x-axis) and the speed at the maximal lactate steady state, MLSS (y-axis). N=16, R2=0,98, Bias=0,12 m/s

In other words: unless you’re using the exact same incremental test protocol that Mader and his team used in 1976, a blood lactate concentration of 4 mmol/l is not a good marker for anaerobic threshold in your (lab) test.

Are you a dedicated sports coach or performance lab professional, striving to optimize your athletes’ performance? Do you want to understand the intricacies of anaerobic threshold assessment and apply the most accurate methods for your team? Don’t rely on the outdated 4 mmol/l lactate threshold. Dive deeper into the science of lactate threshold assessment and maximize your athletes’ potential.

Take advantage of our exclusive offer: Book a FREE 1:1 consultation with INSCYD’s team of experts in your own language, and let us guide you through the nuances of MLSS and IAT for optimal performance assessment. Click the button below and embark on a journey to unleash the full potential of your athletes with INSCYD’s cutting-edge expertise.

Now you’re probably wondering: what was the original protocol?

The original 4 mmol/l test protocol

According to their 1985 publication, there are a couple of factors that determine whether you can use the 4 mmol/l mark to determine the anaerobic threshold. 

  1. Sport: the original test was performed with runners.
  2. Step duration: the original test used 5-minute incremental steps. Using other step durations will under- or overestimate the anaerobic threshold when using the 4 mmol/l mark.
  3. Step intensity: the original test started at 2.4 m/s and increased running speed by 0.4 m/s per step. Different step sizes will affect the results.
  4. Time between steps: the original test used passive rest periods to measure blood lactate. The duration of the rest period affects the lactate curve and therefore the intensity of the 4 mmol/l lactate mark. The original test included passive rest periods of 30 seconds.
  5. Equipment: two different treadmills turned out to result in two different outcomes. The original test used a Siemens treadmill.
  6. The incline of the treadmill: the original test used a treadmill incline of 1%.

The 1985 publication shows that if you don’t check all these boxes, you should not use the 4 mmol/l mark to determine the anaerobic threshold.

Example of what happens when you don’t stick to the original test protocol. If you change the step duration from 5 to 3 minutes, you’ll get a different lactate curve. As a result, you will overestimate the exercise intensity at the maximal lactate steady state (MLSS) or anaerobic threshold (AT).
Example of what happens when you don’t stick to the original test protocol. If you change the step duration from 5 to 3 minutes, you’ll get a different lactate curve. As a result, you will overestimate the exercise intensity at the maximal lactate steady state (MLSS) or anaerobic threshold (AT).

Lactate concentration at anaerobic threshold

We learned that the 4 mmol/l mark is not a good indicator for the anaerobic threshold (AT) if you’re not using the original test protocol. But then, what is the lactate concentration at anaerobic threshold?

Your lactate concentration depends on the exercise intensity, the exercise duration and the initial lactate concentration. As a result, your lactate concentration at threshold intensity could be “anything”. Here’s an example of how you could measure lactate concentrations above 8 mmol/l at threshold intensity:

Go out and do a (very) hard 5 minute effort. After 5 minutes, continue with a 10 minute interval at your AT intensity. Voila, you’re now exercising at your threshold intensity with a lactate concentration that will remain well above 4 mmol/l.

Even if you’re only interested in lactate concentrations in a graded exercise (starting with low lactate concentrations), there’s still not one specific lactate concentration that you’ll find. Ralph Beneke and his colleagues show that in “gold standard” MLSS tests, you can find an AT lactate concentration somewhere between 2 mmol/l to 8 mmol/l.

There is no correlation between MLSS blood lactate concentration (y-axis) and MLSS workload (x-axis). The lactate concentration at MLSS can range somewhere between 2 and 8 mmol/l. (Source).

 As Mader quotes in his 1985 publication:

 

(..) endurance-trained persons probably have their thresholds at lower lactate concentration levels. Work loads in training corresponding to the 4-mmol/l threshold value were poorly tolerated by trained individuals, but well tolerated by untrained persons.”

Wrap up The Future of Anaerobic Threshold

Even though Wikipedia still suggests the 4 mmol/l mark for approximating AT, we now know better. Those who unintentionally founded the 4 mmol/l idea in 1976, already showed that you could not use this mark in any other test protocol in 1985.

Unless you are using the original test protocol in runners, there are better ways to determine the anaerobic threshold. INSCYD performance software enables you to accurately determine AT, while using your preferred (lactate) test protocol. The best part: the results are not limited to AT only. Instead, you get a full 360 metabolic profile. Learn more about the INSCYD test and the INSCYD software.

Don’t settle for outdated methods when it comes to assessing anaerobic threshold. Sports coaches and labs, take advantage of a free consultation with an expert to learn how the latest advancements can transform the way you determine AT and create comprehensive training plans for your athletes. Click the buttons below to schedule free 1:1 consultation on your own language and stay ahead of the competition

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Literature

  • Original paper 1976. Mader A, Liesen H, Heck H, Philippi H, Rost R, Schürch P, Hollmann W (1976) Zur Beurteilung der sportartspezifischen Ausdauerleistungsfähigkeit im Labor. Sportarzt und Sportmedizin 27 (5): 109–112 [LINK]
  • Follow up publication 1985. Heck H, Mader A, Hess G, Mücke S, Müller R & Hollmann W (1985). Justification of the 4-mmol/l lactate threshold. Int J Sports Med 6, 117–130 [LINK]
  • MLSS lactate concentration does not correlate with MLSS workload. Beneke, R., Hütler, M., & Leithäuser, R. M. (2000). Maximal lactate-steady-state independent of performance. Medicine and science in sports and exercise, 32(6), 1135–1139. [LINK]
LOEK VOSSEN

Human Movement Scientist | Content Marketing and Education