(R)-Alpha-Lipoic Acid: Weight Loss with Benefits?

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Reference Bobe G, Michels AJ, Zhang WJ, et al. A randomized controlled trial of long-term (R)-α-lipoic acid supplementation promotes weight loss in overweight or obese adults without altering elevated plasma triglyceride concentrations. J Nutr. 2020;150(9):2336-2345. Study Objective Primary: Evaluate the effectiveness of (R)-alpha-lipoic acid (R-LA) in reducing elevated plasma triglycerides in overweight and obese adults Secondary: Evaluate the effectiveness of alpha-lipoic acid in promoting weight loss and/or improving oxidative stress and/or inflammation Design Randomized, double-blind, placebo-controlled study intervention The trial duration was 24 weeks. Participants received either 2 capsules of 300 mg each 30 minutes before breakfast...

Bezug Bobe G, Michels AJ, Zhang WJ, et al. Eine randomisierte kontrollierte Studie zur langfristigen (R)-α-Liponsäure-Supplementierung fördert die Gewichtsabnahme bei übergewichtigen oder fettleibigen Erwachsenen, ohne die erhöhten Triglyceridkonzentrationen im Plasma zu verändern. J Nutr. 2020;150(9):2336-2345. Studienziel Primär: Bewerten Sie die Wirksamkeit von (R)-Alpha-Liponsäure (R-LA) bei der Reduzierung erhöhter Plasmatriglyceride bei übergewichtigen und fettleibigen Erwachsenen Sekundär: Bewerten Sie die Wirksamkeit von Alpha-Liponsäure bei der Förderung der Gewichtsabnahme und/oder der Verbesserung von oxidativem Stress und/oder Entzündungen Entwurf Randomisierte, doppelblinde, placebokontrollierte Studie Intervention Die Versuchsdauer betrug 24 Wochen. Die Teilnehmer erhielten 30 Minuten vor dem Frühstück entweder 2 Kapseln mit jeweils 300 mg …
Reference Bobe G, Michels AJ, Zhang WJ, et al. A randomized controlled trial of long-term (R)-α-lipoic acid supplementation promotes weight loss in overweight or obese adults without altering elevated plasma triglyceride concentrations. J Nutr. 2020;150(9):2336-2345. Study Objective Primary: Evaluate the effectiveness of (R)-alpha-lipoic acid (R-LA) in reducing elevated plasma triglycerides in overweight and obese adults Secondary: Evaluate the effectiveness of alpha-lipoic acid in promoting weight loss and/or improving oxidative stress and/or inflammation Design Randomized, double-blind, placebo-controlled study intervention The trial duration was 24 weeks. Participants received either 2 capsules of 300 mg each 30 minutes before breakfast...

(R)-Alpha-Lipoic Acid: Weight Loss with Benefits?

Relation

Bobe G, Michels AJ, Zhang WJ, et al. A randomized controlled trial of long-term (R)-α-lipoic acid supplementation promotes weight loss in overweight or obese adults without altering elevated plasma triglyceride concentrations.J Nutr. 2020;150(9):2336-2345.

Study objective

Primary:Evaluate the effectiveness of (R)-alpha-lipoic acid (R-LA) in reducing elevated plasma triglycerides in overweight and obese adults

Secondary:Evaluate the effectiveness of alpha lipoic acid in promoting weight loss and/or improving oxidative stress and/or inflammation

Draft

Randomized, double-blind, placebo-controlled trial

intervention

The duration of the experiment was 24 weeks. Participants received either 2 capsules containing 300 mg R-LA each or matching inert tablets on an empty stomach 30 minutes before breakfast. Researchers asked participants not to change any other aspects of diet or lifestyle over the course of the study.

Participant

The study involved 81 adults (57% women; aged 21 to 60 years; body mass index [BMI] ≥ 25 kg/m2).

All participants had elevated plasma triglycerides (≥100 mg/dL) at baseline.

Study parameters assessed

Primary:

  • Plasma-Triglyceride

Secondary:

  • Körpergewicht und Körperfettmasse
  • Zell- und Plasma-Antioxidantien-Pool und -Kapazität
  • Genexpression antioxidativer Enzyme
  • Lipidperoxidation
  • Zelluläre und plasmatische Entzündungsmarker
  • Blutmarker der Immunüberwachung

Primary outcome measures

Change in plasma triglycerides.

Key insights

  • Die Plasmatriglyzeride nahmen mit der R-LA-Ergänzung nicht ab.
  • Die Behandlungsgruppe hatte nach 24 Wochen eine stärkere Reduktion des BMI als die Placebogruppe (–0,8; P=0,04)
  • Nach 24 Wochen verloren Frauen und adipöse Teilnehmer in der Behandlungsgruppe (BMI ≥ 35) am meisten Gewicht (–5,0 % bzw. –4,8 %; beides). P<0,001) und Körperfett (–9,4 % bzw. –8,6 %; beides P<0,005).
  • Genexpression von Antioxidantien in mononukleären Zellen, exprimiert durch Hämoxygenase 1 (HMOX1) genetische Expression, war in der Behandlungsgruppe nach 24 Wochen höher.
  • Mehrere Marker zur Bewertung von oxidativem Stress und Entzündungen waren in der Behandlungsgruppe nach 24 Wochen niedriger, darunter weniger F2-Isoprostane im Urin (–25 %; P=0,005).

Practice implications

In some people, obesity and overweight are highly correlated with associated health risks, including elevated triglycerides,1.2Inflammation,3and oxidative stress.4

The extent to which these physiological changes may affect overall health5and mortality6is significant and warrants a multidisciplinary approach when working with this patient population.

After 24 weeks, women and obese participants in the treatment group (BMI ≥ 35) lost the most weight.

The road to thoroughly and lastingly implementing fundamental, health-promoting lifestyle changes can be long, arduous, and arduous. It therefore makes sense to use additional tools to improve your BMI. If this support serves directly to improve important physiological factors that might otherwise contribute to eventual pathological changes, it makes even more sense.

Although this study showed no effect on its primary endpoint, the effects observed on various secondary endpoints strongly suggest that R-LA may still fit this bill. The changes in the intervention group may arguably make a more impactful contribution to health than the primary outcome measure.

While this study did not show that R-LA lowered triglycerides, the clear effects on inflammation and oxidative stress that this nutrient appears to have in this patient population make R-LA clinically relevant. This is particularly true when considering the negative effects of inflammation and oxidative stress on hypertriglyceridemia-induced cardiovascular risk.6.7

Theoretically, the lack of effect observed on R-LA's primary outcome measure of plasma triglycerides could be interpreted to mean that there is no benefit from using R-LA. However, triglycerides themselves are not considered directly atherogenic, but rather as biomarkers of risk, as they often correlate with other atherogenic factors.8

In fact, increasing triglycerides can have questionable negative effects when inflammation is under control. Some evidence suggests that significant effects on endpoint markers of cardiovascular disease may occur even if triglycerides increase with treatment when inflammation and oxidative stress improve.9

As always, when treating patients, we should aim for a multi-pronged approach based on fundamental health-promoting principles (diet, exercise, sleep, stress reduction, etc.). However, various real-world circumstances that may come into play during patients' efforts can slow or hinder their progress. Having additional tools like R-LA on board or at the ready can help protect our patients in important ways as they work toward ever-increasing health-promoting lifestyles and improved health status.

  1. Szczygielska A, Widomska S, Jaraszkiewicz M, Knera P, Muc K. Blutfettprofil bei adipösen oder übergewichtigen Patienten. Ann Univ. Mariae Curie Sklodowska Med. 2003;58(2):343-349.
  2. Feingold KR. Fettleibigkeit und Dyslipidämie. In: Feingold KR, Anawalt B, Boyce A, et al, Hrsg. Endotext [Internet]. South Dartmouth, MA: MDText.com, Inc. 2020.
  3. Mraz M, Haluzik M. Die Rolle von Fettgewebe-Immunzellen bei Fettleibigkeit und leichten Entzündungen. J Endocrinol. 2014;222(3):R113-127.
  4. Marseglia L, Manti S, D’Angelo G, et al. Oxidativer Stress bei Fettleibigkeit: eine kritische Komponente bei menschlichen Krankheiten. Int. J. Mol. Sci. 2014;16(1):378-400.
  5. Fernández-Sánchez A, Madrigal-Santillán E, Bautista M, et al. Entzündungen, oxidativer Stress und Fettleibigkeit. Int. J. Mol. Sci. 2011;12(5):3117-3132.
  6. Skalicky J, Muzakova V, Kandar R, Meloun M, Rousar T, Palicka V. Bewertung von oxidativem Stress und Entzündungen bei übergewichtigen Erwachsenen mit metabolischem Syndrom. Clin Chem Lab Med. 2008;46(4):499-505.
  7. Lockman KA, Baren JP, Pemberton CJ, et al. Oxidativer Stress und nicht die Akkumulation von Triglyceriden ist eine Determinante der mitochondrialen Dysfunktion in In-vitro-Modellen der hepatischen zellulären Steatose. Leber Int. 2012;32(7):1079-1092.
  8. Talayero BG, Säcke FM. Die Rolle von Triglyceriden bei Arteriosklerose. Curr Cardiol Rep. 2011;13(6):544-552.
  9. Ornish D, Scherwitz LW, Billings JH, et al. Intensive Lebensstiländerungen zur Umkehrung der koronaren Herzkrankheit. JAMA. 1998;280(23):2001-2007.