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Effects of beta-conglycinin intake on circulating FGF21 levels and brown adipose tissue activity in Japanese young men: a single intake study and a randomized controlled trial



Human brown adipose tissue (BAT) activity has beneficial effects on body composition and glucose metabolism. A previous study reported that beta-conglycinin intake induced postprandial fibroblast growth factor 21 (FGF21) secretion, thereby promoting adipose tissue thermogenesis in mice. Since it has not been evaluated whether beta-conglycinin intake is associated with induced FGF21 secretion and BAT thermogenesis in humans, the current study examined the effects of beta-conglycinin intake on circulating FGF21 level and BAT activity.


Twenty-two healthy young male subjects participated. This study consisted of 2 interventional studies. In one of them, the effects of single beta-conglycinin intake at thermoneutral temperature on circulating FGF21 levels were examined (n = 7). The other study was a single-blinded randomized crossover trial of 2 weeks (n = 14). The subjects were exposed to mild cold conditions using a climatic chamber, and BAT activity was analyzed using thermography. Serum FGF21 level was determined by ELISA in these studies.


In the single intake study, serum FGF21 level was the highest before beta-conglycinin intake and gradually and significantly decreased throughout the 2-h experimental period (P < 0.05). The randomized crossover trial showed that 2-week beta-conglycinin intake did not affect serum FGF21 level and BAT activity, whereas changes (Δ) in baseline levels of serum FGF21 were positively correlated with Δ BAT activity (P < 0.05). In addition, analysis of each group revealed that there was significant correlation between the Δ serum FGF21 level and Δ BAT activity in the beta-conglycinin group (P < 0.05), but not in the placebo group.


This study reveals that although serum FGF21 levels are not increased by a single or short-term intake of beta-conglycinin, the Δ basal FGF21 level is associated with Δ BAT activity. These results suggest that human FGF21 responsiveness is different from that of rodents and support the importance of FGF21 in human BAT thermogenesis.

Trial registration

This study is registered with University Hospital Medical Information Network in Japan (number 000038723,


Brown adipose tissue (BAT) is characterized by a high expression of the mitochondrial uncoupling protein 1, which enhances thermogenic energy expenditure [1, 2]. It has been demonstrated that human BAT has beneficial effects on body composition and glucose metabolism, and the same is true for animals [1,2,3,4,5]. Previous studies have undertaken the strategy of increasing BAT activity through dietary intake activating the sympathetic nervous system [6, 7]. It is therefore necessary to further elucidate the regulatory factors of human BAT activity.

Fibroblast growth factor 21 (FGF21) is a hormonal factor that is primarily secreted by the liver and improves whole-body metabolism [8,9,10,11]. Previous animal studies have shown that FGF21 is related to an increase in browning of the white adipose tissue [12, 13], and, according to some studies, activating of the BAT [12, 14]. Human studies have also reported beneficial effects of FGF21. For instance, ingestion of FGF21 or an analog has been shown to improve glycolipid metabolism [15,16,17]. Moreover, circulating FGF21 levels correlated with the BAT activity during cold exposure in male subjects [18, 19]. It is considered that the increase in circulating FGF21 stimulates BAT thermogenesis. In contrast, in obese rodents and humans, circulating FGF21 is chronically elevated [20, 21], which has been characterized as a FGF21-resistant state [21]. Although these results suggest that basal FGF21 concentration may relate to the thermogenic impairment of the adipose tissue, the association between baseline changes in circulating FGF21 levels and BAT activity has not been examined.

In a previous study, single ingestion of beta-conglycinin, a protein isolated from soy beans, induced postprandial FGF21 secretion in mice [22]. Furthermore, long-term beta-conglycinin intake suppressed high resting level of circulating FGF21, induced adipose tissue thermogenesis, and prevented body fat accumulation in mice fed high fat diets [22, 23]. In addition, interventional human studies have demonstrated that beta-conglycinin intake improves metabolic disorders including dyslipidemia [24] and visceral fat obesity [25]. It is therefore likely that the favorable mechanism of beta-conglycinin intake may be related to BAT activation by FGF21. However, it has not been evaluated whether beta-conglycinin intake is associated with induced FGF21 secretion and BAT thermogenesis in humans.

The purpose of this study was to identify the effects of beta-conglycinin intake on circulating FGF21 levels and BAT activity. This study initially determined whether a single intake of beta-conglycinin affects circulating FGF21 levels in healthy young men. Thereafter, we performed a randomized controlled trial (RCT) to examine the effects of 2-week beta-conglycinin intake on circulating FGF21 concentration and BAT activity.



Twenty-two healthy young male subjects (age 19–22 years) participated in this study. The subjects were recruited personally and through a volunteer club in the Kyoto Prefectural University. The inclusion criteria were being male and having an age of 18–22 years. The exclusion criteria included a history of chronic disease and intake of medication. All participants provided written informed consent before enrolment in the study, which was approved by the ethical committee of the Kyoto Prefectural University (Approved number 175). This study is registered with UMIN (University Hospital Medical Information Network in Japan), number 000038723.

Study design

As shown in Fig. 1, this study consisted of 2 interventional studies performed in the winter of 2019.

Fig 1.
figure 1

Flow diagram of the participants in the study

The first study examined the effects of single beta-conglycinin intake on circulating FGF21 levels without cold exposure. Seven subjects were selected. The single intake study started at 9:00 AM after an overnight fast, and the subjects were seated at rest during the experiment. After resting for 30 min, baseline blood samples were collected, and then subjects took beta-conglycinin tablets containing 10.6 g protein including 9.2 g beta-conglycinin (20 tables of WELLBEST beta-conglycinin; Fuji Industry, Tokyo, Japan). The amount of beta-conglycinin was more than that in previous interventional studies, which examined the effects of beta-conglycinin intake on acute appetite sensation [26], lipid metabolism [24], and visceral obesity [25]. After ingestion, blood samples were collected at 1 h and 2 h after the beta-conglycinin intake. The room temperature was maintained at 24 °C ± 2 °C throughout this study.

The other study was a single blind RCT. One subject did not participate due to lack of time before allocation, and thus 21 subjects were allocated into the beta-conglycinin group (n = 10) or the placebo group (n = 11). Baseline measurements were performed to determine anthropometric characteristics, blood biochemical parameters, daily food intake, and BAT activity. After baseline measurements, 2 subjects from the placebo group were excluded because of difficulties in collecting blood samples due to vasovagal reaction or rough skin surface. The nutritional composition of beta-conglycinin and placebo tablets has been shown in Table 1. Subjects were instructed to take either 20 tablets of WELLBEST beta-conglycinin (Fuji Industry, Tokyo, Japan) in the beta-conglycinin group or 20 tablets of placeplus (Placebo pharmaceutical company, Otsu, Japan) in the placebo group daily. Both groups were instructed to take 10 tablets in the morning and 10 tablets in the evening. All subjects were free-living and were instructed to consume their habitual diet throughout the study, and final measurements were performed after the 2-week interventional period.

Table 1 Nutritional composition of beta-conglycinin and placebo tablets

Baseline and final measurements in the randomized crossover trial

Mild-cold exposure was performed to evaluate BAT activity and serum FGF21 level in the randomized crossover trial. Subjects entered the climatic chamber (TBRR-9A4GX; ESPEC, Osaka, Japan) at 9:00 AM after an overnight fast, and the initial temperature of the climatic chamber was set at 27 °C. They were seated at rest for 30 min, and then baseline body surface temperature was measured as described below. After blood samples were collected, the temperature of the climatic chamber was reduced to 19 °C. The changes in chamber temperature were done within 5 min, and the cold exposure started at 19 °C in the chamber [27, 28]. Thereafter, both body surface temperature and blood samples were collected at 1 h and 2 h of mild-cold exposure. Before and during cold exposure, subjects were asked to rate shivering, cold sensation, and discomfort using a visual analog scale [27].

Measurement of BAT activity

BAT activity was determined as per a previously described method [27]. In brief, body surface temperature was measured using a thermal imaging camera (DE-TC1000T; D-eyes, Osaka, Japan). The supraclavicular temperature adjacent to BAT location on both the right and left sides was measured from each image. Chest temperature was simultaneously measured as a control for underlying BAT depots. The images of body surface temperature were analyzed using a modified (D-eyes) version of the Thermal-Cam v. software (Laon People, Seoul, Korea), and the average of supraclavicular temperature minus chest temperature was estimated as BAT activity. In the previous study, the thermography index was correlated (r = 0.74, P < 0.05) using 18F fluorodeoxyglucose-positron emission tomography/computed tomography, a standardized method for measuring BAT activity in humans [27].

Blood analysis

Blood samples were centrifuged at 3000g for 5 min. Serum was stored at – 80 °C until the time of analysis. The concentrations of serum glucose and triglycerides and the serum enzymatic activities of aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were measured using a Fuji Dry Chem 4000 analyzer (Fuji film, Tokyo, Japan). The serum FGF21 concentration was determined using a commercially available enzyme-linked immunosorbent assay (ELISA) kit (DF2100; R&D Systems, Minneapolis, MN, USA) according to the manufacturer’s instructions. The intra- and inter-assay coefficients of variation reported by the manufacturer were 2.9–3.9% and 5.2–10.9%, respectively.

Anthropometric characteristics and dietary food intake

Body weight and body fat percentage were measured using an electronic scale (V-body HBF-359; Omron, Kyoto, Japan), and body mass index (BMI) was calculated from measurements of height and body weight. Energy, protein, carbohydrate, and fat intake were also assessed using a Food Frequency Questionnaire based on the food groups (FFQg Ver 5.0; Kenpakusha, Tokyo, Japan), which estimates habitual intake by portion size and food frequency [29]. Supplemental nutrients from beta-conglycinin and placebo tablets were added to nutritional intake in the final measurements of the RCT.

Statistical analysis

All statistical analyses were performed using SPSS, version 24.0 (SPSS, Chicago, Illinois, USA). The Kolmogorov-Smirnov test was performed to assess the normality of data distribution. The one-way ANOVA and the post hoc Tukey’s HSD test were used to evaluate the difference in serum FGF21 levels between before, 1 h after, and 2 h after beta-conglycinin intake in the single intake study. Baseline characteristics and changes in variables during the randomized crossover trial were compared using the Student’s t test. Two-way ANOVA analysis (time × group) was used to determine absolute value difference between the groups. Relationships between changes in all variables were determined by the Pearson’s correlation coefficients. All measurements and calculated values have been presented as the mean ± SD, and the level of statistical significance was set at P < 0.05.


In the single intake study, the participating male subjects were young (21.1 years ± 0.7 years) and had a normal BMI (20.1 kg/m2 ± 1.4 kg/m2). The ELISA assay revealed that serum FGF21 level was the highest before beta-conglycinin intake and gradually decreased after single ingestion in the thermoneutral room (Fig. 2). One-way ANOVA revealed that the serum FGF21 levels were significantly lower 2 h after beta-conglycinin intake when compared to the baseline measurement (P < 0.05).

Fig 2.
figure 2

Effects of a single intake of beta-conglycinin on serum FGF21 levels in young male subjects. FGF21, fibroblast growth factor 21

Table 2 summarizes the baseline characteristics of the subjects and the changes in variables during the 2-week randomized controlled trial. The 14 young male subjects had normal BMI, serum metabolic parameters, and nutrient intake. Four subjects did not participate in the final measurements, and 1 subject was excluded because of an abnormal increase in serum FGF21 concentration (+ 509.7 pg/mL during the interventional period) that was more than 5 SD above the mean of the changes in the placebo group. Therefore, the results of 14 subjects were analyzed in total. The final number of subjects was 8 in the beta-conglycinin group and 6 in the placebo group. At baseline measurement, the height was significantly higher in the placebo group compared to the beta-conglycinin group (P < 0.05), whereas there was no statistical significance in other variables between the groups. The 2-week interventional study did not show a statistical difference in any variable including anthropometric characteristics, dietary food intake, and serum biochemical variables between the beta-conglycinin and placebo groups (Table 2).

Table 2 Changes in the variables during 2-week beta-congllycinin and placebo intakes

As shown in Fig. 3, serum FGF21 concentration did not decrease during cold exposure, whereas BAT activity was significantly increased by cold exposure (P < 0.05). There was no significant difference in BAT activity between 1 h and 2 h after cold exposure, indicating that BAT activity had reached a plateau at 1 h cold exposure. The randomized controlled trial found that the absolute values of serum FGF21 concentration and BAT activity were not different between the two groups before and after intervention periods. Moreover, there were no significant changes in baseline serum FGF21 levels and BAT activity 1 h and 2 h after cold exposure between the beta-conglycinin and placebo groups (Table 2). Shivering response, cold sensation, and discomfort were not statistically different between the two groups in this study (data not shown).

Fig 3.
figure 3

Serum FGF21 levels and BAT activity before and during cold exposure in the pre- and post-randomized controlled trials. FGF21, fibroblast growth factor-21; BAT, brown adipose tissue

In turn, the determinants of BAT activity were examined using correlation analysis (Table 3). The length of cold exposure did not increase BAT activity, and serum FGF21 concentration remained steady during cold exposure in the interventional study. Therefore, the changes in BAT activity (Δ BAT activity) 1 h after cold exposure and the changes in baseline serum FGF21 level (Δ baseline FGF21 level) were used as variables. In all subjects, the Δ BAT activity was not associated with changes in anthropometric characteristics and serum biochemical variables, whereas Δ baseline FGF21 level was significantly and positively correlated with Δ BAT activity (Fig. 4a, P < 0.05). In addition, analysis of each group revealed that there was a significant correlation between the changes in Δ baseline FGF21 level and Δ BAT activity in the beta-conglycinin group (Fig. 4b, P < 0.05), but not in the placebo group (Fig. 4c). Although there was no significant correlation in all subjects, the changes in dietary fat amount (Δ fat intake) were significantly and negatively correlated with Δ BAT activity in the beta-conglycinin group (Table 3, P < 0.05).

Table 3 Correlations between BAT activity and other variables in young male subjects
Fig 4.
figure 4

Correlations of the changes in the baseline serum FGF21 levels with BAT activity in young male subjects. Closed circle shows the beta-conglycinin group, and open triangle shows the placebo group. FGF21, fibroblast growth factor 21; BAT, brown adipose tissue


The present study revealed that the single intake of beta-conglycinin did not increase serum FGF21 level, and the serum FGF21 level decreased during a 2-h rest in young men. In addition, a 2-week RCT showed that serum FGF21 concentration and BAT activity were not increased by beta-conglycinin intake. In contrast, the Δ baseline FGF21 level significantly correlated with the Δ BAT activity. These results suggested that the circulating FGF21 concentration was not affected by a single and short-term intake of beta-conglycinin, and basal FGF21 concentration was associated with human BAT activity. Since the significant correlation between Δ baseline FGF21 level and Δ BAT activity was only observed in the beta-conglycinin group, it may be suggested that soy protein intake may modulate BAT activity through FGF21.

It was reported that temporary FGF21 secretion was induced by 6-h fasting in rodents, but 1-week fasting was needed to increase serum FGF21 concentration in humans [30]. The results suggest that FGF21 responsiveness to fasting may differ between rodents and humans. Unlike a previous animal study [22], this human study found that single beta-conglycinin intake does not increase circulating FGF21 level. This might be partly caused by the different FGF21 responsiveness that has been described in fasting conditions [30]. In addition, a human study reported that circulating FGF21 concentration followed a diurnal rhythm, reaching its peak in the early morning and declining after breakfast [31]. Thus, there is a possibility that different circadian rhythms and feeding patterns may lead to different outcomes: rodents are nocturnal animals and fed ad libitum in the laboratory, while humans are diurnal animals with regular meal times. Since this study started in the morning (9:00 AM), with the subjects in starvation to examine how the beta-conglycinin intake would affect FGF21 serum levels, the observed effects may be stronger than the ones caused by beta-conglycinin intake in humans. Moreover, hepatic FGF21 secretion in mice fed beta-conglycinin was elicited by methionine imbalance because of the lower methionine composition of beta-conglycinin [22], whereas the FFQg showed that the subjects of this study had consumed various protein sources before the days of beta-conglycinin intake (data not shown). It is difficult to assume that the dietary protein source is restricted only to beta-conglycinin in humans, and thus the methionine imbalance may not occur frequently. For the above mentioned reasons, it may be difficult to evaluate the single beta-conglycinin intake effect on FGF21 levels in humans.

In contrast, the RCT showed that serum FGF21 levels in the both groups were unchanged during the 2-h cold exposure. The blood sampling in the RCT was performed under fasting condition, and thus dietary suppression of circulating FGF21 level was linked to unchanged serum FGF21 levels during the 2-h rest. In addition, because it was reported that FGF21 secretion from BAT was stimulated by cold exposure in mice [32], the decrease in serum FGF21 concentration by the circadian rhythm might be suppressed by both fasting and the cold exposure in this study. Our RCT results revealed that Δ BAT activity was correlated with Δ baseline FGF21 level only in the beta-conglycinin group. The serum FGF21 levels were decreased, unchanged, or increased in the subjects of the beta-conglycinin group. This result suggested that the response of circulating FGF21 level to beta-conglycinin intake was not consistent. However, the mechanism remains unknown. Further studies will be needed to detail the effect of beta-conglycinin intake on FGF21 metabolism in BAT.

The Δ BAT activity was negatively correlated with fat intake only in the beta-conglycinin group, and thus there is a possibility that dietary fat intake influences BAT activity. To our knowledge, it has not been reported whether dietary fat restriction modulates BAT thermogenesis. Since the FFQg questionnaire only inquired about habitual dietary intake, the effects of fat intake should be investigated in further research using a stricter experimental design. We confirmed no significant correlation between basal levels of serum FGF21 and dietary fat intake in all subjects (r = 0.141, P = 0.631) and in the beta-conglycinin group (r = − 0.472, P = 0.238). Therefore, the dietary fat intake did not affect baseline FGF21 level and the relationship to BAT activity. The sample size of this study was small, making it difficult to identify the individual differences. Large-scale studies will be needed to explore the determining factors of the relationship between BAT activity and FGF21 in the future.

This study has several limitations including small sample size. Young healthy subjects participated in the RCT, and thus the therapeutic efficacy with regards to obesity and metabolic health has not been addressed. In addition, although the RCT performed a short-term intervention because 2 weeks are enough to induce BAT adaptation [4, 6], the confounding factors of chronic elevated FGF21 levels, such as changes in body fat distribution, have also not been addressed [33, 34]. The subjects had a relatively lower BAT activity. Indeed, the average supraclavicular–chest skin temperature was 0.8 °C, while BAT-positive subjects were defined as having approximately > 1.0°C in a previous study [27]. It is necessary to examine the long-term effects of beta-conglycinin intake on BAT activity and to identify the related variables.


Single intake of beta-conglycinin does not increase serum FGF21 levels, indicating that human FGF21 responsiveness is different from rodents. Moreover, although our RCT study revealed that 2-week beta-conglycinin intake did not affect serum FGF21 concentration, the changes in basal changes in FGF21 level and BAT activity were significantly and positively correlated. This result supports the importance of FGF21 in human BAT thermogenesis. Uncovered factors of human BAT activity remain, which may yield new insights into metabolic homeostasis. Therefore, it is necessary to provide novel evidence in future studies.

Availability of data and materials

The datasets analyzed during the current study are available from the corresponding author on reasonable request.



Alanine aminotransferase


Aspartate aminotransferase


Brown adipose tissue


Body mass index


Enzyme-linked immunosorbent assay


Food frequency questionnaire based on food groups


Fibroblast growth factor 21


Randomized controlled trial


  1. Kajimura S, Saito M. A new era in brown adipose tissue biology: molecular control of brown fat development and energy homeostasis. Annu Rev Physiol. 2014;76:225–49.

    Article  CAS  Google Scholar 

  2. Sidossis L, Kajimura S. Brown and beige fat in humans: thermogenic adipocytes that control energy and glucose homeostasis. J Clin Invest. 2015;125(2):478–86.

    Article  Google Scholar 

  3. Yoneshiro T, Aita S, Matsushita M, Kayahara T, Kameya T, Kawai Y, Iwanaga T, Saito M. Recruited brown adipose tissue as an antiobesity agent in humans. J Clin Invest. 2013;123(8):3404–8.

    Article  CAS  Google Scholar 

  4. Hanssen MJ, Hoeks J, Brans B, van der Lans AA, Schaart G, van den Driessche JJ, Jorgensen JA, Boekschoten MV, Hesselink MK, Havekes B, et al. Short-term cold acclimation improves insulin sensitivity in patients with type 2 diabetes mellitus. Nat Med. 2015;21(8):863–5.

    Article  CAS  Google Scholar 

  5. Iwen KA, Backhaus J, Cassens M, Waltl M, Hedesan OC, Merkel M, Heeren J, Sina C, Rademacher L, Windjager A, et al. Cold-induced brown adipose tissue activity alters plasma fatty acids and improves glucose metabolism in men. J Clin Endocrinol Metab. 2017;102(11):4226–34.

    Article  Google Scholar 

  6. Nirengi S, Homma T, Inoue N, Sato H, Yoneshiro T, Matsushita M, Kameya T, Sugie H, Tsuzaki K, Saito M, et al. Assessment of human brown adipose tissue density during daily ingestion of thermogenic capsinoids using near-infrared time-resolved spectroscopy. J Biomed Opt. 2016;21(9):091305.

    Article  Google Scholar 

  7. Saito M, Matsushita M, Yoneshiro T. Brown adipose tissue, diet-induced thermogenesis, and thermogenic food ingredients: from mice to men. Front. Endocrinol. 2016;11:222.

    Article  Google Scholar 

  8. Kharitonenkov A, Shiyanova TL, Koester A, Ford AM, Micanovic R, Galbreath EJ, Sandusky GE, Hammond LJ, Moyers JS, Owens RA, et al. FGF-21 as a novel metabolic regulator. J Clin Invest. 2005;115(6):1627–35.

    Article  CAS  Google Scholar 

  9. Fisher FM, Maratos-Flier E. Understanding the Physiology of FGF21. Annu Rev Physiol. 2016;78:223–41.

    Article  CAS  Google Scholar 

  10. Markan KR, Potthoff MJ. Metabolic fibroblast growth factors (FGFs): mediators of energy homeostasis. Semin Cell Dev Biol. 2016;53:85–93.

    Article  CAS  Google Scholar 

  11. Staiger H, Keuper M, Berti L. Hrabe de Angelis M, Haring HU: fibroblast growth factor 21-metabolic role in mice and men. Endocr Rev. 2017;38(5):468–88.

    Article  Google Scholar 

  12. Martinez-Garza U, Torres-Oteros D, Yarritu-Gallego A, Marrero PF, Haro D, Relat J. Fibroblast growth factor 21 and the adaptive response to nutritional challenges. Int J Mol Sci. 2019:20(19).

  13. Keipert S, Lutter D, Schroeder BO, Brandt D, Stahlman M, Schwarzmayr T, Graf E, Fuchs H, de Angelis MH, Tschop MH, et al. Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice. Nat Commun. 2020;11(1):624.

    Article  CAS  Google Scholar 

  14. Lewis JE, Monnier C, Marshall H, Fowler M, Green R, Cooper S, Chiotellis A, Luckett J, Perkins AC, Coskun T, et al. Whole-body and adipose tissue-specific mechanisms underlying the metabolic effects of fibroblast growth factor 21 in the Siberian hamster. Mol Metab. 2020;31:45–54.

    Article  CAS  Google Scholar 

  15. Gaich G, Chien JY, Fu H, Glass LC, Deeg MA, Holland WL, Kharitonenkov A, Bumol T, Schilske HK, Moller DE. The effects of LY2405319, an FGF21 analog, in obese human subjects with type 2 diabetes. Cell Metab. 2013;18(3):333–40.

    Article  CAS  Google Scholar 

  16. Charles ED, Neuschwander-Tetri BA, Pablo Frias J, Kundu S, Luo Y, Tirucherai GS, Christian R. Pegbelfermin (BMS-986036), pEGylated FGF21, in patients with obesity and type 2 diabetes: results from a randomized phase 2 study. Obesity (Silver Spring). 2019;27(1):41–9.

    Article  CAS  Google Scholar 

  17. Sanyal A, Charles ED, Neuschwander-Tetri BA, Loomba R, Harrison SA, Abdelmalek MF, Lawitz EJ, Halegoua-DeMarzio D, Kundu S, Noviello S, et al. Pegbelfermin (BMS-986036), a PEGylated fibroblast growth factor 21 analogue, in patients with non-alcoholic steatohepatitis: a randomised, double-blind, placebo-controlled, phase 2a trial. Lancet. 2019;392(10165):2705–17.

    Article  Google Scholar 

  18. Hanssen MJ, Broeders E, Samms RJ, Vosselman MJ, van der Lans AA, Cheng CC, Adams AC, van Marken Lichtenbelt WD, Schrauwen P. Serum FGF21 levels are associated with brown adipose tissue activity in humans. Sci Rep. 2015;5:10275.

    Article  CAS  Google Scholar 

  19. Sun L, Yan J, Goh HJ, Govindharajulu P, Verma S, Michael N, Sadananthan SA, Henry CJ, Velan SS, Leow MK. Fibroblast growth factor-21, leptin, and adiponectin responses to acute cold-induced brown adipose tissue activation. J Clin Endocrinol Metab. 2020:105(3).

  20. Zhang X, Yeung DC, Karpisek M, Stejskal D, Zhou ZG, Liu F, Wong RL, Chow WS, Tso AW, Lam KS, et al. Serum FGF21 levels are increased in obesity and are independently associated with the metabolic syndrome in humans. Diabetes. 2008;57(5):1246–53.

    Article  CAS  Google Scholar 

  21. Fisher FM, Chui PC, Antonellis PJ, Bina HA, Kharitonenkov A, Flier JS, Maratos-Flier E. Obesity is a fibroblast growth factor 21 (FGF21)-resistant state. Diabetes. 2010;59(11):2781–9.

    Article  CAS  Google Scholar 

  22. Hashidume T, Kato A, Tanaka T, Miyoshi S, Itoh N, Nakata R, Inoue H, Oikawa A, Nakai Y, Shimizu M, et al. Single ingestion of soy beta-conglycinin induces increased postprandial circulating FGF21 levels exerting beneficial health effects. Sci Rep. 2016;6:28183.

    Article  CAS  Google Scholar 

  23. Taniguchi H, Akiyama N, Ishihara K. Hepatic fat content is associated with fasting-induced fibroblast growth factor 21 secretion in mice fed soy proteins. J Nutr Sci Vitaminol (Tokyo). 2019;65(6):515–25.

    Article  CAS  Google Scholar 

  24. Nishimura M, Ohkawara T, Sato Y, Satoh H, Takahashi Y, Hajika M, Nishihira J. Improvement of triglyceride levels through the intake of enriched-beta-conglycinin soybean (Nanahomare) revealed in a randomized, double-blind, placebo-controlled study. Nutrients. 2016:8(8).

  25. Kohno M, Hirotsuka M, Kito M, Matsuzawa Y. Decreases in serum triacylglycerol and visceral fat mediated by dietary soybean beta-conglycinin. J Atheroscler Thromb. 2006;13(5):247–55.

    Article  CAS  Google Scholar 

  26. Hira T, Mori N, Nakamori T, Furuta H, Asano K, Chiba H, Hara H. Acute effect of soybean beta-conglycinin hydrolysate ingestion on appetite sensations in healthy humans. Appetite. 2011;57(3):765–8.

    Article  CAS  Google Scholar 

  27. Nirengi S, Wakabayashi H, Matsushita M, Domichi M, Suzuki S, Sukino S, Suganuma A, Kawaguchi Y, Hashimoto T, Saito M, et al. An optimal condition for the evaluation of human brown adipose tissue by infrared thermography. PLoS One. 2019;14(8):e0220574.

    Article  CAS  Google Scholar 

  28. Yoneshiro T, Wang Q, Tajima K, Matsushita M, Maki H, Igarashi K, Dai Z, White PJ, McGarrah RW, Ilkayeva OR, et al. BCAA catabolism in brown fat controls energy homeostasis through SLC25A44. Nature. 2019;572(7771):614–9.

    Article  CAS  Google Scholar 

  29. Takahashi K, Yoshimura Y, Kaimoto T, Kunii D, Komatsu T, Yamamoto S: Validation of a food frequency questionnaire based on food groups for estimating individual nutrient intake. Jpn J Nutr 2001, 59(5):221-232. (Japanese).

  30. Fazeli PK, Lun M, Kim SM, Bredella MA, Wright S, Zhang Y, Lee H, Catana C, Klibanski A, Patwari P, et al. FGF21 and the late adaptive response to starvation in humans. J Clin Invest. 2015;125(12):4601–11.

    Article  Google Scholar 

  31. Yu H, Xia F, Lam KS, Wang Y, Bao Y, Zhang J, Gu Y, Zhou P, Lu J, Jia W, et al. Circadian rhythm of circulating fibroblast growth factor 21 is related to diurnal changes in fatty acids in humans. Clin Chem. 2011;57(5):691–700.

    Article  CAS  Google Scholar 

  32. Hondares E, Iglesias R, Giralt A, Gonzalez FJ, Giralt M, Mampel T, Villarroya F. Thermogenic activation induces FGF21 expression and release in brown adipose tissue. J Biol Chem. 2011;286(15):12983–90.

    Article  CAS  Google Scholar 

  33. Taniguchi H, Tanisawa K, Sun X, Cao ZB, Oshima S, Ise R, Sakamoto S, Higuchi M. Cardiorespiratory fitness and visceral fat are key determinants of serum fibroblast growth factor 21 concentration in Japanese men. J Clin Endocrinol Metab. 2014;99(10):E1877–84.

    Article  CAS  Google Scholar 

  34. Taniguchi H, Tanisawa K, Sun X, Kubo T, Higuchi M. Endurance exercise reduces hepatic fat content and serum fibroblast growth factor 21 levels in elderly men. J Clin Endocrinol Metab. 2016;101(1):191–8.

    Article  CAS  Google Scholar 

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The authors thank Sayo Oiso, Kazuo Nagano, and Naoki Matsubara for their assistance in the BAT activity measurements. We would like to thank Editage ( for the English language editing.


This work was supported by the Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (17 K18244, 2017-2019).

Author information

Authors and Affiliations



HT and KS designed the experiments and performed the statistical analyses. HT drafted the manuscript. SW collected blood samples. HT, KS, and HK assisted in the blood collection and analyzed the blood samples. SN assisted measurements of BAT activity. SW, SN, and AH critically reviewed the manuscript. HT supervised the entire study. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Hirokazu Taniguchi.

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All participants provided written informed consent before enrolment in the study, which was approved by the ethical committee of Kyoto Prefectural University (Approved number 175).

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The authors declare that they have no competing interests.

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Taniguchi, H., Shimizu, K., Wada, S. et al. Effects of beta-conglycinin intake on circulating FGF21 levels and brown adipose tissue activity in Japanese young men: a single intake study and a randomized controlled trial. J Physiol Anthropol 39, 17 (2020).

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