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Systematic Reviews and Meta-analysis
91 (
6
); 730-740
doi:
10.25259/IJDVL_1165_2023
pmid:
40826844

Effects of collagen-based supplements on skin’s hydration and elasticity: A systematic review and meta-analysis

Bachelor of Medicine, School of Medicine and Health Sciences, Atma Jaya Catholic University of Indonesia, Jakarta, Indonesia
Department of Pharmacy, School of Medicine and Health Sciences, Atma Jaya Catholic University of Indonesia, Jakarta, Indonesia
Department of Dermatology and Venereology, School of Medicine and Health Sciences, Atma Jaya Catholic University of Indonesia, Jakarta, Indonesia

Corresponding author: Dr. Regina Regina, Department of Dermatology and Venereology, School of Medicine and Health Sciences, Atma Jaya Catholic University of Indonesia, Jakarta, Indonesia. regina@atmajaya.ac.id

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Danessa G, Notario D, Regina R. Effects of collagen-based supplements on skin’s hydration and elasticity during ageing: A systematic review and meta-analysis. Indian J Dermatol Venereol Leprol. 2025;91:730-40. doi: 10.25259/IJDVL_1165_2023

Abstract

Background

Ageing is a degenerative process that affects the entire body. Skin ageing is characterised by a decrease in the levels of collagen, elastin fibre, and hyaluronic acid (HA), resulting in a loss of skin elasticity and hydration. Prior studies suggest that oral collagen supplements can help increase collagen, elastin, and HA levels, ultimately improving skin health.

Objective

To assess the impact of collagen-based supplements on the signs of skin ageing and determine the effective dosage.

Methods

This systematic review and meta-analysis utilized PubMed, Clinical Key, ProQuest, and Cochrane Library databases to identify studies published from 2010 to 2021. It includes ten randomised controlled trials (RCTs) with a total of 646 participants.

Results

The findings indicate that collagen supplements were statistically effective in increasing skin hydration (SMD 1.25 (CI: 0.77−1.74)) and elasticity (SMD 0.61 (CI: 0.21−1.02)). The most commonly administered dose was 4 g/day, with a median dose of 3.5 g/ day.

Limitations

Most of the studies could not control for weather-related factors. The findings are more applicable to females. Moderate heterogeneity (I2 = 55.5-56.5%) may limit generalisability. The risk of bias was generally unclear, and publication bias could not be assessed due to the small number of studies.

Conclusion

Oral administration of collagen supplement in a dose ranging from 1-10 g/day was statistically effective in increasing the skin hydration and elasticity.

Keywords

Collagen
elasticity
hydration
moisture
skin

Introduction

Ageing is a degenerative process caused by a decline in physiological functions.1 Individuals of the same age experience ageing differently due to intrinsic factors (e.g., genetics) and extrinsic factors (e.g., pollution, UV radiation, chemicals, toxins, and lifestyle). As a result, body morphology and physiology vary.1-3 Skin ageing involves a decline in skin quality due to overlapping intrinsic and extrinsic factors.4,5 Visible signs of ageing often drive individuals, to invest in cosmetics and treatments aimed at preventing or reversing their effects.6

Skin ageing involves reduced levels of collagen, elastin fibres, and hyaluronic acid (HA).7,8 Collagen and HA form the extracellular matrix, providing skin structure, while HA maintains hydration, and elastin fibres preserve elasticity.7-9 Their decline leads to reduced skin integrity, moisture loss, wrinkles, and sagging.3,9 Sagging skin (94.3%) and wrinkles (100%) were observed in individuals aged 50-81.10 Kim et al. (2018) suggested that collagen supplements counteract this decline, promoting elastin fibre regeneration and increasing HA levels, thereby improving skin health.7

Hydrolysed collagen supplements act through two pathways. The first involves free amino acids supporting collagen, elastin, and HA synthesis while suppressing MMP-2, an enzyme that degrades type IV collagen, thereby increasing its levels.11 The second involves collagen oligopeptides (Gly-Pro-Hyp) binding to fibroblast receptors, stimulating collagen, elastin, and HA production.12 However, the link between collagen oligopeptides and fibroblast receptors remains unclear.

Research on collagen supplementation and its effects on skin is limited, with mixed findings from previous studies. This has led to interest in systematically evaluating its impact on skin hydration and elasticity. This study aims to assess collagen’s role in reducing age-related declines in skin hydration and elasticity and to determine the effective dosage for these benefits.

Methods

This systematic review and meta-analysis followed PRISMA 2020 guidelines. The study protocol was pre-registered per standard methods. Inclusion criteria: (1) Population: Males and females; studies in English or Indonesian (2010–2021); (2) Intervention: Oral collagen for skin hydration and elasticity; (3) Comparison: Placebo or no supplementation; (4) Outcomes: Skin hydration and elasticity before and after supplementation. Only randomised placebo-controlled trials were included. Studies with incomplete or missing data were excluded.

Major databases (PubMed, Cochrane Library, Clinical Key, and ProQuest) were searched for studies published from 2010 to April 2021. The search used MeSH and Freestyle terms, including (“collagen” AND “oral” AND “skin” AND “placebo” AND (elasticity OR wrinkle) AND (hydration OR moisture)). Minor adjustments were made to fit the syntax of each database. The search process and study selection are detailed in the PRISMA 2020 flow diagram [Figure 1]. Titles and abstracts were manually screened by two independent reviewers based on pre-defined criteria. Full-texts of eligible studies were retrieved and assessed. Disagreements were resolved through discussion or a third reviewer if needed. Study selection details have been presented in the PRISMA 2020 flow diagram [Figure 1].

PRISMA 2020 flow diagram search results.
Figure 1:
PRISMA 2020 flow diagram search results.

Two authors independently extracted data using a predefined form, including study (author, year, country, design, sample size), participant (age, sex, criteria), intervention (collagen type/dosage), outcomes (skin hydration/elasticity before and after), and statistical data (mean, standardised differences (SD), confidence interval (CI), effect sizes). Discrepancies were resolved by consensus. The Cochrane Collaboration’s Risk of Bias Tool was used to assess selection, performance, detection, attrition, and reporting bias. Each was rated as low, unclear, or high risk based on predefined criteria.

Statistical analysis

Meta-analysis was conducted using R software (4.1.1) with the meta and metafor packages. Skin hydration and elasticity were analysed using a random-effects model, with standardised mean differences (SMD) and 95% CIs. SMDs were calculated using the metafor package in R software, with the escalc function used to compute the change scores (post-minus-pre values).

Heterogeneity was assessed using I2 and Tau22). I2 quantifies the proportion of variability due to heterogeneity across studies, with interpretation guided by Higgins’ thresholds: 25% (low), 50% (moderate), and 75% (high). Hydration (I2 = 55.5%) and elasticity (I2 = 56.5%) showed moderate heterogeneity.13 Tau2 values further supported moderate variability for hydration (0.1331, p = 0.0766) and slightly less for elasticity (0.096, p = 0.0729). The higher variability in hydration may reflect methodological differences, sample characteristics, or collagen formulations.

Prediction intervals were used to estimate effects in future studies. Forest plots visualised the results, and publication bias was assessed using funnel plots and Egger’s test. Sensitivity analysis with a leave-one-out approach was performed for hydration and elasticity to test robustness. The meta-analysis was re-run, excluding each study, and pooled SMDs were compared. All data and R code are available upon request.

Result

The results revealed 19 studies (PubMed), 23 studies (Cochrane Library), 33 studies (Clinical Key), and 263 studies (ProQuest), totalling 338 studies. Research screening was conducted, and 10 studies were included in this systematic review. The assessment of bias risk has been listed in Table 1 and the summary of the included studies is presented in Figure 1, Tables 2-5. The studies were conducted between 2014 and 2021 from Italy, Germany, Korea, Japan, China, the U.S., and Slovenia. Participants were mostly female, aged 31 to 62 years. Collagen sources varied, including chicken, bovine, fish, and porcine, with doses ranging from 246 mg/ day to 10,000 mg/day [Table 5].

Table 1: Risk of bias assessment
No. Author [year] Random sequence generation (selection bias) Allocation concealment (selection bias) Blinding of participants and personnel (performance bias) Blinding of outcome assessment (detection bias) Incomplete outcome data (attrition bias) Selective reporting (reporting bias) Overall risk of bias assessment (low, unclear, high)
1 Cerbo et al17 [2015] ? ? ? ? ? + unclear
2 Bolke et al9 [2019] ? ? ? ? + + unclear
3 Czajka et al21 [2018] ? + + + + + unclear
4 Tak et al15 [2021] + ? ? ? + + unclear
5 Zmitek et al19 [2020] + ? ? ? ? + unclear
6 Inoue et al20 [2016] + + + + + + low
7 Schwartz et al18 [2019] + + + + + + low
8 Yoon et al14 [2014] ? ? + ? + + unclear
9 Kim et al7 [2018] ? + ? ? + + unclear
10 Asserin et al16 [2015] ? ? ? ? + + unclear

?: Unclear, +: Low risk.

Table 2: Characteristics of the studies (1)
No Author [year] Level of Evidence; Study Design; Risk of Bias Participant; Inclusion criteria; Intervention setting Intervention group (IG) Control Group (CG)
1. Cerbo et al.17 [2015] 1b; RCT; Unclear Female (n = 30); Moderate/ severe facial photoageing (measured by VAS/ visual analogue scale); Outpatient clinic VISCODERM® Pearls (IBSA FARMACEUTICI ITALIA Srl, Lodi, Italy) containing Pycnogenol 15 mg, collagen (124 mg), chondroitinsulfate 40 mg, glucosamine sulphate > 3%, low-molecular-weight HA 20 mg, coenzyme Q10 10 mg Placebo
2. Bolke et al.9 [2019] 1b; RCT; Unclear Female (n = 72); Age ≥ 35 years, any type healthy skin; Outpatient clinic ELASTEN® (QUIRIS Healthcare, Gütersloh, Germany) containing 2.5 g collagen peptide, 666 mg acerola fruit extract, 80 mg vitamin C, 3 mg zinc, 2.3 mg vitamin E, 50 μg biotin Placebo
3. Czajka et al.21 [2018] 1b; RCT; Unclear Female (n = 91), male (n = 29); Male/ female (volunteer), age between 21-70 years, any body mass index and ethnic, balanced diet, had the ability to understand the study related information and to give written informed consent; Outpatient clinic GOLD COLLAGEN® (MINERVA Research Labs, London, UK) containing hydrolised fish collagen type I 4,000 mg, HA, glucosamine hydrochloride, L-carnitine, maca, and black pepper extract Placebo
4. Tak et al.15 [2021] 1b; RCT; Unclear n = 84; Age between 40-60 years with transepidermal water loss (TEEL) score ≥4 (measured by Tewameter); Outpatient clinic CTP (collagen tripeptide) from Nile Tilapia (Oreochromis niloticus) containing hydrolised collagen 1000 mg Placebo
5. Zmitek et al.19 [2020] 1b; RCT; Unclear

Female (n = 31) age 55.0 ± 7.6 years (CG n = 15), age 53.7 ± 6.2 years (IG n = 16); Caucasian female age between 40-65 years, Fitzpatrick skin type II, III, with signs of skin ageing

(wrinkle/ poor skin tone, dry); Outpatient clinic

Hydrolised collagen syrup (Valens Int. d.o.o, Šenčur, Slovenia) containing hydrolised fish collagen 4000 mg, water-soluble CoQ10 50 mg, vitamin C 80 mg, vitamin A 920 μg, biotin 150 μg Placebo
6. Inoue et al.20 2016] 1b; RCT; Low n = 80 (IG1 n = 28, IG2 n = 26, CG n = 26); Age between 35-55 years, subject conscious of their dry and rough skin, body mass index <30kg/m2, not regularly using other supplements or health foods, no treatment with sex hormones over the prior 3 months, no pregnant; Outpatient clinic IG1: L-CP / low molecular collagen peptide (5000 mg) (Nita Gelatin Inc., Osaka, Japan); IG2: H-CP / high molecular collagen peptide (5000 mg) (Nita Gelatin Inc., Osaka, Japan) Placebo (maltodextrin TK-16, Matsutani Chemical Industry Co., Ltd., Itami, Japan)
7. Schwartz et al.18 [2019] 1b; RCT; Low n = 128 (IG n = 56, CG n = 56); Overall healthy, age between 36-59 years, willing and able to provide consent, any Fitzpatrick skin type, shows sign of skin ageing, doesn’t have skin’s disease, willing to prevent skin product that claim can increase skin hydration, brightening, anti-ageing, willing to arrive at the test center for the study’s scheduled visits, prior to which they would apply no topical treatments, including moisturizers and creams; Outpatient clinic BioCell Collagen (BioCell Technology, Anaheim, CA) containing hydrolised collagen type II 300 mg, glycosaminoglycan 100 mg, chondroitin sulphate, HA 50 mg Placebo
8. Yoon et al.14 2014] 1b; RCT; Unclear n = 44 (IG n = 22, CG n = 22); Healthy female volunteer, age ± 40 years with wrinkle skin level ± 2; Outpatient clinic Astaxanthin capsule (triglyceride moderate chain 480 mg, Haematococcus pluvialis microalgae extract 20 mg), fish collagen tablet (enzymatic hydrolised fish collagen 0.75 g) Placebo
9. Kim et al.7 [2018] 1b; RCT; Unclear Female (n = 53); Female healthy age between 40-60, diagnosed wrinkle in the eye area by dermatologist with global photodamage score between 2-6, willing to follow the research, cooperative during the study; Outpatient clinic LMWCP (low molecular weight collagen peptide) (LMWCP 1000 mg, vitamin C 100 mg, mixed fruit concentrate 3000 mg, mixed flavor 200 mg, expiens 1900 mg, sweetener 12,5 mg; water 43,7 ml) Placebo
10. Asserin et al.16 [2015] 1b; RCT; Unclear Female (n = 33 (IG1n = 11, IG2 n = 11, CG n = 11)); Japanese female age between 40 and 59 years, low skin water content, no pregnant, doesn’t have systemic disease, no intolerance of fish and gluten, doesn’t consume any drugs and food supplements; Outpatient clinic Peptan® fish (10 g) for IG1, porcine (10g) for IG2 (Rousselot BVBA, Ghent, Belgium) Placebo

According to the Oxford Centre for Evidence-Based Medicine, Level 1b refers to an individual randomised controlled trial (RCT) with a narrow confidence interval, indicating high-quality evidence from a single well-designed study. HA: Hyaluronic acid, CG: Control group, IG1: Intervention group 1, H-CP: High collagen peptide, BVBA: Besloten vennootschap met beperkte aansprakelijkheid

Table 3: Characteristics of the studies (1)
No Author [year] Instrument Result (Hydration) Result (Elasticity)
1. Cerbo et al.17 [2015] Hydration & elasticity : Skin Tester (manufactured by Selenia Italia (Pisa, Italy), distributed by Dermal Medical Division (Bologna, Italy)) Significantly increase (IG), no significantly change (CG) Decrease (IG), no significantly change (CG)
2. Bolke et al.9 [2019] Corneometer CM 825 for hydration and Cutometer MPA 580 for elasticity (Courage - Khazaka, Cologne, Germany) Significantly increase (IG), significant change between IG & CG Significantly increase (IG & CG)
3. Czajka et al.21 [2018] Elasticity: SkinLab USB Elasticity Module (DermaLab® Series, Cortex Technology, Hadsund, Denmark). Doesn’t measure hydration. Doesn’t measure hydration. Significantly increase (IG), no change (CG)
4. Tak et al.15 [2021] Corneometer CM 825 for hydration and Cutometer MPA 580 for elasticity (Courage - Khazaka, Cologne, Germany) Increase for both groups (IG > CG) Decrease for both groups
5. Zmitek et al.19 [2020] Hydration & elasticity : DermaLab Series, SkinLab Combo Hydration & Elasticity probe (Cortex Technology ApS, Hadsund, Denmark) Decrease for both groups and no significant change between the groups Decrease for both groups and no significant change between the groups
6. Inoue et al.20 [2016] Elasticity: Cutomater SEM575 (Courage - Khazaka, Cologne, Germany). Doesn’t measure hydration Doesn’t measure hydration. Significantly increase (IG 1 & IG 2), no change (CG)
7. Schwartz et al.18 [2019] MoistureMeterSC (Delfin Technologies, Kuopio, Finland) for hydration and Cutometer MPA 580 (Courage - Khazaka, Cologne, Germany) for elasticity Significantly increase for both groups (IG and CG) Significantly increase for both groups (IG and CG)
8. Yoon et al.14 [2014] Corneometer CM 825 for hydration and Cutometer MPA 580 for elasticity (Courage - Khazaka, Cologne, Germany), Tewameter (Courage - Khazaka Electronic, Cologne, Germany) for transepidermal water loss (TEWL), Increase for both groups (IG and CG) Significantly increase (IG), no change (CG)
9. Kim et al.7 [2018] Corneometer CM 825 for hydration and Cutometer MPA 580 for elasticity (Courage - Khazaka, Cologne, Germany) Significantly increase for both groups (IG > CG) Significantly increase (IG), increase (CG)
10. Asserin et al.16 [2015] Hydration: Corneometer (Courage - Khazaka Electronic, Köln, Germany) for skin moisture & Tewameter (Courage - Khazaka Electronic) for TEWL. Doesn’t measure elasticity. Significantly increase (IG 1 & IG 2), no change (CG) Doesn’t measure elasticity

IG: Intervention group, CG: Control group, USB: Universal serial bus,

Table 4: Characteristics of the studies (2)
No. Study Country Study duration Total participant Subject sex Mean age (years)
1. Cerbo et al.17 [2015] Italy 1 month 30 F 47.5±1.6
2. Bolke et al.9 [2019] Germany 3 month 72 F 50.6±11
3. Czajka et al.21 [2018] Italy 3 month 91 F, M 43±13
4. Tak et al.15 [2021] Korea 3 month 84 F 49.9±6.5
5. Zmitek et al.19 [2020] Slovenia 3 month 31 F 54.4±6.8
6. Inoue et al.20 [2016] China 2 month 80 F 43±4
7. Schwartz et al.18 [2019] America 3 month 128 F 51±5
8. Yoon et al.14 [2014] Korea 3 month 44 F 51±5
9. Kim et al.7 [2018] Korea 3 month 53 F
10. Asserin et al.16 [2015] Japan 2 month 33 F

F: Female, M: Male

Table 5: Collagen supplement dosage
Study Dose/ day Total dose/ day
Cerbo et al.17 [2015] 2x124 mg 246 mg
Bolke et al.9 [2019]ab 2500 mg 2500 mg
Czajka et al.21 l [2018] 4000 mg 4000 mg
Tak et al.15 [2021] 4x1000 mg 4000 mg
Zmitek et al.19 l [2020] 4000 mg 4000 mg
Inoue et al.20 [2016]b 5000 mg 5000 mg
Schwartz et al.18 [2019] 2x300 mg 600 mg
Yoon et al.14 [2014]a 4x750 mg 3000 mg
Kim et al.7 [2018]ab 1000 mg 1000 mg
Asserin et al.16 [2015]a 10000 mg 10000 mg

a: Studies included for hydration meta-analysis, b: Studies that included for elasticity meta-analysis

Discussion

Systematic review

The geographic spread and steady publication of studies from 2014 to 2021 reflect an increasing international focus on oral collagen supplementation and its potential impact on skin aging.

Oral collagen supplements and skin hydration

Four studies (Yoon et al., Kim et al., Bolke et al., and Tak et al.) using the Corneometer CM825 (Courage-Khazaka, Cologne, Germany) consistently showed a significant increase in skin hydration [Table 6].7,9,14,15 Hydrolysed collagen enhances hydration due to its moisture-retaining properties.14 Gly-Pro-Hyp peptide levels peak in the bloodstream 1–2 hours post-consumption, stimulating dermal fibroblast migration and growth.7 While the exact mechanism remains unclear, Asserin et al. suggested fibroblasts recognise Gly-Pro-Hyp, triggering collagen, elastin, and HA synthesis in the epidermis and dermis, improving hydration and elasticity.7,14,16 This mechanism is supported by Tak et al., Cerbo et al., and Asserin et al.1517 Additionally, a clinical study detected Pro-Hyp in urine after collagen ingestion, confirming its stability and ability to reach skin tissue.15

Table 6: Effects of oral collagen-based supplement on skin’s hydration
No Study Group Total subjects Hydration (mean±SD)
Interpretation
Before intervention After intervention
1. Cerbo et al.17 [2015] IG 15 20.3±1.6 33.2±3.2 Significantly increase* (p <0,0001)
CG 15 20.07±1.5 19.9±1.6 No significant change
2. Bolke et al.9 [2019] IG 36 35.0±4.8 44.5±4.4

Significantly increase*

(p <0,0004)

CG 36 33.7±5.1 36.6±5.7
3. Tak et al.15 [2021] IG 36 192.5±21.4 209.0±18.7 Increase (>)
CG 38 199.7±21.9 212.1±16.0 Increase
4. Zmitek et al.19 [2020] IG 16 255.5±65.6 200.0±52.3 Decrease
CG 15 230.6±67.3 194±1±44.4 Decrease
5. Schwartz et al.18 [2019] IG 58 41.84±29.19 61.31±24.53 Significantly increase
CG 55 39.59±23.95 62.08±28.41 Significantly increase
6. Yoon et al.14 [2014] IG 22 46.0±14.0 114.6±14.5 Significantly increase
CG 22 44.5±13.2 98.2±10.4 Significantly increase
7. Kim et al.7 [2018] IG 26 47.79±12.48 61.14±11.31 Increase (>)*(p <0,003)
CG 27 48.43±12.52 53.02±13.59 Increase
8. Asserin et al.16 [2015] IG1 11 51.37±2.79 57.49±3.01 Significantly increase
IG2 11 50.68±1.75 64.83±2.44 Significantly increase*
CG 11 50.55±2.61 52.51±2.6 No significant change
: Significant change between the groups, IG: Intervention group, CG: Control group, IG1: Intervention group 1, IG2: Intervention group 2, SD: Standard deviation

The increase in skin hydration may also be due to the structural similarity between hydrolysed bovine collagen and human collagen. Bovine collagen shares 31% similarity with type I collagen alpha chain I, 18% with type I collagen alpha chain II, and 13% with type III collagen alpha chain I.9 Among collagen sources, bovine collagen exhibits the highest similarity to human collagen.9 Schwartz et al. attributed increased hydration partly to higher water intake from supplements and placebos.18 Tak et al. suggested that seasonal changes from winter to summer (February–June) during Kim et al.’s study may have influenced hydration and elasticity levels.7,15

However, Zmitek et al. found no significant changes in skin hydration after 12 weeks, as measured by the DermaLab Series, SkinLab Combo hydration probe (Cortex Technology Aps, Hadsund, Denmark).19 This contrasts with other studies showing increased hydration. The decline observed in Zmitek et al.’s study is likely due to seasonal changes, transitioning from late autumn to winter.19 Low humidity, combined with colder outdoor temperatures and indoor heating, may have negatively impacted skin hydration.19

Oral collagen supplements and skin elasticity

Three studies (Yoon et al., Bolke et al., and Schwartz et al.) using the Cutometer MPA580 (Courage-Khazaka, Cologne, Germany) consistently reported a significant increase in skin elasticity [Table 7].9,14,18 This improvement is attributed to molecular changes in the dermis’s extracellular matrix.14 Yoon et al. and Kim et al. suggested that hydrolysed collagen enhances elasticity by promoting elastin fibre synthesis and inhibiting MMP-2 and MMP-9, enzymes that degrade elastin.7,14 MMP levels significantly impact elastin and, consequently, skin elasticity.7 Additionally, skin hydration plays a crucial role, as elastin conformation changes only occur in the presence of hydrated proteins.7 These findings align with Kim et al.’s conclusions, further supporting the increase in skin elasticity.7

Table 7: Effects of oral collagen-based supplement on skin’s elasticity
S.No Study Group Total subjects Elasticity (mean±SD)
Interpretation
Before intervention After intervention
1. Cerbo et al.17 [2015] IG 15 12.4±0.9 9.7±1.9 Decrease
CG 15 12.3±0.98 12.5±0.9 No significant change
2. Bolke et al.9 [2019] IG 36 0.69±0.05 0.81±0.04

Significantly increase*

(p <0,0004)

CG 36 0.71±0.06 0.75±0.06 Significantly increase
3. Tak et al.15 [2021] IG 36 0.40±0.11 0.33±0.10 Decrease
CG 38 0.42±0.10 0.36±0.09 Decrease
4. Zmitek et al.19 [2017] IG 16 1.49±0.38 1.38±0.33 Decrease
CG 15 1.53±0.64 1.59±0.68
5. Schwartz et al.18 [2019] IG 58 0.20±0.07 0.40±0.08 Significantly increase*(p<0,05)
CG 55 0.22±0.06 0.34±0.15 Significantly increase
6. Yoon et al.14 [2014] IG 22 0.61±0.06 0.63±0.02 Significantly increase*
CG 22 0.64±0.07 0.62±0.02 No significant change
7. Kim et al.7 [2018] IG 26 0.64±0.14 0.71±0.16

Significantly increase*

(p <0,027)

CG 27 0.63±0.13 0.64±0.15 Increase
8. Czajka et al.21 [2018] IG 61 7.9±0.2 9.8±0.2

Significantly increase*

(p <0,001)

CG 59 6.9±0.3 7.0±0.3 No significant change
9. Inoue et al.20 [2016] IG1 28 0.739±0.058 0.749±0.039 Increase
IG2 26 0.725±0.058 0.767±0.058

Significantly increase*

(p <0,05)

CG 26 0.736±0.060 0.738±0.045 No significant change
: Significant change between the groups, SD: Standard deviation, IG: Intervention group, CG: Control group, IG1: Intervention group 1, IG2: Intervention group 2

Studies by Inoue et al. and Czajka et al. also reported increased skin elasticity.20,21 In older subjects, improvements appeared more gradually, with noticeable effects emerging after 60 days of supplementation, unlike younger participants. Inoue et al. suggested that age-related changes in nutrient absorption may influence skin elasticity in the elderly.20 Notably, among all reviewed studies, only Tak et al. addressed the impact of weather conditions on skin measurements.15 However, despite efforts to control this variable, complete regulation was not achieved.

In contrast, Cerbo et al., Zmitek et al., and Tak et al. reported a decrease in skin elasticity.15,17,19 Zmitek et al. attributed this decline to seasonal changes from late autumn to winter, which likely impacted skin elasticity.19 Tak et al. shared a similar view, suggesting that the transition from winter to autumn contributed to reduced elasticity.15 Weather conditions were considered a potential influencing factor affecting study outcomes.

Collagen supplement dosage

Collagen doses ranged from 246 mg to 10,000 mg per day [Table 5]. While doses below 1,000 mg were used in two studies, the most common dose was 4,000 mg, with an average of 3,500 mg.17,18 However, dosage alone was not a reliable predictor of effectiveness. Notably, three studies using 4,000 mg reported decreased hydration and elasticity, while others using the same dose observed improvements.15,19,21 These discrepancies may be attributed to factors such as study duration or environmental conditions.

Collagen supplement side effects

Of the included studies, nine (Yoon et al., Bolke et al., Tak et al., Zmitek et al., Inoue et al., Schwartz et al., Kim et al., Asserin et al., Czajka et al.) reported no side effects.7,9,1416,18-21 All found collagen supplements to be safe, with no adverse effects observed during the study period.

Meta-analysis

Heterogeneity significantly impacted skin hydration and elasticity outcomes in this meta-analysis. Initially, all relevant studies were included, resulting in high heterogeneity: I2 = 99.8% for hydration [Figure 2] and I2 = 82.4% for elasticity [Figure 3], likely due to variations in study design, interventions, and participant characteristics. Due to this, pooled effect sizes were unreliable. To reduce heterogeneity, we selected methodologically sound studies with the least variability. For hydration, we included Yoon et al. (2014), Asserin et al. (2015), Kim et al. (2018), and Bolke et al. (2019), reducing I2 to 55.5% [Figure 4].7,9,14,16 For elasticity, we included Inoue et al. (2016), Kim et al. (2018), and Bolke et al. (2019), lowering I2 to 56.5% [Figure 5].7,9,20 This approach ensured consistent and interpretable pooled results while maintaining the overall effect of collagen supplementation. To check for potential publication bias, funnel plots for hydration [Figure 6] and elasticity [Figure 7] were also created.

Forest plot of skin hydration (all studies).
Figure 2:
Forest plot of skin hydration (all studies).
Forest plot of skin elasticity (all studies).
Figure 3:
Forest plot of skin elasticity (all studies).
Forest plot of skin hydration (selected studies).
Figure 4:
Forest plot of skin hydration (selected studies).
Forest plot of skin elasticity (selected studies).
Figure 5:
Forest plot of skin elasticity (selected studies).
Funnel plot of skin hydration (all studies). The funnel plot appeared asymmetrical, with only two studies inside the funnel. This may suggest possible publication bias or study differences, but interpretation is limited due to the small number of included studies.
Figure 6:
Funnel plot of skin hydration (all studies). The funnel plot appeared asymmetrical, with only two studies inside the funnel. This may suggest possible publication bias or study differences, but interpretation is limited due to the small number of included studies.
Funnel plot of skin elasticity (all studies).
Figure 7:
Funnel plot of skin elasticity (all studies).

Effect of oral collagen supplements on hydration during ageing

The meta-analysis included studies by Yoon et al. (2014), Asserin et al. (2015), Kim et al. (2018), and Bolke et al. (2019), all of which demonstrated a significant increase in skin hydration following the intervention [Figure 4].7,9,14,16 The pooled SMD for hydration was 1.25 (CI: 0.77–1.74), suggesting a moderate effect. The prediction interval was 0.61 (0.39–2.12), indicating that the effect size in future studies may vary within this range, and the CI reflects the precision of the average effect estimate. Each individual study also contributed to our understanding of the effect size of the intervention. For instance, Yoon et al. (2014) reported an SMD of 1.268, Asserin et al. (2015) an SMD of 1.772, Kim et al. (2018) an SMD of 0.648, and Bolke et al. (2019) an SMD of 1.551, highlighting notable effect sizes of collagen supplementation on skin hydration.7,9,14,16 These findings highlight the positive impact of collagen supplementation on skin hydration, though variations in effect sizes emphasize the need to consider factors such as study design, population characteristics, and intervention protocols when interpreting the pooled estimate.

Effect of oral collagen supplements on elasticity during ageing

The studies included in the meta-analysis were Inoue et al. (2016), Kim et al. (2018), and Bolke et al. (2019), all of which demonstrated a positive effect on skin elasticity following intervention [Figure 5].7,9,20 The pooled SMD for elasticity studies was 0.61 (CI: 0.21−1.02), suggesting a moderate effect. The prediction interval (PI) was 0.61 (-0.12−1.34), indicating that the effect size in future studies may vary within this range and the CI reflects the precision of the average effect estimate. Individual study results included an SMD of 0.238 for Inoue et al. (LCP), 0.578 for Inoue et al. (HCP), 0.452 for Kim et al., and 1.176 for Bolke et al., highlighting the intervention’s consistent positive impact on skin elasticity.7,9,20

Sensitivity analysis was performed for both hydration and elasticity studies. For hydration, the pooled SMDs after excluding each study were: Yoon et al. (2014) 1.2714, Asserin et al. (2015) 1.1496, Kim et al. (2018) 1.4627, and Bolke et al. (2019) 1.1748.7,9,14,16 For elasticity, the values were: Inoue et al. (2016) 0.7389 (L-CP), Inoue et al. (2016) 0.6226 (H-CP), Kim et al. (2018) 0.6640, and Bolke et al. (2019) 0.4124.7,9,20 The consistent pooled effects suggest that the findings are robust and not driven by any single study.

Funnel plots for all studies were created for hydration [Figure 6] and elasticity [Figure 7] analyses. The Egger test for hydration studies showed significant asymmetry (z = 6.160, p < .001), suggesting potential publication bias. However, the bias correction (b = -0.059) was not significant (CI: -0.675, 0.556), indicating minimal impact on the meta-analysis results. In contrast, the Egger test for elasticity studies showed no asymmetry (z = -0.251, p = 0.802), with the bias correction (b = 0.778) also non-significant (CI: -1.220, 2.777), suggesting no publication bias.

Limitations

Many studies in this review couldn’t control the weather-related factors, which may have influenced skin hydration and elasticity outcomes. Only one of the ten studies included both males and females, making the findings more applicable to females. This meta-analysis had moderate heterogeneity (I2 = 55.5–56.5%), likely due to differences in collagen types, study populations, and methods, which may limit generalisability. Most studies had unclear risk of bias, so results should be interpreted with caution. Egger’s test for publication bias wasn’t done due to the small number of studies, as it could yield unreliable results. Larger meta-analyses are needed for more definitive conclusions.

Conclusion

The oral administration of collagen supplements (at doses ranging from 1-10 g/day) is statistically shown to be effective in increasing skin hydration and elasticity, which tend to decrease with the natural process of skin ageing.

Ethical approval

The Institutional Review Board approval is not required.

Declaration of patient consent

Patient’s consent not required as there are no patients in this study.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

Use of artificial intelligence (AI)-assisted technology for manuscript preparation

The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.

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