Endometriosis in Adolescence: A Narrative Review of the Psychological and Clinical Implications
Abstract
:1. Introduction
2. Methods
3. Integrated Insights into Endometriosis and Emotional Well-Being
3.1. Psychological Impact on Adolescence
3.2. Interplay of Biological Mechanisms Between Endometriosis and Mental Health
3.3. Non-Invasive Diagnostic Biomarkers and Digital Tools for Monitoring and Support
3.4. Psychological and Mind–Body Interventions
Category | Diet/Nutritional Factor | Key Components | Reported Effects on Endometriosis |
---|---|---|---|
Specific diets | Mediterranean diet (Ott et al., 2012 [202]) | Rich in olive oil, fish, nuts, legumes, fruits, and vegetables | Linked to lower endometriosis risk, reduced pelvic pain, and inflammation |
Low-FODMAP diet (Moore et al., 2017 [203]; van Haaps et al., 2023 [204]) | Excludes fermentable oligosaccharides, disaccharides, monosaccharides, and polyols (FODMAPs) | Reduces gastrointestinal and abdominal symptoms common in endometriosis (especially if associated with irritable bowel syndrome) | |
Low-nickel diet (Borghini et al., 2020 [205]) | Excludes foods that contain a high amount of nickel | May be recommended to reduce gastrointestinal, extra-intestinal, and gynecological symptoms (especially if nickel allergic contact mucositis is present) | |
Gluten-free diet (Marziali et al., 2012 [206]) | Excludes any foods that contain gluten | May reduce pain in gluten-sensitive individuals with endometriosis | |
Specific nutrients | Omega-3 fatty acids (Nodler et al., 2020 [207]) | Found in fatty fish, flaxseed, and walnuts | Reduces inflammation, pain, and prostaglandin production |
Antioxidants (Mier-Cabrera et al., 2009 [208]; Santanam et al., 2013 [209]) | Vitamins C and E, selenium, and zinc | Mitigates oxidative stress, reduces pain, and enhances symptom relief | |
Vitamin D (Nodler et al., 2020 [207]; Qiu et al., 2020 [210]) | Found in fortified foods, sunlight exposure, and fatty fish | Regulates immune function. There is a negative relationship between vitamin D levels and the severity of endometriosis | |
Food groups | Dairy products (Harris et al., 2013 [211]; Nodler et al., 2020 [212]; Qi et al., 2021 [213]) | Milk, yogurt, and cheese | An optimal intake of total dairy may be associated with a decreased risk of endometriosis |
Red meat (Parazzini et al., 2004 [214]; Yamamoto et al., 2018 [215]) | High intake of processed and red meats | Associated with a higher risk of developing endometriosis and worsened symptoms | |
Soy products (Tsuchiya et al., 2007 [216]) | Isoflavones (phytoestrogens) found in soy milk and tofu | Higher urinary levels of isoflavones may be associated with a reduced risk of advanced but not minimal–mild-stage endometriosis | |
Dietary fibers (Parazzini et al., 2004 [214]; Harris et al., 2018 [217]) | Fruits and vegetables | Reduction in the risk of endometriosis with higher consumption of (not all, some) fruits and vegetables |
4. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Study | Population | Diagnostic Method | Prevalence of Endometriosis |
---|---|---|---|
Zannoni et al., 2024 [16] | Young women (n = 100, 14–24 years) with chronic pelvic pain (CPP) | Ultrasound (US) | 25% (US-diagnosed endometriosis); higher prevalence in young women (20–24 years) compared to adolescents (14–19 years) |
Millischer et al., 2023 [28] | Adolescents (12–20 years) with severe dysmenorrhea | Magnetic resonance imaging | 39.3% (121/345) overall; 20.7% (25/121) with ovarian endometrioma (OMA), 88.4% (107/121) with deep infiltrating endometriosis (DIE) |
Martire et al., 2023 [29] | Young women (12–25 years) with severe dysmenorrhea | US | 35.3% (131/371) overall; 41.2% (54/131) with OMA, 16.8% (22/131) with isolated endometrioma, and 53.4% (70/131) with posterior DIE |
Hirsch et al., 2020 [30] | Adolescents with CPP undergoing laparoscopy | Laparoscopy | 64% (648/1011; range 25–100%) |
Martire et al., 2020 [31] | Adolescents (12–20 years) referred for US | US | At least one US feature of endometriosis in 13.3% (36/270); higher detection in adolescents with dysmenorrhea (21%) and dyspareunia (33%) |
Yeung et al., 2017 [32] | Adolescents with laparoscopically proven endometriosis | Laparoscopy | Histologically confirmed in 39% of cases (448/1148) [Global prevalence: up to 80% of adolescents with CPP who fail to respond to medical treatment] |
Janssen et al., 2013 [33] | Adolescents with CPP | Laparoscopy | 62% (543/880; range 25–100%) |
Opoku-Anane and Laufer, 2012 [34] | Young women (12–21 years) with CPP unresponsive to non-steroidal anti-inflammatory drugs and oral contraceptives | Laparoscopy | 98% (115/117); all patients had either stage I or II endometriosis |
Biomarker Type | Sample Type | Diagnostic Potential | Limitations | References |
---|---|---|---|---|
CA125 (Cancer Antigen 125) | Serum | Useful for detecting advanced disease in some cases | Low specificity for early/mild cases | Agic et al., 2008 [111]; Mihalyi et al., 2010 [112]; Socolov et al., 2010 [113]; Vodolazkaia et al., 2012 [114]; Ozhan et al., 2014 [115]; Choi et al., 2019 [116] |
MicroRNAs (e.g., miR-200 family) | Serum | Early diagnostic potential, stable in blood, non-invasive | Need for further validation and standardization | Teague et al., 2010 [117]; Jia et al., 2013 [118]; Suryawanshi et al., 2013 [119]; Wang et al., 2013 [120]; Cosar et al., 2016 [121]; Nisenblat et al., 2019 [122]; Vanhie et al., 2019 [123]; |
Cytokines (IL-6, TNF-α) | Serum | Can indicate inflammation and the presence of endometriosis | Limited accuracy in differentiating from other diseases | Xavier et al., 2006 [124]; Othman et al., 2008 [125]; Seeber et al., 2008 [126]; Socolov et al., 2010 [113]; Choi et al., 2019 [116] |
Exosomes/extracellular vesicles | Blood, urine, menstrual fluid | Contains proteins, lipids, and RNA markers for diagnosis | Still in the early stages of research | Li et al., 2020 [127]; Zhang et al., 2020 [128]; Shan et al., 2022 [129] |
Menstrual fluid proteins and genes | Menstrual fluid | Non-invasive, specific to endometriosis | Requires more validation and standardized protocols | Ji et al., 2023 [130]; Amanda et al., 2024 [131]; Starodubtseva et al., 2024 [132] |
Vascular Endothelial Growth Factor (VEGF) | Serum, urine | Potential biomarker for early detection and staging | Limited sensitivity in early stages, affected by other conditions | Potlog-Nahari et al., 2004 [133]; Xavier et al., 2006 [124]; Vodolazkaia et al., 2012 [114] |
Long non-coding RNAs | Serum | Emerging role in the diagnosis and prognosis of endometriosis | Limited standardization and variability in findings | Wang et al., 2016 [134]; Qiu et al., 2019 [135] |
Autoantibodies | Serum | Can help in the detection of autoimmune responses associated with endometriosis | Lack of specificity for endometriosis | Nabeta et al., 2009 [136]; Gajbhiye et al., 2012 [137] |
Apoptotic markers (e.g., caspase-3) | Serum | Provides insight into endometrial tissue damage and disease progression | Not widely validated for clinical use | Kaya et al., 2018 [138] |
Treatment | Indication | Mechanism of Action | Key Findings |
---|---|---|---|
Non-steroidal anti-inflammatory drugs | For pain relief in all stages of treatment (Brown et al., 2017 [150]) | Temporarily suppress cyclooxygenase (COX)-1 and COX-2 activity, leading to a reduction in prostaglandin synthesis | Reduces pain effectively without long-term narcotic use [11,151] |
Combined hormonal contraceptives (CHC) (oral, vaginal ring, or transdermal) | First-line treatment to reduce endometriosis-associated dyspareunia, dysmenorrhea, and non-menstrual pain (Brown et al., 2018 [152]; Jensen et al., 2018 [153]; Grandi et al., 2019 [154]) | Suppress follicle-stimulating hormone (FSH) and luteinizing hormone (LH), curbing cell growth and promoting endometrial cell death | Effective in reducing symptoms and suppressing endometriosis [11,151] |
Progestin-only agents (e.g., dienogest) | First-line treatment alternative to CHC, effective in reducing symptoms (Brown et al., 2012 [155]; Petraglia et al., 2012 [156]; Andres et al., 2015 [157]) | Lower FSH and LH levels, inducing shrinkage or regression of endometrial tissue | Reduces pain and promotes endometrial suppression [11,151] |
Levonorgestrel-releasing intrauterine system | Alternative to CHC, provides localized therapy for symptom management (Lan et al., 2013 [158]; Yoost et al., 2013 [159]; Margatho et al., 2020 [160]) | Similar to progestin-only agents, with minimal systemic hormone exposure | Effective for long-term symptom relief, reduces pain [159] |
Gonadotropin-releasing hormone (GnRH) agonists | For refractory cases, often used with add-back therapy (Brown et al., 2010 [161]; Tang et al., 2017 [162]; Veth et al., 2023 [163]) | Prolonged use suppresses steroid hormone production by lowering LH and FSH levels, although initially causes a hormone surge | Need add-back therapy (combination of low-dose hormones) to prevent bone loss and hypoestrogenic symptoms [164,165] |
GnRH antagonists | A second-line treatment (e.g., if CHC or progestogens have been ineffective) owing to their side effect profile (Taylor et al., 2017 [166]; Donnez et al., 2020 [167]; Osuga et al., 2021 [168]) | Competitively binds to GnRH receptors in the pituitary gland, leading to immediate suppression of LH and FSH levels without the initial hormone flare seen with GnRH agonists | Similar to GnRH agonists [169] |
Aromatase inhibitors | For severe cases resistant to other treatments (Ferrero et al., 2011 [170]; Almassinokiani et al., 2014 [171]) | Prevents the transformation of androgens into estrogens, diminishing endometrial cell proliferation | Effective in combination with CHC, progestins, and GnRH agonists or antagonists [172] |
Androgens (e.g., danazol) | Second-line treatment for refractory cases or patients with contraindications to other treatments (Ferrero and Barra, 2022 [173]) | Act as antiestrogens by inhibiting enzymes responsible for steroid production and reducing gonadotropin secretion | Reduces endometriosis symptoms, but typically avoided in adolescents and young women due to long-term androgenic effects [174] |
Selective progesterone receptor modulators | Emerging therapy for pain and lesion reduction (Fu et al., 2017 [175]) | Antagonistic effects on progesterone receptors in the endometrium, leading to the suppression of endometrial proliferation and induction of atrophy, contributing to symptom relief | Reduces endometrial growth with fewer side effects compared to GnRH agonists; long-term safety data are limited, particularly regarding potential endometrial effects, such as changes in endometrial histology [176] |
Surgical management | For refractory cases with severe pain, organ dysfunction, or infertility risk (Tyson et al., 2024 [177]) | Removes endometriotic lesions to relieve symptoms and prevent recurrence | Effective in selected cases but requires specialized surgical expertise; postoperative hormonal therapy reduces recurrence [178] |
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Panvino, F.; Paparella, R.; Pisani, F.; Tarani, F.; Ferraguti, G.; Fiore, M.; Ardizzone, I.; Tarani, L. Endometriosis in Adolescence: A Narrative Review of the Psychological and Clinical Implications. Diagnostics 2025, 15, 548. https://doi.org/10.3390/diagnostics15050548
Panvino F, Paparella R, Pisani F, Tarani F, Ferraguti G, Fiore M, Ardizzone I, Tarani L. Endometriosis in Adolescence: A Narrative Review of the Psychological and Clinical Implications. Diagnostics. 2025; 15(5):548. https://doi.org/10.3390/diagnostics15050548
Chicago/Turabian StylePanvino, Fabiola, Roberto Paparella, Francesco Pisani, Francesca Tarani, Giampiero Ferraguti, Marco Fiore, Ignazio Ardizzone, and Luigi Tarani. 2025. "Endometriosis in Adolescence: A Narrative Review of the Psychological and Clinical Implications" Diagnostics 15, no. 5: 548. https://doi.org/10.3390/diagnostics15050548
APA StylePanvino, F., Paparella, R., Pisani, F., Tarani, F., Ferraguti, G., Fiore, M., Ardizzone, I., & Tarani, L. (2025). Endometriosis in Adolescence: A Narrative Review of the Psychological and Clinical Implications. Diagnostics, 15(5), 548. https://doi.org/10.3390/diagnostics15050548