# Evidence digest — 2026-10-23 (week 2026-10-16..10-23) The day-bounded publication-date query (`endometriosis[Title/Abstract]`, datetype=pdat, 2026-10-16..2026-10-23) returned **23** records. An entrez-date supplement (datetype=edat, 2026-10-17..2026-10-23) returned 42 records, **22** of which were not in the pdat set. The supplement starts the day after the 2026-10-16 digest's edat window, which already ran through 2026-10-16. Of the 45 records screened, **32** are endometriosis-relevant and appear below (1 carry-over, 12 dropped as noise). No Cochrane update and no new guideline. The one new randomized trial in the window is a surgical-adjunct study of vasopressin, and it did not separate ovarian-reserve decline. What stands out is a **comorbidity meta-analysis that rates its own evidence low or very low**, a **narrative review that restates the limit of a normal scan**, a **retrospective frozen-embryo-transfer association with a very large odds ratio**, and a **supplement review whose own conclusion is that supplements should not replace standard treatment**. Prior digest: 2026-10-16 (open as PR #51, updated onto main after the 2026-10-19 data refresh). Every entry below comes from a fetched PubMed record; PMIDs are live. Nothing here changes an OpenEndo repurposing verdict, the Yselty or saliva-diagnostics knowledge pages, or a patient-facing recommendation. ## Diagnostics and imaging - **Non-invasive diagnosis, from imaging to biomarkers and AI** — narrative review, not a systematic review. The authors state that major guidelines now endorse a clinical and imaging-based diagnosis without mandatory laparoscopy. Expert transvaginal ultrasound and MRI are described as identifying ovarian endometrioma and deep endometriosis with high specificity and as mapping disease for surgery. A normal scan does not exclude endometriosis, because superficial peritoneal disease remains largely invisible. No blood, urinary, or endometrial biomarker is described as meeting criteria for clinical use. Circulating miRNA panels are described as having failed independent validation, and a salivary miRNA signature is described as still needing independent validation in a lower-prevalence setting. Radiomics and AI are described as investigational pending external validation, calibration, and demonstrated clinical utility. The abstract gives no new accuracy figures. [PMID 42885805](https://pubmed.ncbi.nlm.nih.gov/42885805/) — *why it matters:* a current restatement of the imaging-first limit already in digest 2026-10-09 (PMID 42833036) and of the miRNA-methods problem in digest 2026-10-16 (PMID 42854833). It is not a new guideline. The saliva Endotest note from digest 2026-09-18 (PMID 42749315) is unchanged: still not an established standard. - **Structured versus free-text MRI reports for deep pelvic endometriosis** — single-centre randomized reader study. Twenty radiology residents were assigned to free-text or structured reporting; five became unavailable before report generation. The remaining 15 readers each reported the same 22 pelvic MRI examinations (330 reports: 154 free-text, 176 structured). The reference was expert imaging consensus, not surgical histology. Structured reporting increased completeness by 8.1 percentage points (95% CI 4.1–12.1) and clinically weighted completeness by 5.6 percentage points (95% CI 1.3–10.0), and took 4.52 minutes longer (95% CI 3.05–5.99). Structured reports also carried more explicit negative discrepancies versus the expert reference (rate ratio 2.94, 95% CI 1.73–4.98), mainly explicit compartment-based negative statements. In an exploratory paired reading, two gynaecologic surgeons scored 44 reports and rated structured reports higher for perceived completeness, usefulness, and adequacy; clarity ratings were similar. [PMID 42891704](https://pubmed.ncbi.nlm.nih.gov/42891704/) — *why it matters:* a reporting-format comparison, not a test of whether MRI detects endometriosis. Higher completeness is not diagnostic accuracy. Single centre, resident readers, imaging reference standard. - **Platelet-to-lymphocyte ratio and CA-125 for endometrioma** — retrospective single-centre case-control study of 645 people having laparoscopic surgery in 2020–2024: 372 with endometriosis and 273 controls with benign ovarian teratomas. Endometrioma was associated with higher platelet-to-lymphocyte ratio (PLR), higher CA-125, and higher products of CA-125 with the neutrophil-to-lymphocyte, monocyte-to-lymphocyte, and platelet-to-lymphocyte ratios. Stage IV had higher platelet counts and higher CA-125 products than stage III. Preoperative bilateral endometrioma and elevated CA-125 were independent factors for stage IV. The authors state that, for people with dysmenorrhoea or pelvic pain, CA-125 had better diagnostic value for ovarian endometrioma than PLR × CA-125. The abstract does not report an AUC. [PMID 42897934](https://pubmed.ncbi.nlm.nih.gov/42897934/) — *why it matters:* another internal blood-marker comparison whose control group is teratoma, not the broader differential of an adnexal mass. The authors' preference for CA-125 is not a new diagnostic standard. Low certainty for any staging claim. - **Uterine corpus flexion angle and the question-mark sign** — mixed prospective-retrospective case-control ultrasound study. Uterine corpus flexion angle (UCFA) rose with revised ASRM stage and with pelvic-adhesion severity. In multivariable regression, adhesion score was the main associate of UCFA (β=0.441), while the uterine flexion angle was mainly associated with baseline uterine position (β=0.508). In an adenomyosis-free endometriosis subgroup of 166, adhesion score remained the main associate (β=0.457). A UCFA cutoff of ≥220° for the sonographic question-mark sign had AUC 0.958. Median UCFA was 179.0° in the benign control group and 178.0° in the normal control group. The abstract does not state the total sample size. [PMID 42902224](https://pubmed.ncbi.nlm.nih.gov/42902224/) — *why it matters:* a proposed numeric definition of a sign sonographers already describe subjectively. The cutoff and the AUC are internal. Not a reporting standard. Epub 2026-07-25; indexed this week. - **Immune-coagulation nomogram for endometriosis-associated ovarian cancer versus endometrioma** — retrospective single-centre study of treatment-naive people having primary surgery, January 2015–February 2025. Histology used Sampson-Scott criteria: endometriosis-associated ovarian cancer n=49, ovarian endometrioma n=146. Median fibrinogen-to-albumin ratio was 0.10 versus 0.07, and median absolute monocyte count was 0.39 versus 0.31×10⁹/L. A model using age, menopausal status, monocyte count, fibrinogen-to-albumin ratio, CA-125, and HE4 had an internal AUC of 0.932 (95% CI 0.887–0.968), higher than HE4 alone (0.835), the fibrinogen-to-albumin ratio (0.786), CA-125 (0.769), and monocyte count (0.657). At a Youden threshold of 0.468, sensitivity was 75.5% and specificity 95.9% (PPV 86.0%, NPV 92.1%). Calibration was acceptable (Hosmer-Lemeshow p=0.225). The authors state that prospective multicentre validation is still required. [PMID 42902392](https://pubmed.ncbi.nlm.nih.gov/42902392/) — *why it matters:* the same class of result as the endometriosis-associated ovarian-malignancy model review in digest 2026-10-09 (PMID 42835309). Internal discrimination is not a usable test. It does not change care. Epub 2026-07-23; indexed this week. - **SEED screening measure, items only** — participatory revision of ENDOPAIN-4D for Canadian young adults aged 18–25. Four Delphi phases. Sixty-five experts took part in the first round; fifteen took part in the working meeting and the second round. The result is a 22-item, five-domain questionnaire named Screening for Early Endometriosis Detection (SEED). No sensitivity, specificity, or cutoff is reported. [PMID 42898862](https://pubmed.ncbi.nlm.nih.gov/42898862/) — *why it matters:* this is the measure whose validation protocol was logged in digest 2026-10-16 (PMID 42869590). It is still not evidence that SEED detects endometriosis. Epub 2026-10-15. ## Surgery - **Vasopressin during laparoscopic endometrioma excision** — randomized trial at one university centre, September 2018–July 2021. Seventy-five women with a unilateral ovarian endometrioma were stratified by baseline anti-Müllerian hormone and assigned to vasopressin-assisted cystectomy or control. The primary outcome was the change in anti-Müllerian hormone at 12 months. Vasopressin shortened bleeding-control time (2.2±2.5 versus 6.5±6.8 minutes, p=0.002). Cyst-stripping time was 8.9±7.9 versus 14.4±13.7 minutes (p=0.054); the abstract calls that reduction significant, and the reported p value is not below 0.05. The 12-month decline in anti-Müllerian hormone did not differ (−0.96±1.11 versus −1.14±0.92 ng/mL, p=0.488). A mixed-effects model found no group-by-time interaction (p=0.816). Histology showed no significant difference in the thickness or proportion of excised ovarian tissue. [PMID 42890533](https://pubmed.ncbi.nlm.nih.gov/42890533/) — *why it matters:* a negative primary result. Shorter electrocoagulation time did not preserve the measured ovarian reserve. It is not a reason to adopt or abandon vasopressin as standard practice. Epub 2026-10-02. - **Nerve-sparing surgery for deep infiltrating endometriosis** — systematic review and meta-analysis (PRISMA 2020; PubMed, Embase, Scopus, and LILACS, January 2000–August 2025). Sixteen studies, 1,623 women with surgically confirmed deep disease. Pooled conversion to open surgery 0.3%, intraoperative complications 1.5%, postoperative complications 9.8%, urinary voiding dysfunction 6.9%, low anterior resection syndrome 10.2%, and postoperative Female Sexual Function Index 22.3. Several functional outcomes were substantially heterogeneous. The authors state that the evidence does not support a conclusion of equivalence or superiority versus conventional surgery. [PMID 42896655](https://pubmed.ncbi.nlm.nih.gov/42896655/) — *why it matters:* a feasibility snapshot, not a comparative verdict. Nerve-sparing is not established here as the better operation. - **Lower urinary tract symptoms in deep endometriosis** — narrative review (PubMed/MEDLINE, English, 2000–July 2026). In women with deep endometriosis who had preoperative urodynamics, pooled estimates were voiding dysfunction in 21% and detrusor overactivity in 15%, with substantial heterogeneity. The authors treat direct urinary-tract involvement, neural dysfunction, inflammation, and surgical injury as separate routes to symptoms, and they state that evidence for neuroinflammatory and nociplastic mechanisms is largely indirect or experimental. They write that nerve-sparing techniques should be considered when surgery is indicated and technically feasible. [PMID 42905159](https://pubmed.ncbi.nlm.nih.gov/42905159/) — *why it matters:* a mechanism map for urinary symptoms, with the authors' own surgical sentence attached. That sentence is their conclusion. It is not an OpenEndo recommendation, and PMID 42896655 does not show that nerve-sparing is superior. - **Headache burden after endometriosis surgery** — single-centre observational study of 88 women who had endometriosis surgery between 3 months and 5 years before enrolment. Participants completed the Headache Impact Test-6 and the 12-item Short Form by recalling their preoperative state and reporting their current state. Prospective preoperative questionnaires were not available. Headache-burden scores were lower, and physical and mental quality-of-life scores were higher, at the postoperative assessment than in the recalled preoperative period, in women with and without migraine (p<0.001). The differences were larger in the migraine group. [PMID 42907837](https://pubmed.ncbi.nlm.nih.gov/42907837/) — *why it matters:* a before/after comparison that depends on remembered preoperative scores. It is not evidence that surgery treats migraine. Epub 2026-07-27; indexed this week. - **Catamenial pneumothorax, two cases** — case report plus literature review. The abstract frames recurrent perimenstrual pneumothorax as under-recognised and presents two cases. It does not give ages, recurrence counts, histology, or a treatment comparison. [PMID 42889145](https://pubmed.ncbi.nlm.nih.gov/42889145/) — *why it matters:* another thoracic-endometriosis case report after the cluster in digest 2026-10-16. Two patients are not a pathway. Epub 2026-10-01. - **Unicornuate uterus, adenomyoma, renal agenesis, and deep endometriosis** — one case, a 39-year-old woman, gravida 1 para 1, previously recorded as uterus didelphys. MRI reclassified the uterus as unicornuate with a left cavitated non-communicating rudimentary horn (ESHRE/ESGE U4a) occupied by a 6 cm adenomyoma, contralateral adenomyosis, a deep endometriotic nodule to the left pelvic sidewall with rectal tenting and no transmural invasion, a left endometrioma, and an absent left kidney. Surgery and histology confirmed the horn, the adenomyoma, adenomyosis, and ovarian endometriosis. She recovered and the abstract describes her as asymptomatic. [PMID 42889881](https://pubmed.ncbi.nlm.nih.gov/42889881/) — *why it matters:* one imaging reclassification. It is not a new standard for Müllerian anomalies. Epub 2026-09-15. - **Endometrioid carcinoma in an endometrioma, with a contralateral borderline tumour** — one case, a 43-year-old woman with endometriosis diagnosed about five years earlier. A left endometrioma grew from 6.1×6.8×5.2 cm (April 2024) to 8.8×9×9.5 cm (April 2025); MRI was O-RADS 5. CA-125 was 408.6 U/mL, CA 19-9 was 643.58 U/mL, and RMI-I was 1225.8. Histology showed grade 2 endometrioid adenocarcinoma arising in a left endometriotic cyst, FIGO IC1. The right ovary looked normal in the operating room and contained a borderline seromucinous tumour. Omentum, peritoneal cytology, and 31 lymph nodes were negative. [PMID 42903660](https://pubmed.ncbi.nlm.nih.gov/42903660/) — *why it matters:* a single oncology case. Interval growth and a suspicious scan are this patient's findings. They are not a screening rule for endometriomas. Epub 2026-10-07. - **Postpartum hemothorax, thoracic endometriosis suggested** — one case, a 34-year-old woman, day 8 after vaginal delivery. An initially clear effusion became a hemothorax. Thoracoscopy showed small hematoma-like lesions on the visceral pleura. Pleural-fluid CA-125 was markedly elevated and pigment-laden macrophages were present. The abstract calls this strongly suggestive of thoracic endometriosis syndrome and does not report endometrial glands and stroma on histology. [PMID 42907392](https://pubmed.ncbi.nlm.nih.gov/42907392/) — *why it matters:* a suggested, not histologically confirmed, thoracic case. One patient. Not a postpartum pathway. ## Mechanisms and biology - **RNF34, PKM2, glycolysis, and a curcumin experiment** — RNF34 was lower in endometriotic tissue and inversely associated with pyruvate kinase M2 (PKM2). RNF34 promoted PKM2 ubiquitination and reduced PKM2 stability, and it suppressed glycolysis, proliferation, migration, and invasion in stromal cells. In a mouse model, RNF34-deficient uterine tissue produced larger lesions, and PKM2 inhibition reduced that increase. Curcumin raised RNF34 and reduced lesion burden; depleting RNF34 weakened those curcumin effects. Preclinical (tissue, cells, mouse). [PMID 42892355](https://pubmed.ncbi.nlm.nih.gov/42892355/) — *why it matters:* a ubiquitin-glycolysis mechanism. The curcumin result is an experiment in that model, not a clinical supplement trial. It does not move any M3 repurposing verdict. - **Peritoneal-fluid extracellular vesicles** — pilot case-control study. Small extracellular vesicles from peritoneal fluid of women with endometriosis (n=7), women without endometriosis having surgery for benign non-inflammatory conditions (n=7), and follicular fluid (n=3). Raman spectra differed between endometriosis and control peritoneal vesicles at 891 cm⁻¹ (proteins) and 968 cm⁻¹ (lipids). Follicular-fluid vesicles were smaller and more rigid in this cohort. The authors call the findings hypothesis-generating and say no diagnostic application can be claimed. [PMID 42891160](https://pubmed.ncbi.nlm.nih.gov/42891160/) — *why it matters:* a methods pilot of 14 peritoneal samples. Not a test. Epub 2026-07-22. - **Rat autologous-transplant model, checked with elagolix** — video protocol. Endometrium sutured to the peritoneal wall of Sprague-Dawley rats formed cystic lesions in 18 of 20 animals at 21 days (90%). Elagolix at 100 mg/kg daily by oral gavage for 4 weeks reduced final lesion volume versus the model group (inhibition rate 86.7%) and lowered serum FSH, LH, and estradiol and peritoneal TNF-α, VEGF, and IL-6. Pain and behaviour were not measured. [PMID 42891579](https://pubmed.ncbi.nlm.nih.gov/42891579/) — *why it matters:* a methods paper. The 100 mg/kg figure is a rat dose in this protocol. It is not a human dose and it is not new evidence about elagolix in people. - **Laparoscopic swine model** — video protocol for autologous endometrial transplantation by laparoscopy, with optional fluorescein nanoparticle labelling and later laparoscopic retrieval. No lesion-take rate and no treatment result are reported. [PMID 42891621](https://pubmed.ncbi.nlm.nih.gov/42891621/) — *why it matters:* a large-animal platform. Not a pathophysiology result. Issue date 2026-10-16 and absent from `weekly/2026-10-16.json`. - **Acute stress and endometriosis pain** — narrative review (English abstract of a Hungarian article). The authors describe the stress-pain relationship as bidirectional and name cognitive appraisal, coping, and pain catastrophising. They suggest that acute psychological stress is more likely to affect short-term pain fluctuation through those psychological routes than through a direct effect, and they state that empirical evidence on the timing is limited. No effect size. [PMID 42893499](https://pubmed.ncbi.nlm.nih.gov/42893499/) — *why it matters:* a framework, not a trial of a psychological treatment. - **Statins in female rodents, including induced endometriosis** — systematic review of preclinical rodent studies (PubMed, Scopus, Embase, Web of Science, LILACS, SciELO; SYRCLE risk of bias). In normocholesterolemic females, statin exposure was associated with ovarian morphological change, including impaired follicular dynamics. In rodents induced to have endometriosis, the abstract reports a reduction in the volume of endometriotic implants. It does not name the statin, the number of endometriosis studies, or a pooled effect. No hyperlipidemic rodent studies were found. [PMID 42900000](https://pubmed.ncbi.nlm.nih.gov/42900000/) — *why it matters:* a preclinical sentence on the statin thread that digest 2026-09-18 logged in humans (PMID 42668641). An unnamed implant reduction without an estimate does not change that observational status and is not an M3 verdict. - **Gut microbiome, symptoms, and taste-receptor variants** — case-only study of 50 women with surgically confirmed endometriosis. Rectal-swab 16S profiles fell into three community types dominated by Bacteroides, Prevotella, or Escherichia-Shigella. Microbiome composition did not differ significantly by stage. Beta diversity was associated with dysmenorrhoea (R²=0.13) and stage (R²=0.12). Variants in TAS2R14 were associated with diversity measures. Lower abundance of short-chain-fatty-acid-producing Lachnospiraceae and Ruminococcaceae was associated with dysmenorrhoea. There is no control group without endometriosis. [PMID 42898479](https://pubmed.ncbi.nlm.nih.gov/42898479/) — *why it matters:* symptom correlations inside one case series. Not a diagnostic microbiome test and not a dietary prescription. Epub 2026-10-05. ## Epidemiology and burden - **Endometriosis and systemic comorbidities** — systematic review and meta-analysis of observational studies (Web of Science and Medline through 31 December 2025; CRD420251258716). Fifty-five studies met inclusion; 48 were pooled. Thirty-two studies covered autoimmune diseases, with study counts that overlap across diseases (systemic lupus erythematosus 14, Sjögren's syndrome 8, rheumatoid arthritis 10, multiple sclerosis 5, celiac disease 5, inflammatory bowel disease 4), plus 17 allergy studies, 13 pain-syndrome studies, and 6 endocrine studies. In cohort studies the pooled risk ratios were 1.81 for systemic lupus erythematosus (95% CI 1.50–2.18), 1.54 for Sjögren's syndrome (1.40–1.71), and 1.71 for rheumatoid arthritis (1.40–2.09). In case-control and cross-sectional studies the pooled odds ratios were 3.93 (2.59–5.98), 3.13 (1.10–8.90), 2.27 (1.75–2.95), 2.30 (1.57–3.37), and 4.50 (1.94–10.42) for those first five, respectively. The inflammatory-bowel-disease odds ratio was 2.82 (95% CI 0.58–13.61); that interval includes 1, so it is not a demonstrated increase even though the abstract lists it with the significant odds ratios. Allergy and pain associations that excluded 1 included asthma (RR 1.27, 1.14–1.40), eczema (OR 1.58, 1.34–1.87), fibromyalgia (RR 1.65, 1.42–1.92), chronic fatigue syndrome (RR 1.41, 1.31–1.51), and irritable bowel syndrome (RR 2.51, 1.55–4.07; OR 3.49, 3.21–3.80). Hypothyroidism (OR 1.89, 0.61–5.90) and hyperthyroidism (OR 0.95, 0.60–1.52) were not significant. GRADE quality was generally low or very low because of bias in the included designs. The authors argue for treating endometriosis as a systemic immuno-inflammatory disease and for multidisciplinary care. [PMID 42901254](https://pubmed.ncbi.nlm.nih.gov/42901254/) — *why it matters:* the largest association map this week, and the authors grade it as weak. Associations are not mechanisms, and the practice sentence is theirs. This digest does not adopt a new disease definition or a new care model. - **Obstetric and neonatal outcomes** — retrospective single-centre cohort of singleton deliveries, 1991–2021, excluding chromosomal abnormalities and congenital malformations. Of 232,476 deliveries, 224 (0.1%) had documented endometriosis. After generalized-estimating-equation adjustment for maternal age, gravidity, and fertility treatment, endometriosis remained associated with caesarean delivery (adjusted OR 2.14, 95% CI 1.62–2.83). Other obstetric and perinatal outcomes that differed before adjustment were not independently associated. Perinatal mortality was comparable in the unadjusted comparison. [PMID 42894015](https://pubmed.ncbi.nlm.nih.gov/42894015/) — *why it matters:* a caesarean association in a cohort whose recorded endometriosis prevalence (0.1%) is far below the usual reproductive-age figure, which is a warning about under-ascertainment. One centre. Not a delivery protocol. Epub 2026-07-22. - **Information needs in Australia** — cross-sectional anonymous online survey, convenience sample via Facebook and women's-health newsletters. Women aged 18 or older, living in Australia, with diagnosed or suspected endometriosis. Of 265 analysed participants from seven states, the highest "strongly agree" information needs were comorbidities (76.98%, 204/265), endometriosis clinics (75.85%, 179/236), and how to deal with dismissal by health professionals (75.54%, 176/233). Open answers also asked for pathogenesis, management including alternatives, public-versus-private care, and costs. [PMID 42893505](https://pubmed.ncbi.nlm.nih.gov/42893505/) — *why it matters:* a map of what this self-selected group says it cannot find. Denominators change by item. It is not an evaluation of an information resource. Epub 2026-10-18. - **Food and supplement spending in Hungary** — cross-sectional mobile-app survey, December 2023–August 2024, 90% response. 1,645 women aged 14–45 years (524 with endometriosis, 1,121 without). Women with endometriosis had smaller households (mean 2.49 versus 2.95) and were more often in the higher spending bands: over €400/month on food in 30% versus 24% (median band €301–€400 versus €251–€300), and supplement costs over €35/month in 22% versus 9% (median band €16–€25 versus €6–€15). Diet adherence and supplement use were also higher. Endometriosis status remained associated with food and supplement expenditure after sociodemographic adjustment. [PMID 42898086](https://pubmed.ncbi.nlm.nih.gov/42898086/) — *why it matters:* a spending difference. It is not evidence that a special diet or a supplement changes symptoms. Epub 2026-09-28. - **What endometriosis randomized trials have been powered to see, 1990–2024** — bibliometric review of 536 endometriosis randomized trials with an English abstract, identified in Dimensions.AI. Medical-management trials were 55.6% (n=298), of which 177 involved a GnRH analogue. Complementary-therapy trials rose from 1 of the medical-management trials in 1990–1999 (0.847%) to 31 (28.7% of medical-management trials) in 2020–2024. The United States and China contributed 70 and 65 trials. Among 445 trials with at least one continuous outcome, 55.7% (n=248) were, at 90% power, sized only for a standardised mean difference the authors class as large or greater. [PMID 42907689](https://pubmed.ncbi.nlm.nih.gov/42907689/) — *why it matters:* a description of the trial literature, including a power limit. It is not itself a treatment result. Epub 2026-07-27. ## Pharmacology and supportive care - **Estetrol 15 mg with drospirenone 3 mg** — systematic review (Cochrane methods, PRISMA; PubMed, Embase, CENTRAL; no language or date limit). Two randomized trials and two observational cohorts, 198 patients in total. Quantitative pooling was not done. Versus placebo, the combination reduced pelvic pain; versus other active hormonal regimens, no significant difference was observed. Dysmenorrhoea improved on the authors' reading. Quality of life, sleep, and global ratings improved. Dyspareunia results were inconsistent. The most common adverse effect was intermenstrual bleeding or spotting. The authors say superiority over other combined hormonal contraceptives remains uncertain. [PMID 42892004](https://pubmed.ncbi.nlm.nih.gov/42892004/) — *why it matters:* a small, unpooled set. "Promising" is the authors' word. It is not a new first-line recommendation and it does not displace a GnRH antagonist or a progestin. Epub 2026-10-15. - **GnRH-agonist plus aromatase-inhibitor pretreatment before frozen embryo transfer** — multicentre retrospective cohort, 2018–2024, at Northwestern University, the University Fertility Clinic in Skive, Denmark, and IVI Rome. Eligible records had endometriosis, adenomyosis, or both, and at least one previous failed conventional frozen transfer. Fifty-one patients contributed 217 cycles: 159 conventional and 58 pretreatment cycles (about two months of GnRH agonist with or followed by an aromatase inhibitor). Most conventional cycles were programmed hormone-replacement cycles (119/159, 75%). Pretreatment was associated with higher odds of live birth (OR 26.7, 95% CI 9.48–75.0). The authors say prospective studies are needed. [PMID 42892070](https://pubmed.ncbi.nlm.nih.gov/42892070/) — *why it matters:* a Danish site is in the cohort, and the odds ratio is the kind of figure that gets repeated without the design. The people in the pretreatment cycles had already failed conventional transfer, the analysis is retrospective, and the interval runs from about 9-fold to 75-fold. That is not a protocol to adopt. - **Nutritional supplements for endometriosis symptoms** — systematic review of 24 clinical trials, 2,019 women. Some trials reported improvements in pain and quality of life, particularly with formulated curcumin or with selenium, alone or with dienogest. Some fertility-related measures improved; pregnancy rates did not. Some combination treatments reduced ovarian endometriosis; supplements did not reduce recurrence after surgery. The authors' conclusion is that supplements may support standard treatment and should not replace it. The PubMed abstract does not report pooled effect sizes. [PMID 42900597](https://pubmed.ncbi.nlm.nih.gov/42900597/) — *why it matters:* the patient-facing item this week. The review's own limit is the one to keep: this is not a reason to replace hormonal or surgical care with a supplement, and it is not an OpenEndo recommendation to start curcumin, selenium, or any other product. The curcumin experiment in PMID 42892355 is a mouse finding and is a different record. - **Dopamine D2 agonists as a non-hormonal idea** — narrative review of cabergoline and quinagolide. The proposed mechanism is reduced VEGF-A signalling and less aberrant angiogenesis. A randomized, double-blind, placebo-controlled pilot of cabergoline for 6 months reduced chronic pelvic pain scores without serious adverse events; the abstract gives no sample size. A post hoc look at quinagolide found regression in 61.3% of lesions, with ovulatory function preserved in 93% of participants. The authors say adequately powered phase 3 trials are still needed. [PMID 42903633](https://pubmed.ncbi.nlm.nih.gov/42903633/) — *why it matters:* early clinical signals without the numbers a decision would need. Cabergoline and quinagolide are not OpenEndo M3 candidates, and this review does not add them. Epub 2026-07-22. - **Diet as support, narrative review** — no new cohort. The abstract discusses an anti-inflammatory pattern (omega-3 fatty acids, cruciferous vegetables, fibre) as distinct from routine food elimination, plus selected supplements and probiotics, and states that diet should be treated as supportive rather than as causal treatment. It gives no study count and no effect size. [PMID 42886549](https://pubmed.ncbi.nlm.nih.gov/42886549/) — *why it matters:* a narrative companion to the supplement review and to the low-FODMAP meta-analysis in digest 2026-10-16 (PMID 42876029), which pooled post-intervention scores rather than controlled effects. Not a diet to prescribe. Issue date 2026-10-16 and absent from `weekly/2026-10-16.json`. ## Notable clinical signals - **No new guideline, Cochrane update, or regulatory decision** this week. Nothing here changes an OpenEndo repurposing verdict. Nothing here is adopted as a patient-facing treatment recommendation. Knowledge pages for Yselty and for saliva diagnostics are unchanged. - **Comorbidity meta-analysis (PMID 42901254)** is the broadest association paper: higher pooled estimates for several autoimmune, allergic, and pain conditions, an inflammatory-bowel-disease interval that includes no effect, thyroid associations that are not significant, and a GRADE rating of low or very low. The authors' call for a systemic disease model and multidisciplinary care is their interpretation. It is not a new care pathway. - **Non-invasive diagnosis (PMID 42885805)** repeats a limit that matters for reading a scan: a normal expert ultrasound or MRI does not exclude superficial disease, and no circulating or endometrial biomarker is described as ready for clinical use, including salivary miRNA. That is a bound on what current tests can claim. It is not a new pathway. - **Frozen-embryo-transfer pretreatment (PMID 42892070)** reports OR 26.7 for live birth after a GnRH-agonist plus aromatase-inhibitor lead-in, in a retrospective series of 51 patients and 217 cycles at three centres, one of them in Skive. The design (already-failed conventional transfers) and the width of the interval are the result. It does not change embryo-transfer practice. - **Supplements (PMID 42900597)** and the diet narrative (PMID 42886549) are the records most likely to be read as advice. The supplement review covers 24 trials and 2,019 women and states that supplements should not replace standard treatment. The diet paper gives no effect size. Neither record is a recommendation to start a product or a diet. - **Estetrol/drospirenone (PMID 42892004)** is 198 patients across four studies, unpooled, with no significant difference versus other active hormonal regimens. **Dopamine agonists (PMID 42903633)** are a pilot and a post hoc analysis without a phase 3 trial. Neither is a new option to adopt. - **Vasopressin (PMID 42890533)** is the week's randomized trial: less time controlling bleeding, no difference in 12-month anti-Müllerian hormone. **Nerve-sparing (PMID 42896655)** reports complication and function rates without a superiority claim; the urinary-symptom review (PMID 42905159) still says nerve-sparing should be considered when feasible. That remains the authors' sentence. - **Two model papers are internal only:** the question-mark angle (PMID 42902224, AUC 0.958, total n not stated) and the ovarian-cancer nomogram (PMID 42902392, internal AUC 0.932, authors: multicentre validation still required). **SEED (PMID 42898862)** is a 22-item draft, not a validated screen. **CA-125 versus a platelet ratio (PMID 42897934)** uses teratoma controls and reports no AUC. - **Case reports** (PMIDs 42889145, 42889881, 42903660, 42907392) are one or two patients. The postpartum hemothorax is suggestive, not histologically confirmed in the abstract. The carcinoma case is one person's imaging and markers. None of these is a pathway. - **RNF34/curcumin (PMID 42892355)**, the rat elagolix protocol (PMID 42891579), the swine protocol (PMID 42891621), peritoneal vesicles (PMID 42891160), the microbiome series (PMID 42898479), and the statin-rodent review (PMID 42900000) are preclinical or case-only. The human statin observation from September is not upgraded. ## Erratum with a known text - **Menstrual-fluid extracellular-vesicle RNA-seq table** — PubMed records this as an erratum for PMID 41924633 (Hum Reprod Open, DOI 10.1093/hropen/hoag020). The PubMed abstract says only that it corrects that article. The Europe PMC full text of the correction (PMC13679381) states that the RNA-seq data deposited as NCBI GEO GSE310627, and shown in the original Supplementary Table S1, came from menstrual-fluid mesenchymal stem cells rather than from menstrual-fluid small extracellular vesicles, because two files from the same cohort had similar names. GEO and the table have been replaced with the vesicle dataset. The correction states that this does not change the results, analyses, conclusions, or scientific message of the original paper. The original paper was not re-read; it is outside this window and not in the weekly snapshots. [PMID 42899171](https://pubmed.ncbi.nlm.nih.gov/42899171/) — *why it matters:* a data-file mix-up that the publisher says leaves the paper's claims in place. Those claims were not re-checked here. ## Carried over / follow-ups checked - **Carry-over, not re-counted:** PMID 42866613 (endometriosis and chronic pain, stress mechanisms) is in `weekly/2026-10-16.json` and was synthesized in digest-2026-10-16. The pdat query returned it again. The record was not re-analyzed. - **No other PMID in this included set** appears in `weekly/2026-09-02.json`, `weekly/2026-09-04.json`, `weekly/2026-09-11.json`, `weekly/2026-09-18.json`, `weekly/2026-09-25.json`, `weekly/2026-10-02.json`, `weekly/2026-10-09.json`, or `weekly/2026-10-16.json` — checked programmatically. - **Issue date 2026-10-16 overlaps the previous window's end date.** PMIDs 42885805, 42886549, 42891579, and 42891621 are included above because they are absent from `weekly/2026-10-16.json`. PMID 42866613, also dated 2026-10-16, is the carry-over. - **Indexed this week with earlier or non-day publication dates, included above because they were not in prior snapshots:** PMIDs 42889145 (epub 2026-10-01), 42889881 (2026 Sep), 42890533 (epub 2026-10-02), 42891160 (epub 2026-07-22), 42892004 (2026-10-15), 42892070 (2026-09-21), 42893505 (publication date "2026 Jan-Dec"), 42894015 (epub 2026-07-22), 42898086 (2026 Nov; epub 2026-09-28), 42898479 (epub 2026-10-05), 42898862 (epub 2026-10-15), 42902224 (epub 2026-07-25), 42902392 (epub 2026-07-23), 42903633 ("2026 Oct", epub 2026-07-22), 42903660 (2026 Dec; epub 2026-10-07), 42907689 and 42907837 (epub 2026-07-27). - **Dropped as noise (12):** - PMID 42889946 — cost-to-baby and national ART utilisation across 22 countries. Endometriosis appears because a coauthor is identified as President of the World Endometriosis Research Foundation, in the disclosures. The analysis is not an endometriosis analysis. - PMID 42891460 — pelvic MRI in 262 people without sexual experience (63 adolescents). Endometriosis is an author keyword. The abstract reports organic versus functional findings and does not give an endometriosis count. - PMID 42892851 — cumulative MUSA features and adenomyosis severity in Kinshasa, 211 women. Endometriosis is an adjustment covariate ("recorded concomitant endometriosis"), not the disease under study. - PMID 42895300 — organoid and assembloid review of female reproductive biology. Endometriosis is one of three modeled conditions. The abstract gives no endometriosis-specific model count or result. - PMID 42895771 — absorption, distribution, metabolism, and excretion of linzagolix in rats and monkeys. Endometriosis is named as an indication alongside uterine fibroids. There is no endometriosis experiment. The Yselty knowledge page is unchanged. - PMID 42896814 — bisphenol A and hormone-associated disorders, 44 studies. Endometriosis is a keyword. The pooled results in the abstract are polycystic ovary syndrome, breast cancer, and benign endometrial disorders. No endometriosis effect size is reported. - PMID 42897337 — prophylactic cefazolin and surgical-site infection after laparoscopic adnexal surgery, 1,678 patients. Endometriosis is a propensity-score covariate. Infection was 1.1% with and without cefazolin. - PMID 42897519 — serum androstenedione and dysmenorrhoea, 139 premenopausal participants. The association the abstract reports is in women without endometriosis. No endometriosis-subgroup effect size is given. - PMID 42900601 — oxidative stress, infertility, and medicinal plants. Endometriosis is one listed cause of female infertility. The abstract gives no endometriosis-specific result. - PMID 42900624 — reversible camptocormia attributed to deep infiltrating endometriosis. The PubMed record has no abstract, so the outcome is not verifiable from the record. - PMID 42904152 — narrative review of paediatric and adolescent gynaecologic ultrasound. Endometriosis is named as one condition for which adult-derived criteria are still used. No endometriosis cohort or accuracy figure. - PMID 42905530 — letter to the editor on a nerve-and-muscle stimulation paper. The PubMed record has no abstract. --- *Sources: PubMed snapshot `weekly/2026-10-23.json` (E-utilities esearch + esummary + efetch). Primary: `endometriosis[Title/Abstract]`, datetype=pdat, 2026-10-16..2026-10-23 (23 records). Supplement: datetype=edat, 2026-10-17..2026-10-23 (42 records, 22 not in the pdat set). 45 records screened, 32 included, 1 carry-over, 12 dropped. The menstrual-fluid erratum text was read from the Europe PMC full text of PMC13679381; the PubMed record itself only names the corrected DOI. Synthesized by Galahad, 2026-10-23. Research infrastructure, not medical advice.*