Evidence map›Paper›PMID 37621818›Full record

ReviewCureus2023

The Comorbidity of Endometriosis and Systemic Lupus Erythematosus: A Systematic Review.

Ranim K Hamouda, Hadia Arzoun, Isra Sahib, Lisbeth Escudero Mendez, Mirra Srinivasan, Shoukrie I Shoukrie, Ravneet K Dhanoa, Ramaneshwar Selvaraj, Jyothirmai Malla, Tharun Yadhav Selvamani and 3 more

Open access · diamondAbstract readReview
In one paragraph

Review in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Endometriosis: An Immunologist's Perspective.International journal of molecular sciences · 2025
    Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Ranim K HamoudaInternal Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Hadia ArzounInternal Medicine, St. Bernards Medical Center, Jonesboro, USA.
Isra SahibInternal Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Lisbeth Escudero MendezPathology, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Mirra SrinivasanInternal Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Shoukrie I ShoukrieOrthopedics and Traumatology, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Ravneet K DhanoaInternal Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Ramaneshwar SelvarajInternal Medicine/Family Medicine/General Surgery, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Jyothirmai MallaInternal Medicine/Family Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Tharun Yadhav SelvamaniGeneral Surgery, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Anam ZahraSurgery, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Sathish VenugopalNeurology, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
Lubna MohammedInternal Medicine, California Institute of Behavioral Neurosciences and Psychology, Fairfield, USA.
California Institute of Behavioral Neurosciences and Psychology (United States) · USSt. Bernards Clopton Clinic · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune diseases manifest in genetically predisposed individuals exposed to certain triggers that aggravate immune dysfunction and result in an exacerbated immune response in the form of hyperactivity to both the humoral and cell-mediated response. The devastating reality apart from the severity of the disease is that multiple immune diseases could co-occur, increasing the patient's physical, psychological, and financial burden. Autoimmune diseases are utterly deranging. One of the dreadful autoimmune diseases is systemic lupus erythematosus (SLE). SLE is a rheumatological disease that affects multiple systems, and there are no predictors to know which system will be affected in the future. It could affect the mucocutaneous system. It could also present with hematological, rheumatological, neuronal, renal, pulmonary, and cardiac manifestations. SLE is prevalent in females, predominantly in the childbearing age group. The pharmacological therapy and bombarding pathophysiology of the disease lead to obstetrical and gynecological complications such as infertility, abortion, miscarriage, and stillbirth. Over the past decade, the autoimmune disease comorbidity increased eminently. One of the common associations is rheumatological diseases (like rheumatoid arthritis, Sjogren syndrome, and SLE) with gynecological diseases (e.g., endometriosis and uterine fibroids). SLE and endometriosis have strong associations, and the prevalence of each condition is relatively high among the female population.

Indexed as

auto immune diseasegeneral gynecologymultisystem involvementrheumatology & autoimmune diseasessystemic lupus erythematosus

Identifiers

PMID37621818
PMCPMC10445410
OpenAlexW4385215967

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.