Matveeva 1990.
Study characteristics | |||
Patient sampling |
Primary objective: to investigate inhibitory and activation motif expression of killer immunoglobulin‐like receptor (KIR) by natural killer (NK) cells, which may be pathogenetically involved in endometriosis Participants: women undergoing laparoscopy for various indications Selection criteria: exclusion criteria: history of pregnancy or history of treatment with GnRH analogues within previous year, complications from apparent pelvic inflammatory disease Study design: cross‐sectional, two‐gate, prospective sample collection |
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Patient characteristics and setting |
Clinical presentation: infertility; all women had regular ovulatory menstrual cycles Age: mean age 30.6 years, range 26‐35 years Number of participants enrolled: 119 participants Number of participants available for analysis: 119/74 participants (in follicular or luteal cycle phase), different number of samples for different tests Setting: National research centre of mother and child health, Ministry of Health Place of study: Moscow, Russia Period of study: not reported Language: Russian |
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Index tests |
Index test: PBMC (CD3, CD4, CD8, CD2), IgA, IgM, IgG Details of the index test procedure as stated: PBMC were measured by flow cytometry using FACScan (Becton Dickinson, USA); serum immunoglobulins were determined by using Manchini method; laboratory technique described Threshold for positive result: not reported Examiners: no information provided, unclear if were blinded to the result of reference standard Interobserver variability: not reported |
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Target condition and reference standard(s) |
Target condition: endometriosis Prevalence of target condition in the sample: n = 62/119 (52%): all stage I‐II; controls n = 57 Reference standard: laparoscopy, n= 119 (100%) Description of positive case definition by reference standard test as reported: staging according to rAFS classification Examiners: no information provided |
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Flow and timing |
Time interval between index test and reference standard: blood samples were collected at surgery Withdrawals: data were not reported for up to 45 participants for some of the index tests, reason not explained |
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Comparative | |||
Key conclusions by the authors | The tested cells did not markedly differ from those in control fertile patients. Serum concentrations of immunoglobulin M were increased in women with endometriosis. Immunoglobulin concentrations widely varied in the peritoneal fluid, with a statistically significant elevation of IgA and IgM in women with tubal‐peritoneal infertility | ||
Conflict of interest | Not reported | ||
Notes | For PBMC (CD3, CD4, CD8, CD2), IgA and IgG there was no statistically significant difference between the groups ‐ no data available for meta‐analysis For IgM there was statistically significant difference between the groups, but there were insufficient data to construct 2 x 2 tables ‐ not included in this review The data for markers measured in peritoneal fluid are not presented in this review The data for a group of healthy women (n = 10) who did not have laparoscopy are not presented in this review |
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Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient Selection | |||
Was a consecutive or random sample of patients enrolled? | Unclear | ||
Did the study avoid inappropriate exclusions? | Unclear | ||
Was a 'two‐gate' design avoided? | Yes | ||
Unclear | High | ||
DOMAIN 2: Index Test All tests | |||
Were the index test results interpreted without knowledge of the results of the reference standard? | Unclear | ||
If a threshold was used, was it pre‐specified? | No | ||
Was a cycle phase considered in interpretation of the result of index test? | Yes | ||
High | Low | ||
DOMAIN 3: Reference Standard | |||
Is the reference standards likely to correctly classify the target condition? | Unclear | ||
Were the reference standard results interpreted without knowledge of the results of the index tests? | Unclear | ||
Unclear | Low | ||
DOMAIN 4: Flow and Timing | |||
Was there an appropriate interval between index test and reference standard? | Yes | ||
Did all patients receive the same reference standard? | Yes | ||
Were all patients included in the analysis? | No | ||
Low |