Modified QUIPS items | Brandt 2014 | Dello Russo 2013 | Derraik 2015 | Gaillard 2014 | Gaillard 2016 | Hochner 2012 | Hrolfsdottir 2015 | Jeffery 2006 | Maftei 2015 | Mingrone 2008 | Oostvogels 2014 | Perng 014 | Sauder 2017 | Tam 2018 | Winham 2006 |
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1. Study participation | |||||||||||||||
Source of target population adequately described for key characteristics including age, gender, pregnancy characteristics | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
The method used to identify the study population is described adequately | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Recruitment period is stated | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | No |
Place of recruitment (setting and location) is stated | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Inclusion and exclusion criteria are clearly defined | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | No |
There is adequate participation in the study by eligible individuals >80%a | No | NA | NA | No | No | No | No | Yes | No | NA | No | No | No | No | NA |
Baseline characteristics of the participants are collected including gestational age, birth weight, age, gender | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Summary: Study participation | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Moderate |
2. Study attrition | |||||||||||||||
All the included patients have outcome data, or the dropout rate is maximum 20%a | No | NA | NA | No | No | No | No | Yes | No | NA | No | No | No | No | NA |
Attempts to collect information on participants who dropped outa | Yes | NA | NA | Yes | Yes | Yes | Yes | Yes | Yes | NA | Yes | Yes | Yes | Yes | NA |
Reasons for lost to follow‐up are describeda | Yes | NA | NA | Yes | Yes | Yes | Yes | Yes | Yes | NA | Yes | Yes | Yes | Yes | NA |
Key characteristics (age, gender, pregnancy characteristics) information on those lost to follow‐upa | Yes | NA | NA | Yes | Yes | Yes | Yes | Yes | Yes | NA | Yes | Yes | Yes | Yes | NA |
There are no important differences between key characteristics and outcomes in participants who completed the study and those who did nota | Unclear | NA | NA | Unclear | Unclear | Yes | Unclear | Unclear | Unclear | NA | Unclear | Unclear | Unclear | Unclear | NA |
Summary: Study attrition | Moderate | NA | NA | Moderate | Moderate | Low | Moderate | Low | Moderate | NA | Moderate | Moderate | Moderate | Moderate | NA |
3. Prognostic factor measurement | |||||||||||||||
Definition of maternal nutritional state (ppBMI and/or GWG) and the method of measurements are clearly described | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Method of measuring of maternal nutritional state is valid and reliableb | Yes | Partly | Partly | Partly | Partly | Partly | Yes | Partly | Partly | Partly | Partly | Partly | Yes | Yes | Yes |
Continuous variables (ppBMI and/or GWG) are reported or appropriate cut points are used (GWG categories in accordance with the IOM recommendations) | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Method and setting of measuring maternal nutritional state are the same for all study participants | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
All the included participants have complete data for the maternal nutritional state | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Appropriate method was used to replace the missing data on maternal nutritional statec | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA |
Summary: Measurement of the maternal nutritional state | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low |
4. Outcome measurement | |||||||||||||||
Definition of outcome: Fasting insulin level | Yes | Yes | Yes | Yes | Yes | Yes | Yes | NA | NA | Yes | NA | NA | Yes | Yes | Yes |
Definition of outcome: HOMA‐IR | NA | Yes | NA | NA | Yes | NA | Yes | Yes | Yes | NA | NA | Yes | Yes | Yes | NA |
Definition of outcome: Fasting glucose level | NA | NA | NA | NA | Yes | Yes | Yes | NA | NA | NA | Yes | NA | NA | Yes | NA |
Valid and reliable measurement of outcome | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Method and setting of outcome measurement is the same for all study participants | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Summary: Outcome measurement | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low |
5. Study confounding | |||||||||||||||
Maternal age, as an important confounder is measured | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Maternal smoking habits during pregnancy, as an important confounder is measured | Yes | Yes | Yes | Yes | Yes | Yes | Yes | No | Yes | No | Yes | Yes | Yes | Yes | No |
Maternal socioeconomic status/maternal educational level, as an important confounder is measured | Yes | Yes | No | Yes | Yes | Yes | Yes | Yes | Yes | No | Yes | Yes | No | No | No |
Birth weight, as an important confounder is measured | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | No | Yes | Yes | Yes | Yes | No | Yes |
Breastfeeding, as an important confounder is measured | No | Yes | No | Yes | Yes | No | No | No | No | No | Yes | Yes | No | Yes | No |
Offspring's age, as an important confounder is measured | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Offspring's adiposity (weight or BMI or fat mass index), as an important confounder is measured | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | No |
The measured confounding factors are clearly defined | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Valid and reliable measurement of confounders | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Method and setting of confounding measurement are the same for all study participants | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
An appropriate method was used for replacing missing confounder data (e.g., imputation) | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA | NA |
Important confounders are accounted for in the study design (e.g., initial assembly of comparable groups or matching) | Partly | Yes | Partly | Yes | Yes | Partly | Partly | Partly | No | No | Yes | Yes | Partly | Partly | No |
Confounders considered important by the authors of the article, are accounted for in the analysis (e.g., appropriate adjustment, stratification, multivariate regression) | No | Yes | No | Yes | Yes | Partly | No | No | No | No | Yes | Partly | No | Partly | No |
Summary: Study confounding | High | Low | High | Low | Low | Moderate | High | High | High | High | Low | Moderate | High | High | High |
6. Statistical analysis and reporting | |||||||||||||||
The analytical strategy is described in detail, the adequacy of the analysis can be judged | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Strategy for model building is appropriate and is based on a conceptual framework or model | Yes | Yes | No | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
The results are reported in detail, no selective reporting can be observed | Yes | Yes | Unclear | Yes | Yes | Yes | Unclear | Yes | Unclear | Unclear | Yes | Yes | Yes | Yes | Unclear |
Summary: Statistical analysis and presentation | Low | Low | Moderate | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low | Low |
Ratings: Items are rated with yes (low risk of bias), unclear (unknown risk of bias), partly (moderate risk of bias) or no (high risk of bias).
For the 1st–4th and the 6th domains: If two of the items were rated as unclear, partly or no, then the specific main domain was considered to carry moderate risk of bias. If three or more of the items were rated as unclear, partly or no, then the specific main domain was considered to be carrying high risk of bias. Because the reasons for lost to follow‐up (dropouts) were described in all prospective studies and they randomly affected the participants, the dropout rate higher than 20% was unlikely to cause selection bias (see domains 1st and 2nd).
For the 5th domain: If maximum one of the items was rated as no plus one or two were rated as partly, then the specific main domain was considered to be carrying moderate risk of bias. If two or more of the items was rated as no, then the specific main domain was considered to be carrying high risk of bias.
Abbreviations: BMI, body mass index; GWG, gestational weight gain; HOMA‐IR, Homeostatic Measurement Assessment for Insulin Resistance; IOM, Institute of Medicine; NA, not applicable due to study design; ppBMI, prepregnancy BMI.
Items only applicable in case of prospective studies. Retrospective ones were not assessed.
In case of self‐reported maternal data the item was rated as partly. If data were measured or obtained from records, the item was rated as yes.
Only those patients were included in the studies, who had appropriate data on maternal nutritional state. Therefore, this item was not assessed.