Introduction
One of the main objectives in dairy farming is to improve milk production and composition. Milking frequency can modify the quality and the amount of milk produced. The substantial increase in milk production, achieved through genetic selection, has compelled dairy producers to increase milking frequency.1,2 Research conducted under controlled conditions and on commercial dairy farms demonstrated a milk production increase (1.72 kg/d) in cows milked 3x compared to those milked twice. This increase was accompanied by a decrease in body condition score.3 Similarly, milk protein yield increased (0.15 kg/d) in cows milked 3x, compared with 2x, as a result of the increased milk production.4 Likewise, milk fat yield also increases in thrice-daily milking. Indeed, Allen et al.5 and Atashi6 found that increasing the frequency of milking from 2x to 3x, boosted milk production (3.46 and 3.69 kg milk/d) and milk fat yield 0.05 kg/d and 0.11 kg/d respectively. These and other studies are summarised in literature reports,1,7 showing the positive response of 3x vs 2x milking at different stages of lactation, and age (primiparous vs multiparous) of the cows. However, an effect of milking frequency on feed intake, parallel to those observed on milk composition and yield, remains debatable. Combining and analysing this information through a meta-analysis would add insight to the production benefits of this management alternative.
The meta-analysis is a powerful statistical tool to cumulate and summarise the knowledge in certain research fields.8 Through a meta-analysis, individual results are combined to identify the overall treatment effects.9 However, analysing data with a meta-analysis is not devoid of problems. Pooling data can create non-linear correlations, multifactorial rather than unifactorial effects, and limited coverage or non-homogeneous data that fails to connect results with the hypothesis tested.8 In contrast, meta-analysis produces effect size estimates with considerable statistical power compared to individual studies, which improves the estimation of the treatment effect. It also combines results of studies that are contrasting, in a way that it weighs those.10 The objective of this study was to combine generated research data in a meta-analysis to provide a more precise estimate of the effect of 2 or 3 times daily milking sessions on the production of dairy cows.
Materials and methods
Literature search
A literature search was performed in PubMed, Google Scholar, and Agricola-USDA, together with citations in reviews or scientific papers for a more comprehensive search. Selected studies had to meet the following criteria: 1) use of lactating dairy cows as experimental units; 2) report information on dry matter intake (DMI), milk production, and milk composition; 3) include contrasts between twice (2x) and thrice (3x) daily milking sessions; and 4) report the standard error, or the standard deviation of the mean for the variables measured. A total of 21 publications were found, but only 14 met the previous criteria for conducting the meta-analysis. Three of the articles used in the meta-analysis were pen studies, and two used Jersey cows and reported two different trials (Table 1). Only a single study used lactating dairy cows on pasture30. The average trial duration was 220+102 milking days.
Author (s) and year | Trials | Cows | Breed | Trial duration (d) | Feeding system | Response variables |
---|---|---|---|---|---|---|
Pearson et al. (1979) 21 | 1 | 26 | H | 182 | Individual | DMI, milk yield, yield of milk fat and protein |
Poole (1982) 22 | 1 | 58 | H | 210 | Individual | DMI, milk yield, percentage of milk fat |
Waterman et al. (1983) 23 | 2 | 48 | H, J | 88 | Individual | Milk yield |
Amos et al. (1985) 24 | 1 | 47 | H | 301 | Individual | DMI, milk yield, percentages of milk fat and protein, yield of milk fat |
DePeters et al. (1985) 25 | 1 | 52 | H | 308 | Individual | DMI, milk yield, percentages of milk fat and protein, yield of milk fat and protein |
Allen et al. (1986) 5 | 1 | 14 | H | 305 | Pen | Milk yield, yield of milk fat |
Gisi et al. (1986) 26 | 1 | 56 | H | 305 | Individual | Milk yield, percentage of milk fat, yield of milk fat |
Barnes et al. (1990) 27 | 1 | 183 | H | 305 | Individual | DMI, milk yield, percentages of milk fat, yield of milk fat |
Economides (1999) 2 | 2 | 142 | H | 53 | Individual | DMI, milk yield, percentages of milk fat and protein |
Smith et al. (2002) 28 | 1 | 20044 | H | 305 | Pen | Milk yield, percentages of milk fat and yield |
McNamara et al. (2008) 29 | 1 | 42 | H | 42 | Individual | DMI, milk yield, percentages of milk fat and protein, yield of milk fat and protein |
Hart et al. (2013) 4 | 1 | 24 | H | 149 | Individual | DMI, milk yield, percentages of milk fat and protein, yield of milk fat and protein |
Phyn et al. (2014) 30 | 1 | 62 | H, H×J | 224 | Individual | Milk yield, percentages of milk fat and protein, yield of milk fat and protein |
Atashi (2015) 6 | 1 | 648 | H | 305 | Pen | Milk yield, yield of milk fat |
DMI: dry matter intake; H: Holstein cows; J: Jersey cows.
It has been reported that milk production response to frequent milking is more pronounced in primiparous than multiparous cows.11,12 In this meta-analysis, data from primiparous and multiparous cows were pooled, because of the impracticality of applying different milking frequencies in large commercial herds.
Parameters and data extraction
The parameters evaluated were DMI, milk production, and percentages and yields of milk fat and protein. The data set included mean, standard deviation, and number of cows per treatment group. Production parameters of the studies used in the meta-analysis averaged 21.40±4.84 kg/d of DMI, 27.44±5.07 kg/d milk yield, 3.71±0.34 % milk fat, 1.01±0.19 kg/d milk fat, 3.15±0.27 % milk protein, and 0.93±0.16 kg/d milk protein. The precision of the estimate was based on the standard deviation for treatment and control groups reported in the article. When the article did not provide the standard deviation, it was calculated by multiplying the standard error of the mean by the square root of the number of cows. Some studies did not report yields of milk fat and protein, and these were estimated from their percentages in milk. In this case, the standard error from their respective milk fat and protein percentages were used. This strategy was adopted to increase the amount of milk fat and protein yield data, which improved the power of the meta-analysis for these parameters.
Statistical analyses
The effects of milking frequency (2x vs 3x) on the production responses of lactating dairy cows were evaluated through a meta-analysis using the fixed and random effects models with the R statistical software program (2015).13 The specific meta-analysis package Metafor was used.14 Each production parameter was first analysed by the fixed effects model to estimate the effect size (ES), 95% confidence interval (CI), and statistical significance of ES. Heterogeneity in experiment level ES was assessed with the Cochran's Q statistic chi-square test,15 which reflects fundamental differences in study design and analytical methods, as well as statistical variation around the response. The analysis of the estimated ES was calculated by the standardised Z-statistic. If the Q test was significant, a random effect model was used.16 The meta-analysis was adapted to a random-effect model since the Q test indicated heterogeneity among ES for all variables (P<0.05). The heterogeneity among studies was evaluated with the I2 statistic,17 which describes the percentage of total variation across studies due to heterogeneity, rather than chance.16 A value higher than 50% is considered substantial heterogeneity.18 For all production response outcomes, the weighted mean difference of 2x, relative to 3x milking, were calculated. Statistical significance was considered at P≤0.05.
The effects of milking frequency on the production response were displayed in forest plots, using the standardised mean difference (SMD) of each parameter according to the random-effect model. Information presented in forest plots also provided the means and 95%CI for primary studies. The weight of each study is calculated by the inverse of the variance of the ES. The SMD shows the difference across studies as an index, and is calculated by dividing the mean difference in each study by the standard deviation of one or both opulations. 16 The SMD of each production response parameter between 2x and 3x was the outcome of interest displayed in the forest plot. The presence of publication bias was investigated using funnel plots, which is a simple scatterplot of the treatment effects estimated from individual studies (horizontal axis) against a measure of study size (vertical axis19), and the Begg's test.20
Meta-regression analysis was used to explore any other source of undetected heterogeneity and to provide greater insight and a more unambiguous interpretation of how study outcomes are not affected by factors other than milking frequency. The variables for meta-regression were year of publication, trial duration, and breed.
Results
Meta-regression analysis demonstrated that the year of publication, the trial duration, and cattle breed did not contribute to the heterogeneity of milk production parameters (P>0.05; Table 2).
Variable | Coefficient | Coefficient 95%CI |
P-value |
---|---|---|---|
DMI (kg/d) | |||
Intercept | 1.706 | [0.712; 2.700] | 0.230 |
Year | −0.190 | [−0.332; −0.048] | 0.333 |
Trial duration | −0.005 | [−0.008; −0.002] | 0.135 |
Milk yield (kg/d) | |||
Intercept | -2.144 | [−6.215; 1.928] | 0.302 |
Year | 0.105 | [-0.107; 0.317] | 0.330 |
Trial duration | −0.007 | [−0.017; 0.002] | 0.132 |
Breed | 0.558 | [−1.559; 2.676] | 0.606 |
Milk fat (%) | |||
Intercept | 0.092 | [−0.140; 0.324] | 0.437 |
Year | −0.002 | [−0.031; 0.027] | 0.911 |
Trial duration | -0.000 | [−0.0007; 0.0007] | 0.988 |
Breed | −0.002 | [−0.236; 0.231] | 0.985 |
Fat yield (kg/d) | |||
Intercept | −0.662 | [−1.452; 0.128] | 0.100 |
Year | 0.052 | [0.005; 0.098] | 0.129 |
Trial duration | −0.001 | [-0.003; 0.0003] | 0.126 |
Breed | 0.378 | [-0.266; 1.022] | 0.250 |
Milk protein (%) | |||
Intercept | −0.121 | [−0.289; 0.047] | 0.157 |
Year | 0.009 | [−0.021; 0.038] | 0.556 |
Trial duration | 0.0002 | [−0.0003; 0.0006] | 0.452 |
Breed | 0.060 | [−0.148; 0.268] | 0.578 |
Protein yield (kg/d) | |||
Intercept | −0.035 | [−0.265; 0.195] | 0.767 |
Year | −0.003 | [−0.027; 0.022] | 0.816 |
Trial duration | −0.0004 | [−0.001; 0.0002] | 0.146 |
Breed | 0.063 | [−0.161; 0.288] | 0.581 |
CI = confidence interval.
Estimates for the differences in production parameters (effect size estimates) for cows milked either 2x or 3x are shown in Table 3. Daily milk production (ES= -0.510; P≤0.0001), milk fat yield (ES=-0.026), and milk protein production (ES=-0.310; P=0.04) was lower 2.23, 0.06, and 0.05 kg/d, respectively, for cows milked 2x. However, milk fat percentage (ES=0.329; P=0.0004) was 0.07 kg/d higher in 2x milking frequency. No effects were found for DMI (ES=0.064; P=0.709) and milk protein percentage (ES=0.026; P=0.460). Heterogeneity in the results among publications (I2 statistic) was moderate for milk fat percentage (I2=48%), and high (I2>50%) for DMI, milk production, milk fat yield, and milk protein yield. No heterogeneity was observed for milk protein percentage (I2=0%). Meta-analysis of multiple studies produce a more precise estimate of the negative (diamond to the left of the dotted line) or positive (diamond to the right) response to milking frequency, and are shown in forest plots (Figures 1 and 2). No significant publication bias was found for the parameters analysed (Figure 3; Begg's test; P>0.05). However, a trend (P=0.071) in publication bias was observed for milk fat percentage. Funnel plots of the effect of milking frequency on production response parameters for assessing publication bias are in Figure 3. Funnel plots showed almost an equal number of studies on every side of the overall ES estimate for DMI, milk production, and percentage and yield of milk fat and protein, which supports the inference that no publication bias existed among studies.
Outcome measured (difference between 2× and 3× milking frequency) |
Weighted mean difference for 2×-3× milking frequencya [95%CI] |
Effect size [95% CI] | I2 (%) |
P-value for effect size | Number of records/ treatment |
|
---|---|---|---|---|---|---|
2×b | 3×b | |||||
DMI (kg/d) | −0.11 [−1.29; 1.07] | 0.064 [−0.271; 0.398] | 59.4 | 0.709 | 288 | 286 |
Milk production (kg/d) | −2.23 [−3.15; −1.30] | −0.510 [−0.739; −0.282] | 69.0 | <0.0001 | 10540 | 10906 |
Milk fat (%) | 0.07 [0.03; 0.11] | 0.329 [0.146; 0.512] | 47.6 | 0.0004 | 10172 | 10538 |
Milk fat yield (kg/d) | −0.06 [−0.15; 0.03] | −0.223 [−0.422; −0.024] | 60.5 | 0.028 | 10516 | 10882 |
Milk protein (%) | 0.001 [−0.02; 0.02] | 0.026 [−0.043; 0.097] | 0.0 | 0.460 | 10022 | 10391 |
Milk protein yield (kg/d) | -0.05 [-0.08, -0.02] | -0.310 [-0.615, -0.004] | 71.3 | 0.047 | 10035 | 10882 |
a Difference between cows milked 2x and 3x, weighted by the precision of the study.
b Milking frequency: 2x = two times per day, 3x = three times per day.
I2 measure de proportion of variability that is explained by differences between the included studies rather than by sampling error in the meta-analysis.
CI: confidence interval.
Discussion
High producing dairy cows in early lactation are most of the time in negative energy balance. During the transition period, they also have reduced appetites which further challenges their ability to fulfil their nutrient requirements. When milking goes from 2x to 3x, the sudden increased yield is not immediately accompanied by a parallel higher nutrient uptake which further challenges this balance. The severity of this discrepancy depends on the cow's genetic potential for milk production, the adequacy of the diet, feed and herd management practices, and the environment. Higher milking frequencies in early lactation, lead to metabolism changes in response to the increased nutrient demand.31 These metabolic changes seem to be dependent not only on the expanded frequency but also on the length of time under the new frequency. If the additional milking is done only up to 21-30 days post-calving, then there are little metabolic changes in response to it.29 This needs to be taken into consideration when designing experiments to evaluate metabolic changes between different frequencies. Three distinct adaptation phases have been proposed through which the mammary gland adapts to increased or decreased milking frequency.32 A first one or acute phase (one to several days), a second one or medium-term phase (days to weeks), and a third one a long-term phase (weeks to months). The first phase is characterised by acute regulatory mechanisms such as feedback inhibition of lactation, leakiness, and the onset of apoptosis. During the second phase, the gland adapts to a state of lower or higher cellular activity (e.g., enzyme activity) and that results in limited metabolic changes.29 The long-term phase results in changes in the mammary parenchyma resulting in changes in cell numbers.
One of the most apparent effects as a result of the increased milking frequency is the mobilisation of body reserves. Research has shown that fat mobilisation is the primary mechanism by which this is accomplished. Higher plasma NEFA and BHBA concentrations, together with losses in BCS are typical as a result of increased milking frequency.33 The later was confirmed by observing reduced BCS, in cows milked 6x when compared to 3x.34 The opposite is also true since decreasing milking frequency improves energy balance, as demonstrated in cows milked 1x with reduced BCS loss, and reduced BW loss during early.29 The metabolic changes that result from the stimulation that happens as a result of additional milkings are complex. They depend on the coordination of nutrient and hormone peripheral signals, with local regulatory mechanisms that adjust rates of nutrients availability to match mammary epithelial cells synthetic capacity.35 Plasma growth hormone and insulin-like growth factor type I (IGF-I) concentrations, were elevated in cows milked six times daily; prolactin and oxytocin also increased, but insulin decreased.36 Post-treatment differences persisted only for insulin and IGF-I. Increased frequency of udder emptying increased milk production and was associated with elevated growth hormone, IGF-I, prolactin, and oxytocin. Similarly, increases in enzyme activity, lactose synthesis, and DNA in the alveolar tissue of the mammary gland have been observed when cows are milked more frequently.37 Meanwhile, the rise of milk production and changes in milk composition with more frequent milking intervals are regulated by local factors within the mammary gland, rather than other physiological mechanisms.7
This has been proven by a few experiments in which the treatment (e.g., 1x or 3x) was applied to two quarters on the same side of the udder, and the other contralateral half was milked 2x as the control. Since the treatments are applied to the same cow, both halves of the udder are under the same environmental and management factors except the milking frequency. Hence, any treatment difference must be solely due to intramammary factors. The intramammary effects of milking frequency on milk yield have ranged from -38% with 1x to +32% with more frequent milking regimens.38
The papers of the present meta-analysis were strictly confined to those that reported DMI, milk production, and milk composition. This selection was an attempt to identify better the effect of increasing milking frequency on milk production ruling out the interference of stage of lactation, feeding system, type and quality of the diets, and lactation number.
Even though milking thrice-daily was proposed since 1920, it is not widely implemented in dairy farms, probably because the variability in production responses, which range between 9 to 39%.39 Benefits of the use of meta-analysis is that multiple studies can be integrated, resolving contradictions among different research, and offer critical insights into the current state of knowledge.40,41 The value of the present meta-analysis is that the positive effect of 3x milking was confirmed for milk production and yields of milk protein and milk fat, without increasing DMI.
With thrice-milking higher milk production is expected to promote an increase in dry matter intake because of energy demands; however, cows milked 3x did not consume more feed.27 Only when milk frequency increased up to 6x, a rise on DMI was observed.43 This was confirmed in earlier research25 where Holstein first lactation cows during a full lactation (44 week) milked twice and three times a day. When older cows were switched from 2 to 3x they produced 17 % more milk over the entire lactation than cows on 2x daily. Dry matter and energy intakes were not affected by three times milking, but gain of body weight was reduced. Cows milked 3x during their first lactation produced 6% more milk than the 2x controls. Dry matter and energy intakes were not affected by 3x milking, but did affect first lactation cows with reduced weight gains over the lactation. No changes in DMI were also reported more recently for cows milked 2x vs 3x. In a large and prolonged experiment,27 Holstein cows were milked twice or thrice daily beginning at calving. Cows yielded approximately 25 and 30% more milk during first and second lactation, respectively, than control cows. Cows milked 3x daily had decreased milk fat percentage and tended to weigh less, suggesting more body tissue was catabolised for milk production, though DMI did not differ from that of cows milked 2x.
Therefore, the present meta-analysis confirms that increasing milking frequency did not affect DMI. Nonetheless, we cannot discard that the lack of effect is not related to the moderate heterogeneity observed for DMI in the present study (I2=59%). One additional explanation is that the metabolic changes that will lead to changes in feed intake depend in the milking frequency, but also on the duration of the new frequency.29 The lack of effect of 3x milking frequency on DMI could be explained if we recall that milk production increase to more frequent milking is mostly due to local regulation at the mammary gland.37,38,42 Indeed, milk yield depends on the number and activity of secretory cells, and increasing the milking frequency reduces the alveoli epithelial cell apoptosis43 and improves enzyme activity and DNA synthesis, making milk production more efficient without the requirement of additional nutrients.37,38,44 These effects are mediated by several galactopoietic hormones like growth hormone, insulin-like growth factor I, oxytocin, and prolactin which blood concentrations are increased in cows that are milked more frequently.37 Specifically, an increase in prolactin secretion and its receptor with 3x milking has been observed.45 Prolactin is essential for the regulation of milk synthesis at the local level as it stimulates lactose synthesis (the primary regulator of milk volume) and has a proliferative effect on mammary gland cells.46 Additionally, prolactin reduces the leakiness of the tight junctions of mammary gland epithelial cells.38 This leakiness increases mammary gland pressure and loss of epithelial cells function that reduce milk secretion.7
As milk fat and protein yields are variables calculated from milk production and milk components percentage, the positive effect of milking frequency on these variables in the present meta-analysis is mostly attributable to the increase in milk volume related to lactose synthesis. Mammary gland ability to extract nutrients is not different between cows milked 2x or 3x, and only an increase in glucose-1-phosphate has been reported when cows are milked thrice per day.47 Therefore, the increase in lactose synthesis could be related to the upregulation of the phosphoglucomutase enzyme that catalyses the synthesis of glucose-1-phosphate as part of the galactose production pathway.47,48
An increase of 2.23 kg per day in milk production without an increase in DMI is highly desirable, since it would result in approximately 468 kg additional milk over a 210-day lactation. Assuming milk prices at close to MX $6.11,49 this could result in an additional MX $2,859 to the producer. It is important however to balance this extra income with the necessary management changes that assure adequate feed bunk management, adding milking shift, and improved milking management to guarantee udder health.39 An economic analysis demonstrated that it is more feasible switching to 3x when cows in 2x milking produce more than 24.5 kg of milk per day.50
Factors such as body condition score, health, reproduction, and economic impact were not included in this meta-analysis, and the authors recommend their study in future research. It has been reported that cows on 1X experienced less negative energy balance than cows on 2x and 3x; however, without a negative effect on reproduction.29 Also, cows on 3x were prone to increased lameness (36%) when compared to 2x.51
Conclusions and implications
Increasing milking frequency from 2x to 3x has a positive effect on milk production and yields of milk fat and milk protein without increasing DMI. The application of 3x milking frequency must consider dairy cow management, labor availability, and milking parlour infrastructure particular to each dairy farm. While the economic results may not justify 3x milking for the entire herd, it certainly could be considered for pens of cows more likely to respond. Future research should consider the energy balance of the cows, animal health, breed and the economic viability when implemented 3x milking frequency in lactating dairy cows.